Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 221496 |
| ensemblid | ENSG00000161904.13 |
| hgncid | 21244 |
| symbol | LEMD2 |
| name | LEM domain nuclear envelope protein 2 |
| refseq_nuc | NM_181336.4 |
| refseq_prot | NP_851853.1 |
| ensembl_nuc | ENST00000293760.10 |
| ensembl_prot | ENSP00000293760.5 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 33771213 |
| end | 33789130 |
| strand | - |
| ver | v1.2 |
| region | chr6:33771213-33789130 |
| region5000 | chr6:33766213-33794130 |
| regionname0 | LEMD2_chr6_33771213_33789130 |
| regionname5000 | LEMD2_chr6_33766213_33794130 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 503 | 358 | 98 | 66 | 147 | 16 | 29 | 108 | LEMD2_chr6_33766213_33794130 | LEMD2 | MAGLS others(498): Show |
chr6 | 33766213 | 33794130 |
| a0002 | 0/0 | 503 | 38 | 1 | 9 | 21 | 2 | 5 | 20 | LEMD2_chr6_33766213_33794130 | LEMD2 | MAGLS others(498): Show |
chr6 | 33766213 | 33794130 |
| a0003 | 0/0 | 503 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | MAGLS others(498): Show |
chr6 | 33766213 | 33794130 |
| a0004 | 0/0 | 503 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | MAGLS others(498): Show |
chr6 | 33766213 | 33794130 |
| a0005 | 0/0 | 503 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | MAGLS others(498): Show |
chr6 | 33766213 | 33794130 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1509 | 349 | 91 | 65 | 146 | 16 | 29 | LEMD2_chr6_33766213_33794130 | LEMD2 | ATGGC others(1504): Show |
chr6 | 33766213 | 33794130 | ||
| a0001c0003 | 0/0 | 1509 | 7 | 6 | 1 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | ATGGC others(1504): Show |
chr6 | 33766213 | 33794130 | ||
| a0001c0007 | 0/0 | 1509 | 1 | 0 | 0 | 1 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | ATGGC others(1504): Show |
chr6 | 33766213 | 33794130 | ||
| a0001c0008 | 0/0 | 1509 | 1 | 1 | 0 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | ATGGC others(1504): Show |
chr6 | 33766213 | 33794130 | ||
| a0002c0002 | 0/0 | 1509 | 38 | 1 | 9 | 21 | 2 | 5 | LEMD2_chr6_33766213_33794130 | LEMD2 | ATGGC others(1504): Show |
chr6 | 33766213 | 33794130 | ||
| a0003c0004 | 0/0 | 1509 | 2 | 0 | 0 | 2 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | ATGGC others(1504): Show |
chr6 | 33766213 | 33794130 | ||
| a0004c0006 | 0/0 | 1509 | 1 | 0 | 1 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | ATGGC others(1504): Show |
chr6 | 33766213 | 33794130 | ||
| a0005c0005 | 0/0 | 1509 | 1 | 1 | 0 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | ATGGC others(1504): Show |
chr6 | 33766213 | 33794130 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2941 | 157 | 19 | 17 | 102 | 4 | 15 | LEMD2_chr6_33766213_33794130 | LEMD2 | GCGGC others(2936): Show |
chr6 | 33766213 | 33794130 |
| a0001c0001t0002 | 0/0 | 2941 | 84 | 16 | 27 | 27 | 8 | 6 | LEMD2_chr6_33766213_33794130 | LEMD2 | GCGGC others(2936): Show |
chr6 | 33766213 | 33794130 |
| a0001c0001t0003 | 1/1 | 2941 | 40 | 20 | 6 | 9 | 3 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | GCGGC others(2936): Show |
chr6 | 33766213 | 33794130 |
| a0001c0001t0004 | 0/0 | 2941 | 34 | 22 | 4 | 2 | 1 | 5 | LEMD2_chr6_33766213_33794130 | LEMD2 | GCGGC others(2936): Show |
chr6 | 33766213 | 33794130 |
| a0001c0001t0005 | 0/0 | 2941 | 1 | 1 | 0 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | GCGGC others(2936): Show |
chr6 | 33766213 | 33794130 |
| a0001c0001t0006 | 0/0 | 2941 | 10 | 7 | 1 | 1 | 0 | 1 | LEMD2_chr6_33766213_33794130 | LEMD2 | GCGGC others(2936): Show |
chr6 | 33766213 | 33794130 |
| a0001c0001t0008 | 0/0 | 2942 | 11 | 4 | 3 | 2 | 0 | 2 | LEMD2_chr6_33766213_33794130 | LEMD2 | GCGGC others(2937): Show |
chr6 | 33766213 | 33794130 |
| a0001c0001t0009 | 0/0 | 2941 | 3 | 1 | 2 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | GCGGC others(2936): Show |
chr6 | 33766213 | 33794130 |
| a0001c0001t0012 | 0/0 | 2941 | 1 | 0 | 0 | 1 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | GCGGC others(2936): Show |
chr6 | 33766213 | 33794130 |
| a0001c0001t0013 | 0/0 | 2941 | 1 | 0 | 0 | 1 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | GCGGC others(2936): Show |
chr6 | 33766213 | 33794130 |
| a0001c0001t0014 | 0/0 | 2942 | 1 | 1 | 0 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | GCGGC others(2937): Show |
chr6 | 33766213 | 33794130 |
| a0001c0001t0015 | 0/0 | 2942 | 1 | 0 | 1 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | GCGGC others(2937): Show |
chr6 | 33766213 | 33794130 |
| a0001c0001t0016 | 0/0 | 2941 | 1 | 0 | 1 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | GCGGC others(2936): Show |
chr6 | 33766213 | 33794130 |
| a0001c0001t0017 | 0/0 | 2942 | 1 | 0 | 1 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | GCGGC others(2937): Show |
chr6 | 33766213 | 33794130 |
| a0001c0001t0018 | 0/0 | 2941 | 1 | 0 | 1 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | GCGGC others(2936): Show |
chr6 | 33766213 | 33794130 |
| a0001c0001t0019 | 0/0 | 2941 | 1 | 0 | 1 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | GCGGC others(2936): Show |
chr6 | 33766213 | 33794130 |
| a0001c0001t0021 | 0/0 | 2927 | 1 | 0 | 0 | 1 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | GCGGC others(2922): Show |
chr6 | 33766213 | 33794130 |
| a0001c0003t0006 | 0/0 | 2941 | 7 | 6 | 1 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | GCGGC others(2936): Show |
chr6 | 33766213 | 33794130 |
| a0001c0007t0001 | 0/0 | 2941 | 1 | 0 | 0 | 1 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | GCGGC others(2936): Show |
chr6 | 33766213 | 33794130 |
| a0001c0008t0006 | 0/0 | 2941 | 1 | 1 | 0 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | GCGGC others(2936): Show |
chr6 | 33766213 | 33794130 |
| a0002c0002t0005 | 0/0 | 2941 | 20 | 1 | 7 | 7 | 2 | 3 | LEMD2_chr6_33766213_33794130 | LEMD2 | GCGGC others(2936): Show |
chr6 | 33766213 | 33794130 |
| a0002c0002t0007 | 0/0 | 2941 | 14 | 0 | 2 | 12 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | GCGGC others(2936): Show |
chr6 | 33766213 | 33794130 |
| a0002c0002t0010 | 0/0 | 2941 | 2 | 0 | 0 | 0 | 0 | 2 | LEMD2_chr6_33766213_33794130 | LEMD2 | GCGGC others(2936): Show |
chr6 | 33766213 | 33794130 |
| a0002c0002t0011 | 0/0 | 2941 | 2 | 0 | 0 | 2 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | GCGGC others(2936): Show |
chr6 | 33766213 | 33794130 |
| a0003c0004t0002 | 0/0 | 2941 | 2 | 0 | 0 | 2 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | GCGGC others(2936): Show |
chr6 | 33766213 | 33794130 |
| a0004c0006t0020 | 0/0 | 2941 | 1 | 0 | 1 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | GCGGC others(2936): Show |
chr6 | 33766213 | 33794130 |
| a0005c0005t0008 | 0/0 | 2942 | 1 | 1 | 0 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | GCGGC others(2937): Show |
chr6 | 33766213 | 33794130 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 31 | 0 | 5 | 18 | 3 | 5 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0001g0007 | 0/0 | 11 | 1 | 0 | 10 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0001g0008 | 0/0 | 10 | 1 | 0 | 7 | 0 | 2 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0001g0009 | 0/0 | 10 | 0 | 0 | 7 | 0 | 3 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0001g0011 | 0/0 | 7 | 3 | 0 | 4 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0001g0012 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0001g0014 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0001g0015 | 0/0 | 6 | 2 | 2 | 0 | 1 | 1 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0001g0018 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0001g0019 | 0/0 | 4 | 3 | 0 | 0 | 0 | 1 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0001g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0001g0027 | 0/0 | 3 | 2 | 0 | 0 | 0 | 1 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0001g0035 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0002g0001 | 0/0 | 33 | 7 | 14 | 6 | 3 | 3 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0002g0004 | 0/0 | 16 | 0 | 0 | 16 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0002g0022 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0002g0023 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0002g0030 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0002g0031 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0002g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0002g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0002g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0003g0003 | 1/1 | 17 | 3 | 3 | 7 | 2 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0003g0006 | 0/0 | 12 | 12 | 0 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0003g0028 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0003g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0003g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0004g0010 | 0/0 | 9 | 3 | 0 | 1 | 0 | 5 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0004g0016 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0004g0017 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0004g0029 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0004g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0004g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0004g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0004g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0004g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0004g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0004g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0005g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0006g0021 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0006g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0006g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0006g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0006g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0006g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0008g0020 | 0/0 | 4 | 0 | 1 | 1 | 0 | 2 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0008g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0008g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0008g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0008g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0008g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0008g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0009g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0009g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0012g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0013g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0014g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0015g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0016g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0017g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0018g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0019g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0001t0021g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0003t0006g0013 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0007t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0001c0008t0006g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0002c0002t0005g0005 | 0/0 | 13 | 0 | 4 | 6 | 1 | 2 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0002c0002t0005g0052 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0002c0002t0005g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0002c0002t0005g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0002c0002t0005g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0002c0002t0005g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0002c0002t0005g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0002c0002t0007g0024 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0002c0002t0007g0025 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0002c0002t0007g0032 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0002c0002t0007g0051 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0002c0002t0007g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0002c0002t0010g0050 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0002c0002t0011g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0002c0002t0011g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0003c0004t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0004c0006t0020g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| a0005c0005t0008g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0031 | EUR | GBR | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0003 | EUR | GBR | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0003 | EUR | GBR | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG00140 | hp2 | a0002 | c0002 | t0005 | g0005 | EUR | GBR | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0028 | EUR | FIN | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | FIN | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG00323 | hp1 | a0002 | c0002 | t0005 | g0154 | EUR | FIN | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0022 | EUR | FIN | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG00408 | hp2 | a0003 | c0004 | t0002 | g0033 | EAS | CHS | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG00423 | hp1 | a0001 | c0001 | t0008 | g0020 | EAS | CHS | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | CHS | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | CHS | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG00558 | hp2 | a0001 | c0001 | t0013 | g0098 | EAS | CHS | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG00597 | hp2 | a0001 | c0001 | t0004 | g0010 | EAS | CHS | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG00642 | hp1 | a0001 | c0001 | t0019 | g0090 | AMR | PUR | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG00642 | hp2 | a0001 | c0001 | t0009 | g0043 | AMR | PUR | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG00733 | hp1 | a0002 | c0002 | t0005 | g0052 | AMR | PUR | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0023 | AMR | PUR | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG00735 | hp2 | a0002 | c0002 | t0005 | g0005 | AMR | PUR | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG00738 | hp1 | a0002 | c0002 | t0005 | g0005 | AMR | PUR | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG00741 | hp2 | a0001 | c0001 | t0004 | g0017 | AMR | PUR | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01069 | hp1 | a0001 | c0001 | t0017 | g0114 | AMR | PUR | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0045 | AMR | PUR | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0028 | AMR | PUR | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0140 | AMR | PUR | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0134 | AMR | PUR | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0045 | AMR | PUR | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0023 | AMR | PUR | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01081 | hp1 | a0001 | c0001 | t0009 | g0043 | AMR | PUR | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01099 | hp1 | a0002 | c0002 | t0005 | g0052 | AMR | PUR | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0132 | AMR | PUR | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0057 | AMR | PUR | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | PUR | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01168 | hp2 | a0002 | c0002 | t0005 | g0151 | AMR | PUR | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01175 | hp2 | a0002 | c0002 | t0005 | g0005 | AMR | PUR | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01192 | hp1 | a0002 | c0002 | t0005 | g0005 | AMR | PUR | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01192 | hp2 | a0001 | c0001 | t0006 | g0106 | AMR | PUR | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01243 | hp1 | a0001 | c0003 | t0006 | g0013 | AMR | PUR | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01255 | hp1 | a0001 | c0001 | t0008 | g0111 | AMR | CLM | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01255 | hp2 | a0001 | c0001 | t0008 | g0125 | AMR | CLM | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | CLM | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | CLM | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01358 | hp2 | a0001 | c0001 | t0016 | g0131 | AMR | CLM | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0031 | AMR | CLM | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01361 | hp2 | a0001 | c0001 | t0004 | g0029 | AMR | CLM | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0023 | AMR | CLM | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | IBS | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0135 | EUR | IBS | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | IBS | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0023 | EUR | IBS | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0042 | AFR | ACB | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0128 | AFR | ACB | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01891 | hp2 | a0001 | c0001 | t0008 | g0112 | AFR | ACB | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0143 | AMR | PEL | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01934 | hp2 | a0001 | c0001 | t0018 | g0089 | AMR | PEL | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01943 | hp1 | a0002 | c0002 | t0007 | g0051 | AMR | PEL | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01975 | hp2 | a0001 | c0001 | t0004 | g0058 | AMR | PEL | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | PEL | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02004 | hp2 | a0004 | c0006 | t0020 | g0100 | AMR | PEL | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02015 | hp1 | a0003 | c0004 | t0002 | g0033 | EAS | KHV | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | KHV | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02040 | hp2 | a0002 | c0002 | t0005 | g0005 | EAS | KHV | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | ACB | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02055 | hp2 | a0001 | c0003 | t0006 | g0013 | AFR | ACB | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | ACB | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0054 | AFR | ACB | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02148 | hp1 | a0001 | c0001 | t0015 | g0109 | AMR | PEL | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02148 | hp2 | a0002 | c0002 | t0007 | g0051 | AMR | PEL | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | CDX | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | CDX | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | ACB | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | ACB | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0049 | AFR | ACB | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02280 | hp1 | a0001 | c0001 | t0014 | g0144 | AFR | ACB | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02451 | hp1 | a0001 | c0001 | t0006 | g0041 | AFR | ACB | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0130 | AFR | GWD | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0010 | AFR | GWD | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0046 | AFR | GWD | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0010 | AFR | GWD | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0129 | AFR | GWD | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02630 | hp2 | a0005 | c0005 | t0008 | g0118 | AFR | GWD | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0120 | AFR | GWD | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0137 | AFR | GWD | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02723 | hp1 | a0001 | c0003 | t0006 | g0013 | AFR | GWD | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0016 | AFR | GWD | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0022 | SAS | PJL | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0028 | AFR | GWD | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0016 | AFR | GWD | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | GWD | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0127 | AFR | GWD | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02886 | hp1 | a0001 | c0001 | t0008 | g0113 | AFR | GWD | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0010 | AFR | GWD | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0016 | AFR | GWD | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0016 | AFR | GWD | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02896 | hp2 | a0001 | c0001 | t0008 | g0044 | AFR | GWD | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02897 | hp1 | a0001 | c0001 | t0008 | g0044 | AFR | GWD | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02897 | hp2 | a0001 | c0001 | t0004 | g0016 | AFR | GWD | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0055 | AFR | ESN | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | ESN | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | ESN | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | ESN | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02970 | hp2 | a0001 | c0003 | t0006 | g0013 | AFR | ESN | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0030 | AFR | ESN | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02976 | hp2 | a0001 | c0001 | t0006 | g0021 | AFR | ESN | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG03017 | hp1 | a0001 | c0001 | t0004 | g0010 | SAS | PJL | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0046 | AFR | GWD | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0029 | AFR | MSL | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0056 | AFR | MSL | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | ESN | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ESN | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG03195 | hp2 | a0001 | c0008 | t0006 | g0147 | AFR | ESN | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG03209 | hp2 | a0001 | c0001 | t0005 | g0108 | AFR | MSL | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0145 | AFR | MSL | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | MSL | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0029 | AFR | MSL | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | MSL | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | MSL | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG03486 | hp2 | a0001 | c0001 | t0006 | g0021 | AFR | MSL | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG03490 | hp2 | a0002 | c0002 | t0010 | g0050 | SAS | PJL | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG03491 | hp1 | a0002 | c0002 | t0005 | g0005 | SAS | PJL | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG03492 | hp1 | a0002 | c0002 | t0010 | g0050 | SAS | PJL | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | ESN | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG03516 | hp2 | a0001 | c0001 | t0006 | g0041 | AFR | ESN | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0017 | AFR | GWD | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | MSL | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG03654 | hp1 | a0002 | c0002 | t0005 | g0005 | SAS | PJL | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0141 | SAS | PJL | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG03688 | hp1 | a0001 | c0001 | t0004 | g0010 | SAS | STU | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | STU | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG03704 | hp2 | a0002 | c0002 | t0005 | g0152 | SAS | PJL | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG03710 | hp2 | a0001 | c0001 | t0004 | g0010 | SAS | PJL | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0010 | SAS | BEB | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG03942 | hp2 | a0001 | c0001 | t0004 | g0010 | SAS | BEB | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | STU | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG04115 | hp2 | a0001 | c0001 | t0006 | g0121 | SAS | STU | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | BEB | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0142 | SAS | BEB | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | STU | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | STU | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG04204 | hp2 | a0001 | c0001 | t0008 | g0020 | SAS | STU | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18522 | hp1 | a0001 | c0001 | t0009 | g0122 | AFR | YRI | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0042 | AFR | YRI | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHB | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18612 | hp2 | a0001 | c0001 | t0006 | g0123 | EAS | CHB | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CHB | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHB | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0117 | AFR | YRI | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18906 | hp2 | a0001 | c0001 | t0006 | g0107 | AFR | YRI | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18940 | hp2 | a0001 | c0001 | t0008 | g0110 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18941 | hp1 | a0002 | c0002 | t0007 | g0025 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18944 | hp2 | a0002 | c0002 | t0007 | g0025 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18952 | hp1 | a0002 | c0002 | t0007 | g0024 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18957 | hp2 | a0001 | c0001 | t0004 | g0059 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18966 | hp2 | a0002 | c0002 | t0007 | g0024 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18967 | hp1 | a0002 | c0002 | t0007 | g0024 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18971 | hp1 | a0001 | c0007 | t0001 | g0146 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18974 | hp1 | a0002 | c0002 | t0007 | g0032 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18978 | hp2 | a0001 | c0001 | t0012 | g0133 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18983 | hp2 | a0002 | c0002 | t0007 | g0032 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18984 | hp2 | a0002 | c0002 | t0005 | g0005 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18988 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18992 | hp1 | a0002 | c0002 | t0005 | g0005 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18993 | hp1 | a0002 | c0002 | t0007 | g0032 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18993 | hp2 | a0002 | c0002 | t0005 | g0153 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18995 | hp2 | a0002 | c0002 | t0007 | g0024 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0115 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA19001 | hp1 | a0002 | c0002 | t0011 | g0148 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA19002 | hp1 | a0002 | c0002 | t0005 | g0005 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA19009 | hp1 | a0002 | c0002 | t0007 | g0149 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA19030 | hp1 | a0001 | c0003 | t0006 | g0013 | AFR | LWK | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA19030 | hp2 | a0001 | c0001 | t0006 | g0021 | AFR | LWK | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0124 | AFR | LWK | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | LWK | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA19054 | hp1 | a0002 | c0002 | t0011 | g0150 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA19055 | hp2 | a0001 | c0001 | t0003 | g0116 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA19056 | hp1 | a0002 | c0002 | t0007 | g0025 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA19077 | hp1 | a0001 | c0001 | t0021 | g0084 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA19083 | hp2 | a0002 | c0002 | t0005 | g0005 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA19085 | hp1 | a0002 | c0002 | t0005 | g0005 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA19087 | hp1 | a0002 | c0002 | t0007 | g0025 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | YRI | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA19240 | hp2 | a0001 | c0003 | t0006 | g0013 | AFR | YRI | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0119 | AFR | ASW | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ASW | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | TSI | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0139 | EUR | TSI | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA20805 | hp1 | a0001 | c0001 | t0004 | g0053 | EUR | TSI | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA20905 | hp1 | a0001 | c0001 | t0008 | g0020 | SAS | GIH | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | GIH | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01123 | hp1 | a0001 | c0001 | t0008 | g0020 | AMR | CLM | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0126 | AFR | ACB | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | ACB | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | ACB | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02559 | hp1 | a0001 | c0003 | t0006 | g0013 | AFR | ACB | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | MSL | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | USA | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0049 | AFR | USA | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | USA | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | USA | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA21309 | hp1 | a0002 | c0002 | t0005 | g0155 | AFR | LWK | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| NA21309 | hp2 | a0001 | c0001 | t0006 | g0021 | AFR | LWK | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0003 | REF | REF | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0003 | REF | REF | LEMD2_chr6_33766213_33794130 | LEMD2 | chr6 | 33766213 | 33794130 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:33780115 | T | C | 1 | a0005 | 1 | HG02630.hp2 | missense_variant | MODERATE | c.995A>G | p.Lys332Arg | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 5/9 | 1009/2941 | 995/1512 | 332/503 | chr6 | 33780115 | |||
| chr6:33781090 | T | C | 1 | a0004 | 1 | HG02004.hp2 | missense_variant | MODERATE | c.917A>G | p.Gln306Arg | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 4/9 | 931/2941 | 917/1512 | 306/503 | chr6 | 33781090 | |||
| chr6:33788755 | G | A | 1 | a0002 | 38 | HG00140.hp2 HG00323.hp1 HG00733.hp1 others(35): Show |
missense_variant | MODERATE | c.362C>T | p.Ala121Val | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 1/9 | 376/2941 | 362/1512 | 121/503 | chr6 | 33788755 | |||
| chr6:33788797 | A | G | 1 | a0003 | 2 | HG00408.hp2 HG02015.hp1 |
missense_variant | MODERATE | c.320T>C | p.Ile107Thr | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 1/9 | 334/2941 | 320/1512 | 107/503 | chr6 | 33788797 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:33788448 | G | C | 1 | a0001c0003 | 7 | HG01243.hp1 HG02055.hp2 HG02559.hp1 others(4): Show |
synonymous_variant | LOW | c.669C>G | p.Leu223Leu | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 1/9 | 683/2941 | 669/1512 | 223/503 | chr6 | 33788448 | |||
| chr6:33788487 | G | A | 1 | a0001c0007 | 1 | NA18971.hp1 | synonymous_variant | LOW | c.630C>T | p.Leu210Leu | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 1/9 | 644/2941 | 630/1512 | 210/503 | chr6 | 33788487 | |||
| chr6:33788655 | G | A | 1 | a0001c0008 | 1 | HG03195.hp2 | synonymous_variant | LOW | c.462C>T | p.Gly154Gly | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 1/9 | 476/2941 | 462/1512 | 154/503 | chr6 | 33788655 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:33771226 | A | C | 1 | a0001c0001t0014 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1402T>G | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 9/9 | 1402 | chr6 | 33771226 | ||||||
| chr6:33771341 | C | CA | 5 | a0001c0001t0008 a0001c0001t0014 a0001c0001t0015 others(2): Show |
15 | HG00423.hp1 HG01069.hp1 HG01123.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1286dupT | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 9/9 | 1286 | chr6 | 33771341 | ||||||
| chr6:33771465 | T | A | 1 | a0002c0002t0011 | 2 | NA19001.hp1 NA19054.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1163A>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 9/9 | 1163 | chr6 | 33771465 | ||||||
| chr6:33771633 | A | T | 1 | a0001c0001t0018 | 1 | HG01934.hp2 | 3_prime_UTR_variant | MODIFIER | c.*995T>A | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 9/9 | 995 | chr6 | 33771633 | ||||||
| chr6:33771634 | G | C | 1 | a0002c0002t0010 | 2 | HG03490.hp2 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*994C>G | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 9/9 | 994 | chr6 | 33771634 | ||||||
| chr6:33771673 | C | T | 1 | a0004c0006t0020 | 1 | HG02004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*955G>A | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 9/9 | 955 | chr6 | 33771673 | ||||||
| chr6:33771692 | A | G | 2 | a0001c0001t0018 a0001c0001t0019 |
2 | HG00642.hp1 HG01934.hp2 |
3_prime_UTR_variant | MODIFIER | c.*936T>C | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 9/9 | 936 | chr6 | 33771692 | ||||||
| chr6:33771731 | G | C | 4 | a0001c0001t0006 a0001c0001t0009 a0001c0003t0006 others(1): Show |
21 | HG00642.hp2 HG01081.hp1 HG01192.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*897C>G | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 9/9 | 897 | chr6 | 33771731 | ||||||
| chr6:33771820 | A | G | 2 | a0002c0002t0007 a0002c0002t0011 |
16 | HG01943.hp1 HG02148.hp2 NA18941.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*808T>C | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 9/9 | 808 | chr6 | 33771820 | ||||||
| chr6:33771938 | CCGCCCGC others(7): Show |
C | 1 | a0001c0001t0021 | 1 | NA19077.hp1 | 3_prime_UTR_variant | MODIFIER | c.*676_*689delCCCCAG others(8): Show |
LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 9/9 | 676 | chr6 | 33771938 | ||||||
| chr6:33771939 | CGCCCGCC others(8): Show |
C | 6 | a0001c0001t0001 a0001c0001t0013 a0001c0001t0018 others(3): Show |
135 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*674_*688delAGCCCC others(9): Show |
LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 9/9 | 674 | chr6 | 33771939 | ||||||
| chr6:33771954 | T | C | 1 | a0001c0001t0021 | 1 | NA19077.hp1 | 3_prime_UTR_variant | MODIFIER | c.*674A>G | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 9/9 | 674 | chr6 | 33771954 | ||||||
| chr6:33771994 | T | C | 1 | a0001c0001t0016 | 1 | HG01358.hp2 | 3_prime_UTR_variant | MODIFIER | c.*634A>G | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 9/9 | 634 | chr6 | 33771994 | ||||||
| chr6:33772065 | G | T | 1 | a0001c0001t0009 | 3 | HG00642.hp2 HG01081.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*563C>A | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 9/9 | 563 | chr6 | 33772065 | ||||||
| chr6:33772183 | A | G | 26 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(23): Show |
360 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(357): Show |
3_prime_UTR_variant | MODIFIER | c.*445T>C | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 9/9 | 445 | chr6 | 33772183 | ||||||
| chr6:33772192 | C | A | 1 | a0001c0001t0014 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*436G>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 9/9 | 436 | chr6 | 33772192 | ||||||
| chr6:33772248 | C | T | 8 | a0001c0001t0001 a0001c0001t0013 a0001c0001t0018 others(5): Show |
165 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(162): Show |
3_prime_UTR_variant | MODIFIER | c.*380G>A | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 9/9 | 380 | chr6 | 33772248 | ||||||
| chr6:33772281 | G | A | 1 | a0001c0001t0015 | 1 | HG02148.hp1 | 3_prime_UTR_variant | MODIFIER | c.*347C>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 9/9 | 347 | chr6 | 33772281 | ||||||
| chr6:33772548 | G | C | 4 | a0001c0001t0002 a0001c0001t0012 a0001c0001t0016 others(1): Show |
88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*80C>G | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 9/9 | 80 | chr6 | 33772548 | ||||||
| chr6:33772556 | G | A | 1 | a0001c0001t0017 | 1 | HG01069.hp1 | 3_prime_UTR_variant | MODIFIER | c.*72C>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 9/9 | 72 | chr6 | 33772556 | ||||||
| chr6:33772604 | C | G | 1 | a0001c0001t0012 | 1 | NA18978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*24G>C | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 9/9 | 24 | chr6 | 33772604 | ||||||
| chr6:33772605 | G | A | 11 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0018 others(8): Show |
201 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(198): Show |
3_prime_UTR_variant | MODIFIER | c.*23C>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 9/9 | 23 | chr6 | 33772605 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:33772815 | C | T | 88 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(85): Show |
216 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.1362-37G>A | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33772815 | |||||||
| chr6:33772882 | T | C | 1 | a0001c0001t0002g0132 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1362-104A>G | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33772882 | |||||||
| chr6:33772927 | AGAG | A | 14 | a0002c0002t0005g0005 a0002c0002t0005g0052 a0002c0002t0005g0151 others(11): Show |
36 | HG00140.hp2 HG00323.hp1 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.1362-152_1362-150d others(5): Show |
LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33772927 | |||||||
| chr6:33773171 | G | A | 3 | a0001c0001t0008g0020 a0001c0001t0008g0110 a0001c0001t0015g0109 |
6 | HG00423.hp1 HG01123.hp1 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.1362-393C>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33773171 | |||||||
| chr6:33773286 | C | T | 7 | a0002c0002t0005g0005 a0002c0002t0005g0052 a0002c0002t0005g0151 others(4): Show |
20 | HG00140.hp2 HG00323.hp1 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.1362-508G>A | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33773286 | |||||||
| chr6:33773380 | C | A | 2 | a0001c0001t0004g0124 a0001c0001t0005g0108 |
2 | HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1362-602G>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33773380 | |||||||
| chr6:33773422 | G | C | 1 | a0001c0001t0006g0041 | 2 | HG02451.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1362-644C>G | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33773422 | |||||||
| chr6:33773512 | A | G | 73 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0022 others(70): Show |
181 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.1362-734T>C | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33773512 | |||||||
| chr6:33773570 | G | A | 4 | a0001c0001t0004g0029 a0001c0001t0004g0046 a0001c0001t0004g0127 others(1): Show |
7 | HG01361.hp2 HG02615.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1362-792C>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33773570 | |||||||
| chr6:33773594 | C | CG | 28 | a0001c0001t0001g0074 a0001c0001t0002g0001 a0001c0001t0002g0004 others(25): Show |
86 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.1362-817dupC | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33773594 | |||||||
| chr6:33773594 | C | CGG | 48 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(45): Show |
130 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.1362-818_1362-817d others(4): Show |
LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33773594 | |||||||
| chr6:33773594 | C | CGGG | 23 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(20): Show |
48 | HG00408.hp1 HG00597.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.1362-819_1362-817d others(5): Show |
LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33773594 | |||||||
| chr6:33773594 | C | T | 1 | a0001c0001t0008g0111 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1362-816G>A | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33773594 | |||||||
| chr6:33773595 | G | A | 1 | a0001c0001t0004g0124 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1362-817C>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33773595 | |||||||
| chr6:33773596 | G | GGT | 14 | a0002c0002t0005g0005 a0002c0002t0005g0052 a0002c0002t0005g0151 others(11): Show |
36 | HG00140.hp2 HG00323.hp1 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.1362-819_1362-818i others(4): Show |
LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33773596 | |||||||
| chr6:33773599 | G | C | 14 | a0002c0002t0005g0005 a0002c0002t0005g0052 a0002c0002t0005g0151 others(11): Show |
36 | HG00140.hp2 HG00323.hp1 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.1362-821C>G | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33773599 | |||||||
| chr6:33773697 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1362-919G>A | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33773697 | |||||||
| chr6:33773746 | G | A | 2 | a0001c0001t0008g0044 a0001c0001t0014g0144 |
3 | HG02280.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1362-968C>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33773746 | |||||||
| chr6:33773785 | C | T | 2 | a0001c0001t0001g0078 a0001c0001t0001g0080 |
2 | NA18979.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.1362-1007G>A | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33773785 | |||||||
| chr6:33773828 | C | A | 1 | a0001c0001t0008g0111 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1362-1050G>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33773828 | |||||||
| chr6:33773939 | A | G | 143 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(140): Show |
355 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(352): Show |
intron_variant | MODIFIER | c.1362-1161T>C | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33773939 | |||||||
| chr6:33773947 | C | T | 7 | a0002c0002t0005g0005 a0002c0002t0005g0052 a0002c0002t0005g0151 others(4): Show |
20 | HG00140.hp2 HG00323.hp1 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.1362-1169G>A | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33773947 | |||||||
| chr6:33774007 | G | C | 1 | a0001c0001t0005g0108 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1362-1229C>G | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33774007 | |||||||
| chr6:33774168 | CT | C | 81 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(78): Show |
203 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.1362-1391delA | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33774168 | |||||||
| chr6:33774177 | T | C | 1 | a0001c0001t0008g0111 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1362-1399A>G | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33774177 | |||||||
| chr6:33774194 | T | G | 1 | a0001c0001t0008g0125 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1362-1416A>C | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33774194 | |||||||
| chr6:33774258 | G | A | 2 | a0001c0001t0008g0044 a0001c0001t0014g0144 |
3 | HG02280.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1362-1480C>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33774258 | |||||||
| chr6:33774296 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1362-1518G>A | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33774296 | |||||||
| chr6:33774320 | T | C | 108 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(105): Show |
249 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(246): Show |
intron_variant | MODIFIER | c.1362-1542A>G | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33774320 | |||||||
| chr6:33774387 | G | C | 1 | a0002c0002t0007g0032 | 3 | NA18974.hp1 NA18983.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.1362-1609C>G | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33774387 | |||||||
| chr6:33774416 | C | T | 40 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0022 others(37): Show |
113 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.1362-1638G>A | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33774416 | |||||||
| chr6:33774430 | A | AT | 12 | a0001c0001t0002g0030 a0001c0001t0003g0115 a0001c0001t0004g0017 others(9): Show |
21 | HG00741.hp2 HG01175.hp1 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.1362-1653dupA | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33774430 | |||||||
| chr6:33774430 | A | ATT | 3 | a0001c0001t0002g0130 a0001c0001t0004g0016 a0001c0001t0004g0054 |
7 | HG02145.hp2 HG02572.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1362-1654_1362-165 others(6): Show |
LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33774430 | |||||||
| chr6:33774430 | AT | A | 75 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(72): Show |
198 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(195): Show |
intron_variant | MODIFIER | c.1362-1653delA | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33774430 | |||||||
| chr6:33774499 | G | A | 10 | a0001c0001t0001g0014 a0001c0001t0001g0036 a0001c0001t0001g0038 others(7): Show |
18 | HG00408.hp1 HG02071.hp2 HG02129.hp1 others(15): Show |
intron_variant | MODIFIER | c.1362-1721C>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33774499 | |||||||
| chr6:33774503 | T | C | 10 | a0001c0001t0004g0016 a0001c0001t0004g0017 a0001c0001t0004g0029 others(7): Show |
20 | HG00741.hp2 HG01255.hp2 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.1362-1725A>G | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33774503 | |||||||
| chr6:33774554 | T | C | 139 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(136): Show |
350 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(347): Show |
intron_variant | MODIFIER | c.1362-1776A>G | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33774554 | |||||||
| chr6:33774626 | C | T | 87 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(84): Show |
215 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.1362-1848G>A | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33774626 | |||||||
| chr6:33774703 | T | C | 1 | a0001c0001t0001g0088 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1362-1925A>G | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33774703 | |||||||
| chr6:33774709 | C | T | 27 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0022 others(24): Show |
88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.1362-1931G>A | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33774709 | |||||||
| chr6:33774712 | G | A | 2 | a0001c0001t0018g0089 a0001c0001t0019g0090 |
2 | HG00642.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.1362-1934C>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33774712 | |||||||
| chr6:33774713 | A | G | 29 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0022 others(26): Show |
90 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.1362-1935T>C | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33774713 | |||||||
| chr6:33774724 | C | T | 8 | a0001c0001t0004g0016 a0001c0001t0004g0017 a0001c0001t0004g0029 others(5): Show |
18 | HG00741.hp2 HG01361.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1362-1946G>A | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33774724 | |||||||
| chr6:33774941 | T | G | 18 | a0001c0001t0008g0112 a0001c0001t0008g0113 a0001c0001t0017g0114 others(15): Show |
40 | HG00140.hp2 HG00323.hp1 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.1361+2013A>C | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33774941 | |||||||
| chr6:33774970 | C | CTGAA | 30 | a0001c0001t0002g0001 a0001c0001t0002g0022 a0001c0001t0002g0030 others(27): Show |
79 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.1361+1980_1361+198 others(8): Show |
LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33774970 | |||||||
| chr6:33774970 | C | CTGAATGA others(1): Show |
7 | a0001c0001t0002g0004 a0001c0001t0002g0023 a0001c0001t0002g0048 others(4): Show |
26 | HG00733.hp2 HG01074.hp2 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.1361+1976_1361+198 others(12): Show |
LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33774970 | |||||||
| chr6:33774970 | C | CTGAATGA others(5): Show |
1 | a0001c0001t0008g0113 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1361+1972_1361+198 others(16): Show |
LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33774970 | |||||||
| chr6:33774970 | CTGAA | C | 62 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(59): Show |
145 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.1361+1980_1361+198 others(8): Show |
LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33774970 | |||||||
| chr6:33774970 | CTGAATGA others(5): Show |
C | 2 | a0001c0001t0008g0044 a0001c0001t0014g0144 |
3 | HG02280.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1361+1972_1361+198 others(16): Show |
LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33774970 | |||||||
| chr6:33774998 | T | A | 1 | a0001c0001t0008g0125 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1361+1956A>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33774998 | |||||||
| chr6:33774999 | A | T | 1 | a0001c0001t0008g0125 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1361+1955T>A | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33774999 | |||||||
| chr6:33775031 | G | A | 1 | a0001c0001t0001g0094 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1361+1923C>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33775031 | |||||||
| chr6:33775061 | T | C | 50 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0022 others(47): Show |
132 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.1361+1893A>G | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33775061 | |||||||
| chr6:33775302 | A | G | 1 | a0001c0001t0003g0117 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1361+1652T>C | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33775302 | |||||||
| chr6:33775316 | C | A | 4 | a0001c0001t0004g0016 a0001c0001t0004g0017 a0001c0001t0004g0054 others(1): Show |
11 | HG00741.hp2 HG02055.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1361+1638G>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33775316 | |||||||
| chr6:33775373 | A | G | 5 | a0001c0001t0008g0020 a0001c0001t0008g0044 a0001c0001t0008g0110 others(2): Show |
9 | HG00423.hp1 HG01123.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.1361+1581T>C | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33775373 | |||||||
| chr6:33775397 | T | C | 146 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(143): Show |
360 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(357): Show |
intron_variant | MODIFIER | c.1361+1557A>G | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33775397 | |||||||
| chr6:33775487 | C | T | 127 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(124): Show |
327 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(324): Show |
intron_variant | MODIFIER | c.1361+1467G>A | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33775487 | |||||||
| chr6:33775584 | G | A | 14 | a0002c0002t0005g0005 a0002c0002t0005g0052 a0002c0002t0005g0151 others(11): Show |
36 | HG00140.hp2 HG00323.hp1 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.1361+1370C>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33775584 | |||||||
| chr6:33775632 | G | A | 1 | a0001c0001t0004g0128 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1361+1322C>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33775632 | |||||||
| chr6:33775665 | A | T | 1 | a0001c0001t0001g0071 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1361+1289T>A | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33775665 | |||||||
| chr6:33775860 | T | G | 1 | a0002c0002t0007g0025 | 4 | NA18941.hp1 NA18944.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.1361+1094A>C | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33775860 | |||||||
| chr6:33775865 | G | A | 1 | a0001c0001t0008g0113 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1361+1089C>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33775865 | |||||||
| chr6:33775873 | G | A | 1 | a0001c0001t0008g0111 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1361+1081C>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33775873 | |||||||
| chr6:33775874 | G | C | 136 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(133): Show |
346 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(343): Show |
intron_variant | MODIFIER | c.1361+1080C>G | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33775874 | |||||||
| chr6:33775908 | C | T | 1 | a0001c0001t0005g0108 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1361+1046G>A | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33775908 | |||||||
| chr6:33775964 | C | T | 15 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0037 others(12): Show |
33 | HG00558.hp2 HG00621.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.1361+990G>A | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33775964 | |||||||
| chr6:33775984 | G | C | 2 | a0001c0001t0002g0137 a0001c0001t0004g0124 |
2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1361+970C>G | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33775984 | |||||||
| chr6:33776052 | G | A | 4 | a0001c0001t0004g0016 a0001c0001t0004g0017 a0001c0001t0004g0054 others(1): Show |
11 | HG00741.hp2 HG02055.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1361+902C>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33776052 | |||||||
| chr6:33776220 | G | A | 26 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0022 others(23): Show |
87 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.1361+734C>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33776220 | |||||||
| chr6:33776380 | G | A | 26 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0022 others(23): Show |
87 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.1361+574C>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33776380 | |||||||
| chr6:33776396 | T | C | 1 | a0001c0001t0002g0138 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1361+558A>G | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33776396 | |||||||
| chr6:33776409 | A | G | 2 | a0001c0001t0008g0112 a0001c0001t0008g0113 |
2 | HG01891.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1361+545T>C | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33776409 | |||||||
| chr6:33776560 | A | G | 2 | a0001c0001t0004g0127 a0001c0001t0004g0145 |
2 | HG02818.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1361+394T>C | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33776560 | |||||||
| chr6:33776608 | T | A | 1 | a0001c0001t0002g0139 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1361+346A>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33776608 | |||||||
| chr6:33776668 | C | G | 1 | a0001c0001t0008g0125 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1361+286G>C | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33776668 | |||||||
| chr6:33776815 | G | C | 2 | a0001c0001t0006g0121 a0001c0001t0006g0123 |
2 | HG04115.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.1361+139C>G | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33776815 | |||||||
| chr6:33776829 | T | C | 3 | a0001c0001t0008g0020 a0001c0001t0008g0110 a0001c0001t0015g0109 |
6 | HG00423.hp1 HG01123.hp1 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.1361+125A>G | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33776829 | |||||||
| chr6:33776870 | C | T | 2 | a0001c0001t0001g0070 a0001c0001t0001g0077 |
2 | NA18970.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.1361+84G>A | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33776870 | |||||||
| chr6:33776892 | G | A | 1 | a0005c0005t0008g0118 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1361+62C>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33776892 | |||||||
| chr6:33776934 | C | T | 73 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(70): Show |
179 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(176): Show |
intron_variant | MODIFIER | c.1361+20G>A | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33776934 | |||||||
| chr6:33776945 | G | A | 1 | a0001c0001t0004g0046 | 2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1361+9C>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 8/8 | chr6 | 33776945 | |||||||
| chr6:33777103 | G | A | 3 | a0001c0001t0001g0095 a0001c0001t0001g0101 a0001c0001t0003g0006 |
14 | HG02080.hp2 HG02145.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1258+35C>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 7/8 | chr6 | 33777103 | |||||||
| chr6:33777105 | C | G | 77 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(74): Show |
190 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(187): Show |
intron_variant | MODIFIER | c.1258+33G>C | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 7/8 | chr6 | 33777105 | |||||||
| chr6:33777272 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1157-33G>A | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 6/8 | chr6 | 33777272 | |||||||
| chr6:33777294 | C | T | 73 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(70): Show |
179 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(176): Show |
intron_variant | MODIFIER | c.1157-55G>A | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 6/8 | chr6 | 33777294 | |||||||
| chr6:33777385 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1157-146C>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 6/8 | chr6 | 33777385 | |||||||
| chr6:33777464 | C | T | 1 | a0001c0001t0008g0112 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1157-225G>A | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 6/8 | chr6 | 33777464 | |||||||
| chr6:33777483 | G | C | 1 | a0001c0001t0004g0124 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1157-244C>G | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 6/8 | chr6 | 33777483 | |||||||
| chr6:33777500 | A | G | 1 | a0001c0001t0014g0144 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1157-261T>C | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 6/8 | chr6 | 33777500 | |||||||
| chr6:33777566 | T | C | 10 | a0001c0001t0006g0021 a0001c0001t0006g0041 a0001c0001t0006g0106 others(7): Show |
21 | HG00642.hp2 HG01081.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.1157-327A>G | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 6/8 | chr6 | 33777566 | |||||||
| chr6:33777620 | G | C | 2 | a0001c0001t0002g0031 a0001c0001t0002g0139 |
4 | HG00099.hp1 HG01361.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.1157-381C>G | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 6/8 | chr6 | 33777620 | |||||||
| chr6:33777765 | G | A | 4 | a0001c0001t0004g0016 a0001c0001t0004g0017 a0001c0001t0004g0054 others(1): Show |
11 | HG00741.hp2 HG02055.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1156+477C>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 6/8 | chr6 | 33777765 | |||||||
| chr6:33778453 | T | C | 1 | a0005c0005t0008g0118 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1011-66A>G | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 5/8 | chr6 | 33778453 | |||||||
| chr6:33778539 | C | T | 1 | a0001c0001t0014g0144 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1011-152G>A | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 5/8 | chr6 | 33778539 | |||||||
| chr6:33778588 | G | A | 2 | a0001c0001t0006g0121 a0001c0001t0006g0123 |
2 | HG04115.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.1011-201C>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 5/8 | chr6 | 33778588 | |||||||
| chr6:33778610 | C | T | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG01081.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1011-223G>A | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 5/8 | chr6 | 33778610 | |||||||
| chr6:33778788 | T | C | 1 | a0001c0001t0001g0064 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1011-401A>G | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 5/8 | chr6 | 33778788 | |||||||
| chr6:33778836 | CATCCATG others(13): Show |
C | 14 | a0002c0002t0005g0005 a0002c0002t0005g0052 a0002c0002t0005g0151 others(11): Show |
36 | HG00140.hp2 HG00323.hp1 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.1011-469_1011-450d others(22): Show |
LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 5/8 | chr6 | 33778836 | |||||||
| chr6:33778920 | G | A | 26 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0022 others(23): Show |
87 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.1011-533C>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 5/8 | chr6 | 33778920 | |||||||
| chr6:33779048 | C | A | 3 | a0001c0001t0001g0039 a0001c0001t0001g0096 a0001c0001t0001g0097 |
4 | HG00735.hp1 HG01496.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.1011-661G>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 5/8 | chr6 | 33779048 | |||||||
| chr6:33779060 | C | T | 1 | a0002c0002t0005g0052 | 2 | HG00733.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.1011-673G>A | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 5/8 | chr6 | 33779060 | |||||||
| chr6:33779102 | G | A | 1 | a0002c0002t0007g0051 | 2 | HG01943.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.1011-715C>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 5/8 | chr6 | 33779102 | |||||||
| chr6:33779137 | G | A | 1 | a0005c0005t0008g0118 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1011-750C>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 5/8 | chr6 | 33779137 | |||||||
| chr6:33779162 | T | C | 1 | a0001c0001t0005g0108 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1011-775A>G | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 5/8 | chr6 | 33779162 | |||||||
| chr6:33779260 | CT | C | 17 | a0001c0001t0001g0099 a0001c0001t0002g0140 a0001c0001t0003g0116 others(14): Show |
39 | HG00140.hp2 HG00323.hp1 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.1010+839delA | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 5/8 | chr6 | 33779260 | |||||||
| chr6:33779373 | A | C | 1 | a0001c0001t0001g0026 | 3 | HG02717.hp2 HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1010+727T>G | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 5/8 | chr6 | 33779373 | |||||||
| chr6:33779463 | C | T | 1 | a0004c0006t0020g0100 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1010+637G>A | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 5/8 | chr6 | 33779463 | |||||||
| chr6:33779464 | G | GA | 3 | a0001c0001t0008g0112 a0001c0001t0008g0113 a0001c0001t0017g0114 |
3 | HG01069.hp1 HG01891.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1010+635dupT | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 5/8 | chr6 | 33779464 | |||||||
| chr6:33779566 | G | A | 5 | a0001c0001t0004g0010 a0001c0001t0004g0053 a0001c0001t0004g0056 others(2): Show |
13 | HG00597.hp2 HG01975.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.1010+534C>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 5/8 | chr6 | 33779566 | |||||||
| chr6:33779696 | T | A | 1 | a0001c0001t0003g0042 | 2 | HG01884.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1010+404A>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 5/8 | chr6 | 33779696 | |||||||
| chr6:33780042 | C | T | 1 | a0001c0001t0004g0124 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1010+58G>A | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 5/8 | chr6 | 33780042 | |||||||
| chr6:33780046 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1010+54G>A | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 5/8 | chr6 | 33780046 | |||||||
| chr6:33780484 | G | A | 4 | a0001c0001t0003g0006 a0001c0001t0003g0028 a0001c0001t0003g0042 others(1): Show |
18 | HG00280.hp1 HG01070.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.931-305C>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 4/8 | chr6 | 33780484 | |||||||
| chr6:33780517 | T | G | 1 | a0001c0001t0002g0129 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.931-338A>C | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 4/8 | chr6 | 33780517 | |||||||
| chr6:33780521 | T | G | 1 | a0001c0001t0002g0129 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.931-342A>C | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 4/8 | chr6 | 33780521 | |||||||
| chr6:33780523 | A | G | 1 | a0001c0001t0002g0129 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.931-344T>C | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 4/8 | chr6 | 33780523 | |||||||
| chr6:33780525 | C | G | 1 | a0001c0001t0002g0129 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.931-346G>C | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 4/8 | chr6 | 33780525 | |||||||
| chr6:33780585 | GT | G | 27 | a0001c0001t0001g0062 a0001c0001t0002g0001 a0001c0001t0002g0004 others(24): Show |
88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.931-407delA | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 4/8 | chr6 | 33780585 | |||||||
| chr6:33780634 | T | C | 2 | a0001c0001t0006g0041 a0001c0003t0006g0013 |
9 | HG01243.hp1 HG02055.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.930+443A>G | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 4/8 | chr6 | 33780634 | |||||||
| chr6:33780700 | G | A | 1 | a0001c0001t0004g0057 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.930+377C>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 4/8 | chr6 | 33780700 | |||||||
| chr6:33780804 | G | A | 1 | a0001c0001t0001g0062 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.930+273C>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 4/8 | chr6 | 33780804 | |||||||
| chr6:33780872 | G | A | 1 | a0001c0001t0002g0141 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.930+205C>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 4/8 | chr6 | 33780872 | |||||||
| chr6:33781054 | T | G | 136 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(133): Show |
346 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(343): Show |
intron_variant | MODIFIER | c.930+23A>C | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 4/8 | chr6 | 33781054 | |||||||
| chr6:33781156 | A | G | 1 | a0001c0008t0006g0147 | 1 | HG03195.hp2 | splice_region_variant&intron_variant | LOW | c.854-3T>C | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 3/8 | chr6 | 33781156 | |||||||
| chr6:33781160 | G | GA | 26 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0022 others(23): Show |
87 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(84): Show |
splice_region_variant&intron_variant | LOW | c.854-8dupT | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 3/8 | chr6 | 33781160 | |||||||
| chr6:33781253 | G | A | 3 | a0001c0001t0001g0019 a0001c0001t0001g0026 a0001c0001t0001g0027 |
10 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.854-100C>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 3/8 | chr6 | 33781253 | |||||||
| chr6:33781374 | A | G | 86 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(83): Show |
214 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.854-221T>C | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 3/8 | chr6 | 33781374 | |||||||
| chr6:33781375 | T | A | 87 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(84): Show |
215 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.854-222A>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 3/8 | chr6 | 33781375 | |||||||
| chr6:33781394 | A | G | 4 | a0001c0001t0004g0016 a0001c0001t0004g0017 a0001c0001t0004g0054 others(1): Show |
11 | HG00741.hp2 HG02055.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.854-241T>C | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 3/8 | chr6 | 33781394 | |||||||
| chr6:33781500 | A | G | 1 | a0001c0001t0001g0062 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.854-347T>C | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 3/8 | chr6 | 33781500 | |||||||
| chr6:33781511 | A | G | 3 | a0001c0001t0004g0016 a0001c0001t0004g0054 a0001c0001t0004g0055 |
7 | HG02145.hp2 HG02723.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.854-358T>C | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 3/8 | chr6 | 33781511 | |||||||
| chr6:33781516 | G | A | 45 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0022 others(42): Show |
120 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.854-363C>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 3/8 | chr6 | 33781516 | |||||||
| chr6:33781749 | G | C | 1 | a0001c0001t0004g0017 | 4 | HG00741.hp2 HG02055.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.854-596C>G | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 3/8 | chr6 | 33781749 | |||||||
| chr6:33781758 | TCCCCTGG others(11): Show |
T | 6 | a0001c0001t0001g0014 a0001c0001t0001g0036 a0001c0001t0001g0071 others(3): Show |
12 | HG00408.hp1 HG02129.hp1 NA18747.hp1 others(9): Show |
intron_variant | MODIFIER | c.854-623_854-606del others(18): Show |
LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 3/8 | chr6 | 33781758 | |||||||
| chr6:33781902 | C | T | 1 | a0001c0001t0001g0070 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.854-749G>A | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 3/8 | chr6 | 33781902 | |||||||
| chr6:33781909 | A | G | 136 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(133): Show |
346 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(343): Show |
intron_variant | MODIFIER | c.854-756T>C | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 3/8 | chr6 | 33781909 | |||||||
| chr6:33781962 | G | A | 91 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(88): Show |
226 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.854-809C>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 3/8 | chr6 | 33781962 | |||||||
| chr6:33782015 | A | G | 1 | a0001c0003t0006g0013 | 7 | HG01243.hp1 HG02055.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.854-862T>C | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 3/8 | chr6 | 33782015 | |||||||
| chr6:33782045 | C | CTGAA | 2 | a0001c0001t0006g0041 a0001c0003t0006g0013 |
9 | HG01243.hp1 HG02055.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.854-896_854-893dup others(4): Show |
LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 3/8 | chr6 | 33782045 | |||||||
| chr6:33782057 | G | C | 91 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(88): Show |
226 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.854-904C>G | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 3/8 | chr6 | 33782057 | |||||||
| chr6:33782127 | A | G | 2 | a0001c0001t0009g0043 a0001c0001t0009g0122 |
3 | HG00642.hp2 HG01081.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.854-974T>C | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 3/8 | chr6 | 33782127 | |||||||
| chr6:33782189 | G | GGACCAC | 8 | a0002c0002t0005g0153 a0002c0002t0007g0024 a0002c0002t0007g0025 others(5): Show |
17 | HG01943.hp1 HG02148.hp2 NA18941.hp1 others(14): Show |
intron_variant | MODIFIER | c.854-1042_854-1037d others(8): Show |
LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 3/8 | chr6 | 33782189 | |||||||
| chr6:33782201 | T | C | 91 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(88): Show |
226 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.854-1048A>G | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 3/8 | chr6 | 33782201 | |||||||
| chr6:33782254 | A | G | 15 | a0002c0002t0005g0005 a0002c0002t0005g0052 a0002c0002t0005g0151 others(12): Show |
38 | HG00140.hp2 HG00323.hp1 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.854-1101T>C | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 3/8 | chr6 | 33782254 | |||||||
| chr6:33782303 | G | A | 2 | a0001c0001t0008g0044 a0001c0001t0008g0111 |
3 | HG01255.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.854-1150C>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 3/8 | chr6 | 33782303 | |||||||
| chr6:33782309 | A | G | 136 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(133): Show |
346 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(343): Show |
intron_variant | MODIFIER | c.854-1156T>C | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 3/8 | chr6 | 33782309 | |||||||
| chr6:33782393 | T | A | 1 | a0001c0001t0001g0040 | 2 | NA18950.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.854-1240A>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 3/8 | chr6 | 33782393 | |||||||
| chr6:33782417 | T | C | 1 | a0005c0005t0008g0118 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.854-1264A>G | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 3/8 | chr6 | 33782417 | |||||||
| chr6:33782774 | T | C | 1 | a0001c0001t0008g0125 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.853+1578A>G | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 3/8 | chr6 | 33782774 | |||||||
| chr6:33782841 | G | A | 1 | a0001c0001t0004g0059 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.853+1511C>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 3/8 | chr6 | 33782841 | |||||||
| chr6:33782903 | G | C | 1 | a0001c0001t0014g0144 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.853+1449C>G | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 3/8 | chr6 | 33782903 | |||||||
| chr6:33782918 | C | T | 1 | a0001c0001t0006g0121 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.853+1434G>A | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 3/8 | chr6 | 33782918 | |||||||
| chr6:33783154 | T | C | 66 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(63): Show |
163 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(160): Show |
intron_variant | MODIFIER | c.853+1198A>G | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 3/8 | chr6 | 33783154 | |||||||
| chr6:33783163 | T | A | 91 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(88): Show |
226 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.853+1189A>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 3/8 | chr6 | 33783163 | |||||||
| chr6:33783225 | C | T | 1 | a0001c0001t0001g0068 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.853+1127G>A | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 3/8 | chr6 | 33783225 | |||||||
| chr6:33783226 | G | A | 28 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0022 others(25): Show |
89 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.853+1126C>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 3/8 | chr6 | 33783226 | |||||||
| chr6:33783276 | C | T | 4 | a0001c0001t0008g0112 a0001c0001t0008g0113 a0001c0001t0017g0114 others(1): Show |
4 | HG01069.hp1 HG01891.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.853+1076G>A | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 3/8 | chr6 | 33783276 | |||||||
| chr6:33783345 | G | C | 73 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(70): Show |
178 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.853+1007C>G | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 3/8 | chr6 | 33783345 | |||||||
| chr6:33783364 | T | C | 1 | a0001c0001t0002g0142 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.853+988A>G | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 3/8 | chr6 | 33783364 | |||||||
| chr6:33783464 | T | C | 1 | a0001c0001t0004g0046 | 2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.853+888A>G | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 3/8 | chr6 | 33783464 | |||||||
| chr6:33783484 | G | A | 28 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0022 others(25): Show |
89 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.853+868C>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 3/8 | chr6 | 33783484 | |||||||
| chr6:33783620 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.853+732C>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 3/8 | chr6 | 33783620 | |||||||
| chr6:33783696 | T | G | 1 | a0005c0005t0008g0118 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.853+656A>C | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 3/8 | chr6 | 33783696 | |||||||
| chr6:33783829 | C | T | 4 | a0001c0001t0004g0029 a0001c0001t0004g0046 a0001c0001t0004g0127 others(1): Show |
7 | HG01361.hp2 HG02615.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.853+523G>A | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 3/8 | chr6 | 33783829 | |||||||
| chr6:33783840 | A | G | 1 | a0001c0001t0014g0144 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.853+512T>C | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 3/8 | chr6 | 33783840 | |||||||
| chr6:33783947 | C | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0061 |
5 | HG00558.hp1 NA18982.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.853+405G>A | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 3/8 | chr6 | 33783947 | |||||||
| chr6:33783990 | A | G | 145 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(142): Show |
359 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(356): Show |
intron_variant | MODIFIER | c.853+362T>C | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 3/8 | chr6 | 33783990 | |||||||
| chr6:33784007 | C | G | 34 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0022 others(31): Show |
98 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.853+345G>C | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 3/8 | chr6 | 33784007 | |||||||
| chr6:33784168 | G | A | 26 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0022 others(23): Show |
87 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.853+184C>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 3/8 | chr6 | 33784168 | |||||||
| chr6:33784236 | A | G | 91 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(88): Show |
226 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.853+116T>C | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 3/8 | chr6 | 33784236 | |||||||
| chr6:33784294 | G | A | 1 | a0005c0005t0008g0118 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.853+58C>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 3/8 | chr6 | 33784294 | |||||||
| chr6:33784515 | A | C | 3 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0105 |
3 | HG00544.hp1 HG00544.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.778-88T>G | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33784515 | |||||||
| chr6:33784609 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.778-182C>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33784609 | |||||||
| chr6:33784640 | A | C | 1 | a0001c0001t0001g0067 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.778-213T>G | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33784640 | |||||||
| chr6:33784773 | G | A | 28 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0022 others(25): Show |
89 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.778-346C>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33784773 | |||||||
| chr6:33784782 | C | T | 4 | a0001c0001t0004g0029 a0001c0001t0004g0046 a0001c0001t0004g0127 others(1): Show |
7 | HG01361.hp2 HG02615.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.778-355G>A | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33784782 | |||||||
| chr6:33784804 | G | A | 1 | a0001c0001t0008g0125 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.778-377C>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33784804 | |||||||
| chr6:33784832 | G | A | 1 | a0001c0001t0014g0144 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.778-405C>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33784832 | |||||||
| chr6:33784883 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.778-456G>A | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33784883 | |||||||
| chr6:33784946 | C | T | 6 | a0001c0001t0005g0108 a0001c0001t0008g0020 a0001c0001t0008g0044 others(3): Show |
10 | HG00423.hp1 HG01123.hp1 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.778-519G>A | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33784946 | |||||||
| chr6:33784950 | C | G | 1 | a0001c0001t0001g0066 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.778-523G>C | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33784950 | |||||||
| chr6:33785100 | C | T | 1 | a0001c0001t0002g0126 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.778-673G>A | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33785100 | |||||||
| chr6:33785112 | G | A | 1 | a0001c0001t0002g0143 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.778-685C>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33785112 | |||||||
| chr6:33785126 | A | C | 1 | a0001c0001t0001g0066 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.778-699T>G | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33785126 | |||||||
| chr6:33785147 | T | C | 1 | a0001c0001t0008g0044 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.778-720A>G | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33785147 | |||||||
| chr6:33785321 | T | A | 1 | a0001c0001t0003g0119 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.778-894A>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33785321 | |||||||
| chr6:33785425 | G | A | 1 | a0001c0001t0002g0120 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.778-998C>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33785425 | |||||||
| chr6:33785502 | T | A | 1 | a0001c0001t0008g0044 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.778-1075A>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33785502 | |||||||
| chr6:33785514 | A | G | 1 | a0001c0001t0008g0044 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.778-1087T>C | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33785514 | |||||||
| chr6:33785517 | G | T | 1 | a0001c0001t0008g0044 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.778-1090C>A | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33785517 | |||||||
| chr6:33785519 | C | T | 1 | a0001c0001t0008g0044 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.778-1092G>A | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33785519 | |||||||
| chr6:33785520 | A | T | 1 | a0001c0001t0008g0044 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.778-1093T>A | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33785520 | |||||||
| chr6:33785522 | G | T | 1 | a0001c0001t0008g0044 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.778-1095C>A | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33785522 | |||||||
| chr6:33785524 | A | C | 1 | a0001c0001t0008g0044 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.778-1097T>G | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33785524 | |||||||
| chr6:33785525 | A | T | 1 | a0001c0001t0008g0044 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.778-1098T>A | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33785525 | |||||||
| chr6:33785526 | C | G | 1 | a0001c0001t0008g0044 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.778-1099G>C | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33785526 | |||||||
| chr6:33785527 | A | C | 1 | a0001c0001t0008g0044 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.778-1100T>G | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33785527 | |||||||
| chr6:33785528 | A | C | 1 | a0001c0001t0008g0044 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.778-1101T>G | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33785528 | |||||||
| chr6:33785530 | T | G | 1 | a0001c0001t0008g0044 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.778-1103A>C | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33785530 | |||||||
| chr6:33785531 | G | A | 1 | a0001c0001t0008g0044 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.778-1104C>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33785531 | |||||||
| chr6:33785532 | T | G | 1 | a0001c0001t0008g0044 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.778-1105A>C | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33785532 | |||||||
| chr6:33785534 | C | G | 1 | a0001c0001t0008g0044 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.778-1107G>C | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33785534 | |||||||
| chr6:33785539 | C | G | 1 | a0001c0001t0008g0044 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.778-1112G>C | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33785539 | |||||||
| chr6:33785544 | G | A | 1 | a0001c0001t0008g0044 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.778-1117C>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33785544 | |||||||
| chr6:33785545 | T | G | 1 | a0001c0001t0008g0044 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.778-1118A>C | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33785545 | |||||||
| chr6:33785546 | G | T | 1 | a0001c0001t0008g0044 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.778-1119C>A | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33785546 | |||||||
| chr6:33785547 | G | A | 1 | a0001c0001t0008g0044 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.778-1120C>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33785547 | |||||||
| chr6:33785552 | G | A | 1 | a0001c0001t0008g0044 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.778-1125C>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33785552 | |||||||
| chr6:33785556 | C | A | 1 | a0001c0001t0008g0044 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.778-1129G>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33785556 | |||||||
| chr6:33785558 | T | G | 1 | a0001c0001t0008g0044 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.778-1131A>C | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33785558 | |||||||
| chr6:33785559 | TTAGAGAT others(372): Show |
T | 1 | a0001c0001t0008g0044 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.777+796_778-1133de others(1): Show |
LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33785559 | |||||||
| chr6:33785896 | G | A | 87 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(84): Show |
215 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.777+838C>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33785896 | |||||||
| chr6:33785945 | G | C | 1 | a0001c0001t0014g0144 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.777+789C>G | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33785945 | |||||||
| chr6:33785947 | A | C | 1 | a0001c0001t0008g0044 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.777+787T>G | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33785947 | |||||||
| chr6:33785948 | G | T | 1 | a0001c0001t0008g0044 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.777+786C>A | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33785948 | |||||||
| chr6:33785952 | T | C | 1 | a0001c0001t0008g0044 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.777+782A>G | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33785952 | |||||||
| chr6:33785953 | G | T | 1 | a0001c0001t0008g0044 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.777+781C>A | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33785953 | |||||||
| chr6:33785954 | G | C | 1 | a0001c0001t0008g0044 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.777+780C>G | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33785954 | |||||||
| chr6:33785963 | C | T | 1 | a0001c0001t0008g0044 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.777+771G>A | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33785963 | |||||||
| chr6:33785965 | A | C | 1 | a0001c0001t0008g0044 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.777+769T>G | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33785965 | |||||||
| chr6:33785967 | G | T | 1 | a0001c0001t0008g0044 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.777+767C>A | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33785967 | |||||||
| chr6:33785968 | C | A | 1 | a0001c0001t0008g0044 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.777+766G>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33785968 | |||||||
| chr6:33785969 | G | A | 2 | a0001c0001t0001g0103 a0001c0001t0001g0104 |
2 | HG01346.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.777+765C>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33785969 | |||||||
| chr6:33785971 | C | T | 1 | a0001c0001t0008g0044 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.777+763G>A | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33785971 | |||||||
| chr6:33785973 | T | A | 1 | a0001c0001t0008g0044 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.777+761A>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33785973 | |||||||
| chr6:33785974 | T | C | 1 | a0001c0001t0008g0044 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.777+760A>G | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33785974 | |||||||
| chr6:33785975 | T | A | 1 | a0001c0001t0008g0044 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.777+759A>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33785975 | |||||||
| chr6:33785979 | T | C | 1 | a0001c0001t0008g0044 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.777+755A>G | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33785979 | |||||||
| chr6:33785981 | C | A | 1 | a0001c0001t0008g0044 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.777+753G>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33785981 | |||||||
| chr6:33785982 | C | G | 1 | a0001c0001t0008g0044 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.777+752G>C | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33785982 | |||||||
| chr6:33785983 | C | T | 1 | a0001c0001t0008g0044 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.777+751G>A | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33785983 | |||||||
| chr6:33785988 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.777+746G>A | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33785988 | |||||||
| chr6:33786071 | C | G | 1 | a0001c0001t0008g0125 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.777+663G>C | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33786071 | |||||||
| chr6:33786207 | C | T | 1 | a0001c0001t0004g0124 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.777+527G>A | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33786207 | |||||||
| chr6:33786210 | C | CTTCCCCA others(17): Show |
91 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(88): Show |
226 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.777+523_777+524ins others(24): Show |
LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33786210 | |||||||
| chr6:33786418 | T | C | 1 | a0002c0002t0005g0155 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.777+316A>G | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33786418 | |||||||
| chr6:33786420 | A | C | 1 | a0001c0001t0001g0060 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.777+314T>G | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33786420 | |||||||
| chr6:33786524 | T | C | 7 | a0002c0002t0005g0005 a0002c0002t0005g0052 a0002c0002t0005g0151 others(4): Show |
20 | HG00140.hp2 HG00323.hp1 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.777+210A>G | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33786524 | |||||||
| chr6:33786619 | A | G | 91 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(88): Show |
226 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.777+115T>C | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33786619 | |||||||
| chr6:33786628 | A | G | 6 | a0001c0001t0006g0021 a0001c0001t0006g0121 a0001c0001t0006g0123 others(3): Show |
10 | HG00642.hp2 HG01081.hp1 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.777+106T>C | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33786628 | |||||||
| chr6:33786646 | T | G | 1 | a0001c0001t0004g0145 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.777+88A>C | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 2/8 | chr6 | 33786646 | |||||||
| chr6:33786815 | G | A | 66 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(63): Show |
163 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(160): Show |
intron_variant | MODIFIER | c.737-41C>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 1/8 | chr6 | 33786815 | |||||||
| chr6:33787040 | T | C | 76 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(73): Show |
188 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(185): Show |
intron_variant | MODIFIER | c.737-266A>G | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 1/8 | chr6 | 33787040 | |||||||
| chr6:33787044 | C | A | 1 | a0001c0001t0002g0049 | 2 | HG02258.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.737-270G>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 1/8 | chr6 | 33787044 | |||||||
| chr6:33787068 | G | C | 1 | a0001c0001t0001g0105 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.737-294C>G | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 1/8 | chr6 | 33787068 | |||||||
| chr6:33787167 | C | G | 1 | a0001c0001t0005g0108 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.737-393G>C | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 1/8 | chr6 | 33787167 | |||||||
| chr6:33787226 | TAAAGCAT others(14): Show |
T | 3 | a0001c0001t0003g0006 a0001c0001t0003g0028 a0001c0001t0003g0042 |
17 | HG00280.hp1 HG01070.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.737-473_737-453del others(21): Show |
LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 1/8 | chr6 | 33787226 | |||||||
| chr6:33787339 | TCA | T | 91 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(88): Show |
226 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.737-567_737-566del others(2): Show |
LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 1/8 | chr6 | 33787339 | |||||||
| chr6:33787412 | G | T | 1 | a0001c0001t0004g0053 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.737-638C>A | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 1/8 | chr6 | 33787412 | |||||||
| chr6:33787764 | G | A | 134 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(131): Show |
343 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.736+617C>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 1/8 | chr6 | 33787764 | |||||||
| chr6:33787934 | G | C | 134 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(131): Show |
343 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.736+447C>G | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 1/8 | chr6 | 33787934 | |||||||
| chr6:33788061 | G | T | 4 | a0001c0001t0006g0041 a0001c0001t0006g0106 a0001c0001t0006g0107 others(1): Show |
11 | HG01192.hp2 HG01243.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.736+320C>A | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 1/8 | chr6 | 33788061 | |||||||
| chr6:33788103 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.736+278C>T | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 1/8 | chr6 | 33788103 | |||||||
| chr6:33788113 | T | C | 55 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(52): Show |
132 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(129): Show |
intron_variant | MODIFIER | c.736+268A>G | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 1/8 | chr6 | 33788113 | |||||||
| chr6:33788249 | C | T | 91 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(88): Show |
226 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.736+132G>A | LEMD2 | ENSG00000161904.13 | transcript | ENST00000293760.10 | protein_coding | 1/8 | chr6 | 33788249 |