Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 167410 |
| ensemblid | ENSG00000145721.12 |
| hgncid | 18581 |
| symbol | LIX1 |
| name | limb and CNS expressed 1 |
| refseq_nuc | NM_153234.5 |
| refseq_prot | NP_694966.3 |
| ensembl_nuc | ENST00000274382.9 |
| ensembl_prot | ENSP00000274382.4 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 97091867 |
| end | 97142611 |
| strand | - |
| ver | v1.2 |
| region | chr5:97091867-97142611 |
| region5000 | chr5:97086867-97147611 |
| regionname0 | LIX1_chr5_97091867_97142611 |
| regionname5000 | LIX1_chr5_97086867_97147611 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 282 | 354 | 86 | 68 | 146 | 16 | 36 | 124 | LIX1_chr5_97086867_97147611 | LIX1 | MDRTL others(277): Show |
chr5 | 97086867 | 97147611 |
| a0002 | 0/0 | 282 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | MDRTL others(277): Show |
chr5 | 97086867 | 97147611 |
| a0003 | 0/0 | 282 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | MDRTL others(277): Show |
chr5 | 97086867 | 97147611 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 846 | 350 | 82 | 68 | 146 | 16 | 36 | LIX1_chr5_97086867_97147611 | LIX1 | ATGGA others(841): Show |
chr5 | 97086867 | 97147611 | ||
| a0001c0002 | 0/0 | 846 | 4 | 4 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | ATGGA others(841): Show |
chr5 | 97086867 | 97147611 | ||
| a0002c0003 | 0/0 | 846 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | ATGGA others(841): Show |
chr5 | 97086867 | 97147611 | ||
| a0003c0004 | 0/0 | 846 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | ATGGA others(841): Show |
chr5 | 97086867 | 97147611 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3765 | 160 | 35 | 34 | 66 | 7 | 17 | LIX1_chr5_97086867_97147611 | LIX1 | ACTCT others(3760): Show |
chr5 | 97086867 | 97147611 |
| a0001c0001t0002 | 0/0 | 3767 | 101 | 26 | 16 | 45 | 2 | 12 | LIX1_chr5_97086867_97147611 | LIX1 | ACTCT others(3762): Show |
chr5 | 97086867 | 97147611 |
| a0001c0001t0003 | 0/0 | 3767 | 20 | 0 | 1 | 16 | 0 | 3 | LIX1_chr5_97086867_97147611 | LIX1 | ACTCT others(3762): Show |
chr5 | 97086867 | 97147611 |
| a0001c0001t0004 | 0/1 | 3766 | 15 | 1 | 2 | 5 | 5 | 1 | LIX1_chr5_97086867_97147611 | LIX1 | ACTCT others(3761): Show |
chr5 | 97086867 | 97147611 |
| a0001c0001t0005 | 0/0 | 3764 | 8 | 1 | 4 | 3 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | ACTCT others(3759): Show |
chr5 | 97086867 | 97147611 |
| a0001c0001t0006 | 0/0 | 3766 | 6 | 5 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | ACTCT others(3761): Show |
chr5 | 97086867 | 97147611 |
| a0001c0001t0007 | 0/0 | 3766 | 5 | 1 | 3 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | ACTCT others(3761): Show |
chr5 | 97086867 | 97147611 |
| a0001c0001t0008 | 0/0 | 3766 | 5 | 3 | 2 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | ACTCT others(3761): Show |
chr5 | 97086867 | 97147611 |
| a0001c0001t0009 | 0/0 | 3765 | 4 | 0 | 3 | 0 | 0 | 1 | LIX1_chr5_97086867_97147611 | LIX1 | ACTCT others(3760): Show |
chr5 | 97086867 | 97147611 |
| a0001c0001t0010 | 0/0 | 3764 | 4 | 0 | 1 | 0 | 2 | 1 | LIX1_chr5_97086867_97147611 | LIX1 | ACTCT others(3759): Show |
chr5 | 97086867 | 97147611 |
| a0001c0001t0011 | 0/0 | 3767 | 4 | 0 | 0 | 4 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | ACTCT others(3762): Show |
chr5 | 97086867 | 97147611 |
| a0001c0001t0012 | 0/0 | 3768 | 3 | 0 | 1 | 2 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | ACTCT others(3763): Show |
chr5 | 97086867 | 97147611 |
| a0001c0001t0013 | 0/0 | 3769 | 3 | 2 | 1 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | ACTCT others(3764): Show |
chr5 | 97086867 | 97147611 |
| a0001c0001t0014 | 0/0 | 3768 | 2 | 2 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | ACTCT others(3763): Show |
chr5 | 97086867 | 97147611 |
| a0001c0001t0015 | 0/0 | 3767 | 2 | 2 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | ACTCT others(3762): Show |
chr5 | 97086867 | 97147611 |
| a0001c0001t0016 | 0/0 | 3765 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | ACTCT others(3760): Show |
chr5 | 97086867 | 97147611 |
| a0001c0001t0017 | 0/0 | 3765 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | ACTCT others(3760): Show |
chr5 | 97086867 | 97147611 |
| a0001c0001t0018 | 0/0 | 3767 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | ACTCT others(3762): Show |
chr5 | 97086867 | 97147611 |
| a0001c0001t0019 | 0/0 | 3767 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | ACTCT others(3762): Show |
chr5 | 97086867 | 97147611 |
| a0001c0001t0020 | 0/0 | 3767 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | ACTCT others(3762): Show |
chr5 | 97086867 | 97147611 |
| a0001c0001t0021 | 0/0 | 3768 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | ACTCT others(3763): Show |
chr5 | 97086867 | 97147611 |
| a0001c0001t0022 | 0/0 | 3768 | 1 | 0 | 0 | 0 | 0 | 1 | LIX1_chr5_97086867_97147611 | LIX1 | ACTCT others(3763): Show |
chr5 | 97086867 | 97147611 |
| a0001c0001t0023 | 0/0 | 3769 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | ACTCT others(3764): Show |
chr5 | 97086867 | 97147611 |
| a0001c0002t0002 | 0/0 | 3767 | 4 | 4 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | ACTCT others(3762): Show |
chr5 | 97086867 | 97147611 |
| a0002c0003t0002 | 0/0 | 3767 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | ACTCT others(3762): Show |
chr5 | 97086867 | 97147611 |
| a0003c0004t0003 | 0/0 | 3767 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | ACTCT others(3762): Show |
chr5 | 97086867 | 97147611 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 9 | 0 | 0 | 8 | 0 | 1 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0003 | 0/0 | 9 | 0 | 4 | 5 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0006 | 0/0 | 5 | 1 | 2 | 0 | 1 | 1 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0009 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0010 | 0/0 | 3 | 2 | 0 | 0 | 0 | 1 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0040 | 1/0 | 2 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0001 | 0/0 | 16 | 1 | 3 | 10 | 0 | 2 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0004 | 0/0 | 5 | 1 | 2 | 1 | 0 | 1 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0044 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0003g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0003g0037 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0003g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0004g0014 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0004g0036 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0004g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0004g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0004g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0004g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0004g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0004g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0004g0211 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0004g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0004g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0005g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0005g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0005g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0005g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0005g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0005g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0005g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0006g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0006g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0006g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0006g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0006g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0007g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0007g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0007g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0007g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0007g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0008g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0008g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0008g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0008g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0008g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0009g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0009g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0009g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0009g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0010g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0010g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0010g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0010g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0011g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0011g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0012g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0012g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0012g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0013g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0013g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0013g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0014g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0014g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0015g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0015g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0016g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0017g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0018g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0019g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0020g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0021g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0022g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0001t0023g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0002t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0002t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0002t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0001c0002t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0002c0003t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| a0003c0004t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0004 | g0014 | EUR | GBR | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0179 | EUR | GBR | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0217 | EUR | GBR | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0036 | EUR | GBR | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0212 | EUR | FIN | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | FIN | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | CHS | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0037 | AMR | PUR | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG00642 | hp2 | a0001 | c0001 | t0009 | g0052 | AMR | PUR | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG00735 | hp1 | a0001 | c0001 | t0012 | g0174 | AMR | PUR | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0055 | AMR | PUR | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0172 | AMR | PUR | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG00738 | hp2 | a0001 | c0001 | t0007 | g0216 | AMR | PUR | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0044 | AMR | PUR | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG01069 | hp1 | a0001 | c0001 | t0005 | g0115 | AMR | PUR | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG01069 | hp2 | a0001 | c0001 | t0005 | g0028 | AMR | PUR | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG01071 | hp2 | a0001 | c0001 | t0005 | g0028 | AMR | PUR | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG01109 | hp1 | a0001 | c0001 | t0008 | g0099 | AMR | PUR | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0119 | AMR | PUR | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG01175 | hp1 | a0001 | c0001 | t0004 | g0169 | AMR | PUR | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG01243 | hp1 | a0001 | c0001 | t0013 | g0163 | AMR | PUR | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG01255 | hp2 | a0001 | c0001 | t0008 | g0259 | AMR | CLM | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG01256 | hp2 | a0001 | c0001 | t0005 | g0201 | AMR | CLM | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0038 | AMR | CLM | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0038 | AMR | CLM | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0230 | AMR | CLM | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0183 | AMR | CLM | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG01433 | hp2 | a0001 | c0001 | t0009 | g0050 | AMR | CLM | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0118 | AMR | CLM | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | CLM | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG01515 | hp1 | a0001 | c0001 | t0004 | g0014 | EUR | IBS | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG01516 | hp1 | a0001 | c0001 | t0010 | g0080 | EUR | IBS | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG01516 | hp2 | a0001 | c0001 | t0004 | g0036 | EUR | IBS | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG01517 | hp1 | a0001 | c0001 | t0004 | g0014 | EUR | IBS | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG01517 | hp2 | a0001 | c0001 | t0010 | g0079 | EUR | IBS | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG01884 | hp1 | a0001 | c0001 | t0008 | g0130 | AFR | ACB | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG01884 | hp2 | a0001 | c0002 | t0002 | g0255 | AFR | ACB | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG01891 | hp1 | a0001 | c0002 | t0002 | g0236 | AFR | ACB | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | ACB | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PEL | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0150 | AMR | PEL | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG01975 | hp1 | a0001 | c0001 | t0007 | g0117 | AMR | PEL | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | PEL | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG01981 | hp2 | a0001 | c0001 | t0007 | g0250 | AMR | PEL | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG01993 | hp1 | a0001 | c0001 | t0004 | g0051 | AMR | PEL | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02004 | hp2 | a0001 | c0001 | t0009 | g0048 | AMR | PEL | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02027 | hp2 | a0001 | c0001 | t0012 | g0165 | EAS | KHV | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0030 | AFR | ACB | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | ACB | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | KHV | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02071 | hp2 | a0001 | c0001 | t0021 | g0164 | EAS | KHV | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02080 | hp2 | a0002 | c0003 | t0002 | g0152 | EAS | KHV | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0184 | EAS | KHV | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0166 | AFR | ACB | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0176 | AMR | PEL | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CDX | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02155 | hp2 | a0003 | c0004 | t0003 | g0121 | EAS | CDX | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | CDX | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | CDX | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0220 | AFR | ACB | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02258 | hp2 | a0001 | c0001 | t0005 | g0252 | AFR | ACB | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02451 | hp1 | a0001 | c0001 | t0006 | g0206 | AFR | ACB | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02451 | hp2 | a0001 | c0001 | t0013 | g0072 | AFR | ACB | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | KHV | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0041 | AFR | GWD | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0070 | AFR | GWD | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0160 | SAS | PJL | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02622 | hp1 | a0001 | c0001 | t0008 | g0107 | AFR | GWD | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02622 | hp2 | a0001 | c0001 | t0018 | g0188 | AFR | GWD | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02630 | hp1 | a0001 | c0001 | t0013 | g0182 | AFR | GWD | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0257 | AFR | GWD | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | GWD | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0224 | SAS | PJL | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0158 | SAS | PJL | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02738 | hp2 | a0001 | c0001 | t0022 | g0075 | SAS | PJL | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0143 | AFR | GWD | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | GWD | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0157 | AFR | GWD | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02886 | hp1 | a0001 | c0001 | t0006 | g0205 | AFR | GWD | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0151 | AFR | GWD | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02896 | hp1 | a0001 | c0001 | t0014 | g0122 | AFR | GWD | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0141 | AFR | ESN | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02922 | hp2 | a0001 | c0002 | t0002 | g0189 | AFR | ESN | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0254 | AFR | ESN | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ESN | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0153 | AFR | ESN | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | ESN | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0162 | SAS | PJL | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0225 | SAS | PJL | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG03041 | hp1 | a0001 | c0001 | t0006 | g0035 | AFR | GWD | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0041 | AFR | MSL | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ESN | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG03139 | hp2 | a0001 | c0002 | t0002 | g0237 | AFR | ESN | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ESN | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG03195 | hp2 | a0001 | c0001 | t0006 | g0191 | AFR | ESN | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | MSL | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | MSL | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | MSL | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0032 | AFR | MSL | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG03453 | hp1 | a0001 | c0001 | t0023 | g0253 | AFR | MSL | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0186 | AFR | MSL | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG03540 | hp2 | a0001 | c0001 | t0015 | g0234 | AFR | GWD | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG03579 | hp1 | a0001 | c0001 | t0017 | g0124 | AFR | MSL | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG03579 | hp2 | a0001 | c0001 | t0015 | g0129 | AFR | MSL | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0046 | SAS | PJL | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0037 | SAS | PJL | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | STU | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | STU | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0229 | SAS | PJL | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG03710 | hp1 | a0001 | c0001 | t0009 | g0071 | SAS | PJL | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0144 | SAS | BEB | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG03831 | hp2 | a0001 | c0001 | t0004 | g0246 | SAS | BEB | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | BEB | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG03927 | hp2 | a0001 | c0001 | t0010 | g0087 | SAS | BEB | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | STU | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | STU | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | BEB | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0145 | SAS | STU | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0173 | SAS | STU | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | STU | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | STU | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0138 | SAS | STU | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | STU | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | YRI | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | CHB | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | CHB | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | CHB | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | YRI | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18906 | hp2 | a0001 | c0001 | t0014 | g0123 | AFR | YRI | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18946 | hp2 | a0001 | c0001 | t0016 | g0251 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18948 | hp1 | a0001 | c0001 | t0005 | g0089 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18948 | hp2 | a0001 | c0001 | t0019 | g0067 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18949 | hp1 | a0001 | c0001 | t0004 | g0238 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18953 | hp2 | a0001 | c0001 | t0011 | g0015 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0227 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18959 | hp2 | a0001 | c0001 | t0007 | g0249 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18963 | hp1 | a0001 | c0001 | t0005 | g0091 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18967 | hp2 | a0001 | c0001 | t0006 | g0078 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18971 | hp2 | a0001 | c0001 | t0011 | g0015 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18972 | hp2 | a0001 | c0001 | t0003 | g0207 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18980 | hp1 | a0001 | c0001 | t0011 | g0015 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18986 | hp2 | a0001 | c0001 | t0005 | g0106 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18987 | hp1 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18991 | hp2 | a0001 | c0001 | t0003 | g0221 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA19000 | hp1 | a0001 | c0001 | t0012 | g0132 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA19000 | hp2 | a0001 | c0001 | t0011 | g0142 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA19006 | hp2 | a0001 | c0001 | t0003 | g0228 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0044 | AFR | LWK | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | LWK | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | LWK | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0187 | AFR | LWK | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0231 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA19067 | hp2 | a0001 | c0001 | t0004 | g0057 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA19072 | hp1 | a0001 | c0001 | t0004 | g0105 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA19078 | hp2 | a0001 | c0001 | t0004 | g0200 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0223 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA19088 | hp1 | a0001 | c0001 | t0004 | g0192 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0126 | EAS | JPT | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0175 | AFR | YRI | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA19240 | hp2 | a0001 | c0001 | t0008 | g0131 | AFR | YRI | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0222 | EUR | TSI | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0209 | EUR | TSI | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0022 | EUR | TSI | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0056 | EUR | TSI | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | GIH | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG01123 | hp1 | a0001 | c0001 | t0010 | g0065 | AMR | CLM | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0069 | AFR | ACB | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02486 | hp2 | a0001 | c0001 | t0007 | g0120 | AFR | ACB | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0030 | AFR | ACB | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG02559 | hp2 | a0001 | c0001 | t0020 | g0260 | AFR | ACB | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | MSL | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG03471 | hp2 | a0001 | c0001 | t0006 | g0035 | AFR | MSL | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | USA | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | USA | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0127 | AFR | USA | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | USA | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0054 | AFR | LWK | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | LWK | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0004 | g0211 | REF | REF | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0040 | REF | REF | LIX1_chr5_97086867_97147611 | LIX1 | chr5 | 97086867 | 97147611 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:97094954 | G | A | 1 | a0002 | 1 | HG02080.hp2 | missense_variant | MODERATE | c.643C>T | p.Arg215Trp | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 6/6 | 678/3765 | 643/849 | 215/282 | chr5 | 97094954 | |||
| chr5:97094990 | G | A | 1 | a0003 | 1 | HG02155.hp2 | missense_variant | MODERATE | c.607C>T | p.Arg203Cys | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 6/6 | 642/3765 | 607/849 | 203/282 | chr5 | 97094990 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:97105244 | C | T | 1 | a0001c0002 | 4 | HG01884.hp2 HG01891.hp1 HG02922.hp2 others(1): Show |
synonymous_variant | LOW | c.429G>A | p.Gly143Gly | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/6 | 464/3765 | 429/849 | 143/282 | chr5 | 97105244 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:97091920 | T | C | 18 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0007 others(15): Show |
157 | HG00099.hp2 HG00609.hp2 HG00621.hp1 others(154): Show |
3_prime_UTR_variant | MODIFIER | c.*2828A>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 6/6 | 2828 | chr5 | 97091920 | ||||||
| chr5:97091994 | C | A | 18 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0007 others(15): Show |
157 | HG00099.hp2 HG00609.hp2 HG00621.hp1 others(154): Show |
3_prime_UTR_variant | MODIFIER | c.*2754G>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 6/6 | 2754 | chr5 | 97091994 | ||||||
| chr5:97092035 | C | G | 1 | a0001c0001t0023 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2713G>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 6/6 | 2713 | chr5 | 97092035 | ||||||
| chr5:97092072 | G | A | 3 | a0001c0001t0003 a0001c0001t0022 a0003c0004t0003 |
22 | HG00642.hp1 HG02083.hp2 HG02155.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2676C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 6/6 | 2676 | chr5 | 97092072 | ||||||
| chr5:97092148 | AC | A | 1 | a0001c0001t0010 | 4 | HG01123.hp1 HG01516.hp1 HG01517.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2599delG | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 6/6 | 2599 | chr5 | 97092148 | ||||||
| chr5:97092396 | G | GA | 3 | a0001c0001t0006 a0001c0001t0013 a0001c0001t0023 |
10 | HG01243.hp1 HG02451.hp1 HG02451.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2351dupT | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 6/6 | 2351 | chr5 | 97092396 | ||||||
| chr5:97092461 | T | A | 1 | a0001c0001t0020 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2287A>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 6/6 | 2287 | chr5 | 97092461 | ||||||
| chr5:97092663 | A | G | 1 | a0001c0001t0019 | 1 | NA18948.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2085T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 6/6 | 2085 | chr5 | 97092663 | ||||||
| chr5:97092768 | G | T | 1 | a0001c0001t0018 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1980C>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 6/6 | 1980 | chr5 | 97092768 | ||||||
| chr5:97092847 | A | G | 1 | a0001c0001t0018 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1901T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 6/6 | 1901 | chr5 | 97092847 | ||||||
| chr5:97092956 | G | T | 1 | a0001c0001t0011 | 4 | NA18953.hp2 NA18971.hp2 NA18980.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1792C>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 6/6 | 1792 | chr5 | 97092956 | ||||||
| chr5:97093181 | T | C | 2 | a0001c0001t0014 a0001c0001t0017 |
3 | HG02896.hp1 HG03579.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1567A>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 6/6 | 1567 | chr5 | 97093181 | ||||||
| chr5:97093288 | G | T | 1 | a0001c0001t0016 | 1 | NA18946.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1460C>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 6/6 | 1460 | chr5 | 97093288 | ||||||
| chr5:97093619 | T | TA | 3 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0008 |
24 | HG00099.hp1 HG00140.hp2 HG00738.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1128dupT | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 6/6 | 1128 | chr5 | 97093619 | ||||||
| chr5:97093619 | T | TAA | 10 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0011 others(7): Show |
136 | HG00099.hp2 HG00609.hp2 HG00621.hp1 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*1127_*1128dupTT | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 6/6 | 1128 | chr5 | 97093619 | ||||||
| chr5:97093619 | T | TAAA | 6 | a0001c0001t0012 a0001c0001t0013 a0001c0001t0014 others(3): Show |
11 | HG00735.hp1 HG01243.hp1 HG02027.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1126_*1128dupTTT | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 6/6 | 1128 | chr5 | 97093619 | ||||||
| chr5:97093619 | TA | T | 1 | a0001c0001t0005 | 8 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1128delT | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 6/6 | 1128 | chr5 | 97093619 | ||||||
| chr5:97093892 | T | G | 2 | a0001c0001t0008 a0001c0001t0015 |
7 | HG01109.hp1 HG01255.hp2 HG01884.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*856A>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 6/6 | 856 | chr5 | 97093892 | ||||||
| chr5:97093942 | C | T | 1 | a0001c0001t0009 | 4 | HG00642.hp2 HG01433.hp2 HG02004.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*806G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 6/6 | 806 | chr5 | 97093942 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:97095093 | C | T | 4 | a0001c0001t0002g0038 a0001c0001t0002g0055 a0001c0001t0002g0222 others(1): Show |
5 | HG00735.hp2 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.562-58G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 5/5 | chr5 | 97095093 | |||||||
| chr5:97095128 | T | C | 74 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0008 others(71): Show |
103 | HG00099.hp2 HG00609.hp2 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.562-93A>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 5/5 | chr5 | 97095128 | |||||||
| chr5:97095390 | C | T | 1 | a0001c0001t0002g0162 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.562-355G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 5/5 | chr5 | 97095390 | |||||||
| chr5:97095734 | G | A | 30 | a0001c0001t0001g0096 a0001c0001t0003g0018 a0001c0001t0003g0037 others(27): Show |
34 | HG00642.hp1 HG00738.hp2 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.562-699C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 5/5 | chr5 | 97095734 | |||||||
| chr5:97095968 | T | A | 118 | a0001c0001t0001g0096 a0001c0001t0001g0171 a0001c0001t0002g0001 others(115): Show |
153 | HG00099.hp2 HG00609.hp2 HG00621.hp1 others(150): Show |
intron_variant | MODIFIER | c.561+842A>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 5/5 | chr5 | 97095968 | |||||||
| chr5:97096220 | A | T | 1 | a0001c0001t0003g0228 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.561+590T>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 5/5 | chr5 | 97096220 | |||||||
| chr5:97096233 | G | T | 1 | a0001c0001t0001g0217 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.561+577C>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 5/5 | chr5 | 97096233 | |||||||
| chr5:97096317 | T | TG | 6 | a0001c0001t0001g0012 a0001c0001t0001g0063 a0001c0001t0001g0092 others(3): Show |
8 | HG02630.hp2 HG02717.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.561+492dupC | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 5/5 | chr5 | 97096317 | |||||||
| chr5:97096725 | C | T | 2 | a0001c0001t0001g0149 a0001c0001t0001g0190 |
2 | HG01891.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.561+85G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 5/5 | chr5 | 97096725 | |||||||
| chr5:97096800 | A | G | 1 | a0001c0001t0001g0023 | 2 | NA18983.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.561+10T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 5/5 | chr5 | 97096800 | |||||||
| chr5:97097263 | G | C | 1 | a0001c0001t0001g0245 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.484-376C>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97097263 | |||||||
| chr5:97097459 | C | T | 1 | a0001c0001t0005g0091 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.484-572G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97097459 | |||||||
| chr5:97097546 | C | T | 1 | a0001c0001t0020g0260 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.484-659G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97097546 | |||||||
| chr5:97097760 | T | A | 32 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(29): Show |
50 | HG00140.hp1 HG00323.hp2 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.484-873A>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97097760 | |||||||
| chr5:97097764 | A | G | 1 | a0001c0001t0002g0161 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.484-877T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97097764 | |||||||
| chr5:97097838 | A | C | 4 | a0001c0001t0007g0117 a0001c0001t0007g0216 a0001c0001t0007g0249 others(1): Show |
4 | HG00738.hp2 HG01975.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.484-951T>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97097838 | |||||||
| chr5:97097959 | C | A | 89 | a0001c0001t0001g0171 a0001c0001t0001g0208 a0001c0001t0002g0001 others(86): Show |
120 | HG00099.hp2 HG00609.hp2 HG00621.hp1 others(117): Show |
intron_variant | MODIFIER | c.484-1072G>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97097959 | |||||||
| chr5:97098030 | C | G | 1 | a0001c0001t0001g0125 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.484-1143G>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97098030 | |||||||
| chr5:97098051 | C | T | 7 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0059 others(4): Show |
9 | HG02258.hp2 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.484-1164G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97098051 | |||||||
| chr5:97098052 | G | T | 1 | a0001c0001t0004g0105 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.484-1165C>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97098052 | |||||||
| chr5:97098314 | C | T | 20 | a0001c0001t0003g0018 a0001c0001t0003g0037 a0001c0001t0003g0039 others(17): Show |
24 | HG00642.hp1 HG02083.hp2 HG02155.hp2 others(21): Show |
intron_variant | MODIFIER | c.484-1427G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97098314 | |||||||
| chr5:97098473 | A | G | 89 | a0001c0001t0001g0171 a0001c0001t0001g0208 a0001c0001t0002g0001 others(86): Show |
120 | HG00099.hp2 HG00609.hp2 HG00621.hp1 others(117): Show |
intron_variant | MODIFIER | c.484-1586T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97098473 | |||||||
| chr5:97098549 | G | C | 4 | a0001c0001t0007g0117 a0001c0001t0007g0216 a0001c0001t0007g0249 others(1): Show |
4 | HG00738.hp2 HG01975.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.484-1662C>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97098549 | |||||||
| chr5:97098743 | A | G | 20 | a0001c0001t0003g0018 a0001c0001t0003g0037 a0001c0001t0003g0039 others(17): Show |
24 | HG00642.hp1 HG02083.hp2 HG02155.hp2 others(21): Show |
intron_variant | MODIFIER | c.484-1856T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97098743 | |||||||
| chr5:97099098 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.484-2211C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97099098 | |||||||
| chr5:97099099 | T | A | 5 | a0001c0001t0002g0141 a0001c0001t0002g0143 a0001c0001t0002g0157 others(2): Show |
5 | HG00738.hp1 HG02145.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.484-2212A>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97099099 | |||||||
| chr5:97099132 | TG | T | 126 | a0001c0001t0001g0096 a0001c0001t0001g0171 a0001c0001t0001g0208 others(123): Show |
162 | HG00099.hp2 HG00609.hp2 HG00621.hp1 others(159): Show |
intron_variant | MODIFIER | c.484-2246delC | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97099132 | |||||||
| chr5:97099160 | C | T | 1 | a0001c0001t0002g0158 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.484-2273G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97099160 | |||||||
| chr5:97099199 | G | A | 2 | a0001c0001t0002g0146 a0001c0001t0002g0170 |
2 | NA18964.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.484-2312C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97099199 | |||||||
| chr5:97099237 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.484-2350G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97099237 | |||||||
| chr5:97099639 | C | A | 1 | a0001c0001t0001g0203 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.484-2752G>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97099639 | |||||||
| chr5:97099729 | C | T | 1 | a0001c0001t0002g0222 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.484-2842G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97099729 | |||||||
| chr5:97099747 | A | G | 1 | a0001c0001t0002g0119 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.484-2860T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97099747 | |||||||
| chr5:97099762 | G | A | 4 | a0001c0001t0006g0035 a0001c0001t0006g0191 a0001c0001t0006g0205 others(1): Show |
5 | HG02451.hp1 HG02886.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.484-2875C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97099762 | |||||||
| chr5:97099768 | C | T | 7 | a0001c0001t0008g0099 a0001c0001t0008g0107 a0001c0001t0008g0130 others(4): Show |
7 | HG01109.hp1 HG01255.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.484-2881G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97099768 | |||||||
| chr5:97099814 | G | A | 4 | a0001c0001t0006g0035 a0001c0001t0006g0191 a0001c0001t0006g0205 others(1): Show |
5 | HG02451.hp1 HG02886.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.484-2927C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97099814 | |||||||
| chr5:97099815 | C | G | 4 | a0001c0001t0006g0035 a0001c0001t0006g0191 a0001c0001t0006g0205 others(1): Show |
5 | HG02451.hp1 HG02886.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.484-2928G>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97099815 | |||||||
| chr5:97099853 | A | G | 1 | a0001c0001t0007g0120 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.484-2966T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97099853 | |||||||
| chr5:97100074 | T | C | 1 | a0001c0001t0007g0120 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.484-3187A>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97100074 | |||||||
| chr5:97100176 | C | G | 20 | a0001c0001t0003g0018 a0001c0001t0003g0037 a0001c0001t0003g0039 others(17): Show |
24 | HG00642.hp1 HG02083.hp2 HG02155.hp2 others(21): Show |
intron_variant | MODIFIER | c.484-3289G>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97100176 | |||||||
| chr5:97100303 | C | T | 1 | a0001c0001t0014g0123 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.484-3416G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97100303 | |||||||
| chr5:97100343 | T | G | 2 | a0001c0001t0002g0146 a0001c0001t0002g0170 |
2 | NA18964.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.484-3456A>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97100343 | |||||||
| chr5:97100364 | A | G | 141 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0059 others(138): Show |
179 | HG00099.hp2 HG00609.hp2 HG00621.hp1 others(176): Show |
intron_variant | MODIFIER | c.484-3477T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97100364 | |||||||
| chr5:97100428 | C | G | 1 | a0001c0001t0009g0071 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.484-3541G>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97100428 | |||||||
| chr5:97100477 | A | G | 7 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0059 others(4): Show |
9 | HG02258.hp2 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.484-3590T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97100477 | |||||||
| chr5:97100569 | C | G | 1 | a0001c0001t0002g0136 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.484-3682G>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97100569 | |||||||
| chr5:97100869 | C | T | 93 | a0001c0001t0001g0149 a0001c0001t0001g0171 a0001c0001t0001g0190 others(90): Show |
124 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(121): Show |
intron_variant | MODIFIER | c.484-3982G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97100869 | |||||||
| chr5:97100893 | GA | G | 106 | a0001c0001t0001g0013 a0001c0001t0001g0042 a0001c0001t0001g0043 others(103): Show |
141 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(138): Show |
intron_variant | MODIFIER | c.484-4007delT | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97100893 | |||||||
| chr5:97100922 | A | T | 4 | a0001c0001t0001g0009 a0001c0001t0001g0110 a0001c0001t0001g0202 others(1): Show |
6 | HG01070.hp2 HG01071.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.484-4035T>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97100922 | |||||||
| chr5:97100986 | G | A | 3 | a0001c0001t0002g0141 a0001c0001t0002g0143 a0001c0001t0002g0166 |
3 | HG02145.hp2 HG02809.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.484-4099C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97100986 | |||||||
| chr5:97101078 | A | AAGGTGAG others(2): Show |
3 | a0001c0001t0014g0122 a0001c0001t0014g0123 a0001c0001t0017g0124 |
3 | HG02896.hp1 HG03579.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.483+4103_483+4111d others(11): Show |
LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97101078 | |||||||
| chr5:97101210 | G | T | 1 | a0001c0001t0001g0096 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.483+3980C>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97101210 | |||||||
| chr5:97101238 | T | C | 93 | a0001c0001t0001g0149 a0001c0001t0001g0171 a0001c0001t0001g0190 others(90): Show |
124 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(121): Show |
intron_variant | MODIFIER | c.483+3952A>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97101238 | |||||||
| chr5:97101396 | C | T | 2 | a0001c0001t0001g0045 a0001c0001t0001g0256 |
3 | HG02647.hp2 HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.483+3794G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97101396 | |||||||
| chr5:97101445 | A | C | 1 | a0001c0001t0001g0104 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.483+3745T>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97101445 | |||||||
| chr5:97101509 | C | T | 1 | a0001c0001t0002g0160 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.483+3681G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97101509 | |||||||
| chr5:97101522 | A | G | 4 | a0001c0001t0006g0035 a0001c0001t0006g0191 a0001c0001t0006g0205 others(1): Show |
5 | HG02451.hp1 HG02886.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.483+3668T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97101522 | |||||||
| chr5:97101733 | C | T | 7 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0059 others(4): Show |
9 | HG02258.hp2 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.483+3457G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97101733 | |||||||
| chr5:97101829 | G | C | 4 | a0001c0002t0002g0189 a0001c0002t0002g0236 a0001c0002t0002g0237 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.483+3361C>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97101829 | |||||||
| chr5:97102059 | C | A | 4 | a0001c0002t0002g0189 a0001c0002t0002g0236 a0001c0002t0002g0237 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.483+3131G>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97102059 | |||||||
| chr5:97102123 | C | G | 1 | a0001c0001t0001g0090 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.483+3067G>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97102123 | |||||||
| chr5:97102169 | G | T | 1 | a0001c0001t0002g0069 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.483+3021C>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97102169 | |||||||
| chr5:97102186 | C | G | 93 | a0001c0001t0001g0086 a0001c0001t0001g0149 a0001c0001t0001g0190 others(90): Show |
124 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(121): Show |
intron_variant | MODIFIER | c.483+3004G>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97102186 | |||||||
| chr5:97102197 | G | T | 4 | a0001c0002t0002g0189 a0001c0002t0002g0236 a0001c0002t0002g0237 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.483+2993C>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97102197 | |||||||
| chr5:97102402 | T | A | 1 | a0001c0001t0002g0175 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.483+2788A>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97102402 | |||||||
| chr5:97102484 | A | G | 4 | a0001c0002t0002g0189 a0001c0002t0002g0236 a0001c0002t0002g0237 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.483+2706T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97102484 | |||||||
| chr5:97102515 | A | G | 1 | a0001c0001t0002g0180 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.483+2675T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97102515 | |||||||
| chr5:97102532 | T | G | 2 | a0001c0001t0003g0039 a0001c0001t0003g0219 |
3 | NA18977.hp1 NA18983.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.483+2658A>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97102532 | |||||||
| chr5:97102727 | GA | G | 4 | a0001c0001t0007g0117 a0001c0001t0007g0216 a0001c0001t0007g0249 others(1): Show |
4 | HG00738.hp2 HG01975.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.483+2462delT | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97102727 | |||||||
| chr5:97102729 | CT | C | 17 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0095 others(14): Show |
23 | HG00323.hp2 HG00733.hp1 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.483+2460delA | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97102729 | |||||||
| chr5:97102751 | C | T | 7 | a0001c0001t0008g0099 a0001c0001t0008g0107 a0001c0001t0008g0130 others(4): Show |
7 | HG01109.hp1 HG01255.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.483+2439G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97102751 | |||||||
| chr5:97102983 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.483+2207C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97102983 | |||||||
| chr5:97103103 | G | GTTTTTTA others(20): Show |
4 | a0001c0002t0002g0189 a0001c0002t0002g0236 a0001c0002t0002g0237 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.483+2086_483+2087i others(29): Show |
LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97103103 | |||||||
| chr5:97103104 | A | G | 4 | a0001c0002t0002g0189 a0001c0002t0002g0236 a0001c0002t0002g0237 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.483+2086T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97103104 | |||||||
| chr5:97103105 | C | T | 4 | a0001c0002t0002g0189 a0001c0002t0002g0236 a0001c0002t0002g0237 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.483+2085G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97103105 | |||||||
| chr5:97103230 | A | G | 4 | a0001c0002t0002g0189 a0001c0002t0002g0236 a0001c0002t0002g0237 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.483+1960T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97103230 | |||||||
| chr5:97103292 | G | A | 8 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0059 others(5): Show |
10 | HG02258.hp2 HG02486.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.483+1898C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97103292 | |||||||
| chr5:97103366 | T | C | 7 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0059 others(4): Show |
9 | HG02258.hp2 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.483+1824A>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97103366 | |||||||
| chr5:97103410 | C | T | 1 | a0001c0001t0001g0096 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.483+1780G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97103410 | |||||||
| chr5:97103539 | G | A | 7 | a0001c0001t0001g0012 a0001c0001t0001g0063 a0001c0001t0001g0092 others(4): Show |
9 | HG01243.hp2 HG02630.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.483+1651C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97103539 | |||||||
| chr5:97103632 | C | T | 1 | a0001c0001t0001g0241 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.483+1558G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97103632 | |||||||
| chr5:97103715 | T | C | 2 | a0001c0001t0001g0242 a0001c0001t0002g0068 |
2 | HG01243.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.483+1475A>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97103715 | |||||||
| chr5:97103730 | C | G | 5 | a0001c0001t0001g0009 a0001c0001t0001g0110 a0001c0001t0001g0190 others(2): Show |
7 | HG01070.hp2 HG01071.hp1 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.483+1460G>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97103730 | |||||||
| chr5:97103744 | T | C | 1 | a0001c0001t0001g0241 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.483+1446A>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97103744 | |||||||
| chr5:97103748 | G | A | 4 | a0001c0001t0001g0009 a0001c0001t0001g0110 a0001c0001t0001g0202 others(1): Show |
6 | HG01070.hp2 HG01071.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.483+1442C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97103748 | |||||||
| chr5:97103761 | G | C | 1 | a0001c0001t0002g0150 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.483+1429C>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97103761 | |||||||
| chr5:97103761 | G | T | 4 | a0001c0001t0001g0009 a0001c0001t0001g0110 a0001c0001t0001g0202 others(1): Show |
6 | HG01070.hp2 HG01071.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.483+1429C>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97103761 | |||||||
| chr5:97103762 | G | C | 1 | a0001c0001t0002g0150 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.483+1428C>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97103762 | |||||||
| chr5:97103826 | A | G | 1 | a0001c0001t0002g0159 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.483+1364T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97103826 | |||||||
| chr5:97103858 | A | G | 1 | a0001c0001t0001g0197 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.483+1332T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97103858 | |||||||
| chr5:97103913 | C | A | 3 | a0001c0001t0014g0122 a0001c0001t0014g0123 a0001c0001t0017g0124 |
3 | HG02896.hp1 HG03579.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.483+1277G>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97103913 | |||||||
| chr5:97103914 | A | G | 3 | a0001c0001t0014g0122 a0001c0001t0014g0123 a0001c0001t0017g0124 |
3 | HG02896.hp1 HG03579.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.483+1276T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97103914 | |||||||
| chr5:97103959 | C | T | 1 | a0001c0001t0007g0120 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.483+1231G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97103959 | |||||||
| chr5:97103971 | G | GA | 7 | a0001c0001t0001g0095 a0001c0001t0001g0101 a0001c0001t0001g0198 others(4): Show |
7 | HG01123.hp1 HG01175.hp2 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.483+1218dupT | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97103971 | |||||||
| chr5:97103971 | GA | G | 21 | a0001c0001t0001g0208 a0001c0001t0002g0167 a0001c0001t0002g0224 others(18): Show |
25 | HG00642.hp1 HG02155.hp2 HG02559.hp2 others(22): Show |
intron_variant | MODIFIER | c.483+1218delT | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97103971 | |||||||
| chr5:97103971 | GAA | G | 109 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0059 others(106): Show |
143 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(140): Show |
intron_variant | MODIFIER | c.483+1217_483+1218d others(4): Show |
LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97103971 | |||||||
| chr5:97104087 | G | C | 1 | a0001c0001t0001g0168 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.483+1103C>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97104087 | |||||||
| chr5:97104093 | T | A | 145 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0045 others(142): Show |
183 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(180): Show |
intron_variant | MODIFIER | c.483+1097A>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97104093 | |||||||
| chr5:97104218 | C | T | 1 | a0001c0001t0015g0129 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.483+972G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97104218 | |||||||
| chr5:97104327 | C | T | 1 | a0001c0001t0002g0158 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.483+863G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97104327 | |||||||
| chr5:97104359 | GAGTTA | G | 4 | a0001c0002t0002g0189 a0001c0002t0002g0236 a0001c0002t0002g0237 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.483+826_483+830del others(5): Show |
LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97104359 | |||||||
| chr5:97104472 | C | T | 139 | a0001c0001t0001g0045 a0001c0001t0001g0096 a0001c0001t0001g0125 others(136): Show |
176 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(173): Show |
intron_variant | MODIFIER | c.483+718G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97104472 | |||||||
| chr5:97104491 | T | C | 94 | a0001c0001t0001g0149 a0001c0001t0001g0168 a0001c0001t0001g0171 others(91): Show |
125 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.483+699A>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97104491 | |||||||
| chr5:97104598 | A | G | 2 | a0001c0001t0002g0178 a0001c0001t0002g0185 |
2 | NA19063.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.483+592T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97104598 | |||||||
| chr5:97104685 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.483+505C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97104685 | |||||||
| chr5:97104791 | T | C | 1 | a0001c0001t0006g0205 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.483+399A>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97104791 | |||||||
| chr5:97104824 | T | C | 1 | a0001c0001t0001g0242 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.483+366A>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97104824 | |||||||
| chr5:97104884 | G | T | 4 | a0001c0002t0002g0189 a0001c0002t0002g0236 a0001c0002t0002g0237 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.483+306C>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97104884 | |||||||
| chr5:97104934 | C | A | 4 | a0001c0002t0002g0189 a0001c0002t0002g0236 a0001c0002t0002g0237 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.483+256G>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97104934 | |||||||
| chr5:97105007 | C | T | 4 | a0001c0002t0002g0189 a0001c0002t0002g0236 a0001c0002t0002g0237 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.483+183G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 4/5 | chr5 | 97105007 | |||||||
| chr5:97105441 | C | A | 4 | a0001c0002t0002g0189 a0001c0002t0002g0236 a0001c0002t0002g0237 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.388-156G>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 3/5 | chr5 | 97105441 | |||||||
| chr5:97105635 | C | T | 2 | a0001c0001t0001g0116 a0001c0001t0005g0115 |
2 | HG01069.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.388-350G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 3/5 | chr5 | 97105635 | |||||||
| chr5:97105648 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.388-363C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 3/5 | chr5 | 97105648 | |||||||
| chr5:97105687 | T | G | 185 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(182): Show |
245 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(242): Show |
intron_variant | MODIFIER | c.388-402A>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 3/5 | chr5 | 97105687 | |||||||
| chr5:97105689 | A | G | 1 | a0001c0001t0001g0096 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.388-404T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 3/5 | chr5 | 97105689 | |||||||
| chr5:97105872 | A | G | 216 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(213): Show |
300 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(297): Show |
intron_variant | MODIFIER | c.388-587T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 3/5 | chr5 | 97105872 | |||||||
| chr5:97105892 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.388-607G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 3/5 | chr5 | 97105892 | |||||||
| chr5:97105947 | C | T | 4 | a0001c0002t0002g0189 a0001c0002t0002g0236 a0001c0002t0002g0237 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.388-662G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 3/5 | chr5 | 97105947 | |||||||
| chr5:97106076 | A | T | 1 | a0001c0001t0001g0024 | 2 | NA18747.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.388-791T>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 3/5 | chr5 | 97106076 | |||||||
| chr5:97106088 | G | A | 8 | a0001c0001t0001g0125 a0001c0001t0008g0099 a0001c0001t0008g0107 others(5): Show |
8 | HG01109.hp1 HG01255.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.388-803C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 3/5 | chr5 | 97106088 | |||||||
| chr5:97106096 | AT | A | 7 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0059 others(4): Show |
9 | HG02258.hp2 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.388-812delA | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 3/5 | chr5 | 97106096 | |||||||
| chr5:97106108 | G | A | 1 | a0001c0001t0002g0170 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.388-823C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 3/5 | chr5 | 97106108 | |||||||
| chr5:97106179 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.388-894G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 3/5 | chr5 | 97106179 | |||||||
| chr5:97106408 | G | A | 1 | a0001c0001t0002g0119 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.387+952C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 3/5 | chr5 | 97106408 | |||||||
| chr5:97106704 | T | C | 1 | a0001c0001t0001g0096 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.387+656A>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 3/5 | chr5 | 97106704 | |||||||
| chr5:97106711 | TA | T | 7 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0059 others(4): Show |
9 | HG02258.hp2 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.387+648delT | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 3/5 | chr5 | 97106711 | |||||||
| chr5:97106758 | A | C | 4 | a0001c0001t0006g0035 a0001c0001t0006g0191 a0001c0001t0006g0205 others(1): Show |
5 | HG02451.hp1 HG02886.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.387+602T>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 3/5 | chr5 | 97106758 | |||||||
| chr5:97106760 | G | A | 7 | a0001c0001t0001g0012 a0001c0001t0001g0063 a0001c0001t0001g0092 others(4): Show |
9 | HG01243.hp2 HG02630.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.387+600C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 3/5 | chr5 | 97106760 | |||||||
| chr5:97106865 | C | T | 4 | a0001c0002t0002g0189 a0001c0002t0002g0236 a0001c0002t0002g0237 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.387+495G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 3/5 | chr5 | 97106865 | |||||||
| chr5:97106878 | G | A | 4 | a0001c0002t0002g0189 a0001c0002t0002g0236 a0001c0002t0002g0237 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.387+482C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 3/5 | chr5 | 97106878 | |||||||
| chr5:97106988 | C | T | 4 | a0001c0002t0002g0189 a0001c0002t0002g0236 a0001c0002t0002g0237 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.387+372G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 3/5 | chr5 | 97106988 | |||||||
| chr5:97107038 | A | G | 4 | a0001c0002t0002g0189 a0001c0002t0002g0236 a0001c0002t0002g0237 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.387+322T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 3/5 | chr5 | 97107038 | |||||||
| chr5:97107131 | A | G | 4 | a0001c0001t0006g0035 a0001c0001t0006g0191 a0001c0001t0006g0205 others(1): Show |
5 | HG02451.hp1 HG02886.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.387+229T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 3/5 | chr5 | 97107131 | |||||||
| chr5:97107212 | G | T | 4 | a0001c0002t0002g0189 a0001c0002t0002g0236 a0001c0002t0002g0237 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.387+148C>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 3/5 | chr5 | 97107212 | |||||||
| chr5:97107253 | T | A | 111 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0059 others(108): Show |
145 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(142): Show |
intron_variant | MODIFIER | c.387+107A>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 3/5 | chr5 | 97107253 | |||||||
| chr5:97107581 | C | T | 3 | a0001c0001t0002g0032 a0001c0001t0002g0069 a0001c0001t0002g0070 |
4 | HG02486.hp1 HG02572.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.247-81G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97107581 | |||||||
| chr5:97107652 | G | A | 1 | a0001c0001t0002g0134 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.247-152C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97107652 | |||||||
| chr5:97107860 | G | GA | 7 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0059 others(4): Show |
9 | HG02258.hp2 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.247-361dupT | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97107860 | |||||||
| chr5:97107933 | C | G | 4 | a0001c0002t0002g0189 a0001c0002t0002g0236 a0001c0002t0002g0237 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.247-433G>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97107933 | |||||||
| chr5:97107948 | T | G | 2 | a0001c0001t0001g0045 a0001c0001t0001g0256 |
3 | HG02647.hp2 HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.247-448A>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97107948 | |||||||
| chr5:97108002 | C | A | 4 | a0001c0002t0002g0189 a0001c0002t0002g0236 a0001c0002t0002g0237 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.247-502G>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97108002 | |||||||
| chr5:97108065 | G | T | 1 | a0001c0001t0001g0083 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.247-565C>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97108065 | |||||||
| chr5:97108279 | G | A | 2 | a0001c0002t0002g0189 a0001c0002t0002g0255 |
2 | HG01884.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.247-779C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97108279 | |||||||
| chr5:97108319 | T | A | 1 | a0001c0001t0001g0061 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.247-819A>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97108319 | |||||||
| chr5:97108407 | C | G | 4 | a0001c0002t0002g0189 a0001c0002t0002g0236 a0001c0002t0002g0237 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.247-907G>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97108407 | |||||||
| chr5:97108453 | CT | C | 4 | a0001c0002t0002g0189 a0001c0002t0002g0236 a0001c0002t0002g0237 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.247-954delA | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97108453 | |||||||
| chr5:97108602 | G | C | 1 | a0001c0001t0002g0235 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.247-1102C>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97108602 | |||||||
| chr5:97108634 | G | A | 2 | a0001c0001t0008g0099 a0001c0001t0008g0107 |
2 | HG01109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.247-1134C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97108634 | |||||||
| chr5:97108710 | C | T | 3 | a0001c0001t0001g0045 a0001c0001t0001g0256 a0001c0001t0002g0157 |
4 | HG02647.hp2 HG02809.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.247-1210G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97108710 | |||||||
| chr5:97108721 | G | A | 1 | a0001c0001t0001g0171 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.247-1221C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97108721 | |||||||
| chr5:97109056 | C | T | 4 | a0001c0002t0002g0189 a0001c0002t0002g0236 a0001c0002t0002g0237 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.247-1556G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97109056 | |||||||
| chr5:97109087 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.247-1587T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97109087 | |||||||
| chr5:97109190 | G | A | 93 | a0001c0001t0001g0149 a0001c0001t0001g0168 a0001c0001t0001g0171 others(90): Show |
124 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(121): Show |
intron_variant | MODIFIER | c.247-1690C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97109190 | |||||||
| chr5:97109320 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.247-1820G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97109320 | |||||||
| chr5:97109622 | A | G | 1 | a0001c0001t0007g0120 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.247-2122T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97109622 | |||||||
| chr5:97109638 | T | TTGCAGTG others(11): Show |
4 | a0001c0002t0002g0189 a0001c0002t0002g0236 a0001c0002t0002g0237 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.247-2139_247-2138i others(20): Show |
LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97109638 | |||||||
| chr5:97109662 | T | C | 22 | a0001c0001t0002g0224 a0001c0001t0002g0226 a0001c0001t0003g0018 others(19): Show |
26 | HG00642.hp1 HG02083.hp2 HG02155.hp2 others(23): Show |
intron_variant | MODIFIER | c.247-2162A>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97109662 | |||||||
| chr5:97109923 | T | C | 93 | a0001c0001t0001g0149 a0001c0001t0001g0168 a0001c0001t0001g0171 others(90): Show |
124 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(121): Show |
intron_variant | MODIFIER | c.247-2423A>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97109923 | |||||||
| chr5:97109957 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.247-2457T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97109957 | |||||||
| chr5:97109975 | G | A | 5 | a0001c0001t0002g0034 a0001c0001t0006g0035 a0001c0001t0006g0191 others(2): Show |
7 | HG02055.hp2 HG02451.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.247-2475C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97109975 | |||||||
| chr5:97109998 | G | A | 104 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0059 others(101): Show |
137 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(134): Show |
intron_variant | MODIFIER | c.247-2498C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97109998 | |||||||
| chr5:97110017 | C | T | 4 | a0001c0002t0002g0189 a0001c0002t0002g0236 a0001c0002t0002g0237 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.247-2517G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97110017 | |||||||
| chr5:97110055 | G | A | 4 | a0001c0002t0002g0189 a0001c0002t0002g0236 a0001c0002t0002g0237 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.247-2555C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97110055 | |||||||
| chr5:97110371 | G | C | 20 | a0001c0001t0002g0224 a0001c0001t0002g0226 a0001c0001t0003g0018 others(17): Show |
24 | HG00642.hp1 HG02083.hp2 HG02155.hp2 others(21): Show |
intron_variant | MODIFIER | c.247-2871C>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97110371 | |||||||
| chr5:97110387 | G | T | 1 | a0001c0001t0001g0103 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.247-2887C>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97110387 | |||||||
| chr5:97110400 | T | C | 1 | a0001c0001t0001g0096 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.247-2900A>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97110400 | |||||||
| chr5:97110421 | G | T | 8 | a0001c0001t0001g0125 a0001c0001t0008g0099 a0001c0001t0008g0107 others(5): Show |
8 | HG01109.hp1 HG01255.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.247-2921C>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97110421 | |||||||
| chr5:97110443 | T | A | 108 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0059 others(105): Show |
141 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(138): Show |
intron_variant | MODIFIER | c.247-2943A>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97110443 | |||||||
| chr5:97110477 | T | C | 1 | a0001c0001t0001g0056 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.247-2977A>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97110477 | |||||||
| chr5:97110484 | G | A | 1 | a0001c0001t0002g0172 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.247-2984C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97110484 | |||||||
| chr5:97110570 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.247-3070C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97110570 | |||||||
| chr5:97110585 | T | C | 1 | a0001c0001t0002g0173 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.247-3085A>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97110585 | |||||||
| chr5:97110624 | A | T | 1 | a0001c0001t0002g0127 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.247-3124T>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97110624 | |||||||
| chr5:97110691 | G | A | 128 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0059 others(125): Show |
165 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(162): Show |
intron_variant | MODIFIER | c.247-3191C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97110691 | |||||||
| chr5:97110769 | T | C | 20 | a0001c0001t0002g0224 a0001c0001t0002g0226 a0001c0001t0003g0018 others(17): Show |
24 | HG00642.hp1 HG02083.hp2 HG02155.hp2 others(21): Show |
intron_variant | MODIFIER | c.247-3269A>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97110769 | |||||||
| chr5:97110809 | A | G | 6 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0095 others(3): Show |
12 | HG00323.hp2 HG00733.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.247-3309T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97110809 | |||||||
| chr5:97111033 | C | A | 2 | a0001c0001t0001g0202 a0001c0001t0005g0201 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.247-3533G>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97111033 | |||||||
| chr5:97111146 | C | T | 3 | a0001c0001t0003g0018 a0001c0001t0003g0207 a0001c0001t0003g0228 |
5 | NA18947.hp2 NA18972.hp2 NA19006.hp2 others(2): Show |
intron_variant | MODIFIER | c.247-3646G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97111146 | |||||||
| chr5:97111278 | A | T | 4 | a0001c0001t0006g0035 a0001c0001t0006g0191 a0001c0001t0006g0205 others(1): Show |
5 | HG02451.hp1 HG02886.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.247-3778T>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97111278 | |||||||
| chr5:97111297 | C | T | 1 | a0001c0001t0001g0096 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.247-3797G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97111297 | |||||||
| chr5:97111347 | G | A | 4 | a0001c0001t0006g0035 a0001c0001t0006g0191 a0001c0001t0006g0205 others(1): Show |
5 | HG02451.hp1 HG02886.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.247-3847C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97111347 | |||||||
| chr5:97111418 | A | C | 22 | a0001c0001t0002g0224 a0001c0001t0002g0226 a0001c0001t0003g0018 others(19): Show |
26 | HG00642.hp1 HG02083.hp2 HG02155.hp2 others(23): Show |
intron_variant | MODIFIER | c.247-3918T>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97111418 | |||||||
| chr5:97111421 | A | C | 4 | a0001c0001t0006g0035 a0001c0001t0006g0191 a0001c0001t0006g0205 others(1): Show |
5 | HG02451.hp1 HG02886.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.247-3921T>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97111421 | |||||||
| chr5:97111453 | C | G | 4 | a0001c0001t0007g0117 a0001c0001t0007g0216 a0001c0001t0007g0249 others(1): Show |
4 | HG00738.hp2 HG01975.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.247-3953G>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97111453 | |||||||
| chr5:97111650 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.247-4150A>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97111650 | |||||||
| chr5:97111704 | G | A | 1 | a0001c0001t0008g0131 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.247-4204C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97111704 | |||||||
| chr5:97111836 | C | G | 4 | a0001c0001t0006g0035 a0001c0001t0006g0191 a0001c0001t0006g0205 others(1): Show |
5 | HG02451.hp1 HG02886.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.247-4336G>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97111836 | |||||||
| chr5:97111933 | G | A | 1 | a0001c0001t0001g0027 | 2 | HG01261.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.247-4433C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97111933 | |||||||
| chr5:97112096 | T | C | 3 | a0001c0001t0001g0021 a0001c0001t0001g0214 a0001c0001t0005g0091 |
4 | NA18963.hp1 NA18963.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.247-4596A>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97112096 | |||||||
| chr5:97112097 | G | T | 1 | a0001c0001t0015g0234 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.247-4597C>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97112097 | |||||||
| chr5:97112107 | C | T | 2 | a0001c0001t0002g0147 a0001c0001t0007g0120 |
2 | HG02486.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.247-4607G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97112107 | |||||||
| chr5:97112130 | T | C | 4 | a0001c0002t0002g0189 a0001c0002t0002g0236 a0001c0002t0002g0237 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.247-4630A>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97112130 | |||||||
| chr5:97112200 | A | G | 1 | a0001c0001t0001g0248 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.247-4700T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97112200 | |||||||
| chr5:97112233 | C | T | 4 | a0001c0001t0007g0117 a0001c0001t0007g0216 a0001c0001t0007g0249 others(1): Show |
4 | HG00738.hp2 HG01975.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.247-4733G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97112233 | |||||||
| chr5:97112269 | G | T | 1 | a0001c0001t0001g0021 | 2 | NA19009.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.247-4769C>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97112269 | |||||||
| chr5:97112592 | C | T | 4 | a0001c0001t0006g0035 a0001c0001t0006g0191 a0001c0001t0006g0205 others(1): Show |
5 | HG02451.hp1 HG02886.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.247-5092G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97112592 | |||||||
| chr5:97112630 | C | G | 4 | a0001c0001t0007g0117 a0001c0001t0007g0216 a0001c0001t0007g0249 others(1): Show |
4 | HG00738.hp2 HG01975.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.247-5130G>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97112630 | |||||||
| chr5:97112709 | T | G | 1 | a0001c0001t0002g0235 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.247-5209A>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97112709 | |||||||
| chr5:97112798 | TA | T | 11 | a0001c0001t0001g0043 a0001c0001t0001g0059 a0001c0001t0001g0077 others(8): Show |
12 | HG01070.hp2 HG01975.hp2 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.247-5299delT | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97112798 | |||||||
| chr5:97112798 | TAA | T | 12 | a0001c0001t0001g0042 a0001c0001t0001g0096 a0001c0001t0002g0038 others(9): Show |
14 | HG01255.hp2 HG01257.hp1 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.247-5300_247-5299d others(4): Show |
LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97112798 | |||||||
| chr5:97112798 | TAAA | T | 99 | a0001c0001t0001g0125 a0001c0001t0001g0149 a0001c0001t0001g0168 others(96): Show |
130 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(127): Show |
intron_variant | MODIFIER | c.247-5301_247-5299d others(5): Show |
LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97112798 | |||||||
| chr5:97112798 | TAAAA | T | 27 | a0001c0001t0002g0186 a0001c0001t0002g0224 a0001c0001t0002g0226 others(24): Show |
31 | HG00642.hp1 HG00738.hp2 HG01975.hp1 others(28): Show |
intron_variant | MODIFIER | c.247-5302_247-5299d others(6): Show |
LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97112798 | |||||||
| chr5:97113300 | C | G | 4 | a0001c0002t0002g0189 a0001c0002t0002g0236 a0001c0002t0002g0237 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.247-5800G>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97113300 | |||||||
| chr5:97113339 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.247-5839C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97113339 | |||||||
| chr5:97113521 | A | G | 4 | a0001c0002t0002g0189 a0001c0002t0002g0236 a0001c0002t0002g0237 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.247-6021T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97113521 | |||||||
| chr5:97113695 | G | A | 8 | a0001c0001t0001g0125 a0001c0001t0008g0099 a0001c0001t0008g0107 others(5): Show |
8 | HG01109.hp1 HG01255.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.247-6195C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97113695 | |||||||
| chr5:97113715 | C | T | 2 | a0001c0001t0001g0049 a0001c0001t0001g0085 |
2 | HG01074.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.247-6215G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97113715 | |||||||
| chr5:97113717 | C | G | 3 | a0001c0001t0001g0011 a0001c0001t0001g0076 a0001c0001t0005g0089 |
5 | NA18948.hp1 NA18954.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.247-6217G>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97113717 | |||||||
| chr5:97113733 | G | A | 94 | a0001c0001t0001g0149 a0001c0001t0001g0168 a0001c0001t0001g0171 others(91): Show |
125 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.247-6233C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97113733 | |||||||
| chr5:97113850 | C | T | 1 | a0001c0001t0001g0247 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.247-6350G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97113850 | |||||||
| chr5:97113879 | A | G | 1 | a0002c0003t0002g0152 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.247-6379T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97113879 | |||||||
| chr5:97113985 | C | A | 3 | a0001c0001t0001g0149 a0001c0001t0001g0190 a0001c0001t0002g0151 |
3 | HG01891.hp2 HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.247-6485G>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97113985 | |||||||
| chr5:97114018 | A | G | 22 | a0001c0001t0002g0224 a0001c0001t0002g0226 a0001c0001t0003g0018 others(19): Show |
26 | HG00642.hp1 HG02083.hp2 HG02155.hp2 others(23): Show |
intron_variant | MODIFIER | c.247-6518T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97114018 | |||||||
| chr5:97114260 | A | G | 7 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0059 others(4): Show |
9 | HG02258.hp2 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.247-6760T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97114260 | |||||||
| chr5:97114281 | T | C | 2 | a0001c0001t0001g0116 a0001c0001t0005g0115 |
2 | HG01069.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.247-6781A>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97114281 | |||||||
| chr5:97114325 | C | A | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.247-6825G>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97114325 | |||||||
| chr5:97114512 | C | T | 4 | a0001c0001t0006g0035 a0001c0001t0006g0191 a0001c0001t0006g0205 others(1): Show |
5 | HG02451.hp1 HG02886.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.247-7012G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97114512 | |||||||
| chr5:97114623 | T | C | 1 | a0001c0001t0001g0064 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.247-7123A>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97114623 | |||||||
| chr5:97114666 | C | T | 1 | a0001c0001t0012g0174 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.247-7166G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97114666 | |||||||
| chr5:97114738 | C | T | 1 | a0001c0001t0002g0146 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.247-7238G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97114738 | |||||||
| chr5:97114786 | C | T | 1 | a0001c0001t0007g0120 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.247-7286G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97114786 | |||||||
| chr5:97114809 | T | C | 2 | a0001c0001t0009g0050 a0001c0001t0009g0052 |
2 | HG00642.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.247-7309A>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97114809 | |||||||
| chr5:97114929 | A | G | 1 | a0001c0001t0002g0156 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.247-7429T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97114929 | |||||||
| chr5:97114996 | C | T | 1 | a0001c0001t0001g0109 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.247-7496G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97114996 | |||||||
| chr5:97115077 | C | T | 1 | a0001c0001t0001g0096 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.247-7577G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97115077 | |||||||
| chr5:97115361 | T | C | 1 | a0001c0001t0012g0174 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.247-7861A>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97115361 | |||||||
| chr5:97115525 | C | T | 22 | a0001c0001t0002g0224 a0001c0001t0002g0226 a0001c0001t0003g0018 others(19): Show |
26 | HG00642.hp1 HG02083.hp2 HG02155.hp2 others(23): Show |
intron_variant | MODIFIER | c.247-8025G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97115525 | |||||||
| chr5:97115590 | T | G | 8 | a0001c0001t0002g0031 a0001c0001t0002g0128 a0001c0001t0002g0133 others(5): Show |
9 | NA18947.hp1 NA18948.hp2 NA18949.hp2 others(6): Show |
intron_variant | MODIFIER | c.247-8090A>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97115590 | |||||||
| chr5:97115665 | T | C | 1 | a0001c0001t0022g0075 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.247-8165A>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97115665 | |||||||
| chr5:97115690 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.247-8190G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97115690 | |||||||
| chr5:97115703 | G | GTGCC | 4 | a0001c0002t0002g0189 a0001c0002t0002g0236 a0001c0002t0002g0237 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.247-8207_247-8204d others(6): Show |
LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97115703 | |||||||
| chr5:97115712 | A | G | 1 | a0001c0001t0002g0254 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.247-8212T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97115712 | |||||||
| chr5:97115713 | A | G | 22 | a0001c0001t0002g0224 a0001c0001t0002g0226 a0001c0001t0003g0018 others(19): Show |
26 | HG00642.hp1 HG02083.hp2 HG02155.hp2 others(23): Show |
intron_variant | MODIFIER | c.247-8213T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97115713 | |||||||
| chr5:97115756 | T | TA | 89 | a0001c0001t0001g0056 a0001c0001t0001g0149 a0001c0001t0001g0168 others(86): Show |
120 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(117): Show |
intron_variant | MODIFIER | c.247-8257dupT | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97115756 | |||||||
| chr5:97115771 | A | G | 1 | a0001c0001t0003g0223 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.247-8271T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97115771 | |||||||
| chr5:97116150 | C | T | 1 | a0001c0001t0001g0247 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.246+8316G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97116150 | |||||||
| chr5:97116184 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.246+8282C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97116184 | |||||||
| chr5:97116276 | A | G | 132 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0059 others(129): Show |
169 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(166): Show |
intron_variant | MODIFIER | c.246+8190T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97116276 | |||||||
| chr5:97116303 | G | A | 1 | a0001c0001t0007g0120 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.246+8163C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97116303 | |||||||
| chr5:97116347 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.246+8119G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97116347 | |||||||
| chr5:97116354 | A | G | 4 | a0001c0001t0007g0117 a0001c0001t0007g0216 a0001c0001t0007g0249 others(1): Show |
4 | HG00738.hp2 HG01975.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+8112T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97116354 | |||||||
| chr5:97116438 | G | C | 1 | a0001c0001t0004g0238 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.246+8028C>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97116438 | |||||||
| chr5:97116465 | A | G | 1 | a0001c0001t0002g0218 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.246+8001T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97116465 | |||||||
| chr5:97116503 | G | T | 4 | a0001c0001t0007g0117 a0001c0001t0007g0216 a0001c0001t0007g0249 others(1): Show |
4 | HG00738.hp2 HG01975.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+7963C>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97116503 | |||||||
| chr5:97116550 | A | G | 1 | a0001c0001t0002g0154 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.246+7916T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97116550 | |||||||
| chr5:97116641 | G | A | 136 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0059 others(133): Show |
174 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(171): Show |
intron_variant | MODIFIER | c.246+7825C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97116641 | |||||||
| chr5:97116798 | T | C | 4 | a0001c0001t0007g0117 a0001c0001t0007g0216 a0001c0001t0007g0249 others(1): Show |
4 | HG00738.hp2 HG01975.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+7668A>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97116798 | |||||||
| chr5:97116937 | G | C | 16 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0019 others(13): Show |
26 | HG02300.hp2 NA18943.hp1 NA18944.hp2 others(23): Show |
intron_variant | MODIFIER | c.246+7529C>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97116937 | |||||||
| chr5:97117036 | G | A | 1 | a0001c0001t0002g0226 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.246+7430C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97117036 | |||||||
| chr5:97117045 | T | C | 4 | a0001c0002t0002g0189 a0001c0002t0002g0236 a0001c0002t0002g0237 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+7421A>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97117045 | |||||||
| chr5:97117381 | C | T | 2 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
2 | HG03669.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.246+7085G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97117381 | |||||||
| chr5:97117601 | G | A | 146 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0042 others(143): Show |
186 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(183): Show |
intron_variant | MODIFIER | c.246+6865C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97117601 | |||||||
| chr5:97117779 | G | A | 1 | a0001c0001t0002g0175 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.246+6687C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97117779 | |||||||
| chr5:97117790 | C | T | 1 | a0001c0001t0003g0229 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.246+6676G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97117790 | |||||||
| chr5:97117814 | G | C | 4 | a0001c0001t0001g0003 a0001c0001t0001g0111 a0001c0001t0001g0244 others(1): Show |
12 | HG01255.hp1 HG01943.hp2 HG02148.hp1 others(9): Show |
intron_variant | MODIFIER | c.246+6652C>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97117814 | |||||||
| chr5:97117866 | C | T | 7 | a0001c0001t0008g0099 a0001c0001t0008g0107 a0001c0001t0008g0130 others(4): Show |
7 | HG01109.hp1 HG01255.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.246+6600G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97117866 | |||||||
| chr5:97117921 | GAA | G | 140 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0042 others(137): Show |
179 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(176): Show |
intron_variant | MODIFIER | c.246+6543_246+6544d others(4): Show |
LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97117921 | |||||||
| chr5:97117921 | GAAA | G | 6 | a0001c0001t0003g0039 a0001c0001t0003g0219 a0001c0002t0002g0189 others(3): Show |
7 | HG01884.hp2 HG01891.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.246+6542_246+6544d others(5): Show |
LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97117921 | |||||||
| chr5:97117925 | A | G | 2 | a0001c0001t0008g0259 a0001c0001t0015g0234 |
2 | HG01255.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.246+6541T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97117925 | |||||||
| chr5:97117984 | T | C | 4 | a0001c0001t0006g0035 a0001c0001t0006g0191 a0001c0001t0006g0205 others(1): Show |
5 | HG02451.hp1 HG02886.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.246+6482A>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97117984 | |||||||
| chr5:97118240 | C | G | 4 | a0001c0002t0002g0189 a0001c0002t0002g0236 a0001c0002t0002g0237 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+6226G>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97118240 | |||||||
| chr5:97118250 | C | T | 137 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0042 others(134): Show |
176 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(173): Show |
intron_variant | MODIFIER | c.246+6216G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97118250 | |||||||
| chr5:97118365 | AATAAG | A | 20 | a0001c0001t0002g0224 a0001c0001t0002g0226 a0001c0001t0003g0018 others(17): Show |
24 | HG00642.hp1 HG02083.hp2 HG02155.hp2 others(21): Show |
intron_variant | MODIFIER | c.246+6096_246+6100d others(7): Show |
LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97118365 | |||||||
| chr5:97118500 | T | TA | 34 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(31): Show |
52 | HG00323.hp2 HG00733.hp1 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.246+5965dupT | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97118500 | |||||||
| chr5:97118627 | G | A | 4 | a0001c0002t0002g0189 a0001c0002t0002g0236 a0001c0002t0002g0237 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+5839C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97118627 | |||||||
| chr5:97118698 | A | C | 1 | a0001c0001t0002g0033 | 2 | NA18943.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.246+5768T>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97118698 | |||||||
| chr5:97118701 | T | A | 4 | a0001c0002t0002g0189 a0001c0002t0002g0236 a0001c0002t0002g0237 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+5765A>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97118701 | |||||||
| chr5:97118820 | G | T | 1 | a0001c0001t0001g0096 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.246+5646C>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97118820 | |||||||
| chr5:97118824 | G | T | 1 | a0001c0001t0007g0250 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.246+5642C>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97118824 | |||||||
| chr5:97118892 | T | C | 1 | a0001c0001t0022g0075 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.246+5574A>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97118892 | |||||||
| chr5:97118931 | T | G | 1 | a0001c0001t0003g0227 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.246+5535A>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97118931 | |||||||
| chr5:97119043 | T | G | 1 | a0001c0001t0002g0034 | 2 | HG02055.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.246+5423A>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97119043 | |||||||
| chr5:97119070 | G | A | 1 | a0001c0001t0002g0041 | 2 | HG02572.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.246+5396C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97119070 | |||||||
| chr5:97119085 | C | T | 1 | a0001c0001t0001g0241 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.246+5381G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97119085 | |||||||
| chr5:97119117 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.246+5349T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97119117 | |||||||
| chr5:97119199 | G | A | 1 | a0001c0001t0008g0107 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.246+5267C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97119199 | |||||||
| chr5:97119270 | G | A | 1 | a0001c0001t0001g0242 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.246+5196C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97119270 | |||||||
| chr5:97119474 | C | G | 7 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0059 others(4): Show |
9 | HG02258.hp2 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.246+4992G>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97119474 | |||||||
| chr5:97119831 | A | G | 1 | a0001c0001t0001g0096 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.246+4635T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97119831 | |||||||
| chr5:97120032 | C | T | 6 | a0001c0001t0007g0117 a0001c0001t0007g0216 a0001c0001t0007g0249 others(3): Show |
6 | HG00738.hp2 HG01975.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.246+4434G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97120032 | |||||||
| chr5:97120274 | T | A | 1 | a0001c0001t0001g0245 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.246+4192A>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97120274 | |||||||
| chr5:97120326 | G | A | 3 | a0001c0001t0001g0177 a0001c0001t0002g0150 a0001c0001t0002g0176 |
3 | HG01928.hp2 HG02004.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.246+4140C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97120326 | |||||||
| chr5:97120367 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.246+4099T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97120367 | |||||||
| chr5:97120453 | C | T | 138 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0042 others(135): Show |
177 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(174): Show |
intron_variant | MODIFIER | c.246+4013G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97120453 | |||||||
| chr5:97120635 | T | A | 1 | a0001c0001t0004g0200 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.246+3831A>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97120635 | |||||||
| chr5:97120730 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.246+3736C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97120730 | |||||||
| chr5:97120826 | C | A | 1 | a0001c0001t0006g0206 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.246+3640G>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97120826 | |||||||
| chr5:97121120 | T | C | 4 | a0001c0002t0002g0189 a0001c0002t0002g0236 a0001c0002t0002g0237 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+3346A>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97121120 | |||||||
| chr5:97121679 | A | G | 4 | a0001c0002t0002g0189 a0001c0002t0002g0236 a0001c0002t0002g0237 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+2787T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97121679 | |||||||
| chr5:97122017 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.246+2449G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97122017 | |||||||
| chr5:97122059 | C | T | 1 | a0001c0001t0001g0096 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.246+2407G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97122059 | |||||||
| chr5:97122179 | C | A | 2 | a0001c0001t0002g0178 a0001c0001t0002g0185 |
2 | NA19063.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.246+2287G>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97122179 | |||||||
| chr5:97122274 | A | G | 1 | a0001c0001t0020g0260 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.246+2192T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97122274 | |||||||
| chr5:97122284 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.246+2182C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97122284 | |||||||
| chr5:97122379 | C | T | 1 | a0001c0001t0001g0096 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.246+2087G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97122379 | |||||||
| chr5:97122560 | T | A | 1 | a0001c0001t0003g0228 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.246+1906A>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97122560 | |||||||
| chr5:97122711 | A | T | 1 | a0001c0001t0002g0153 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.246+1755T>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97122711 | |||||||
| chr5:97122836 | T | C | 1 | a0001c0001t0002g0151 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.246+1630A>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97122836 | |||||||
| chr5:97122978 | T | C | 1 | a0001c0001t0004g0246 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.246+1488A>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97122978 | |||||||
| chr5:97123115 | T | C | 1 | a0001c0001t0001g0109 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.246+1351A>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97123115 | |||||||
| chr5:97123211 | G | A | 1 | a0001c0002t0002g0237 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.246+1255C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97123211 | |||||||
| chr5:97123290 | G | T | 1 | a0001c0002t0002g0236 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.246+1176C>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97123290 | |||||||
| chr5:97123294 | G | A | 1 | a0001c0001t0003g0229 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.246+1172C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97123294 | |||||||
| chr5:97123359 | C | T | 1 | a0001c0001t0018g0188 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.246+1107G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97123359 | |||||||
| chr5:97123381 | C | T | 1 | a0001c0001t0018g0188 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.246+1085G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97123381 | |||||||
| chr5:97123540 | C | T | 1 | a0002c0003t0002g0152 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.246+926G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97123540 | |||||||
| chr5:97123604 | G | A | 4 | a0001c0001t0007g0120 a0001c0001t0008g0130 a0001c0001t0008g0131 others(1): Show |
4 | HG01884.hp1 HG02486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+862C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97123604 | |||||||
| chr5:97123605 | A | C | 4 | a0001c0001t0007g0117 a0001c0001t0007g0216 a0001c0001t0007g0249 others(1): Show |
4 | HG00738.hp2 HG01975.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+861T>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97123605 | |||||||
| chr5:97123701 | C | A | 1 | a0001c0001t0001g0027 | 2 | HG01261.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.246+765G>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97123701 | |||||||
| chr5:97123738 | C | T | 2 | a0001c0001t0001g0045 a0001c0001t0001g0256 |
3 | HG02647.hp2 HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.246+728G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97123738 | |||||||
| chr5:97123804 | G | A | 1 | a0001c0001t0004g0200 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.246+662C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97123804 | |||||||
| chr5:97123969 | C | T | 4 | a0001c0001t0007g0117 a0001c0001t0007g0216 a0001c0001t0007g0249 others(1): Show |
4 | HG00738.hp2 HG01975.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+497G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97123969 | |||||||
| chr5:97124067 | A | G | 1 | a0001c0001t0003g0231 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.246+399T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97124067 | |||||||
| chr5:97124092 | C | T | 2 | a0001c0001t0001g0053 a0001c0001t0001g0210 |
2 | HG02698.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.246+374G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97124092 | |||||||
| chr5:97124251 | G | T | 1 | a0001c0001t0001g0209 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.246+215C>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97124251 | |||||||
| chr5:97124450 | A | T | 1 | a0001c0001t0001g0084 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.246+16T>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 2/5 | chr5 | 97124450 | |||||||
| chr5:97124862 | G | A | 4 | a0001c0001t0001g0020 a0001c0001t0001g0047 a0001c0001t0001g0066 others(1): Show |
5 | HG00741.hp1 HG01099.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.83-233C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97124862 | |||||||
| chr5:97124880 | G | A | 139 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0042 others(136): Show |
179 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(176): Show |
intron_variant | MODIFIER | c.83-251C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97124880 | |||||||
| chr5:97124885 | G | T | 1 | a0001c0001t0009g0071 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.83-256C>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97124885 | |||||||
| chr5:97124928 | G | A | 1 | a0001c0001t0002g0179 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.83-299C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97124928 | |||||||
| chr5:97125018 | A | T | 4 | a0001c0001t0007g0117 a0001c0001t0007g0216 a0001c0001t0007g0249 others(1): Show |
4 | HG00738.hp2 HG01975.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.83-389T>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97125018 | |||||||
| chr5:97125268 | C | T | 7 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0059 others(4): Show |
9 | HG02258.hp2 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.83-639G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97125268 | |||||||
| chr5:97125666 | G | C | 2 | a0001c0001t0001g0045 a0001c0001t0001g0256 |
3 | HG02647.hp2 HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.83-1037C>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97125666 | |||||||
| chr5:97125830 | T | C | 4 | a0001c0002t0002g0189 a0001c0002t0002g0236 a0001c0002t0002g0237 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.83-1201A>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97125830 | |||||||
| chr5:97125867 | G | A | 2 | a0001c0001t0002g0180 a0001c0001t0002g0181 |
2 | HG02071.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.83-1238C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97125867 | |||||||
| chr5:97125960 | A | C | 4 | a0001c0002t0002g0189 a0001c0002t0002g0236 a0001c0002t0002g0237 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.83-1331T>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97125960 | |||||||
| chr5:97126134 | T | A | 13 | a0001c0001t0001g0096 a0001c0001t0002g0118 a0001c0001t0007g0117 others(10): Show |
13 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.83-1505A>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97126134 | |||||||
| chr5:97126265 | C | A | 1 | a0001c0001t0009g0048 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.83-1636G>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97126265 | |||||||
| chr5:97126540 | G | A | 195 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(192): Show |
256 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(253): Show |
intron_variant | MODIFIER | c.83-1911C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97126540 | |||||||
| chr5:97126637 | C | CT | 31 | a0001c0001t0001g0081 a0001c0001t0001g0149 a0001c0001t0001g0190 others(28): Show |
33 | HG01496.hp1 HG01891.hp2 HG01928.hp2 others(30): Show |
intron_variant | MODIFIER | c.83-2009dupA | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97126637 | |||||||
| chr5:97126637 | CT | C | 8 | a0001c0001t0001g0062 a0001c0001t0007g0117 a0001c0001t0007g0120 others(5): Show |
8 | HG00738.hp2 HG01169.hp2 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.83-2009delA | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97126637 | |||||||
| chr5:97126641 | T | C | 2 | a0001c0001t0001g0096 a0001c0001t0001g0242 |
2 | HG01243.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.83-2012A>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97126641 | |||||||
| chr5:97126679 | G | A | 1 | a0001c0001t0002g0046 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.83-2050C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97126679 | |||||||
| chr5:97126693 | G | A | 4 | a0001c0002t0002g0189 a0001c0002t0002g0236 a0001c0002t0002g0237 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.83-2064C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97126693 | |||||||
| chr5:97126709 | G | A | 1 | a0001c0001t0007g0250 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.83-2080C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97126709 | |||||||
| chr5:97126891 | G | A | 1 | a0001c0001t0009g0052 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.83-2262C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97126891 | |||||||
| chr5:97126892 | C | T | 1 | a0001c0001t0009g0052 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.83-2263G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97126892 | |||||||
| chr5:97126913 | C | T | 1 | a0001c0001t0009g0050 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.83-2284G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97126913 | |||||||
| chr5:97127093 | T | A | 1 | a0001c0001t0002g0183 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.83-2464A>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97127093 | |||||||
| chr5:97127335 | A | G | 149 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0042 others(146): Show |
189 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(186): Show |
intron_variant | MODIFIER | c.83-2706T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97127335 | |||||||
| chr5:97127515 | C | A | 1 | a0001c0001t0001g0204 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.83-2886G>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97127515 | |||||||
| chr5:97127515 | C | T | 24 | a0001c0001t0001g0217 a0001c0001t0002g0038 a0001c0001t0002g0055 others(21): Show |
29 | HG00140.hp1 HG00642.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.83-2886G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97127515 | |||||||
| chr5:97127520 | C | T | 1 | a0001c0001t0002g0041 | 2 | HG02572.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.83-2891G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97127520 | |||||||
| chr5:97127521 | A | G | 149 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0042 others(146): Show |
189 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(186): Show |
intron_variant | MODIFIER | c.83-2892T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97127521 | |||||||
| chr5:97127563 | G | A | 1 | a0001c0001t0002g0135 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.83-2934C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97127563 | |||||||
| chr5:97127566 | G | A | 4 | a0001c0001t0007g0117 a0001c0001t0007g0216 a0001c0001t0007g0249 others(1): Show |
4 | HG00738.hp2 HG01975.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.83-2937C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97127566 | |||||||
| chr5:97127731 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.83-3102C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97127731 | |||||||
| chr5:97127794 | G | A | 4 | a0001c0001t0007g0117 a0001c0001t0007g0216 a0001c0001t0007g0249 others(1): Show |
4 | HG00738.hp2 HG01975.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.83-3165C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97127794 | |||||||
| chr5:97127831 | G | A | 1 | a0001c0001t0002g0041 | 2 | HG02572.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.83-3202C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97127831 | |||||||
| chr5:97127847 | T | A | 10 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0059 others(7): Show |
12 | HG01255.hp2 HG02258.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.83-3218A>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97127847 | |||||||
| chr5:97127879 | G | T | 1 | a0001c0001t0002g0145 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.83-3250C>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97127879 | |||||||
| chr5:97128076 | G | A | 4 | a0001c0002t0002g0189 a0001c0002t0002g0236 a0001c0002t0002g0237 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.83-3447C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97128076 | |||||||
| chr5:97128275 | T | C | 1 | a0001c0001t0001g0240 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.83-3646A>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97128275 | |||||||
| chr5:97128582 | T | C | 4 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0258 others(1): Show |
6 | HG02258.hp2 HG02647.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.83-3953A>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97128582 | |||||||
| chr5:97128764 | A | G | 2 | a0001c0001t0010g0079 a0001c0001t0010g0080 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.83-4135T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97128764 | |||||||
| chr5:97128841 | G | T | 1 | a0001c0001t0002g0144 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.83-4212C>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97128841 | |||||||
| chr5:97128929 | C | T | 1 | a0001c0001t0003g0231 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.83-4300G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97128929 | |||||||
| chr5:97128956 | C | T | 1 | a0001c0001t0001g0022 | 2 | HG03927.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.83-4327G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97128956 | |||||||
| chr5:97129016 | T | C | 1 | a0001c0001t0001g0090 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.83-4387A>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97129016 | |||||||
| chr5:97129174 | C | G | 124 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0047 others(121): Show |
161 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(158): Show |
intron_variant | MODIFIER | c.83-4545G>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97129174 | |||||||
| chr5:97129393 | C | T | 1 | a0001c0001t0001g0241 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.83-4764G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97129393 | |||||||
| chr5:97129525 | A | G | 1 | a0001c0001t0003g0221 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.83-4896T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97129525 | |||||||
| chr5:97129669 | G | A | 8 | a0001c0001t0001g0096 a0001c0001t0002g0118 a0001c0001t0007g0117 others(5): Show |
8 | HG00738.hp2 HG01496.hp1 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.83-5040C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97129669 | |||||||
| chr5:97129674 | A | G | 1 | a0001c0001t0004g0257 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.83-5045T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97129674 | |||||||
| chr5:97129677 | A | G | 1 | a0001c0001t0001g0096 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.83-5048T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97129677 | |||||||
| chr5:97129729 | T | C | 1 | a0001c0001t0003g0231 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.83-5100A>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97129729 | |||||||
| chr5:97129859 | T | C | 1 | a0001c0001t0002g0136 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.83-5230A>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97129859 | |||||||
| chr5:97129919 | C | T | 140 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0042 others(137): Show |
180 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(177): Show |
intron_variant | MODIFIER | c.83-5290G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97129919 | |||||||
| chr5:97129986 | A | G | 4 | a0001c0002t0002g0189 a0001c0002t0002g0236 a0001c0002t0002g0237 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.83-5357T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97129986 | |||||||
| chr5:97130167 | C | A | 4 | a0001c0001t0007g0117 a0001c0001t0007g0216 a0001c0001t0007g0249 others(1): Show |
4 | HG00738.hp2 HG01975.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.83-5538G>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97130167 | |||||||
| chr5:97130211 | G | C | 1 | a0001c0001t0001g0096 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.83-5582C>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97130211 | |||||||
| chr5:97130240 | G | C | 3 | a0001c0001t0006g0035 a0001c0001t0006g0205 a0001c0001t0006g0206 |
4 | HG02451.hp1 HG02886.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.83-5611C>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97130240 | |||||||
| chr5:97130249 | C | T | 6 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0077 others(3): Show |
12 | HG02300.hp2 NA18943.hp1 NA18946.hp2 others(9): Show |
intron_variant | MODIFIER | c.83-5620G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97130249 | |||||||
| chr5:97130446 | C | T | 139 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0042 others(136): Show |
179 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(176): Show |
intron_variant | MODIFIER | c.83-5817G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97130446 | |||||||
| chr5:97130536 | A | G | 1 | a0001c0001t0007g0120 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.83-5907T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97130536 | |||||||
| chr5:97130912 | C | T | 140 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0042 others(137): Show |
180 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(177): Show |
intron_variant | MODIFIER | c.83-6283G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97130912 | |||||||
| chr5:97131061 | C | T | 1 | a0001c0001t0002g0054 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.83-6432G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97131061 | |||||||
| chr5:97131236 | CAT | C | 10 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0059 others(7): Show |
12 | HG01255.hp2 HG02258.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.83-6609_83-6608del others(2): Show |
LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97131236 | |||||||
| chr5:97131237 | A | T | 1 | a0001c0001t0001g0096 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.83-6608T>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97131237 | |||||||
| chr5:97131302 | T | C | 1 | a0001c0002t0002g0237 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.83-6673A>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97131302 | |||||||
| chr5:97131499 | T | C | 10 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0059 others(7): Show |
12 | HG01255.hp2 HG02258.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.83-6870A>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97131499 | |||||||
| chr5:97131549 | CT | C | 139 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0042 others(136): Show |
179 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(176): Show |
intron_variant | MODIFIER | c.83-6921delA | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97131549 | |||||||
| chr5:97131693 | C | A | 1 | a0001c0001t0018g0188 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.83-7064G>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97131693 | |||||||
| chr5:97132052 | G | T | 152 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0042 others(149): Show |
192 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(189): Show |
intron_variant | MODIFIER | c.83-7423C>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97132052 | |||||||
| chr5:97132130 | C | T | 4 | a0001c0002t0002g0189 a0001c0002t0002g0236 a0001c0002t0002g0237 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.83-7501G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97132130 | |||||||
| chr5:97132154 | C | T | 1 | a0001c0001t0002g0143 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.83-7525G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97132154 | |||||||
| chr5:97132408 | G | A | 1 | a0001c0001t0001g0022 | 2 | HG03927.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.83-7779C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97132408 | |||||||
| chr5:97132504 | A | G | 1 | a0001c0001t0002g0220 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.83-7875T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97132504 | |||||||
| chr5:97132531 | C | A | 2 | a0001c0001t0001g0045 a0001c0001t0001g0256 |
3 | HG02647.hp2 HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.83-7902G>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97132531 | |||||||
| chr5:97132620 | C | T | 1 | a0001c0001t0001g0023 | 2 | NA18983.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.83-7991G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97132620 | |||||||
| chr5:97132685 | C | T | 1 | a0001c0001t0003g0219 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.83-8056G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97132685 | |||||||
| chr5:97132821 | T | C | 1 | a0001c0001t0006g0191 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.83-8192A>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97132821 | |||||||
| chr5:97133450 | A | T | 1 | a0001c0001t0001g0256 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.83-8821T>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97133450 | |||||||
| chr5:97133474 | T | C | 1 | a0001c0001t0009g0052 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.83-8845A>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97133474 | |||||||
| chr5:97133485 | C | T | 12 | a0001c0001t0001g0096 a0001c0001t0002g0118 a0001c0001t0007g0117 others(9): Show |
12 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.83-8856G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97133485 | |||||||
| chr5:97133520 | T | A | 162 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0022 others(159): Show |
205 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(202): Show |
intron_variant | MODIFIER | c.83-8891A>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97133520 | |||||||
| chr5:97133669 | G | C | 13 | a0001c0001t0001g0096 a0001c0001t0002g0118 a0001c0001t0007g0117 others(10): Show |
13 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.82+8826C>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97133669 | |||||||
| chr5:97133816 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.82+8679C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97133816 | |||||||
| chr5:97133882 | C | T | 2 | a0001c0001t0011g0015 a0001c0001t0011g0142 |
4 | NA18953.hp2 NA18971.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.82+8613G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97133882 | |||||||
| chr5:97133896 | A | G | 1 | a0001c0001t0018g0188 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.82+8599T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97133896 | |||||||
| chr5:97134043 | C | A | 1 | a0001c0001t0002g0127 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.82+8452G>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97134043 | |||||||
| chr5:97134044 | T | C | 13 | a0001c0001t0001g0096 a0001c0001t0002g0118 a0001c0001t0007g0117 others(10): Show |
13 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.82+8451A>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97134044 | |||||||
| chr5:97134120 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.82+8375G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97134120 | |||||||
| chr5:97134139 | A | G | 1 | a0001c0001t0007g0120 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.82+8356T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97134139 | |||||||
| chr5:97134236 | C | T | 1 | a0001c0001t0002g0141 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.82+8259G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97134236 | |||||||
| chr5:97134307 | G | A | 13 | a0001c0001t0001g0096 a0001c0001t0002g0118 a0001c0001t0007g0117 others(10): Show |
13 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.82+8188C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97134307 | |||||||
| chr5:97134366 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.82+8129G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97134366 | |||||||
| chr5:97134419 | A | C | 145 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0042 others(142): Show |
185 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(182): Show |
intron_variant | MODIFIER | c.82+8076T>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97134419 | |||||||
| chr5:97134562 | A | G | 1 | a0001c0001t0001g0096 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.82+7933T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97134562 | |||||||
| chr5:97134565 | A | G | 1 | a0001c0001t0002g0140 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.82+7930T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97134565 | |||||||
| chr5:97134694 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.82+7801C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97134694 | |||||||
| chr5:97134696 | A | T | 2 | a0001c0001t0002g0068 a0001c0001t0002g0139 |
2 | NA18977.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.82+7799T>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97134696 | |||||||
| chr5:97134723 | T | G | 1 | a0001c0001t0001g0111 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.82+7772A>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97134723 | |||||||
| chr5:97134882 | A | G | 1 | a0001c0001t0001g0258 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.82+7613T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97134882 | |||||||
| chr5:97135044 | T | C | 4 | a0001c0002t0002g0189 a0001c0002t0002g0236 a0001c0002t0002g0237 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.82+7451A>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97135044 | |||||||
| chr5:97135556 | C | T | 1 | a0001c0001t0007g0120 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.82+6939G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97135556 | |||||||
| chr5:97135595 | G | C | 1 | a0001c0001t0001g0215 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.82+6900C>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97135595 | |||||||
| chr5:97135693 | C | T | 4 | a0001c0001t0007g0117 a0001c0001t0007g0216 a0001c0001t0007g0249 others(1): Show |
4 | HG00738.hp2 HG01975.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.82+6802G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97135693 | |||||||
| chr5:97135806 | G | A | 1 | a0001c0001t0007g0120 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.82+6689C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97135806 | |||||||
| chr5:97135873 | A | G | 4 | a0001c0001t0007g0117 a0001c0001t0007g0216 a0001c0001t0007g0249 others(1): Show |
4 | HG00738.hp2 HG01975.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.82+6622T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97135873 | |||||||
| chr5:97136161 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.82+6334A>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97136161 | |||||||
| chr5:97136195 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.82+6300C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97136195 | |||||||
| chr5:97136286 | C | G | 1 | a0001c0001t0003g0037 | 2 | HG00642.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.82+6209G>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97136286 | |||||||
| chr5:97136297 | C | G | 1 | a0001c0001t0002g0138 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.82+6198G>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97136297 | |||||||
| chr5:97136360 | G | T | 4 | a0001c0001t0007g0117 a0001c0001t0007g0216 a0001c0001t0007g0249 others(1): Show |
4 | HG00738.hp2 HG01975.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.82+6135C>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97136360 | |||||||
| chr5:97136429 | C | A | 6 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(3): Show |
7 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.82+6066G>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97136429 | |||||||
| chr5:97136493 | T | C | 164 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0022 others(161): Show |
207 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(204): Show |
intron_variant | MODIFIER | c.82+6002A>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97136493 | |||||||
| chr5:97136606 | A | G | 1 | a0001c0001t0001g0096 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.82+5889T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97136606 | |||||||
| chr5:97136637 | T | C | 1 | a0001c0001t0007g0120 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.82+5858A>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97136637 | |||||||
| chr5:97136638 | A | G | 1 | a0001c0001t0004g0192 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.82+5857T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97136638 | |||||||
| chr5:97136756 | G | A | 4 | a0001c0002t0002g0189 a0001c0002t0002g0236 a0001c0002t0002g0237 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.82+5739C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97136756 | |||||||
| chr5:97136904 | T | A | 2 | a0001c0001t0002g0118 a0001c0001t0020g0260 |
2 | HG01496.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.82+5591A>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97136904 | |||||||
| chr5:97136950 | T | G | 1 | a0001c0001t0005g0091 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.82+5545A>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97136950 | |||||||
| chr5:97137137 | C | T | 1 | a0001c0001t0007g0120 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.82+5358G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97137137 | |||||||
| chr5:97137204 | AACAGCAA others(4): Show |
A | 1 | a0001c0001t0002g0034 | 2 | HG02055.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.82+5280_82+5290del others(11): Show |
LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97137204 | |||||||
| chr5:97137219 | C | A | 1 | a0001c0001t0001g0242 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.82+5276G>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97137219 | |||||||
| chr5:97137366 | G | A | 9 | a0001c0001t0001g0012 a0001c0001t0001g0045 a0001c0001t0001g0063 others(6): Show |
12 | HG01243.hp2 HG02630.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.82+5129C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97137366 | |||||||
| chr5:97137602 | G | C | 1 | a0001c0001t0001g0243 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.82+4893C>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97137602 | |||||||
| chr5:97137720 | G | A | 25 | a0001c0001t0001g0217 a0001c0001t0002g0038 a0001c0001t0002g0055 others(22): Show |
30 | HG00140.hp1 HG00642.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.82+4775C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97137720 | |||||||
| chr5:97137757 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.82+4738C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97137757 | |||||||
| chr5:97138162 | C | A | 1 | a0001c0001t0001g0096 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.82+4333G>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97138162 | |||||||
| chr5:97138247 | C | T | 1 | a0001c0001t0002g0137 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.82+4248G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97138247 | |||||||
| chr5:97138520 | C | A | 1 | a0001c0001t0002g0127 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.82+3975G>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97138520 | |||||||
| chr5:97138580 | C | A | 2 | a0001c0001t0002g0185 a0001c0001t0002g0235 |
2 | NA18967.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.82+3915G>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97138580 | |||||||
| chr5:97138625 | T | C | 4 | a0001c0001t0002g0044 a0001c0001t0002g0186 a0001c0001t0002g0187 others(1): Show |
5 | HG00741.hp2 HG02965.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.82+3870A>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97138625 | |||||||
| chr5:97138655 | A | G | 8 | a0001c0001t0002g0031 a0001c0001t0002g0128 a0001c0001t0002g0133 others(5): Show |
9 | NA18947.hp1 NA18948.hp2 NA18949.hp2 others(6): Show |
intron_variant | MODIFIER | c.82+3840T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97138655 | |||||||
| chr5:97138789 | C | T | 1 | a0001c0001t0001g0076 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.82+3706G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97138789 | |||||||
| chr5:97138861 | A | G | 2 | a0001c0001t0001g0047 a0001c0001t0001g0066 |
2 | HG00741.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.82+3634T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97138861 | |||||||
| chr5:97138880 | T | G | 1 | a0001c0001t0002g0034 | 2 | HG02055.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.82+3615A>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97138880 | |||||||
| chr5:97138928 | T | C | 3 | a0001c0001t0008g0130 a0001c0001t0008g0131 a0001c0001t0015g0129 |
3 | HG01884.hp1 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.82+3567A>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97138928 | |||||||
| chr5:97139005 | AT | A | 6 | a0001c0001t0001g0019 a0001c0001t0007g0117 a0001c0001t0007g0216 others(3): Show |
8 | HG00738.hp2 HG01975.hp1 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.82+3489delA | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97139005 | |||||||
| chr5:97139306 | A | G | 1 | a0001c0001t0001g0096 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.82+3189T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97139306 | |||||||
| chr5:97139323 | T | C | 12 | a0001c0001t0001g0019 a0001c0001t0001g0096 a0001c0001t0007g0117 others(9): Show |
14 | HG00738.hp2 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.82+3172A>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97139323 | |||||||
| chr5:97139475 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.82+3020C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97139475 | |||||||
| chr5:97139596 | A | G | 1 | a0001c0001t0001g0096 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.82+2899T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97139596 | |||||||
| chr5:97139755 | T | C | 2 | a0001c0001t0001g0190 a0001c0001t0006g0191 |
2 | HG01891.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.82+2740A>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97139755 | |||||||
| chr5:97139938 | T | C | 1 | a0001c0001t0001g0022 | 2 | HG03927.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.82+2557A>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97139938 | |||||||
| chr5:97140399 | C | G | 1 | a0001c0001t0002g0119 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.82+2096G>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97140399 | |||||||
| chr5:97140415 | G | A | 1 | a0001c0001t0001g0056 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.82+2080C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97140415 | |||||||
| chr5:97140431 | C | G | 150 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(147): Show |
191 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(188): Show |
intron_variant | MODIFIER | c.82+2064G>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97140431 | |||||||
| chr5:97140534 | A | G | 3 | a0001c0001t0008g0130 a0001c0001t0008g0131 a0001c0001t0015g0129 |
3 | HG01884.hp1 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.82+1961T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97140534 | |||||||
| chr5:97140804 | G | A | 6 | a0001c0001t0001g0019 a0001c0001t0007g0117 a0001c0001t0007g0216 others(3): Show |
8 | HG00738.hp2 HG01975.hp1 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.82+1691C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97140804 | |||||||
| chr5:97140830 | C | T | 4 | a0001c0001t0007g0117 a0001c0001t0007g0216 a0001c0001t0007g0249 others(1): Show |
4 | HG00738.hp2 HG01975.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.82+1665G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97140830 | |||||||
| chr5:97141041 | A | G | 9 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0059 others(6): Show |
11 | HG01496.hp1 HG02258.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.82+1454T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97141041 | |||||||
| chr5:97141118 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.82+1377C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97141118 | |||||||
| chr5:97141127 | A | G | 1 | a0001c0001t0010g0065 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.82+1368T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97141127 | |||||||
| chr5:97141127 | AT | A | 46 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0013 others(43): Show |
74 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.82+1367delA | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97141127 | |||||||
| chr5:97141170 | G | T | 1 | a0001c0001t0002g0128 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.82+1325C>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97141170 | |||||||
| chr5:97141252 | T | C | 1 | a0001c0001t0001g0029 | 2 | NA19070.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.82+1243A>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97141252 | |||||||
| chr5:97141281 | T | C | 6 | a0001c0001t0001g0019 a0001c0001t0007g0117 a0001c0001t0007g0216 others(3): Show |
8 | HG00738.hp2 HG01975.hp1 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.82+1214A>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97141281 | |||||||
| chr5:97141412 | A | C | 1 | a0001c0001t0001g0064 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.82+1083T>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97141412 | |||||||
| chr5:97141497 | A | G | 45 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0059 others(42): Show |
53 | HG00140.hp1 HG00621.hp1 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.82+998T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97141497 | |||||||
| chr5:97141528 | T | C | 1 | a0001c0001t0001g0258 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.82+967A>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97141528 | |||||||
| chr5:97141557 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.82+938G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97141557 | |||||||
| chr5:97141616 | A | AT | 84 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(81): Show |
137 | HG00099.hp1 HG00323.hp2 HG00609.hp1 others(134): Show |
intron_variant | MODIFIER | c.82+878_82+879insA | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97141616 | |||||||
| chr5:97141617 | C | T | 212 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(209): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(296): Show |
intron_variant | MODIFIER | c.82+878G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97141617 | |||||||
| chr5:97141873 | A | C | 1 | a0001c0001t0003g0058 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.82+622T>G | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97141873 | |||||||
| chr5:97141898 | C | T | 1 | a0001c0001t0002g0008 | 3 | NA18942.hp2 NA18978.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.82+597G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97141898 | |||||||
| chr5:97141906 | A | G | 1 | a0001c0001t0004g0057 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.82+589T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97141906 | |||||||
| chr5:97142105 | T | A | 1 | a0001c0001t0002g0041 | 2 | HG02572.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.82+390A>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97142105 | |||||||
| chr5:97142297 | A | G | 10 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0001g0053 others(7): Show |
10 | HG00642.hp2 HG00735.hp2 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.82+198T>C | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97142297 | |||||||
| chr5:97142298 | G | A | 12 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0045 others(9): Show |
16 | HG00741.hp2 HG01255.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.82+197C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97142298 | |||||||
| chr5:97142397 | G | A | 1 | a0001c0001t0020g0260 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.82+98C>T | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97142397 | |||||||
| chr5:97142481 | C | T | 1 | a0001c0001t0002g0046 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.82+14G>A | LIX1 | ENSG00000145721.12 | transcript | ENST00000274382.9 | protein_coding | 1/5 | chr5 | 97142481 |