Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79825 |
| ensemblid | ENSG00000114654.8 |
| hgncid | 25692 |
| symbol | EFCC1 |
| name | EF-hand and coiled-coil domain containing 1 |
| refseq_nuc | NM_001377500.1 |
| refseq_prot | NP_001364429.1 |
| ensembl_nuc | ENST00000683648.1 |
| ensembl_prot | ENSP00000507795.1 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 129001304 |
| end | 129040742 |
| strand | + |
| ver | v1.2 |
| region | chr3:129001304-129040742 |
| region5000 | chr3:128996304-129045742 |
| regionname0 | EFCC1_chr3_129001304_129040742 |
| regionname5000 | EFCC1_chr3_128996304_129045742 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 599 | 136 | 50 | 25 | 55 | 1 | 5 | 41 | EFCC1_chr3_128996304_129045742 | EFCC1 | MEPVS others(594): Show |
chr3 | 128996304 | 129045742 |
| a0002 | 1/0 | 599 | 84 | 4 | 23 | 37 | 4 | 15 | 25 | EFCC1_chr3_128996304_129045742 | EFCC1 | MEPVS others(594): Show |
chr3 | 128996304 | 129045742 |
| a0003 | 0/0 | 599 | 79 | 18 | 18 | 23 | 5 | 15 | 16 | EFCC1_chr3_128996304_129045742 | EFCC1 | MEPVS others(594): Show |
chr3 | 128996304 | 129045742 |
| a0004 | 0/0 | 599 | 16 | 9 | 0 | 5 | 0 | 2 | 4 | EFCC1_chr3_128996304_129045742 | EFCC1 | MEPVS others(594): Show |
chr3 | 128996304 | 129045742 |
| a0005 | 0/0 | 599 | 14 | 0 | 0 | 13 | 0 | 1 | 10 | EFCC1_chr3_128996304_129045742 | EFCC1 | MEPVS others(594): Show |
chr3 | 128996304 | 129045742 |
| a0006 | 0/0 | 599 | 13 | 8 | 5 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | MEPVS others(594): Show |
chr3 | 128996304 | 129045742 |
| a0007 | 0/0 | 599 | 5 | 0 | 0 | 4 | 0 | 1 | 3 | EFCC1_chr3_128996304_129045742 | EFCC1 | MEPVS others(594): Show |
chr3 | 128996304 | 129045742 |
| a0008 | 0/0 | 599 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | EFCC1_chr3_128996304_129045742 | EFCC1 | MEPVS others(594): Show |
chr3 | 128996304 | 129045742 |
| a0009 | 0/0 | 599 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | MEPVS others(594): Show |
chr3 | 128996304 | 129045742 |
| a0010 | 0/0 | 339 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | MEPVS others(334): Show |
chr3 | 128996304 | 129045742 |
| a0011 | 0/0 | 599 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | MEPVS others(594): Show |
chr3 | 128996304 | 129045742 |
| a0012 | 0/0 | 599 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EFCC1_chr3_128996304_129045742 | EFCC1 | MEPVS others(594): Show |
chr3 | 128996304 | 129045742 |
| a0013 | 0/1 | 599 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | MEPVS others(594): Show |
chr3 | 128996304 | 129045742 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1797 | 135 | 50 | 25 | 54 | 1 | 5 | EFCC1_chr3_128996304_129045742 | EFCC1 | ATGGA others(1792): Show |
chr3 | 128996304 | 129045742 | ||
| a0001c0011 | 0/0 | 1797 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | ATGGA others(1792): Show |
chr3 | 128996304 | 129045742 | ||
| a0002c0002 | 1/0 | 1797 | 84 | 4 | 23 | 37 | 4 | 15 | EFCC1_chr3_128996304_129045742 | EFCC1 | ATGGA others(1792): Show |
chr3 | 128996304 | 129045742 | ||
| a0003c0003 | 0/0 | 1797 | 75 | 17 | 18 | 23 | 5 | 12 | EFCC1_chr3_128996304_129045742 | EFCC1 | ATGGA others(1792): Show |
chr3 | 128996304 | 129045742 | ||
| a0003c0008 | 0/0 | 1797 | 3 | 0 | 0 | 0 | 0 | 3 | EFCC1_chr3_128996304_129045742 | EFCC1 | ATGGA others(1792): Show |
chr3 | 128996304 | 129045742 | ||
| a0003c0016 | 0/0 | 1797 | 1 | 1 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | ATGGA others(1792): Show |
chr3 | 128996304 | 129045742 | ||
| a0004c0004 | 0/0 | 1797 | 16 | 9 | 0 | 5 | 0 | 2 | EFCC1_chr3_128996304_129045742 | EFCC1 | ATGGA others(1792): Show |
chr3 | 128996304 | 129045742 | ||
| a0005c0005 | 0/0 | 1797 | 14 | 0 | 0 | 13 | 0 | 1 | EFCC1_chr3_128996304_129045742 | EFCC1 | ATGGA others(1792): Show |
chr3 | 128996304 | 129045742 | ||
| a0006c0006 | 0/0 | 1797 | 13 | 8 | 5 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | ATGGA others(1792): Show |
chr3 | 128996304 | 129045742 | ||
| a0007c0007 | 0/0 | 1797 | 5 | 0 | 0 | 4 | 0 | 1 | EFCC1_chr3_128996304_129045742 | EFCC1 | ATGGA others(1792): Show |
chr3 | 128996304 | 129045742 | ||
| a0008c0009 | 0/0 | 1797 | 2 | 0 | 0 | 2 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | ATGGA others(1792): Show |
chr3 | 128996304 | 129045742 | ||
| a0009c0014 | 0/0 | 1797 | 1 | 0 | 1 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | ATGGA others(1792): Show |
chr3 | 128996304 | 129045742 | ||
| a0010c0010 | 0/0 | 1325 | 1 | 1 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | ATGGA others(1320): Show |
chr3 | 128996304 | 129045742 | ||
| a0011c0015 | 0/0 | 1797 | 1 | 0 | 0 | 0 | 0 | 1 | EFCC1_chr3_128996304_129045742 | EFCC1 | ATGGA others(1792): Show |
chr3 | 128996304 | 129045742 | ||
| a0012c0013 | 0/0 | 1797 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | ATGGA others(1792): Show |
chr3 | 128996304 | 129045742 | ||
| a0013c0012 | 0/1 | 1797 | 1 | 0 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | ATGGA others(1792): Show |
chr3 | 128996304 | 129045742 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3019 | 110 | 26 | 24 | 54 | 1 | 5 | EFCC1_chr3_128996304_129045742 | EFCC1 | AGACG others(3014): Show |
chr3 | 128996304 | 129045742 |
| a0001c0001t0002 | 0/0 | 3019 | 3 | 3 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | AGACG others(3014): Show |
chr3 | 128996304 | 129045742 |
| a0001c0001t0003 | 0/0 | 3019 | 5 | 5 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | AGACG others(3014): Show |
chr3 | 128996304 | 129045742 |
| a0001c0001t0004 | 0/0 | 3019 | 6 | 5 | 1 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | AGACG others(3014): Show |
chr3 | 128996304 | 129045742 |
| a0001c0001t0005 | 0/0 | 3019 | 4 | 4 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | AGACG others(3014): Show |
chr3 | 128996304 | 129045742 |
| a0001c0001t0006 | 0/0 | 3019 | 3 | 3 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | AGACG others(3014): Show |
chr3 | 128996304 | 129045742 |
| a0001c0001t0007 | 0/0 | 3019 | 2 | 2 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | AGACG others(3014): Show |
chr3 | 128996304 | 129045742 |
| a0001c0001t0010 | 0/0 | 3019 | 1 | 1 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | AGACG others(3014): Show |
chr3 | 128996304 | 129045742 |
| a0001c0001t0012 | 0/0 | 3019 | 1 | 1 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | AGACG others(3014): Show |
chr3 | 128996304 | 129045742 |
| a0001c0011t0001 | 0/0 | 3019 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | AGACG others(3014): Show |
chr3 | 128996304 | 129045742 |
| a0002c0002t0001 | 1/0 | 3019 | 81 | 3 | 23 | 36 | 4 | 14 | EFCC1_chr3_128996304_129045742 | EFCC1 | AGACG others(3014): Show |
chr3 | 128996304 | 129045742 |
| a0002c0002t0003 | 0/0 | 3019 | 1 | 1 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | AGACG others(3014): Show |
chr3 | 128996304 | 129045742 |
| a0002c0002t0011 | 0/0 | 3019 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | AGACG others(3014): Show |
chr3 | 128996304 | 129045742 |
| a0002c0002t0014 | 0/0 | 3019 | 1 | 0 | 0 | 0 | 0 | 1 | EFCC1_chr3_128996304_129045742 | EFCC1 | AGACG others(3014): Show |
chr3 | 128996304 | 129045742 |
| a0003c0003t0001 | 0/0 | 3019 | 63 | 10 | 13 | 23 | 5 | 12 | EFCC1_chr3_128996304_129045742 | EFCC1 | AGACG others(3014): Show |
chr3 | 128996304 | 129045742 |
| a0003c0003t0002 | 0/0 | 3019 | 7 | 6 | 1 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | AGACG others(3014): Show |
chr3 | 128996304 | 129045742 |
| a0003c0003t0008 | 0/0 | 3019 | 2 | 1 | 1 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | AGACG others(3014): Show |
chr3 | 128996304 | 129045742 |
| a0003c0003t0009 | 0/0 | 3019 | 2 | 0 | 2 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | AGACG others(3014): Show |
chr3 | 128996304 | 129045742 |
| a0003c0003t0013 | 0/0 | 3019 | 1 | 0 | 1 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | AGACG others(3014): Show |
chr3 | 128996304 | 129045742 |
| a0003c0008t0001 | 0/0 | 3019 | 3 | 0 | 0 | 0 | 0 | 3 | EFCC1_chr3_128996304_129045742 | EFCC1 | AGACG others(3014): Show |
chr3 | 128996304 | 129045742 |
| a0003c0016t0001 | 0/0 | 3019 | 1 | 1 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | AGACG others(3014): Show |
chr3 | 128996304 | 129045742 |
| a0004c0004t0001 | 0/0 | 3019 | 12 | 5 | 0 | 5 | 0 | 2 | EFCC1_chr3_128996304_129045742 | EFCC1 | AGACG others(3014): Show |
chr3 | 128996304 | 129045742 |
| a0004c0004t0003 | 0/0 | 3019 | 4 | 4 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | AGACG others(3014): Show |
chr3 | 128996304 | 129045742 |
| a0005c0005t0001 | 0/0 | 3019 | 14 | 0 | 0 | 13 | 0 | 1 | EFCC1_chr3_128996304_129045742 | EFCC1 | AGACG others(3014): Show |
chr3 | 128996304 | 129045742 |
| a0006c0006t0001 | 0/0 | 3019 | 13 | 8 | 5 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | AGACG others(3014): Show |
chr3 | 128996304 | 129045742 |
| a0007c0007t0001 | 0/0 | 3019 | 5 | 0 | 0 | 4 | 0 | 1 | EFCC1_chr3_128996304_129045742 | EFCC1 | AGACG others(3014): Show |
chr3 | 128996304 | 129045742 |
| a0008c0009t0001 | 0/0 | 3019 | 2 | 0 | 0 | 2 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | AGACG others(3014): Show |
chr3 | 128996304 | 129045742 |
| a0009c0014t0001 | 0/0 | 3019 | 1 | 0 | 1 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | AGACG others(3014): Show |
chr3 | 128996304 | 129045742 |
| a0010c0010t0001 | 0/0 | 2547 | 1 | 1 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | AGACG others(2542): Show |
chr3 | 128996304 | 129045742 |
| a0011c0015t0001 | 0/0 | 3019 | 1 | 0 | 0 | 0 | 0 | 1 | EFCC1_chr3_128996304_129045742 | EFCC1 | AGACG others(3014): Show |
chr3 | 128996304 | 129045742 |
| a0012c0013t0001 | 0/0 | 3019 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | AGACG others(3014): Show |
chr3 | 128996304 | 129045742 |
| a0013c0012t0001 | 0/1 | 3019 | 1 | 0 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | AGACG others(3014): Show |
chr3 | 128996304 | 129045742 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 9 | 0 | 1 | 8 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0010 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0012 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0003g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0004g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0004g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0004g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0004g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0004g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0005g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0006g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0006g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0006g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0007g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0007g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0010g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0001t0012g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0001c0011t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0002c0002t0001g0001 | 1/0 | 16 | 1 | 8 | 1 | 1 | 4 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0002c0002t0001g0005 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0002c0002t0001g0006 | 0/0 | 7 | 0 | 1 | 5 | 0 | 1 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0002c0002t0001g0014 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0002c0002t0001g0017 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0002c0002t0001g0018 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0002c0002t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0002c0002t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0002c0002t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0002c0002t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0002c0002t0001g0030 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0002c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0002c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0002c0002t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0002c0002t0011g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0002c0002t0014g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0003c0003t0001g0004 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0003c0003t0001g0007 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0003c0003t0001g0008 | 0/0 | 5 | 0 | 1 | 1 | 2 | 1 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0003c0003t0001g0009 | 0/0 | 6 | 1 | 3 | 0 | 0 | 2 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0003c0003t0001g0022 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0003c0003t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0003c0003t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0003c0003t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0003c0003t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0003c0003t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0003c0003t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0003c0003t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0003c0003t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0003c0003t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0003c0003t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0003c0003t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0003c0003t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0003c0003t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0003c0003t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0003c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0003c0003t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0003c0003t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0003c0003t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0003c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0003c0003t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0003c0003t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0003c0003t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0003c0003t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0003c0003t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0003c0003t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0003c0003t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0003c0003t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0003c0003t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0003c0003t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0003c0003t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0003c0003t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0003c0003t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0003c0003t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0003c0003t0002g0024 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0003c0003t0002g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0003c0003t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0003c0003t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0003c0003t0008g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0003c0003t0008g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0003c0003t0009g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0003c0003t0009g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0003c0003t0013g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0003c0008t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0003c0008t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0003c0008t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0003c0016t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0004c0004t0001g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0004c0004t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0004c0004t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0004c0004t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0004c0004t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0004c0004t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0004c0004t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0004c0004t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0004c0004t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0004c0004t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0004c0004t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0004c0004t0003g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0004c0004t0003g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0005c0005t0001g0005 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0005c0005t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0005c0005t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0005c0005t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0005c0005t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0005c0005t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0005c0005t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0005c0005t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0006c0006t0001g0002 | 0/0 | 10 | 6 | 4 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0006c0006t0001g0045 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0006c0006t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0007c0007t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0007c0007t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0007c0007t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0007c0007t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0008c0009t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0009c0014t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0010c0010t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0011c0015t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0012c0013t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| a0013c0012t0001g0182 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0055 | EUR | GBR | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG00099 | hp2 | a0003 | c0003 | t0001 | g0022 | EUR | GBR | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0014 | EUR | GBR | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG00140 | hp2 | a0003 | c0003 | t0001 | g0022 | EUR | GBR | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG00280 | hp1 | a0003 | c0003 | t0001 | g0143 | EUR | FIN | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG00280 | hp2 | a0002 | c0002 | t0001 | g0014 | EUR | FIN | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0001 | EUR | FIN | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG00323 | hp2 | a0003 | c0003 | t0001 | g0008 | EUR | FIN | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG00408 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | CHS | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG00408 | hp2 | a0007 | c0007 | t0001 | g0025 | EAS | CHS | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | CHS | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0059 | EAS | CHS | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG00558 | hp1 | a0005 | c0005 | t0001 | g0013 | EAS | CHS | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG00597 | hp1 | a0003 | c0003 | t0001 | g0007 | EAS | CHS | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | CHS | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | CHS | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG00639 | hp2 | a0003 | c0003 | t0002 | g0024 | AMR | PUR | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG00642 | hp1 | a0003 | c0003 | t0001 | g0036 | AMR | PUR | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | CHS | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG00673 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | CHS | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0014 | AMR | PUR | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG00735 | hp2 | a0006 | c0006 | t0001 | g0002 | AMR | PUR | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0030 | AMR | PUR | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG00738 | hp2 | a0006 | c0006 | t0001 | g0002 | AMR | PUR | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0027 | AMR | PUR | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG00741 | hp2 | a0003 | c0003 | t0001 | g0009 | AMR | PUR | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG01069 | hp1 | a0003 | c0003 | t0001 | g0197 | AMR | PUR | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG01070 | hp1 | a0003 | c0003 | t0001 | g0037 | AMR | PUR | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG01071 | hp1 | a0003 | c0003 | t0001 | g0037 | AMR | PUR | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG01074 | hp2 | a0002 | c0002 | t0001 | g0018 | AMR | PUR | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG01081 | hp2 | a0003 | c0003 | t0001 | g0144 | AMR | PUR | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG01109 | hp1 | a0003 | c0003 | t0001 | g0187 | AMR | PUR | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG01167 | hp1 | a0006 | c0006 | t0001 | g0002 | AMR | PUR | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG01167 | hp2 | a0003 | c0003 | t0009 | g0004 | AMR | PUR | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG01168 | hp1 | a0002 | c0002 | t0001 | g0088 | AMR | PUR | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0027 | AMR | PUR | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG01169 | hp1 | a0006 | c0006 | t0001 | g0002 | AMR | PUR | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG01169 | hp2 | a0002 | c0002 | t0001 | g0014 | AMR | PUR | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG01192 | hp1 | a0003 | c0003 | t0001 | g0036 | AMR | PUR | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG01243 | hp1 | a0006 | c0006 | t0001 | g0045 | AMR | PUR | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG01243 | hp2 | a0003 | c0003 | t0001 | g0141 | AMR | PUR | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG01258 | hp2 | a0003 | c0003 | t0009 | g0007 | AMR | CLM | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG01346 | hp2 | a0003 | c0003 | t0008 | g0174 | AMR | CLM | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG01358 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG01358 | hp2 | a0003 | c0003 | t0001 | g0009 | AMR | CLM | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG01361 | hp1 | a0003 | c0003 | t0001 | g0022 | AMR | CLM | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0079 | AMR | CLM | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG01433 | hp2 | a0003 | c0003 | t0001 | g0009 | AMR | CLM | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG01515 | hp1 | a0003 | c0003 | t0001 | g0008 | EUR | IBS | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0142 | EUR | IBS | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG01884 | hp1 | a0003 | c0003 | t0002 | g0043 | AFR | ACB | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG01884 | hp2 | a0003 | c0003 | t0008 | g0122 | AFR | ACB | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG01891 | hp1 | a0003 | c0003 | t0001 | g0193 | AFR | ACB | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG01928 | hp2 | a0002 | c0002 | t0001 | g0018 | AMR | PEL | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG01934 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG01934 | hp2 | a0002 | c0002 | t0001 | g0029 | AMR | PEL | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG01952 | hp1 | a0009 | c0014 | t0001 | g0011 | AMR | PEL | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG01978 | hp1 | a0003 | c0003 | t0013 | g0008 | AMR | PEL | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0069 | AMR | PEL | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0006 | AMR | PEL | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02015 | hp1 | a0003 | c0003 | t0001 | g0112 | EAS | KHV | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02055 | hp1 | a0004 | c0004 | t0003 | g0214 | AFR | ACB | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0205 | AFR | ACB | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02056 | hp2 | a0004 | c0004 | t0001 | g0220 | EAS | KHV | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02071 | hp1 | a0003 | c0003 | t0001 | g0007 | EAS | KHV | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02071 | hp2 | a0003 | c0003 | t0001 | g0008 | EAS | KHV | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02074 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | KHV | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02074 | hp2 | a0003 | c0003 | t0001 | g0124 | EAS | KHV | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0052 | EAS | KHV | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0058 | EAS | KHV | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02129 | hp1 | a0003 | c0003 | t0001 | g0107 | EAS | KHV | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02132 | hp2 | a0003 | c0003 | t0001 | g0007 | EAS | KHV | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02135 | hp1 | a0005 | c0005 | t0001 | g0005 | EAS | KHV | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0073 | EAS | KHV | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02145 | hp1 | a0001 | c0001 | t0006 | g0177 | AFR | ACB | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02145 | hp2 | a0002 | c0002 | t0001 | g0070 | AFR | ACB | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02148 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02165 | hp1 | a0002 | c0002 | t0001 | g0066 | EAS | CDX | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | CDX | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02257 | hp1 | a0006 | c0006 | t0001 | g0002 | AFR | ACB | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | ACB | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02258 | hp1 | a0004 | c0004 | t0003 | g0222 | AFR | ACB | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02258 | hp2 | a0001 | c0001 | t0005 | g0015 | AFR | ACB | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02273 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02273 | hp2 | a0002 | c0002 | t0001 | g0029 | AMR | PEL | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02293 | hp1 | a0002 | c0002 | t0001 | g0082 | AMR | PEL | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02300 | hp1 | a0003 | c0003 | t0001 | g0008 | AMR | PEL | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0074 | AMR | PEL | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02451 | hp2 | a0004 | c0004 | t0003 | g0215 | AFR | ACB | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02523 | hp2 | a0005 | c0005 | t0001 | g0005 | EAS | KHV | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02572 | hp1 | a0002 | c0002 | t0001 | g0071 | AFR | GWD | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02615 | hp1 | a0003 | c0003 | t0001 | g0041 | AFR | GWD | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0202 | AFR | GWD | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0137 | AFR | GWD | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02647 | hp1 | a0003 | c0003 | t0001 | g0155 | AFR | GWD | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02647 | hp2 | a0006 | c0006 | t0001 | g0216 | AFR | GWD | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0078 | SAS | PJL | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02683 | hp2 | a0004 | c0004 | t0001 | g0211 | SAS | PJL | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02717 | hp1 | a0006 | c0006 | t0001 | g0002 | AFR | GWD | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02717 | hp2 | a0010 | c0010 | t0001 | g0163 | AFR | GWD | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02723 | hp1 | a0001 | c0001 | t0007 | g0179 | AFR | GWD | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0173 | AFR | GWD | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02738 | hp1 | a0002 | c0002 | t0001 | g0081 | SAS | PJL | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02738 | hp2 | a0005 | c0005 | t0001 | g0005 | SAS | PJL | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02818 | hp1 | a0003 | c0003 | t0001 | g0041 | AFR | GWD | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02818 | hp2 | a0001 | c0001 | t0010 | g0203 | AFR | GWD | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02886 | hp1 | a0003 | c0003 | t0001 | g0171 | AFR | GWD | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02895 | hp1 | a0006 | c0006 | t0001 | g0002 | AFR | GWD | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | GWD | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0208 | AFR | GWD | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02896 | hp2 | a0003 | c0003 | t0002 | g0024 | AFR | GWD | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02897 | hp1 | a0003 | c0003 | t0002 | g0024 | AFR | GWD | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | GWD | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02922 | hp2 | a0004 | c0004 | t0001 | g0016 | AFR | ESN | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02965 | hp1 | a0003 | c0003 | t0001 | g0009 | AFR | ESN | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | ESN | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02970 | hp1 | a0001 | c0001 | t0005 | g0015 | AFR | ESN | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02970 | hp2 | a0004 | c0004 | t0001 | g0016 | AFR | ESN | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | ESN | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG03017 | hp1 | a0003 | c0003 | t0001 | g0154 | SAS | PJL | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG03017 | hp2 | a0003 | c0003 | t0001 | g0009 | SAS | PJL | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG03041 | hp2 | a0001 | c0001 | t0006 | g0176 | AFR | GWD | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | MSL | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG03139 | hp1 | a0003 | c0003 | t0001 | g0140 | AFR | ESN | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG03195 | hp1 | a0006 | c0006 | t0001 | g0002 | AFR | ESN | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG03195 | hp2 | a0001 | c0001 | t0006 | g0175 | AFR | ESN | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG03209 | hp1 | a0003 | c0003 | t0002 | g0043 | AFR | MSL | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG03209 | hp2 | a0004 | c0004 | t0001 | g0016 | AFR | MSL | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG03239 | hp2 | a0003 | c0003 | t0001 | g0009 | SAS | PJL | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG03453 | hp1 | a0002 | c0002 | t0003 | g0093 | AFR | MSL | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG03486 | hp1 | a0006 | c0006 | t0001 | g0002 | AFR | MSL | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0206 | AFR | MSL | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG03516 | hp1 | a0001 | c0001 | t0005 | g0015 | AFR | ESN | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG03579 | hp1 | a0003 | c0003 | t0002 | g0204 | AFR | MSL | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG03579 | hp2 | a0003 | c0003 | t0001 | g0172 | AFR | MSL | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0006 | SAS | PJL | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG03654 | hp2 | a0003 | c0003 | t0001 | g0188 | SAS | PJL | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG03669 | hp2 | a0003 | c0003 | t0001 | g0145 | SAS | PJL | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG03688 | hp1 | a0003 | c0003 | t0001 | g0189 | SAS | STU | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG03688 | hp2 | a0002 | c0002 | t0001 | g0054 | SAS | STU | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0017 | SAS | PJL | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG03704 | hp2 | a0003 | c0008 | t0001 | g0225 | SAS | PJL | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG03831 | hp1 | a0007 | c0007 | t0001 | g0053 | SAS | BEB | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | BEB | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG03834 | hp1 | a0003 | c0003 | t0001 | g0181 | SAS | BEB | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG03834 | hp2 | a0002 | c0002 | t0014 | g0067 | SAS | BEB | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG03927 | hp1 | a0003 | c0003 | t0001 | g0196 | SAS | BEB | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG03927 | hp2 | a0011 | c0015 | t0001 | g0218 | SAS | BEB | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG03942 | hp1 | a0003 | c0008 | t0001 | g0224 | SAS | BEB | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0072 | SAS | BEB | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG04115 | hp1 | a0003 | c0003 | t0001 | g0008 | SAS | STU | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG04115 | hp2 | a0003 | c0003 | t0001 | g0007 | SAS | STU | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG04184 | hp1 | a0003 | c0003 | t0001 | g0165 | SAS | BEB | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG04184 | hp2 | a0002 | c0002 | t0001 | g0080 | SAS | BEB | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | STU | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG04199 | hp2 | a0003 | c0003 | t0001 | g0161 | SAS | STU | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | STU | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG04204 | hp2 | a0003 | c0008 | t0001 | g0223 | SAS | STU | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0005 | SAS | STU | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG04228 | hp2 | a0004 | c0004 | t0001 | g0213 | SAS | STU | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | YRI | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0044 | AFR | YRI | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0086 | EAS | CHB | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | CHB | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | CHB | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0089 | EAS | CHB | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | YRI | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | YRI | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0091 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA18944 | hp2 | a0005 | c0005 | t0001 | g0061 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA18945 | hp1 | a0005 | c0005 | t0001 | g0013 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA18945 | hp2 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA18946 | hp1 | a0002 | c0002 | t0001 | g0087 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA18949 | hp1 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA18950 | hp1 | a0004 | c0004 | t0001 | g0217 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA18951 | hp2 | a0002 | c0002 | t0001 | g0051 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA18952 | hp1 | a0002 | c0002 | t0001 | g0092 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA18952 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA18953 | hp2 | a0003 | c0003 | t0001 | g0149 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA18954 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA18957 | hp1 | a0003 | c0003 | t0001 | g0156 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA18957 | hp2 | a0005 | c0005 | t0001 | g0013 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA18959 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA18959 | hp2 | a0001 | c0011 | t0001 | g0032 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA18963 | hp1 | a0002 | c0002 | t0001 | g0083 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA18965 | hp1 | a0002 | c0002 | t0001 | g0077 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA18965 | hp2 | a0008 | c0009 | t0001 | g0033 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA18973 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA18974 | hp1 | a0002 | c0002 | t0001 | g0057 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA18975 | hp2 | a0002 | c0002 | t0001 | g0049 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA18980 | hp1 | a0007 | c0007 | t0001 | g0085 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA18982 | hp1 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA18983 | hp1 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA18983 | hp2 | a0005 | c0005 | t0001 | g0064 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA18984 | hp1 | a0002 | c0002 | t0001 | g0075 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA18984 | hp2 | a0003 | c0003 | t0001 | g0123 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA18988 | hp1 | a0002 | c0002 | t0011 | g0076 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA18991 | hp1 | a0002 | c0002 | t0001 | g0090 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA18991 | hp2 | a0005 | c0005 | t0001 | g0050 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA18992 | hp1 | a0003 | c0003 | t0001 | g0166 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA18992 | hp2 | a0005 | c0005 | t0001 | g0005 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA18995 | hp2 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA19002 | hp2 | a0005 | c0005 | t0001 | g0068 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA19003 | hp2 | a0002 | c0002 | t0001 | g0084 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA19005 | hp1 | a0012 | c0013 | t0001 | g0108 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0063 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA19007 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA19009 | hp1 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA19009 | hp2 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA19010 | hp1 | a0003 | c0003 | t0001 | g0125 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA19011 | hp1 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA19030 | hp1 | a0003 | c0003 | t0002 | g0201 | AFR | LWK | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA19030 | hp2 | a0004 | c0004 | t0003 | g0221 | AFR | LWK | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA19043 | hp1 | a0003 | c0003 | t0001 | g0136 | AFR | LWK | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA19043 | hp2 | a0001 | c0001 | t0012 | g0167 | AFR | LWK | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA19056 | hp1 | a0005 | c0005 | t0001 | g0056 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA19056 | hp2 | a0003 | c0003 | t0001 | g0159 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA19057 | hp1 | a0003 | c0003 | t0001 | g0153 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA19057 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA19058 | hp1 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA19060 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA19063 | hp1 | a0004 | c0004 | t0001 | g0219 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA19065 | hp2 | a0005 | c0005 | t0001 | g0013 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA19066 | hp2 | a0004 | c0004 | t0001 | g0209 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA19068 | hp1 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA19068 | hp2 | a0005 | c0005 | t0001 | g0060 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA19077 | hp1 | a0007 | c0007 | t0001 | g0065 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA19081 | hp1 | a0003 | c0003 | t0001 | g0007 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA19082 | hp1 | a0002 | c0002 | t0001 | g0048 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA19082 | hp2 | a0002 | c0002 | t0001 | g0062 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA19084 | hp1 | a0007 | c0007 | t0001 | g0025 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA19084 | hp2 | a0008 | c0009 | t0001 | g0033 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA19087 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA19091 | hp1 | a0004 | c0004 | t0001 | g0212 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0199 | AFR | YRI | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0200 | AFR | YRI | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA20129 | hp1 | a0001 | c0001 | t0005 | g0015 | AFR | ASW | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA20129 | hp2 | a0004 | c0004 | t0001 | g0210 | AFR | ASW | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0030 | SAS | GIH | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0005 | SAS | GIH | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG01123 | hp2 | a0001 | c0001 | t0004 | g0207 | AMR | CLM | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02109 | hp1 | a0003 | c0003 | t0001 | g0169 | AFR | ACB | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02486 | hp1 | a0006 | c0006 | t0001 | g0002 | AFR | ACB | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0044 | AFR | ACB | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG02559 | hp2 | a0001 | c0001 | t0007 | g0178 | AFR | ACB | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG03471 | hp1 | a0006 | c0006 | t0001 | g0045 | AFR | MSL | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | MSL | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG06807 | hp1 | a0004 | c0004 | t0001 | g0016 | AFR | USA | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| HG06807 | hp2 | a0003 | c0016 | t0001 | g0170 | AFR | USA | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | USA | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | USA | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| homoSapiens | chm13v2 | a0013 | c0012 | t0001 | g0182 | REF | REF | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0001 | REF | REF | EFCC1_chr3_128996304_129045742 | EFCC1 | chr3 | 128996304 | 129045742 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:129001644 | A | G | 9 | a0001 a0003 a0004 others(6): Show |
250 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(247): Show |
missense_variant | MODERATE | c.16A>G | p.Thr6Ala | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 1/8 | 341/3019 | 16/1800 | 6/599 | chr3 | 129001644 | |||
| chr3:129002068 | C | T | 1 | a0011 | 1 | HG03927.hp2 | missense_variant | MODERATE | c.440C>T | p.Ala147Val | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 1/8 | 765/3019 | 440/1800 | 147/599 | chr3 | 129002068 | |||
| chr3:129003842 | G | A | 3 | a0004 a0006 a0011 |
30 | HG00735.hp2 HG00738.hp2 HG01167.hp1 others(27): Show |
missense_variant | MODERATE | c.745G>A | p.Gly249Arg | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/8 | 1070/3019 | 745/1800 | 249/599 | chr3 | 129003842 | |||
| chr3:129003863 | G | A | 1 | a0008 | 2 | NA18965.hp2 NA19084.hp2 |
missense_variant | MODERATE | c.766G>A | p.Glu256Lys | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/8 | 1091/3019 | 766/1800 | 256/599 | chr3 | 129003863 | |||
| chr3:129003923 | C | A | 1 | a0005 | 14 | HG00558.hp1 HG02135.hp1 HG02523.hp2 others(11): Show |
missense_variant | MODERATE | c.826C>A | p.Arg276Ser | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/8 | 1151/3019 | 826/1800 | 276/599 | chr3 | 129003923 | |||
| chr3:129004074 | A | G | 1 | a0009 | 1 | HG01952.hp1 | missense_variant | MODERATE | c.977A>G | p.Tyr326Cys | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/8 | 1302/3019 | 977/1800 | 326/599 | chr3 | 129004074 | |||
| chr3:129026309 | CTGTCCCT others(8739): Show |
C | 1 | a0010 | 1 | HG02717.hp2 | exon_loss_variant | HIGH | c.981-4393_1452+726d others(2): Show |
EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 3/8 | chr3 | 129026309 | |||||||
| chr3:129030807 | C | T | 1 | a0001 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.1085C>T | p.Pro362Leu | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 3/8 | 1410/3019 | 1085/1800 | 362/599 | chr3 | 129030807 | |||
| chr3:129032827 | G | A | 1 | a0003 | 2 | HG01167.hp2 HG01258.hp2 |
missense_variant | MODERATE | c.1147G>A | p.Glu383Lys | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 4/8 | 1472/3019 | 1147/1800 | 383/599 | chr3 | 129032827 | |||
| chr3:129034181 | C | T | 1 | a0005 | 2 | HG00558.hp1 HG02523.hp2 |
missense_variant | MODERATE | c.1304C>T | p.Ala435Val | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 5/8 | 1629/3019 | 1304/1800 | 435/599 | chr3 | 129034181 | |||
| chr3:129034297 | G | A | 1 | a0003 | 1 | HG02647.hp1 | missense_variant | MODERATE | c.1420G>A | p.Gly474Ser | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 5/8 | 1745/3019 | 1420/1800 | 474/599 | chr3 | 129034297 | |||
| chr3:129037110 | G | A | 3 | a0003 a0006 a0007 |
97 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(94): Show |
missense_variant | MODERATE | c.1586G>A | p.Arg529Gln | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 6/8 | 1911/3019 | 1586/1800 | 529/599 | chr3 | 129037110 | |||
| chr3:129038855 | A | G | 1 | a0012 | 1 | NA19005.hp1 | missense_variant | MODERATE | c.1618A>G | p.Lys540Glu | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 7/8 | 1943/3019 | 1618/1800 | 540/599 | chr3 | 129038855 | |||
| chr3:129040742 | A | G | 1 | a0001 | 1 | HG02818.hp2 | splice_region_variant | LOW | c.*894A>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 8/8 | chr3 | 129040742 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:129002030 | C | T | 1 | a0003c0016 | 1 | HG06807.hp2 | synonymous_variant | LOW | c.402C>T | p.Arg134Arg | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 1/8 | 727/3019 | 402/1800 | 134/599 | chr3 | 129002030 | |||
| chr3:129002294 | G | A | 4 | a0003c0008 a0004c0004 a0006c0006 others(1): Show |
33 | HG00735.hp2 HG00738.hp2 HG01167.hp1 others(30): Show |
synonymous_variant | LOW | c.666G>A | p.Gln222Gln | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 1/8 | 991/3019 | 666/1800 | 222/599 | chr3 | 129002294 | |||
| chr3:129030730 | G | A | 1 | a0001c0001 | 4 | HG02258.hp2 HG02970.hp1 HG03516.hp1 others(1): Show |
synonymous_variant | LOW | c.1008G>A | p.Pro336Pro | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 3/8 | 1333/3019 | 1008/1800 | 336/599 | chr3 | 129030730 | |||
| chr3:129037057 | G | C | 1 | a0001c0011 | 1 | NA18959.hp2 | synonymous_variant | LOW | c.1533G>C | p.Leu511Leu | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 6/8 | 1858/3019 | 1533/1800 | 511/599 | chr3 | 129037057 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:129001380 | C | A | 1 | a0001c0001t0007 | 2 | HG02559.hp2 HG02723.hp1 |
5_prime_UTR_variant | MODIFIER | c.-249C>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 1/8 | 249 | chr3 | 129001380 | ||||||
| chr3:129001481 | G | A | 1 | a0001c0001t0004 | 6 | HG01123.hp2 HG02055.hp2 HG02486.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-148G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 1/8 | 148 | chr3 | 129001481 | ||||||
| chr3:129001611 | G | A | 3 | a0001c0001t0002 a0001c0001t0010 a0003c0003t0002 |
11 | HG00639.hp2 HG01884.hp1 HG02622.hp2 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-18G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 1/8 | 18 | chr3 | 129001611 | ||||||
| chr3:129001618 | G | A | 1 | a0002c0002t0011 | 1 | NA18988.hp1 | 5_prime_UTR_variant | MODIFIER | c.-11G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 1/8 | 11 | chr3 | 129001618 | ||||||
| chr3:129040145 | C | T | 1 | a0002c0002t0014 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*297C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 8/8 | 297 | chr3 | 129040145 | ||||||
| chr3:129040170 | A | G | 1 | a0003c0003t0009 | 2 | HG01167.hp2 HG01258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*322A>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 8/8 | 322 | chr3 | 129040170 | ||||||
| chr3:129040385 | T | C | 1 | a0001c0001t0005 | 4 | HG02258.hp2 HG02970.hp1 HG03516.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*537T>C | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 8/8 | 537 | chr3 | 129040385 | ||||||
| chr3:129040435 | G | A | 1 | a0001c0001t0006 | 3 | HG02145.hp1 HG03041.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*587G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 8/8 | 587 | chr3 | 129040435 | ||||||
| chr3:129040439 | T | C | 4 | a0001c0001t0003 a0001c0001t0006 a0002c0002t0003 others(1): Show |
13 | HG02055.hp1 HG02145.hp1 HG02258.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*591T>C | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 8/8 | 591 | chr3 | 129040439 | ||||||
| chr3:129040448 | A | G | 1 | a0003c0003t0013 | 1 | HG01978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*600A>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 8/8 | 600 | chr3 | 129040448 | ||||||
| chr3:129040615 | G | A | 1 | a0003c0003t0008 | 2 | HG01346.hp2 HG01884.hp2 |
3_prime_UTR_variant | MODIFIER | c.*767G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 8/8 | 767 | chr3 | 129040615 | ||||||
| chr3:129040634 | G | A | 1 | a0001c0001t0012 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*786G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 8/8 | 786 | chr3 | 129040634 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:129002343 | G | C | 2 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.696+19G>C | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 1/7 | chr3 | 129002343 | |||||||
| chr3:129002391 | C | T | 20 | a0003c0008t0001g0223 a0003c0008t0001g0224 a0003c0008t0001g0225 others(17): Show |
33 | HG00735.hp2 HG00738.hp2 HG01167.hp1 others(30): Show |
intron_variant | MODIFIER | c.696+67C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 1/7 | chr3 | 129002391 | |||||||
| chr3:129002467 | A | C | 170 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(167): Show |
250 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.696+143A>C | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 1/7 | chr3 | 129002467 | |||||||
| chr3:129002563 | A | G | 35 | a0001c0001t0001g0198 a0001c0001t0002g0199 a0001c0001t0002g0200 others(32): Show |
52 | HG00639.hp2 HG00735.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.696+239A>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 1/7 | chr3 | 129002563 | |||||||
| chr3:129003218 | G | C | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | NA19012.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.697-576G>C | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 1/7 | chr3 | 129003218 | |||||||
| chr3:129003239 | T | G | 170 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(167): Show |
250 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.697-555T>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 1/7 | chr3 | 129003239 | |||||||
| chr3:129003272 | G | A | 20 | a0003c0008t0001g0223 a0003c0008t0001g0224 a0003c0008t0001g0225 others(17): Show |
33 | HG00735.hp2 HG00738.hp2 HG01167.hp1 others(30): Show |
intron_variant | MODIFIER | c.697-522G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 1/7 | chr3 | 129003272 | |||||||
| chr3:129003469 | T | C | 170 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(167): Show |
250 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.697-325T>C | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 1/7 | chr3 | 129003469 | |||||||
| chr3:129003510 | G | C | 1 | a0002c0002t0001g0048 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.697-284G>C | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 1/7 | chr3 | 129003510 | |||||||
| chr3:129003514 | C | A | 1 | a0001c0001t0001g0096 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.697-280C>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 1/7 | chr3 | 129003514 | |||||||
| chr3:129004115 | A | G | 36 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0023 others(33): Show |
56 | HG00323.hp2 HG00423.hp2 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.980+38A>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129004115 | |||||||
| chr3:129004143 | G | A | 1 | a0002c0002t0001g0049 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.980+66G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129004143 | |||||||
| chr3:129004164 | C | T | 1 | a0003c0003t0001g0196 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.980+87C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129004164 | |||||||
| chr3:129004212 | C | T | 13 | a0001c0001t0002g0199 a0001c0001t0002g0200 a0001c0001t0002g0202 others(10): Show |
17 | HG00639.hp2 HG01123.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.980+135C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129004212 | |||||||
| chr3:129004372 | C | A | 73 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0023 others(70): Show |
113 | HG00323.hp2 HG00423.hp2 HG00639.hp2 others(110): Show |
intron_variant | MODIFIER | c.980+295C>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129004372 | |||||||
| chr3:129004416 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.980+339C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129004416 | |||||||
| chr3:129004433 | A | G | 1 | a0001c0001t0001g0168 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.980+356A>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129004433 | |||||||
| chr3:129004522 | C | T | 1 | a0002c0002t0003g0093 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.980+445C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129004522 | |||||||
| chr3:129004686 | G | A | 1 | a0005c0005t0001g0050 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.980+609G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129004686 | |||||||
| chr3:129004718 | T | C | 10 | a0001c0001t0003g0173 a0001c0001t0006g0175 a0001c0001t0006g0176 others(7): Show |
11 | HG01346.hp2 HG02109.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.980+641T>C | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129004718 | |||||||
| chr3:129005132 | G | A | 2 | a0002c0002t0001g0051 a0002c0002t0001g0052 |
2 | HG02083.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.980+1055G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129005132 | |||||||
| chr3:129005201 | C | A | 48 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0019 others(45): Show |
68 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.980+1124C>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129005201 | |||||||
| chr3:129005220 | G | A | 3 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0005g0015 |
6 | HG02258.hp2 HG02622.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.980+1143G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129005220 | |||||||
| chr3:129005223 | G | A | 8 | a0001c0001t0002g0199 a0001c0001t0002g0200 a0001c0001t0002g0202 others(5): Show |
11 | HG00639.hp2 HG01884.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.980+1146G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129005223 | |||||||
| chr3:129005232 | A | T | 8 | a0001c0001t0001g0012 a0001c0001t0001g0023 a0001c0001t0001g0042 others(5): Show |
15 | HG01891.hp1 HG02109.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.980+1155A>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129005232 | |||||||
| chr3:129005353 | C | T | 25 | a0001c0001t0001g0011 a0001c0001t0001g0180 a0001c0001t0001g0183 others(22): Show |
38 | HG00323.hp2 HG00423.hp2 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.980+1276C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129005353 | |||||||
| chr3:129005474 | T | A | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.980+1397T>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129005474 | |||||||
| chr3:129005965 | C | A | 25 | a0002c0002t0001g0005 a0002c0002t0001g0051 a0002c0002t0001g0052 others(22): Show |
35 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.980+1888C>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129005965 | |||||||
| chr3:129005983 | T | G | 1 | a0001c0001t0001g0135 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.980+1906T>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129005983 | |||||||
| chr3:129006033 | A | G | 3 | a0001c0001t0001g0168 a0001c0001t0007g0178 a0001c0001t0007g0179 |
3 | HG02559.hp2 HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.980+1956A>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129006033 | |||||||
| chr3:129006139 | A | G | 2 | a0001c0001t0007g0178 a0001c0001t0007g0179 |
2 | HG02559.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.980+2062A>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129006139 | |||||||
| chr3:129006247 | C | T | 1 | a0005c0005t0001g0068 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.980+2170C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129006247 | |||||||
| chr3:129006268 | G | A | 28 | a0001c0001t0001g0195 a0001c0001t0001g0198 a0001c0001t0002g0199 others(25): Show |
44 | HG00639.hp2 HG00642.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.980+2191G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129006268 | |||||||
| chr3:129006379 | C | T | 1 | a0001c0001t0012g0167 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.980+2302C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129006379 | |||||||
| chr3:129006534 | T | C | 1 | a0002c0002t0001g0069 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.980+2457T>C | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129006534 | |||||||
| chr3:129006723 | A | G | 78 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0019 others(75): Show |
114 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.980+2646A>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129006723 | |||||||
| chr3:129006747 | G | C | 1 | a0002c0002t0001g0070 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.980+2670G>C | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129006747 | |||||||
| chr3:129006787 | C | T | 2 | a0004c0004t0003g0221 a0004c0004t0003g0222 |
2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.980+2710C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129006787 | |||||||
| chr3:129006894 | AAAG | A | 8 | a0001c0001t0002g0199 a0001c0001t0002g0200 a0001c0001t0002g0202 others(5): Show |
11 | HG00639.hp2 HG01884.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.980+2821_980+2823d others(5): Show |
EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 129006894 | ||||||
| chr3:129007187 | A | G | 29 | a0001c0001t0001g0195 a0001c0001t0001g0198 a0001c0001t0002g0199 others(26): Show |
45 | HG00639.hp2 HG00642.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.980+3110A>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129007187 | |||||||
| chr3:129007302 | G | A | 2 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
2 | HG00423.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.980+3225G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129007302 | |||||||
| chr3:129007423 | T | C | 170 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(167): Show |
250 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.980+3346T>C | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129007423 | |||||||
| chr3:129007582 | G | A | 1 | a0001c0001t0001g0102 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.980+3505G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129007582 | |||||||
| chr3:129007593 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0194 |
4 | HG02109.hp2 HG02572.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.980+3516C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129007593 | |||||||
| chr3:129007626 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.980+3549G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129007626 | |||||||
| chr3:129007709 | G | A | 2 | a0002c0002t0001g0054 a0007c0007t0001g0053 |
2 | HG03688.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.980+3632G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129007709 | |||||||
| chr3:129007848 | T | C | 18 | a0001c0001t0007g0179 a0004c0004t0001g0016 a0004c0004t0001g0209 others(15): Show |
31 | HG00735.hp2 HG00738.hp2 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.980+3771T>C | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129007848 | |||||||
| chr3:129007931 | T | C | 5 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 others(2): Show |
5 | HG01952.hp2 HG01975.hp1 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.980+3854T>C | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129007931 | |||||||
| chr3:129008080 | C | A | 2 | a0001c0001t0001g0103 a0001c0001t0001g0104 |
2 | HG01952.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.980+4003C>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129008080 | |||||||
| chr3:129008100 | C | T | 1 | a0002c0002t0014g0067 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.980+4023C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129008100 | |||||||
| chr3:129008152 | C | G | 1 | a0002c0002t0001g0092 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.980+4075C>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129008152 | |||||||
| chr3:129008263 | C | T | 17 | a0004c0004t0001g0016 a0004c0004t0001g0209 a0004c0004t0001g0210 others(14): Show |
30 | HG00735.hp2 HG00738.hp2 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.980+4186C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129008263 | |||||||
| chr3:129008292 | T | A | 4 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(1): Show |
4 | NA18982.hp2 NA19005.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.980+4215T>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129008292 | |||||||
| chr3:129008380 | C | G | 25 | a0001c0001t0001g0011 a0001c0001t0001g0180 a0001c0001t0001g0183 others(22): Show |
38 | HG00323.hp2 HG00423.hp2 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.980+4303C>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129008380 | |||||||
| chr3:129008473 | T | C | 76 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0023 others(73): Show |
116 | HG00323.hp2 HG00423.hp2 HG00639.hp2 others(113): Show |
intron_variant | MODIFIER | c.980+4396T>C | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129008473 | |||||||
| chr3:129008602 | G | A | 2 | a0002c0002t0001g0071 a0002c0002t0003g0093 |
2 | HG02572.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.980+4525G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129008602 | |||||||
| chr3:129008628 | TG | T | 6 | a0001c0001t0001g0096 a0001c0001t0001g0138 a0001c0001t0003g0021 others(3): Show |
8 | HG00639.hp1 HG01981.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.980+4553delG | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 129008628 | ||||||
| chr3:129008835 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.980+4758C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129008835 | |||||||
| chr3:129009007 | G | A | 1 | a0002c0002t0001g0072 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.980+4930G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129009007 | |||||||
| chr3:129009091 | A | G | 3 | a0002c0002t0001g0089 a0002c0002t0001g0090 a0002c0002t0001g0091 |
3 | NA18747.hp2 NA18941.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.980+5014A>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129009091 | |||||||
| chr3:129009108 | C | T | 1 | a0003c0003t0001g0166 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.980+5031C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129009108 | |||||||
| chr3:129009210 | G | A | 2 | a0004c0004t0003g0221 a0004c0004t0003g0222 |
2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.980+5133G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129009210 | |||||||
| chr3:129009324 | G | A | 5 | a0001c0001t0001g0195 a0001c0001t0001g0198 a0002c0002t0001g0026 others(2): Show |
6 | HG00408.hp1 HG00642.hp2 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.980+5247G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129009324 | |||||||
| chr3:129009368 | T | C | 17 | a0001c0001t0001g0012 a0001c0001t0001g0023 a0001c0001t0001g0042 others(14): Show |
25 | HG01346.hp2 HG02055.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.980+5291T>C | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129009368 | |||||||
| chr3:129009559 | A | G | 2 | a0002c0002t0003g0093 a0004c0004t0001g0220 |
2 | HG02056.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.980+5482A>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129009559 | |||||||
| chr3:129009659 | C | T | 2 | a0002c0002t0001g0014 a0002c0002t0001g0088 |
5 | HG00140.hp1 HG00280.hp2 HG00735.hp1 others(2): Show |
intron_variant | MODIFIER | c.980+5582C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129009659 | |||||||
| chr3:129009679 | A | C | 4 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0168 others(1): Show |
4 | HG02280.hp2 HG02630.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.980+5602A>C | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129009679 | |||||||
| chr3:129009714 | G | A | 4 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0168 others(1): Show |
4 | HG02280.hp2 HG02630.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.980+5637G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129009714 | |||||||
| chr3:129009780 | G | A | 1 | a0002c0002t0003g0093 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.980+5703G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129009780 | |||||||
| chr3:129009839 | C | T | 2 | a0001c0001t0001g0168 a0002c0002t0003g0093 |
2 | HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.980+5762C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129009839 | |||||||
| chr3:129009867 | G | A | 2 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.980+5790G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129009867 | |||||||
| chr3:129010116 | G | A | 4 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0168 others(1): Show |
4 | HG02280.hp2 HG02630.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.980+6039G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129010116 | |||||||
| chr3:129010259 | A | G | 4 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0168 others(1): Show |
4 | HG02280.hp2 HG02630.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.980+6182A>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129010259 | |||||||
| chr3:129010267 | C | T | 1 | a0002c0002t0001g0066 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.980+6190C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129010267 | |||||||
| chr3:129010346 | G | T | 1 | a0003c0008t0001g0225 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.980+6269G>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129010346 | |||||||
| chr3:129010440 | A | T | 1 | a0007c0007t0001g0065 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.980+6363A>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129010440 | |||||||
| chr3:129010495 | C | T | 1 | a0002c0002t0003g0093 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.980+6418C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129010495 | |||||||
| chr3:129010511 | G | T | 1 | a0003c0003t0002g0204 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.980+6434G>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129010511 | |||||||
| chr3:129010538 | G | A | 1 | a0001c0001t0002g0199 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.980+6461G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129010538 | |||||||
| chr3:129010581 | A | C | 1 | a0005c0005t0001g0064 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.980+6504A>C | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129010581 | |||||||
| chr3:129010656 | C | G | 4 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0168 others(1): Show |
4 | HG02280.hp2 HG02630.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.980+6579C>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129010656 | |||||||
| chr3:129010684 | A | G | 58 | a0001c0001t0001g0023 a0001c0001t0001g0042 a0001c0001t0001g0046 others(55): Show |
82 | HG00639.hp2 HG00642.hp2 HG00735.hp2 others(79): Show |
intron_variant | MODIFIER | c.980+6607A>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129010684 | |||||||
| chr3:129010723 | C | T | 1 | a0001c0001t0007g0178 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.980+6646C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129010723 | |||||||
| chr3:129010740 | C | T | 4 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0168 others(1): Show |
4 | HG02280.hp2 HG02630.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.980+6663C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129010740 | |||||||
| chr3:129010774 | T | A | 3 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0005g0015 |
6 | HG02258.hp2 HG02622.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.980+6697T>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129010774 | |||||||
| chr3:129010781 | G | A | 4 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0168 others(1): Show |
4 | HG02280.hp2 HG02630.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.980+6704G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129010781 | |||||||
| chr3:129011025 | C | G | 4 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0168 others(1): Show |
4 | HG02280.hp2 HG02630.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.980+6948C>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129011025 | |||||||
| chr3:129011068 | A | G | 1 | a0007c0007t0001g0065 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.980+6991A>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129011068 | |||||||
| chr3:129011069 | G | A | 1 | a0007c0007t0001g0065 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.980+6992G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129011069 | |||||||
| chr3:129011150 | T | G | 2 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.980+7073T>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129011150 | |||||||
| chr3:129011186 | A | C | 6 | a0001c0001t0002g0202 a0001c0001t0010g0203 a0003c0003t0002g0024 others(3): Show |
9 | HG00639.hp2 HG01884.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.980+7109A>C | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129011186 | |||||||
| chr3:129011195 | T | G | 1 | a0001c0001t0001g0195 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.980+7118T>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129011195 | |||||||
| chr3:129011263 | G | A | 1 | a0003c0003t0001g0169 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.980+7186G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129011263 | |||||||
| chr3:129011316 | C | T | 2 | a0002c0002t0001g0062 a0002c0002t0001g0063 |
2 | NA19005.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.980+7239C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129011316 | |||||||
| chr3:129011463 | A | G | 4 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0168 others(1): Show |
4 | HG02280.hp2 HG02630.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.980+7386A>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129011463 | |||||||
| chr3:129011503 | A | G | 4 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0168 others(1): Show |
4 | HG02280.hp2 HG02630.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.980+7426A>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129011503 | |||||||
| chr3:129011545 | C | T | 4 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0168 others(1): Show |
4 | HG02280.hp2 HG02630.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.980+7468C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129011545 | |||||||
| chr3:129011550 | CA | C | 5 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0004g0208 others(2): Show |
8 | HG02258.hp2 HG02622.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.980+7489delA | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 129011550 | ||||||
| chr3:129011561 | A | C | 1 | a0007c0007t0001g0065 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.980+7484A>C | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129011561 | |||||||
| chr3:129011573 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.980+7496A>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129011573 | |||||||
| chr3:129011592 | G | A | 1 | a0002c0002t0001g0073 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.980+7515G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129011592 | |||||||
| chr3:129011611 | C | G | 32 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0134 others(29): Show |
49 | HG00639.hp2 HG00735.hp2 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.980+7534C>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129011611 | |||||||
| chr3:129011643 | C | T | 2 | a0003c0003t0001g0189 a0003c0003t0001g0196 |
2 | HG03688.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.980+7566C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129011643 | |||||||
| chr3:129011690 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.980+7613C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129011690 | |||||||
| chr3:129011744 | G | A | 2 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.980+7667G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129011744 | |||||||
| chr3:129012109 | C | T | 1 | a0001c0001t0001g0132 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.980+8032C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129012109 | |||||||
| chr3:129012135 | T | C | 1 | a0005c0005t0001g0064 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.980+8058T>C | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129012135 | |||||||
| chr3:129012163 | T | C | 4 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0168 others(1): Show |
4 | HG02280.hp2 HG02630.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.980+8086T>C | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129012163 | |||||||
| chr3:129012425 | G | A | 4 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0168 others(1): Show |
4 | HG02280.hp2 HG02630.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.980+8348G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129012425 | |||||||
| chr3:129012474 | A | G | 4 | a0001c0001t0006g0175 a0001c0001t0006g0176 a0001c0001t0006g0177 others(1): Show |
5 | HG02145.hp1 HG02615.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.980+8397A>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129012474 | |||||||
| chr3:129012582 | C | G | 2 | a0002c0002t0001g0030 a0002c0002t0001g0070 |
3 | HG00738.hp1 HG02145.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.980+8505C>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129012582 | |||||||
| chr3:129012594 | C | A | 1 | a0003c0003t0001g0181 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.980+8517C>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129012594 | |||||||
| chr3:129012594 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.980+8517C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129012594 | |||||||
| chr3:129012760 | G | A | 15 | a0001c0001t0001g0011 a0001c0001t0001g0180 a0001c0001t0001g0183 others(12): Show |
27 | HG00323.hp2 HG00423.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.980+8683G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129012760 | |||||||
| chr3:129013105 | G | A | 1 | a0003c0003t0001g0112 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.980+9028G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129013105 | |||||||
| chr3:129013150 | G | T | 1 | a0001c0001t0001g0131 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.980+9073G>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129013150 | |||||||
| chr3:129013190 | G | A | 7 | a0001c0001t0002g0199 a0001c0001t0002g0202 a0001c0001t0010g0203 others(4): Show |
10 | HG00639.hp2 HG01884.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.980+9113G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129013190 | |||||||
| chr3:129013197 | T | C | 5 | a0001c0001t0001g0023 a0001c0001t0001g0042 a0001c0001t0001g0190 others(2): Show |
8 | HG02109.hp2 HG02257.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.980+9120T>C | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129013197 | |||||||
| chr3:129013247 | GA | G | 3 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0005g0015 |
6 | HG02258.hp2 HG02622.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.980+9177delA | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 129013247 | ||||||
| chr3:129013336 | G | C | 59 | a0001c0001t0001g0023 a0001c0001t0001g0042 a0001c0001t0001g0046 others(56): Show |
83 | HG00639.hp2 HG00642.hp2 HG00735.hp2 others(80): Show |
intron_variant | MODIFIER | c.980+9259G>C | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129013336 | |||||||
| chr3:129013340 | T | G | 1 | a0001c0001t0001g0113 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.980+9263T>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129013340 | |||||||
| chr3:129013542 | T | C | 2 | a0001c0001t0007g0178 a0001c0001t0007g0179 |
2 | HG02559.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.980+9465T>C | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129013542 | |||||||
| chr3:129013555 | A | G | 2 | a0001c0001t0001g0099 a0001c0001t0001g0130 |
2 | HG02165.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.980+9478A>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129013555 | |||||||
| chr3:129013607 | C | G | 4 | a0001c0001t0001g0195 a0001c0001t0001g0198 a0002c0002t0001g0071 others(1): Show |
4 | HG00642.hp2 HG01069.hp1 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.980+9530C>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129013607 | |||||||
| chr3:129013630 | A | G | 58 | a0001c0001t0001g0023 a0001c0001t0001g0042 a0001c0001t0001g0046 others(55): Show |
82 | HG00639.hp2 HG00642.hp2 HG00735.hp2 others(79): Show |
intron_variant | MODIFIER | c.980+9553A>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129013630 | |||||||
| chr3:129013724 | C | T | 3 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 |
3 | NA18951.hp1 NA18974.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.980+9647C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129013724 | |||||||
| chr3:129013756 | C | T | 28 | a0001c0001t0001g0134 a0001c0001t0002g0199 a0001c0001t0002g0202 others(25): Show |
45 | HG00639.hp2 HG00735.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.980+9679C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129013756 | |||||||
| chr3:129013985 | G | A | 1 | a0003c0003t0001g0022 | 3 | HG00099.hp2 HG00140.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.980+9908G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129013985 | |||||||
| chr3:129014211 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.980+10134G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129014211 | |||||||
| chr3:129014218 | A | G | 4 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0168 others(1): Show |
4 | HG02280.hp2 HG02630.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.980+10141A>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129014218 | |||||||
| chr3:129014429 | C | A | 58 | a0001c0001t0001g0023 a0001c0001t0001g0042 a0001c0001t0001g0046 others(55): Show |
82 | HG00639.hp2 HG00642.hp2 HG00735.hp2 others(79): Show |
intron_variant | MODIFIER | c.980+10352C>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129014429 | |||||||
| chr3:129014434 | G | A | 15 | a0001c0001t0001g0023 a0001c0001t0001g0042 a0001c0001t0001g0190 others(12): Show |
19 | HG01346.hp2 HG02109.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.980+10357G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129014434 | |||||||
| chr3:129014456 | G | T | 2 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.980+10379G>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129014456 | |||||||
| chr3:129014531 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.980+10454G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129014531 | |||||||
| chr3:129014533 | C | T | 2 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.980+10456C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129014533 | |||||||
| chr3:129014725 | C | T | 16 | a0001c0001t0001g0134 a0004c0004t0001g0016 a0004c0004t0001g0209 others(13): Show |
29 | HG00735.hp2 HG00738.hp2 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.980+10648C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129014725 | |||||||
| chr3:129014838 | G | A | 3 | a0001c0001t0001g0139 a0003c0003t0001g0140 a0003c0003t0001g0141 |
3 | HG01243.hp2 HG01255.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.980+10761G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129014838 | |||||||
| chr3:129014840 | C | T | 1 | a0003c0003t0001g0165 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.980+10763C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129014840 | |||||||
| chr3:129015102 | C | T | 31 | a0001c0001t0001g0134 a0001c0001t0001g0164 a0001c0001t0001g0168 others(28): Show |
48 | HG00639.hp2 HG00735.hp2 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.980+11025C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129015102 | |||||||
| chr3:129015247 | T | A | 4 | a0001c0001t0001g0192 a0001c0001t0007g0178 a0001c0001t0007g0179 others(1): Show |
4 | HG01891.hp1 HG02559.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.980+11170T>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129015247 | |||||||
| chr3:129015267 | C | A | 4 | a0001c0001t0001g0195 a0001c0001t0001g0198 a0002c0002t0001g0071 others(1): Show |
4 | HG00642.hp2 HG01069.hp1 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.980+11190C>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129015267 | |||||||
| chr3:129015330 | C | A | 1 | a0001c0001t0001g0168 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.980+11253C>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129015330 | |||||||
| chr3:129015394 | A | G | 4 | a0001c0001t0001g0192 a0001c0001t0007g0178 a0001c0001t0007g0179 others(1): Show |
4 | HG01891.hp1 HG02559.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.980+11317A>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129015394 | |||||||
| chr3:129015400 | T | C | 2 | a0001c0001t0001g0146 a0002c0002t0001g0055 |
2 | HG00099.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.980+11323T>C | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129015400 | |||||||
| chr3:129015413 | C | A | 3 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0005g0015 |
6 | HG02258.hp2 HG02622.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.980+11336C>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129015413 | |||||||
| chr3:129015422 | G | A | 15 | a0001c0001t0001g0023 a0001c0001t0001g0042 a0001c0001t0001g0190 others(12): Show |
19 | HG01346.hp2 HG02109.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.980+11345G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129015422 | |||||||
| chr3:129015422 | G | T | 3 | a0001c0001t0001g0040 a0002c0002t0001g0087 a0002c0002t0003g0093 |
4 | HG01069.hp2 HG01071.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.980+11345G>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129015422 | |||||||
| chr3:129015435 | G | A | 17 | a0001c0001t0001g0134 a0001c0001t0001g0164 a0004c0004t0001g0016 others(14): Show |
30 | HG00735.hp2 HG00738.hp2 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.980+11358G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129015435 | |||||||
| chr3:129015649 | T | A | 1 | a0001c0001t0001g0168 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.980+11572T>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129015649 | |||||||
| chr3:129015802 | C | T | 1 | a0003c0003t0001g0193 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.980+11725C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129015802 | |||||||
| chr3:129015977 | A | G | 61 | a0001c0001t0001g0023 a0001c0001t0001g0042 a0001c0001t0001g0046 others(58): Show |
86 | HG00639.hp2 HG00642.hp2 HG00735.hp2 others(83): Show |
intron_variant | MODIFIER | c.980+11900A>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129015977 | |||||||
| chr3:129016026 | G | A | 1 | a0001c0001t0001g0183 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.980+11949G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129016026 | |||||||
| chr3:129016057 | A | G | 4 | a0001c0001t0001g0195 a0001c0001t0001g0198 a0002c0002t0001g0071 others(1): Show |
4 | HG00642.hp2 HG01069.hp1 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.980+11980A>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129016057 | |||||||
| chr3:129016156 | G | A | 1 | a0003c0003t0001g0036 | 2 | HG00642.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.980+12079G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129016156 | |||||||
| chr3:129016307 | C | T | 1 | a0002c0002t0003g0093 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.980+12230C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129016307 | |||||||
| chr3:129016502 | G | A | 22 | a0001c0001t0001g0023 a0001c0001t0001g0042 a0001c0001t0001g0097 others(19): Show |
29 | HG01346.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.980+12425G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129016502 | |||||||
| chr3:129016513 | C | A | 1 | a0001c0001t0001g0168 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.980+12436C>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129016513 | |||||||
| chr3:129016534 | G | A | 17 | a0001c0001t0001g0134 a0001c0001t0001g0164 a0004c0004t0001g0016 others(14): Show |
30 | HG00735.hp2 HG00738.hp2 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.980+12457G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129016534 | |||||||
| chr3:129017060 | C | T | 2 | a0001c0001t0001g0168 a0002c0002t0003g0093 |
2 | HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.980+12983C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129017060 | |||||||
| chr3:129017419 | C | T | 1 | a0003c0003t0001g0188 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.981-13284C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129017419 | |||||||
| chr3:129017420 | G | T | 1 | a0001c0001t0001g0194 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.981-13283G>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129017420 | |||||||
| chr3:129017481 | G | T | 2 | a0001c0001t0003g0173 a0003c0003t0008g0174 |
2 | HG01346.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.981-13222G>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129017481 | |||||||
| chr3:129017505 | G | A | 4 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0168 others(1): Show |
4 | HG02280.hp2 HG02630.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.981-13198G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129017505 | |||||||
| chr3:129017552 | C | T | 1 | a0001c0001t0001g0035 | 2 | HG02523.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.981-13151C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129017552 | |||||||
| chr3:129017587 | C | T | 1 | a0001c0001t0001g0035 | 2 | HG02523.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.981-13116C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129017587 | |||||||
| chr3:129017745 | C | CCT | 61 | a0001c0001t0001g0023 a0001c0001t0001g0042 a0001c0001t0001g0046 others(58): Show |
86 | HG00639.hp2 HG00642.hp2 HG00735.hp2 others(83): Show |
intron_variant | MODIFIER | c.981-12958_981-1295 others(6): Show |
EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129017745 | |||||||
| chr3:129017767 | C | T | 4 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0168 others(1): Show |
4 | HG02280.hp2 HG02630.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.981-12936C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129017767 | |||||||
| chr3:129017886 | T | G | 4 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0168 others(1): Show |
4 | HG02280.hp2 HG02630.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.981-12817T>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129017886 | |||||||
| chr3:129018029 | A | G | 1 | a0002c0002t0003g0093 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.981-12674A>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129018029 | |||||||
| chr3:129018274 | G | A | 22 | a0001c0001t0001g0023 a0001c0001t0001g0042 a0001c0001t0001g0097 others(19): Show |
29 | HG01346.hp2 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.981-12429G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129018274 | |||||||
| chr3:129018308 | G | C | 1 | a0002c0002t0001g0026 | 2 | HG00408.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.981-12395G>C | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129018308 | |||||||
| chr3:129018477 | T | C | 3 | a0001c0001t0001g0142 a0002c0002t0001g0027 a0002c0002t0001g0074 |
4 | HG00741.hp1 HG01168.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.981-12226T>C | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129018477 | |||||||
| chr3:129018505 | G | A | 28 | a0001c0001t0001g0134 a0001c0001t0001g0164 a0001c0001t0002g0199 others(25): Show |
45 | HG00639.hp2 HG00735.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.981-12198G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129018505 | |||||||
| chr3:129018536 | T | C | 1 | a0002c0002t0001g0075 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.981-12167T>C | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129018536 | |||||||
| chr3:129018567 | G | A | 1 | a0001c0001t0001g0194 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.981-12136G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129018567 | |||||||
| chr3:129018593 | C | T | 28 | a0001c0001t0001g0134 a0001c0001t0001g0164 a0001c0001t0002g0199 others(25): Show |
45 | HG00639.hp2 HG00735.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.981-12110C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129018593 | |||||||
| chr3:129018872 | C | T | 31 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0134 others(28): Show |
48 | HG00639.hp2 HG00735.hp2 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.981-11831C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129018872 | |||||||
| chr3:129019012 | G | A | 5 | a0001c0001t0001g0195 a0001c0001t0001g0198 a0002c0002t0001g0071 others(2): Show |
5 | HG00642.hp2 HG01069.hp1 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.981-11691G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129019012 | |||||||
| chr3:129019032 | G | A | 1 | a0002c0002t0001g0028 | 2 | NA18945.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.981-11671G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129019032 | |||||||
| chr3:129019083 | G | T | 1 | a0001c0001t0001g0012 | 5 | HG02451.hp1 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.981-11620G>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129019083 | |||||||
| chr3:129019173 | T | C | 2 | a0001c0001t0001g0168 a0002c0002t0003g0093 |
2 | HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.981-11530T>C | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129019173 | |||||||
| chr3:129019189 | G | C | 1 | a0003c0003t0001g0193 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.981-11514G>C | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129019189 | |||||||
| chr3:129019209 | G | A | 1 | a0004c0004t0001g0209 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.981-11494G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129019209 | |||||||
| chr3:129019315 | A | C | 1 | a0002c0002t0001g0086 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.981-11388A>C | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129019315 | |||||||
| chr3:129019342 | G | A | 1 | a0003c0003t0001g0189 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.981-11361G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129019342 | |||||||
| chr3:129019420 | C | G | 1 | a0004c0004t0001g0217 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.981-11283C>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129019420 | |||||||
| chr3:129019475 | G | A | 2 | a0001c0001t0001g0147 a0003c0003t0001g0166 |
2 | HG00673.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.981-11228G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129019475 | |||||||
| chr3:129019764 | C | CT | 36 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0001t0001g0094 others(33): Show |
51 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.981-10918dupT | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 129019764 | ||||||
| chr3:129019764 | C | CTT | 59 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0020 others(56): Show |
91 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.981-10919_981-1091 others(6): Show |
EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 129019764 | ||||||
| chr3:129019764 | CT | C | 10 | a0001c0001t0001g0184 a0001c0001t0001g0192 a0001c0001t0002g0199 others(7): Show |
10 | HG01081.hp1 HG01168.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.981-10918delT | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 129019764 | ||||||
| chr3:129019900 | C | A | 4 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0168 others(1): Show |
4 | HG02280.hp2 HG02630.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.981-10803C>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129019900 | |||||||
| chr3:129020058 | C | G | 10 | a0001c0001t0003g0173 a0001c0001t0006g0175 a0001c0001t0006g0176 others(7): Show |
11 | HG01346.hp2 HG02109.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.981-10645C>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129020058 | |||||||
| chr3:129020172 | G | C | 3 | a0001c0001t0001g0139 a0003c0003t0001g0140 a0003c0003t0001g0141 |
3 | HG01243.hp2 HG01255.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.981-10531G>C | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129020172 | |||||||
| chr3:129020277 | A | T | 2 | a0001c0001t0001g0162 a0010c0010t0001g0163 |
2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.981-10426A>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129020277 | |||||||
| chr3:129020312 | C | A | 1 | a0002c0002t0001g0073 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.981-10391C>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129020312 | |||||||
| chr3:129020337 | C | G | 18 | a0001c0001t0001g0023 a0001c0001t0001g0042 a0001c0001t0001g0190 others(15): Show |
22 | HG00642.hp2 HG01069.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.981-10366C>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129020337 | |||||||
| chr3:129020339 | A | G | 2 | a0003c0003t0001g0140 a0003c0003t0001g0141 |
2 | HG01243.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.981-10364A>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129020339 | |||||||
| chr3:129020375 | A | G | 3 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0002c0002t0003g0093 |
3 | HG02280.hp2 HG02630.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.981-10328A>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129020375 | |||||||
| chr3:129020701 | C | T | 18 | a0001c0001t0001g0023 a0001c0001t0001g0042 a0001c0001t0001g0190 others(15): Show |
22 | HG00642.hp2 HG01069.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.981-10002C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129020701 | |||||||
| chr3:129020785 | G | T | 1 | a0001c0001t0001g0150 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.981-9918G>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129020785 | |||||||
| chr3:129021505 | C | T | 1 | a0003c0003t0001g0169 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.981-9198C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129021505 | |||||||
| chr3:129021561 | T | C | 29 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0134 others(26): Show |
36 | HG00639.hp2 HG01123.hp2 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.981-9142T>C | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129021561 | |||||||
| chr3:129021622 | A | ACTC | 28 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0134 others(25): Show |
35 | HG00639.hp2 HG01123.hp2 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.981-9079_981-9078i others(5): Show |
EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 129021622 | ||||||
| chr3:129021885 | T | A | 1 | a0002c0002t0001g0057 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.981-8818T>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129021885 | |||||||
| chr3:129022019 | C | T | 4 | a0001c0001t0001g0116 a0001c0001t0001g0127 a0001c0001t0001g0128 others(1): Show |
4 | HG02293.hp2 NA18951.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.981-8684C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129022019 | |||||||
| chr3:129022020 | G | A | 1 | a0003c0003t0001g0171 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.981-8683G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129022020 | |||||||
| chr3:129022028 | C | T | 2 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.981-8675C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129022028 | |||||||
| chr3:129022029 | G | A | 4 | a0001c0001t0001g0116 a0001c0001t0001g0127 a0001c0001t0001g0128 others(1): Show |
4 | HG02293.hp2 NA18951.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.981-8674G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129022029 | |||||||
| chr3:129022063 | C | T | 5 | a0001c0001t0004g0044 a0001c0001t0004g0205 a0001c0001t0004g0206 others(2): Show |
6 | HG01123.hp2 HG02055.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.981-8640C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129022063 | |||||||
| chr3:129022196 | A | G | 8 | a0001c0001t0001g0114 a0001c0001t0001g0198 a0001c0001t0006g0175 others(5): Show |
8 | HG01109.hp2 HG01243.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.981-8507A>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129022196 | |||||||
| chr3:129022221 | T | G | 9 | a0001c0001t0001g0038 a0001c0001t0001g0042 a0001c0001t0001g0139 others(6): Show |
15 | HG01123.hp2 HG01255.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.981-8482T>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129022221 | |||||||
| chr3:129022224 | G | A | 1 | a0002c0002t0001g0078 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.981-8479G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129022224 | |||||||
| chr3:129022228 | G | C | 87 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0031 others(84): Show |
121 | HG00280.hp1 HG00408.hp2 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.981-8475G>C | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129022228 | |||||||
| chr3:129022270 | T | C | 11 | a0001c0001t0004g0206 a0003c0003t0001g0041 a0003c0003t0001g0155 others(8): Show |
24 | HG00639.hp2 HG00735.hp2 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.981-8433T>C | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129022270 | |||||||
| chr3:129022421 | A | G | 1 | a0002c0002t0001g0071 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.981-8282A>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129022421 | |||||||
| chr3:129022463 | C | T | 1 | a0001c0001t0010g0203 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.981-8240C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129022463 | |||||||
| chr3:129022509 | C | T | 6 | a0001c0001t0001g0115 a0002c0002t0001g0006 a0002c0002t0001g0028 others(3): Show |
13 | HG00609.hp1 HG00673.hp2 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.981-8194C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129022509 | |||||||
| chr3:129022646 | G | T | 26 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0094 others(23): Show |
29 | HG00642.hp2 HG01069.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.981-8057G>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129022646 | |||||||
| chr3:129022780 | C | T | 1 | a0001c0001t0001g0097 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.981-7923C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129022780 | |||||||
| chr3:129022799 | A | G | 32 | a0001c0001t0001g0023 a0001c0001t0001g0042 a0001c0001t0001g0046 others(29): Show |
46 | HG00280.hp1 HG00323.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.981-7904A>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129022799 | |||||||
| chr3:129022807 | C | T | 1 | a0004c0004t0001g0213 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.981-7896C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129022807 | |||||||
| chr3:129022835 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.981-7868G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129022835 | |||||||
| chr3:129022864 | G | A | 14 | a0001c0001t0001g0126 a0001c0001t0001g0183 a0001c0001t0001g0186 others(11): Show |
24 | HG00280.hp1 HG00323.hp2 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.981-7839G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129022864 | |||||||
| chr3:129022943 | A | C | 47 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0094 others(44): Show |
65 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.981-7760A>C | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129022943 | |||||||
| chr3:129023166 | A | C | 1 | a0001c0001t0010g0203 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.981-7537A>C | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129023166 | |||||||
| chr3:129023310 | C | CT | 39 | a0001c0001t0001g0023 a0001c0001t0001g0042 a0001c0001t0001g0101 others(36): Show |
53 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.981-7376dupT | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 129023310 | ||||||
| chr3:129023310 | C | CTT | 19 | a0001c0001t0001g0039 a0001c0001t0001g0094 a0001c0001t0001g0095 others(16): Show |
23 | HG02015.hp2 HG02056.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.981-7377_981-7376d others(4): Show |
EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 129023310 | ||||||
| chr3:129023310 | CT | C | 6 | a0001c0001t0001g0105 a0001c0001t0001g0119 a0001c0001t0010g0203 others(3): Show |
8 | HG02818.hp2 HG03704.hp1 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.981-7376delT | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 129023310 | ||||||
| chr3:129023369 | T | G | 1 | a0001c0001t0001g0047 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.981-7334T>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129023369 | |||||||
| chr3:129023382 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.981-7321G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129023382 | |||||||
| chr3:129023394 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.981-7309T>C | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129023394 | |||||||
| chr3:129023430 | G | A | 3 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0005g0015 |
6 | HG02258.hp2 HG02622.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.981-7273G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129023430 | |||||||
| chr3:129023454 | G | A | 2 | a0001c0001t0001g0046 a0001c0001t0001g0198 |
2 | HG01109.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.981-7249G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129023454 | |||||||
| chr3:129023523 | G | A | 31 | a0001c0001t0001g0023 a0001c0001t0001g0042 a0001c0001t0001g0114 others(28): Show |
45 | HG00280.hp1 HG00323.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.981-7180G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129023523 | |||||||
| chr3:129023622 | G | A | 1 | a0003c0003t0001g0037 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.981-7081G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129023622 | |||||||
| chr3:129023708 | T | G | 3 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0198 |
3 | HG01109.hp2 HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.981-6995T>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129023708 | |||||||
| chr3:129023796 | G | A | 1 | a0002c0002t0001g0089 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.981-6907G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129023796 | |||||||
| chr3:129023950 | C | A | 1 | a0001c0001t0001g0120 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.981-6753C>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129023950 | |||||||
| chr3:129023965 | T | C | 45 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0094 others(42): Show |
63 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.981-6738T>C | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129023965 | |||||||
| chr3:129024530 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0097 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.981-6157_981-6146d others(14): Show |
EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 129024530 | ||||||
| chr3:129024540 | GA | G | 12 | a0001c0001t0003g0021 a0001c0001t0003g0137 a0001c0001t0003g0173 others(9): Show |
14 | HG02055.hp1 HG02145.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.981-6152delA | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 129024540 | ||||||
| chr3:129024607 | A | G | 31 | a0001c0001t0001g0023 a0001c0001t0001g0042 a0001c0001t0001g0114 others(28): Show |
45 | HG00280.hp1 HG00323.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.981-6096A>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129024607 | |||||||
| chr3:129024854 | T | C | 2 | a0002c0002t0001g0086 a0004c0004t0001g0217 |
2 | NA18612.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.981-5849T>C | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129024854 | |||||||
| chr3:129024922 | G | A | 3 | a0001c0001t0001g0142 a0002c0002t0001g0027 a0002c0002t0001g0074 |
4 | HG00741.hp1 HG01168.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.981-5781G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129024922 | |||||||
| chr3:129025107 | C | G | 1 | a0001c0001t0010g0203 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.981-5596C>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129025107 | |||||||
| chr3:129025112 | G | A | 1 | a0001c0001t0002g0200 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.981-5591G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129025112 | |||||||
| chr3:129025280 | C | T | 13 | a0001c0001t0001g0039 a0001c0001t0001g0094 a0001c0001t0001g0095 others(10): Show |
14 | HG02015.hp2 HG02056.hp2 HG02683.hp2 others(11): Show |
intron_variant | MODIFIER | c.981-5423C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129025280 | |||||||
| chr3:129025298 | C | T | 1 | a0008c0009t0001g0033 | 2 | NA18965.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.981-5405C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129025298 | |||||||
| chr3:129025337 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.981-5366G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129025337 | |||||||
| chr3:129025370 | A | G | 121 | a0001c0001t0001g0023 a0001c0001t0001g0039 a0001c0001t0001g0040 others(118): Show |
175 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.981-5333A>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129025370 | |||||||
| chr3:129025377 | G | A | 1 | a0001c0001t0001g0109 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.981-5326G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129025377 | |||||||
| chr3:129025388 | C | T | 20 | a0001c0001t0001g0023 a0001c0001t0001g0042 a0001c0001t0001g0135 others(17): Show |
33 | HG00280.hp1 HG00323.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.981-5315C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129025388 | |||||||
| chr3:129025543 | A | G | 2 | a0005c0005t0001g0060 a0005c0005t0001g0061 |
2 | NA18944.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.981-5160A>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129025543 | |||||||
| chr3:129025748 | CCCCAGGG others(2): Show |
C | 31 | a0001c0001t0001g0023 a0001c0001t0001g0042 a0001c0001t0001g0114 others(28): Show |
45 | HG00280.hp1 HG00323.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.981-4951_981-4943d others(11): Show |
EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 129025748 | ||||||
| chr3:129025785 | C | T | 2 | a0001c0001t0001g0038 a0001c0001t0001g0152 |
3 | HG02976.hp1 HG03516.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.981-4918C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129025785 | |||||||
| chr3:129025892 | T | C | 120 | a0001c0001t0001g0023 a0001c0001t0001g0039 a0001c0001t0001g0040 others(117): Show |
174 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.981-4811T>C | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129025892 | |||||||
| chr3:129025949 | C | G | 1 | a0004c0004t0003g0215 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.981-4754C>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129025949 | |||||||
| chr3:129026282 | A | T | 2 | a0001c0001t0001g0103 a0001c0001t0001g0104 |
2 | HG01952.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.981-4421A>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129026282 | |||||||
| chr3:129026509 | C | G | 2 | a0003c0003t0008g0122 a0003c0003t0008g0174 |
2 | HG01346.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.981-4194C>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129026509 | |||||||
| chr3:129026691 | T | G | 1 | a0001c0001t0010g0203 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.981-4012T>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129026691 | |||||||
| chr3:129026815 | G | T | 1 | a0001c0001t0001g0168 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.981-3888G>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129026815 | |||||||
| chr3:129026919 | T | G | 1 | a0001c0001t0010g0203 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.981-3784T>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129026919 | |||||||
| chr3:129027099 | A | G | 1 | a0002c0002t0001g0075 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.981-3604A>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129027099 | |||||||
| chr3:129027130 | A | AGGGGGTC others(11): Show |
1 | a0001c0001t0010g0203 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.981-3573_981-3572i others(20): Show |
EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129027130 | |||||||
| chr3:129027137 | G | C | 1 | a0001c0001t0010g0203 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.981-3566G>C | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129027137 | |||||||
| chr3:129027138 | A | T | 1 | a0001c0001t0010g0203 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.981-3565A>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129027138 | |||||||
| chr3:129027139 | A | G | 1 | a0001c0001t0010g0203 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.981-3564A>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129027139 | |||||||
| chr3:129027139 | AACGCCTG others(3): Show |
A | 3 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0198 |
3 | HG01109.hp2 HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.981-3549_981-3540d others(12): Show |
EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 129027139 | ||||||
| chr3:129027141 | C | G | 1 | a0001c0001t0010g0203 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.981-3562C>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129027141 | |||||||
| chr3:129027145 | T | C | 1 | a0001c0001t0010g0203 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.981-3558T>C | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129027145 | |||||||
| chr3:129027147 | C | G | 1 | a0001c0001t0010g0203 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.981-3556C>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129027147 | |||||||
| chr3:129027149 | G | A | 1 | a0001c0001t0010g0203 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.981-3554G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129027149 | |||||||
| chr3:129027325 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.981-3378G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129027325 | |||||||
| chr3:129027365 | C | T | 5 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0019 others(2): Show |
5 | HG01070.hp2 HG01074.hp1 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.981-3338C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129027365 | |||||||
| chr3:129027381 | G | A | 1 | a0001c0001t0002g0200 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.981-3322G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129027381 | |||||||
| chr3:129027715 | T | C | 3 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0005g0015 |
6 | HG02258.hp2 HG02622.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.981-2988T>C | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129027715 | |||||||
| chr3:129027796 | A | G | 1 | a0002c0002t0001g0006 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.981-2907A>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129027796 | |||||||
| chr3:129027888 | A | T | 1 | a0005c0005t0001g0050 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.981-2815A>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129027888 | |||||||
| chr3:129027909 | G | A | 1 | a0003c0003t0001g0172 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.981-2794G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129027909 | |||||||
| chr3:129028081 | C | CT | 6 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0168 others(3): Show |
10 | HG00642.hp1 HG01192.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.981-2608dupT | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 129028081 | ||||||
| chr3:129028081 | CT | C | 46 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(43): Show |
65 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.981-2608delT | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 129028081 | ||||||
| chr3:129028195 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.981-2508C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129028195 | |||||||
| chr3:129028225 | A | T | 1 | a0003c0003t0001g0036 | 2 | HG00642.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.981-2478A>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129028225 | |||||||
| chr3:129028396 | T | A | 1 | a0002c0002t0001g0080 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.981-2307T>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129028396 | |||||||
| chr3:129028526 | G | C | 118 | a0001c0001t0001g0023 a0001c0001t0001g0039 a0001c0001t0001g0040 others(115): Show |
172 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.981-2177G>C | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129028526 | |||||||
| chr3:129028578 | C | T | 2 | a0002c0002t0001g0014 a0002c0002t0001g0088 |
5 | HG00140.hp1 HG00280.hp2 HG00735.hp1 others(2): Show |
intron_variant | MODIFIER | c.981-2125C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129028578 | |||||||
| chr3:129028604 | C | T | 2 | a0001c0001t0002g0199 a0004c0004t0001g0016 |
5 | HG02922.hp2 HG02970.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.981-2099C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129028604 | |||||||
| chr3:129028641 | C | CT | 3 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0005g0015 |
6 | HG02258.hp2 HG02622.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.981-2052dupT | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 129028641 | ||||||
| chr3:129028641 | CTTTTTTT | C | 21 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0094 others(18): Show |
24 | HG00642.hp2 HG01069.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.981-2058_981-2052d others(9): Show |
EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 129028641 | ||||||
| chr3:129028651 | T | C | 56 | a0001c0001t0001g0023 a0001c0001t0001g0042 a0001c0001t0001g0114 others(53): Show |
85 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.981-2052T>C | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129028651 | |||||||
| chr3:129028676 | A | C | 1 | a0001c0001t0010g0203 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.981-2027A>C | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129028676 | |||||||
| chr3:129028891 | T | G | 1 | a0001c0001t0001g0010 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.981-1812T>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129028891 | |||||||
| chr3:129028895 | C | G | 1 | a0001c0001t0001g0135 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.981-1808C>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129028895 | |||||||
| chr3:129028921 | G | A | 13 | a0001c0001t0001g0039 a0001c0001t0001g0094 a0001c0001t0001g0095 others(10): Show |
14 | HG02015.hp2 HG02056.hp2 HG02683.hp2 others(11): Show |
intron_variant | MODIFIER | c.981-1782G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129028921 | |||||||
| chr3:129029018 | T | G | 1 | a0003c0008t0001g0225 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.981-1685T>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129029018 | |||||||
| chr3:129029171 | G | A | 2 | a0001c0001t0002g0199 a0004c0004t0001g0016 |
5 | HG02922.hp2 HG02970.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.981-1532G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129029171 | |||||||
| chr3:129029241 | T | C | 1 | a0001c0001t0001g0190 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.981-1462T>C | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129029241 | |||||||
| chr3:129029305 | A | C | 118 | a0001c0001t0001g0023 a0001c0001t0001g0039 a0001c0001t0001g0040 others(115): Show |
172 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.981-1398A>C | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129029305 | |||||||
| chr3:129029585 | G | GT | 116 | a0001c0001t0001g0011 a0001c0001t0001g0023 a0001c0001t0001g0039 others(113): Show |
166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.981-1108dupT | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 129029585 | ||||||
| chr3:129029735 | C | T | 39 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0019 others(36): Show |
57 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.981-968C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129029735 | |||||||
| chr3:129029794 | A | G | 1 | a0001c0001t0001g0034 | 2 | NA18979.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.981-909A>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129029794 | |||||||
| chr3:129029886 | TA | T | 7 | a0001c0001t0001g0011 a0001c0001t0001g0035 a0001c0001t0001g0104 others(4): Show |
7 | HG01952.hp2 HG02895.hp2 NA18906.hp1 others(4): Show |
intron_variant | MODIFIER | c.981-804delA | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 129029886 | ||||||
| chr3:129029887 | A | T | 2 | a0002c0002t0001g0083 a0003c0003t0001g0009 |
2 | HG03017.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.981-816A>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129029887 | |||||||
| chr3:129029991 | C | A | 1 | a0003c0003t0001g0036 | 2 | HG00642.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.981-712C>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129029991 | |||||||
| chr3:129029992 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.981-711G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129029992 | |||||||
| chr3:129030694 | C | T | 2 | a0003c0003t0008g0122 a0003c0003t0008g0174 |
2 | HG01346.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.981-9C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 2/7 | chr3 | 129030694 | |||||||
| chr3:129031009 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1138+149C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 3/7 | chr3 | 129031009 | |||||||
| chr3:129031016 | C | T | 1 | a0002c0002t0001g0058 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1138+156C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 3/7 | chr3 | 129031016 | |||||||
| chr3:129031308 | A | G | 1 | a0001c0001t0002g0199 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1138+448A>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 3/7 | chr3 | 129031308 | |||||||
| chr3:129031441 | C | A | 1 | a0001c0001t0005g0015 | 4 | HG02258.hp2 HG02970.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1138+581C>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 3/7 | chr3 | 129031441 | |||||||
| chr3:129031449 | A | G | 1 | a0001c0001t0001g0035 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1138+589A>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 3/7 | chr3 | 129031449 | |||||||
| chr3:129031686 | G | A | 1 | a0003c0003t0001g0154 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1138+826G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 3/7 | chr3 | 129031686 | |||||||
| chr3:129031714 | G | A | 1 | a0003c0003t0001g0189 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1138+854G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 3/7 | chr3 | 129031714 | |||||||
| chr3:129031939 | G | A | 1 | a0004c0004t0001g0219 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1139-880G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 3/7 | chr3 | 129031939 | |||||||
| chr3:129031944 | T | C | 1 | a0002c0002t0001g0058 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1139-875T>C | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 3/7 | chr3 | 129031944 | |||||||
| chr3:129031996 | C | A | 1 | a0003c0003t0002g0043 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1139-823C>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 3/7 | chr3 | 129031996 | |||||||
| chr3:129032222 | G | A | 1 | a0003c0003t0001g0136 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1139-597G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 3/7 | chr3 | 129032222 | |||||||
| chr3:129032259 | G | C | 51 | a0001c0001t0001g0183 a0001c0001t0001g0186 a0003c0003t0001g0004 others(48): Show |
87 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.1139-560G>C | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 3/7 | chr3 | 129032259 | |||||||
| chr3:129032375 | C | T | 60 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0019 others(57): Show |
81 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.1139-444C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 3/7 | chr3 | 129032375 | |||||||
| chr3:129032425 | A | G | 1 | a0005c0005t0001g0068 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1139-394A>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 3/7 | chr3 | 129032425 | |||||||
| chr3:129032431 | T | G | 1 | a0005c0005t0001g0013 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1139-388T>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 3/7 | chr3 | 129032431 | |||||||
| chr3:129032474 | C | T | 1 | a0002c0002t0001g0028 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1139-345C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 3/7 | chr3 | 129032474 | |||||||
| chr3:129033106 | G | T | 1 | a0002c0002t0001g0029 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1286+140G>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 4/7 | chr3 | 129033106 | |||||||
| chr3:129033172 | G | T | 11 | a0001c0001t0003g0021 a0001c0001t0003g0137 a0001c0001t0003g0173 others(8): Show |
13 | HG02055.hp1 HG02145.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1286+206G>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 4/7 | chr3 | 129033172 | |||||||
| chr3:129033213 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1286+247C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 4/7 | chr3 | 129033213 | |||||||
| chr3:129033352 | C | T | 1 | a0001c0001t0002g0200 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1286+386C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 4/7 | chr3 | 129033352 | |||||||
| chr3:129033464 | C | T | 17 | a0001c0001t0001g0039 a0001c0001t0001g0094 a0001c0001t0001g0095 others(14): Show |
18 | HG02015.hp2 HG02056.hp2 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.1286+498C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 4/7 | chr3 | 129033464 | |||||||
| chr3:129033468 | T | C | 1 | a0002c0002t0001g0058 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1286+502T>C | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 4/7 | chr3 | 129033468 | |||||||
| chr3:129033485 | G | C | 11 | a0001c0001t0003g0021 a0001c0001t0003g0137 a0001c0001t0003g0173 others(8): Show |
13 | HG02055.hp1 HG02145.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1286+519G>C | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 4/7 | chr3 | 129033485 | |||||||
| chr3:129033912 | A | G | 1 | a0001c0001t0005g0015 | 4 | HG02258.hp2 HG02970.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1287-252A>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 4/7 | chr3 | 129033912 | |||||||
| chr3:129034047 | C | T | 1 | a0005c0005t0001g0005 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1287-117C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 4/7 | chr3 | 129034047 | |||||||
| chr3:129034143 | G | A | 1 | a0002c0002t0001g0014 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1287-21G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 4/7 | chr3 | 129034143 | |||||||
| chr3:129034714 | G | A | 19 | a0001c0001t0001g0023 a0001c0001t0001g0042 a0001c0001t0001g0046 others(16): Show |
23 | HG01109.hp2 HG01123.hp2 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.1452+385G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 5/7 | chr3 | 129034714 | |||||||
| chr3:129034788 | C | T | 1 | a0002c0002t0001g0030 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1452+459C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 5/7 | chr3 | 129034788 | |||||||
| chr3:129034867 | C | T | 1 | a0001c0001t0005g0015 | 4 | HG02258.hp2 HG02970.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1452+538C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 5/7 | chr3 | 129034867 | |||||||
| chr3:129035282 | G | A | 1 | a0003c0003t0002g0201 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1452+953G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 5/7 | chr3 | 129035282 | |||||||
| chr3:129035338 | G | A | 1 | a0004c0004t0001g0016 | 4 | HG02922.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1452+1009G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 5/7 | chr3 | 129035338 | |||||||
| chr3:129035449 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1452+1120C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 5/7 | chr3 | 129035449 | |||||||
| chr3:129035615 | T | C | 1 | a0003c0003t0001g0159 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1452+1286T>C | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 5/7 | chr3 | 129035615 | |||||||
| chr3:129035944 | T | G | 123 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0019 others(120): Show |
184 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.1453-1033T>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 5/7 | chr3 | 129035944 | |||||||
| chr3:129035961 | T | C | 1 | a0001c0001t0007g0179 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1453-1016T>C | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 5/7 | chr3 | 129035961 | |||||||
| chr3:129036063 | T | C | 1 | a0001c0001t0005g0015 | 4 | HG02258.hp2 HG02970.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1453-914T>C | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 5/7 | chr3 | 129036063 | |||||||
| chr3:129036375 | G | A | 1 | a0001c0001t0001g0034 | 2 | NA18979.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.1453-602G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 5/7 | chr3 | 129036375 | |||||||
| chr3:129036517 | G | A | 1 | a0001c0001t0005g0015 | 4 | HG02258.hp2 HG02970.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1453-460G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 5/7 | chr3 | 129036517 | |||||||
| chr3:129036576 | G | A | 1 | a0003c0003t0001g0187 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1453-401G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 5/7 | chr3 | 129036576 | |||||||
| chr3:129036664 | T | A | 8 | a0001c0001t0001g0115 a0002c0002t0001g0006 a0002c0002t0001g0028 others(5): Show |
15 | HG00609.hp1 HG00673.hp2 HG02004.hp2 others(12): Show |
intron_variant | MODIFIER | c.1453-313T>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 5/7 | chr3 | 129036664 | |||||||
| chr3:129036841 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1453-136G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 5/7 | chr3 | 129036841 | |||||||
| chr3:129036971 | T | C | 159 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0019 others(156): Show |
232 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(229): Show |
splice_region_variant&intron_variant | LOW | c.1453-6T>C | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 5/7 | chr3 | 129036971 | |||||||
| chr3:129037119 | T | C | 1 | a0002c0002t0001g0090 | 1 | NA18991.hp1 | splice_donor_variant&intron_variant | HIGH | c.1593+2T>C | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 6/7 | chr3 | 129037119 | |||||||
| chr3:129037128 | G | A | 58 | a0003c0003t0001g0004 a0003c0003t0001g0007 a0003c0003t0001g0008 others(55): Show |
97 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.1593+11G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 6/7 | chr3 | 129037128 | |||||||
| chr3:129037261 | C | T | 1 | a0002c0002t0001g0052 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1593+144C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 6/7 | chr3 | 129037261 | |||||||
| chr3:129037263 | G | A | 1 | a0002c0002t0001g0080 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1593+146G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 6/7 | chr3 | 129037263 | |||||||
| chr3:129037385 | G | A | 1 | a0003c0003t0001g0197 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1593+268G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 6/7 | chr3 | 129037385 | |||||||
| chr3:129037459 | A | T | 1 | a0002c0002t0001g0058 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1593+342A>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 6/7 | chr3 | 129037459 | |||||||
| chr3:129037612 | GA | G | 3 | a0001c0001t0006g0175 a0001c0001t0006g0176 a0001c0001t0006g0177 |
3 | HG02145.hp1 HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1593+499delA | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 129037612 | ||||||
| chr3:129037668 | A | C | 1 | a0003c0008t0001g0223 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1593+551A>C | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 6/7 | chr3 | 129037668 | |||||||
| chr3:129037817 | T | G | 1 | a0001c0001t0003g0137 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1593+700T>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 6/7 | chr3 | 129037817 | |||||||
| chr3:129037898 | C | CA | 7 | a0001c0001t0001g0019 a0001c0001t0001g0127 a0003c0003t0001g0007 others(4): Show |
8 | HG00280.hp1 HG01981.hp1 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1593+797dupA | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 129037898 | ||||||
| chr3:129038063 | CA | C | 155 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0023 others(152): Show |
226 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.1594-754delA | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 129038063 | ||||||
| chr3:129038147 | T | C | 1 | a0001c0001t0001g0191 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1594-684T>C | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 6/7 | chr3 | 129038147 | |||||||
| chr3:129038472 | T | A | 5 | a0001c0001t0001g0040 a0001c0001t0001g0131 a0001c0001t0001g0151 others(2): Show |
7 | HG01069.hp2 HG01071.hp2 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.1594-359T>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 6/7 | chr3 | 129038472 | |||||||
| chr3:129038717 | C | G | 121 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0019 others(118): Show |
182 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.1594-114C>G | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 6/7 | chr3 | 129038717 | |||||||
| chr3:129039033 | G | A | 1 | a0002c0002t0001g0058 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1663+133G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 7/7 | chr3 | 129039033 | |||||||
| chr3:129039127 | C | T | 1 | a0001c0001t0005g0015 | 4 | HG02258.hp2 HG02970.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1663+227C>T | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 7/7 | chr3 | 129039127 | |||||||
| chr3:129039281 | G | A | 3 | a0001c0001t0001g0168 a0001c0001t0002g0199 a0004c0004t0001g0016 |
6 | HG02922.hp2 HG02970.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.1663+381G>A | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 7/7 | chr3 | 129039281 | |||||||
| chr3:129039622 | G | C | 14 | a0001c0001t0002g0199 a0001c0001t0003g0021 a0001c0001t0003g0137 others(11): Show |
19 | HG02055.hp1 HG02145.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.1664-90G>C | EFCC1 | ENSG00000114654.8 | transcript | ENST00000683648.1 | protein_coding | 7/7 | chr3 | 129039622 |