Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4277 |
| ensemblid | ENSG00000204516.10 |
| hgncid | 7091 |
| symbol | MICB |
| name | MHC class I polypeptide-related sequence B |
| refseq_nuc | NM_005931.5 |
| refseq_prot | NP_005922.2 |
| ensembl_nuc | ENST00000252229.7 |
| ensembl_prot | ENSP00000252229.6 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 31498145 |
| end | 31511124 |
| strand | + |
| ver | v1.2 |
| region | chr6:31498145-31511124 |
| region5000 | chr6:31493145-31516124 |
| regionname0 | MICB_chr6_31498145_31511124 |
| regionname5000 | MICB_chr6_31493145_31516124 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 383 | 252 | 34 | 46 | 134 | 11 | 27 | 111 | MICB_chr6_31493145_31516124 | MICB | MGLGR others(378): Show |
chr6 | 31493145 | 31516124 |
| a0002 | 0/1 | 383 | 89 | 27 | 18 | 30 | 1 | 12 | 23 | MICB_chr6_31493145_31516124 | MICB | MGLGR others(378): Show |
chr6 | 31493145 | 31516124 |
| a0003 | 0/0 | 383 | 54 | 11 | 9 | 28 | 2 | 4 | 22 | MICB_chr6_31493145_31516124 | MICB | MGLGR others(378): Show |
chr6 | 31493145 | 31516124 |
| a0004 | 0/0 | 383 | 27 | 10 | 6 | 7 | 2 | 2 | 3 | MICB_chr6_31493145_31516124 | MICB | MGLGR others(378): Show |
chr6 | 31493145 | 31516124 |
| a0005 | 0/0 | 383 | 13 | 4 | 1 | 4 | 1 | 3 | 0 | MICB_chr6_31493145_31516124 | MICB | MGLGR others(378): Show |
chr6 | 31493145 | 31516124 |
| a0006 | 0/0 | 192 | 9 | 1 | 2 | 6 | 0 | 0 | 4 | MICB_chr6_31493145_31516124 | MICB | MGLGR others(187): Show |
chr6 | 31493145 | 31516124 |
| a0007 | 0/0 | 383 | 8 | 2 | 0 | 5 | 1 | 0 | 3 | MICB_chr6_31493145_31516124 | MICB | MGLGR others(378): Show |
chr6 | 31493145 | 31516124 |
| a0008 | 0/0 | 383 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | MGLGR others(378): Show |
chr6 | 31493145 | 31516124 |
| a0009 | 0/0 | 383 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MICB_chr6_31493145_31516124 | MICB | MGLGR others(378): Show |
chr6 | 31493145 | 31516124 |
| a0010 | 0/0 | 383 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MICB_chr6_31493145_31516124 | MICB | MGLGR others(378): Show |
chr6 | 31493145 | 31516124 |
| a0011 | 0/0 | 383 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | MGLGR others(378): Show |
chr6 | 31493145 | 31516124 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1149 | 207 | 32 | 44 | 105 | 10 | 16 | MICB_chr6_31493145_31516124 | MICB | ATGGG others(1144): Show |
chr6 | 31493145 | 31516124 | ||
| a0001c0004 | 0/0 | 1149 | 40 | 0 | 0 | 29 | 1 | 10 | MICB_chr6_31493145_31516124 | MICB | ATGGG others(1144): Show |
chr6 | 31493145 | 31516124 | ||
| a0001c0009 | 0/0 | 1149 | 4 | 2 | 1 | 0 | 0 | 1 | MICB_chr6_31493145_31516124 | MICB | ATGGG others(1144): Show |
chr6 | 31493145 | 31516124 | ||
| a0001c0012 | 0/0 | 1149 | 1 | 0 | 1 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | ATGGG others(1144): Show |
chr6 | 31493145 | 31516124 | ||
| a0002c0002 | 0/1 | 1149 | 87 | 26 | 18 | 29 | 1 | 12 | MICB_chr6_31493145_31516124 | MICB | ATGGG others(1144): Show |
chr6 | 31493145 | 31516124 | ||
| a0002c0013 | 0/0 | 1149 | 1 | 1 | 0 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | ATGGG others(1144): Show |
chr6 | 31493145 | 31516124 | ||
| a0002c0017 | 0/0 | 1149 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | ATGGG others(1144): Show |
chr6 | 31493145 | 31516124 | ||
| a0003c0003 | 0/0 | 1149 | 53 | 10 | 9 | 28 | 2 | 4 | MICB_chr6_31493145_31516124 | MICB | ATGGG others(1144): Show |
chr6 | 31493145 | 31516124 | ||
| a0003c0011 | 0/0 | 1149 | 1 | 1 | 0 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | ATGGG others(1144): Show |
chr6 | 31493145 | 31516124 | ||
| a0004c0005 | 0/0 | 1149 | 27 | 10 | 6 | 7 | 2 | 2 | MICB_chr6_31493145_31516124 | MICB | ATGGG others(1144): Show |
chr6 | 31493145 | 31516124 | ||
| a0005c0006 | 0/0 | 1149 | 13 | 4 | 1 | 4 | 1 | 3 | MICB_chr6_31493145_31516124 | MICB | ATGGG others(1144): Show |
chr6 | 31493145 | 31516124 | ||
| a0006c0007 | 0/0 | 1149 | 9 | 1 | 2 | 6 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | ATGGG others(1144): Show |
chr6 | 31493145 | 31516124 | ||
| a0007c0008 | 0/0 | 1149 | 8 | 2 | 0 | 5 | 1 | 0 | MICB_chr6_31493145_31516124 | MICB | ATGGG others(1144): Show |
chr6 | 31493145 | 31516124 | ||
| a0008c0010 | 0/0 | 1149 | 4 | 4 | 0 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | ATGGG others(1144): Show |
chr6 | 31493145 | 31516124 | ||
| a0009c0014 | 0/0 | 1149 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | ATGGG others(1144): Show |
chr6 | 31493145 | 31516124 | ||
| a0010c0016 | 0/0 | 1149 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | ATGGG others(1144): Show |
chr6 | 31493145 | 31516124 | ||
| a0011c0015 | 0/0 | 1149 | 1 | 1 | 0 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | ATGGG others(1144): Show |
chr6 | 31493145 | 31516124 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2414 | 183 | 28 | 33 | 101 | 6 | 15 | MICB_chr6_31493145_31516124 | MICB | ATTCA others(2409): Show |
chr6 | 31493145 | 31516124 |
| a0001c0001t0003 | 0/0 | 2408 | 11 | 1 | 5 | 1 | 3 | 1 | MICB_chr6_31493145_31516124 | MICB | ATTCA others(2403): Show |
chr6 | 31493145 | 31516124 |
| a0001c0001t0005 | 0/0 | 2408 | 6 | 1 | 4 | 0 | 1 | 0 | MICB_chr6_31493145_31516124 | MICB | ATTCA others(2403): Show |
chr6 | 31493145 | 31516124 |
| a0001c0001t0009 | 0/0 | 2414 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | ATTCA others(2409): Show |
chr6 | 31493145 | 31516124 |
| a0001c0001t0010 | 0/0 | 2402 | 1 | 1 | 0 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | ATTCA others(2397): Show |
chr6 | 31493145 | 31516124 |
| a0001c0001t0011 | 0/0 | 2414 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | ATTCA others(2409): Show |
chr6 | 31493145 | 31516124 |
| a0001c0001t0012 | 0/0 | 2414 | 1 | 1 | 0 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | ATTCA others(2409): Show |
chr6 | 31493145 | 31516124 |
| a0001c0001t0013 | 0/0 | 2414 | 1 | 0 | 1 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | ATTCA others(2409): Show |
chr6 | 31493145 | 31516124 |
| a0001c0001t0014 | 0/0 | 2414 | 1 | 0 | 1 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | ATTCA others(2409): Show |
chr6 | 31493145 | 31516124 |
| a0001c0001t0015 | 0/0 | 2414 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | ATTCA others(2409): Show |
chr6 | 31493145 | 31516124 |
| a0001c0004t0001 | 0/0 | 2414 | 40 | 0 | 0 | 29 | 1 | 10 | MICB_chr6_31493145_31516124 | MICB | ATTCA others(2409): Show |
chr6 | 31493145 | 31516124 |
| a0001c0009t0007 | 0/0 | 2414 | 4 | 2 | 1 | 0 | 0 | 1 | MICB_chr6_31493145_31516124 | MICB | ATTCA others(2409): Show |
chr6 | 31493145 | 31516124 |
| a0001c0012t0003 | 0/0 | 2408 | 1 | 0 | 1 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | ATTCA others(2403): Show |
chr6 | 31493145 | 31516124 |
| a0002c0002t0001 | 0/1 | 2414 | 74 | 21 | 15 | 29 | 1 | 7 | MICB_chr6_31493145_31516124 | MICB | ATTCA others(2409): Show |
chr6 | 31493145 | 31516124 |
| a0002c0002t0004 | 0/0 | 2413 | 11 | 3 | 3 | 0 | 0 | 5 | MICB_chr6_31493145_31516124 | MICB | ATTCA others(2408): Show |
chr6 | 31493145 | 31516124 |
| a0002c0002t0008 | 0/0 | 2414 | 2 | 2 | 0 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | ATTCA others(2409): Show |
chr6 | 31493145 | 31516124 |
| a0002c0013t0001 | 0/0 | 2414 | 1 | 1 | 0 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | ATTCA others(2409): Show |
chr6 | 31493145 | 31516124 |
| a0002c0017t0001 | 0/0 | 2414 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | ATTCA others(2409): Show |
chr6 | 31493145 | 31516124 |
| a0003c0003t0002 | 0/0 | 2416 | 49 | 10 | 9 | 25 | 2 | 3 | MICB_chr6_31493145_31516124 | MICB | ATTCA others(2411): Show |
chr6 | 31493145 | 31516124 |
| a0003c0003t0006 | 0/0 | 2416 | 4 | 0 | 0 | 3 | 0 | 1 | MICB_chr6_31493145_31516124 | MICB | ATTCA others(2411): Show |
chr6 | 31493145 | 31516124 |
| a0003c0011t0002 | 0/0 | 2416 | 1 | 1 | 0 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | ATTCA others(2411): Show |
chr6 | 31493145 | 31516124 |
| a0004c0005t0001 | 0/0 | 2414 | 27 | 10 | 6 | 7 | 2 | 2 | MICB_chr6_31493145_31516124 | MICB | ATTCA others(2409): Show |
chr6 | 31493145 | 31516124 |
| a0005c0006t0002 | 0/0 | 2416 | 12 | 3 | 1 | 4 | 1 | 3 | MICB_chr6_31493145_31516124 | MICB | ATTCA others(2411): Show |
chr6 | 31493145 | 31516124 |
| a0005c0006t0016 | 0/0 | 2416 | 1 | 1 | 0 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | ATTCA others(2411): Show |
chr6 | 31493145 | 31516124 |
| a0006c0007t0002 | 0/0 | 2416 | 9 | 1 | 2 | 6 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | ATTCA others(2411): Show |
chr6 | 31493145 | 31516124 |
| a0007c0008t0001 | 0/0 | 2414 | 8 | 2 | 0 | 5 | 1 | 0 | MICB_chr6_31493145_31516124 | MICB | ATTCA others(2409): Show |
chr6 | 31493145 | 31516124 |
| a0008c0010t0002 | 0/0 | 2416 | 4 | 4 | 0 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | ATTCA others(2411): Show |
chr6 | 31493145 | 31516124 |
| a0009c0014t0001 | 0/0 | 2414 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | ATTCA others(2409): Show |
chr6 | 31493145 | 31516124 |
| a0010c0016t0006 | 0/0 | 2416 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | ATTCA others(2411): Show |
chr6 | 31493145 | 31516124 |
| a0011c0015t0001 | 0/0 | 2414 | 1 | 1 | 0 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | ATTCA others(2409): Show |
chr6 | 31493145 | 31516124 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 37 | 0 | 9 | 28 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0001g0002 | 0/0 | 27 | 1 | 5 | 15 | 1 | 5 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0001g0004 | 0/0 | 17 | 3 | 0 | 13 | 0 | 1 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0001g0008 | 0/0 | 9 | 8 | 1 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0001g0010 | 0/0 | 7 | 6 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0001g0012 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0001g0013 | 0/0 | 6 | 2 | 3 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0001g0016 | 0/0 | 6 | 0 | 4 | 0 | 1 | 1 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0001g0022 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0001g0026 | 0/0 | 4 | 0 | 0 | 0 | 0 | 4 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0001g0027 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0001g0029 | 0/0 | 3 | 0 | 0 | 1 | 1 | 1 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0001g0031 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0001g0036 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0001g0037 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0001g0058 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0001g0059 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0003g0011 | 0/0 | 8 | 1 | 3 | 1 | 3 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0005g0025 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0005g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0005g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0009g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0010g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0011g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0012g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0013g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0014g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0001t0015g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0004t0001g0003 | 0/0 | 20 | 0 | 0 | 19 | 0 | 1 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0004t0001g0017 | 0/0 | 5 | 0 | 0 | 3 | 0 | 2 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0004t0001g0023 | 0/0 | 4 | 0 | 0 | 1 | 0 | 3 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0004t0001g0046 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0004t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0004t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0004t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0004t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0004t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0004t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0004t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0004t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0009t0007g0045 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0009t0007g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0009t0007g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0001c0012t0003g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0002c0002t0001g0005 | 0/0 | 15 | 1 | 5 | 8 | 0 | 1 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0002c0002t0001g0007 | 0/0 | 9 | 0 | 1 | 8 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0002c0002t0001g0015 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0002c0002t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0002c0002t0001g0032 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0002c0002t0001g0035 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0002c0002t0001g0052 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0002c0002t0001g0053 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0002c0002t0001g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0002c0002t0001g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0002c0002t0001g0056 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0002c0002t0001g0057 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0002c0002t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0002c0002t0001g0131 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0002c0002t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0002c0002t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0002c0002t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0002c0002t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0002c0002t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0002c0002t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0002c0002t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0002c0002t0004g0018 | 0/0 | 5 | 0 | 0 | 0 | 0 | 5 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0002c0002t0004g0033 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0002c0002t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0002c0002t0004g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0002c0002t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0002c0002t0008g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0002c0013t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0002c0017t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0003c0003t0002g0006 | 0/0 | 13 | 1 | 1 | 11 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0003c0003t0002g0009 | 0/0 | 9 | 2 | 3 | 4 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0003c0003t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0003c0003t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0003c0003t0002g0038 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0003c0003t0002g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0003c0003t0002g0061 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0003c0003t0002g0062 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0003c0003t0002g0063 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0003c0003t0002g0064 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0003c0003t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0003c0003t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0003c0003t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0003c0003t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0003c0003t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0003c0003t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0003c0003t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0003c0003t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0003c0003t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0003c0003t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0003c0003t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0003c0003t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0003c0003t0006g0021 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0003c0011t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0004c0005t0001g0019 | 0/0 | 5 | 0 | 3 | 0 | 2 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0004c0005t0001g0020 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0004c0005t0001g0034 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0004c0005t0001g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0004c0005t0001g0051 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0004c0005t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0004c0005t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0004c0005t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0004c0005t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0004c0005t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0004c0005t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0004c0005t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0004c0005t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0004c0005t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0004c0005t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0005c0006t0002g0014 | 0/0 | 6 | 1 | 0 | 2 | 0 | 3 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0005c0006t0002g0043 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0005c0006t0002g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0005c0006t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0005c0006t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0005c0006t0016g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0006c0007t0002g0030 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0006c0007t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0006c0007t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0006c0007t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0006c0007t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0006c0007t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0006c0007t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0007c0008t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0007c0008t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0007c0008t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0007c0008t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0007c0008t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0007c0008t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0007c0008t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0008c0010t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0008c0010t0002g0028 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0009c0014t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0010c0016t0006g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| a0011c0015t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0011 | EUR | GBR | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG00099 | hp2 | a0004 | c0005 | t0001 | g0019 | EUR | GBR | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG00140 | hp1 | a0005 | c0006 | t0002 | g0043 | EUR | GBR | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG00140 | hp2 | a0003 | c0003 | t0002 | g0182 | EUR | GBR | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG00280 | hp1 | a0004 | c0005 | t0001 | g0019 | EUR | FIN | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | FIN | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG00323 | hp1 | a0007 | c0008 | t0001 | g0136 | EUR | FIN | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG00323 | hp2 | a0002 | c0002 | t0001 | g0056 | EUR | FIN | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG00408 | hp1 | a0002 | c0002 | t0001 | g0054 | EAS | CHS | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | CHS | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG00438 | hp1 | a0003 | c0003 | t0002 | g0006 | EAS | CHS | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG00558 | hp2 | a0003 | c0003 | t0006 | g0021 | EAS | CHS | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG00597 | hp1 | a0002 | c0017 | t0001 | g0148 | EAS | CHS | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | CHS | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG00621 | hp1 | a0003 | c0003 | t0002 | g0006 | EAS | CHS | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | CHS | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0011 | AMR | PUR | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG00639 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | PUR | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG00642 | hp1 | a0001 | c0001 | t0005 | g0025 | AMR | PUR | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0053 | AMR | PUR | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG00673 | hp1 | a0001 | c0004 | t0001 | g0023 | EAS | CHS | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG00673 | hp2 | a0006 | c0007 | t0002 | g0087 | EAS | CHS | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG00733 | hp1 | a0001 | c0001 | t0005 | g0025 | AMR | PUR | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG00733 | hp2 | a0001 | c0012 | t0003 | g0180 | AMR | PUR | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG00735 | hp1 | a0002 | c0002 | t0004 | g0121 | AMR | PUR | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0107 | AMR | PUR | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG00738 | hp2 | a0004 | c0005 | t0001 | g0019 | AMR | PUR | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG00741 | hp1 | a0001 | c0001 | t0013 | g0060 | AMR | PUR | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01069 | hp1 | a0004 | c0005 | t0001 | g0019 | AMR | PUR | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | PUR | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01070 | hp1 | a0003 | c0003 | t0002 | g0048 | AMR | PUR | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01070 | hp2 | a0004 | c0005 | t0001 | g0110 | AMR | PUR | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01071 | hp1 | a0003 | c0003 | t0002 | g0048 | AMR | PUR | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | PUR | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01074 | hp1 | a0001 | c0009 | t0007 | g0045 | AMR | PUR | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0053 | AMR | PUR | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | PUR | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01106 | hp2 | a0003 | c0003 | t0002 | g0173 | AMR | PUR | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01109 | hp2 | a0004 | c0005 | t0001 | g0051 | AMR | PUR | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01167 | hp1 | a0002 | c0002 | t0004 | g0033 | AMR | PUR | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01167 | hp2 | a0006 | c0007 | t0002 | g0030 | AMR | PUR | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01168 | hp1 | a0002 | c0002 | t0001 | g0113 | AMR | PUR | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01169 | hp1 | a0002 | c0002 | t0004 | g0033 | AMR | PUR | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01169 | hp2 | a0002 | c0002 | t0001 | g0052 | AMR | PUR | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01175 | hp2 | a0003 | c0003 | t0002 | g0006 | AMR | PUR | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01243 | hp1 | a0004 | c0005 | t0001 | g0020 | AMR | PUR | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01255 | hp1 | a0003 | c0003 | t0002 | g0009 | AMR | CLM | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01256 | hp1 | a0003 | c0003 | t0002 | g0009 | AMR | CLM | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01256 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | CLM | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01257 | hp1 | a0003 | c0003 | t0002 | g0181 | AMR | CLM | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01257 | hp2 | a0001 | c0001 | t0005 | g0025 | AMR | CLM | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01258 | hp1 | a0003 | c0003 | t0002 | g0062 | AMR | CLM | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | CLM | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | CLM | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0152 | AMR | CLM | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01358 | hp1 | a0002 | c0002 | t0001 | g0057 | AMR | CLM | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0159 | AMR | CLM | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01433 | hp1 | a0004 | c0005 | t0001 | g0019 | AMR | CLM | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01496 | hp2 | a0003 | c0003 | t0002 | g0009 | AMR | CLM | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0011 | EUR | IBS | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0169 | EUR | IBS | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0070 | EUR | IBS | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0071 | EUR | IBS | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0011 | EUR | IBS | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01884 | hp1 | a0008 | c0010 | t0002 | g0028 | AFR | ACB | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01891 | hp2 | a0002 | c0002 | t0001 | g0015 | AFR | ACB | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01934 | hp2 | a0005 | c0006 | t0002 | g0090 | AMR | PEL | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01952 | hp1 | a0002 | c0002 | t0001 | g0007 | AMR | PEL | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0052 | AMR | PEL | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0145 | EAS | KHV | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0154 | EAS | KHV | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02040 | hp1 | a0004 | c0005 | t0001 | g0119 | EAS | KHV | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02055 | hp1 | a0002 | c0002 | t0001 | g0144 | AFR | ACB | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02055 | hp2 | a0003 | c0003 | t0002 | g0006 | AFR | ACB | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02056 | hp2 | a0006 | c0007 | t0002 | g0084 | EAS | KHV | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02071 | hp2 | a0003 | c0003 | t0002 | g0176 | EAS | KHV | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02074 | hp2 | a0001 | c0001 | t0009 | g0001 | EAS | KHV | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02080 | hp1 | a0004 | c0005 | t0001 | g0034 | EAS | KHV | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02080 | hp2 | a0005 | c0006 | t0002 | g0014 | EAS | KHV | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02083 | hp1 | a0007 | c0008 | t0001 | g0114 | EAS | KHV | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02083 | hp2 | a0005 | c0006 | t0002 | g0014 | EAS | KHV | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02129 | hp1 | a0004 | c0005 | t0001 | g0124 | EAS | KHV | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02129 | hp2 | a0005 | c0006 | t0002 | g0092 | EAS | KHV | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0117 | EAS | KHV | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02145 | hp1 | a0001 | c0009 | t0007 | g0045 | AFR | ACB | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02148 | hp1 | a0001 | c0001 | t0005 | g0167 | AMR | PEL | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02155 | hp1 | a0007 | c0008 | t0001 | g0115 | EAS | CDX | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | CDX | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0011 | AFR | ACB | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02273 | hp2 | a0001 | c0001 | t0014 | g0042 | AMR | PEL | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02280 | hp1 | a0003 | c0003 | t0002 | g0175 | AFR | ACB | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02280 | hp2 | a0002 | c0002 | t0001 | g0032 | AFR | ACB | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02300 | hp2 | a0006 | c0007 | t0002 | g0030 | AMR | PEL | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02523 | hp1 | a0004 | c0005 | t0001 | g0118 | EAS | KHV | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02572 | hp1 | a0002 | c0002 | t0001 | g0141 | AFR | GWD | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02602 | hp1 | a0001 | c0004 | t0001 | g0003 | SAS | PJL | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0108 | SAS | PJL | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02622 | hp1 | a0001 | c0001 | t0010 | g0072 | AFR | GWD | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02622 | hp2 | a0004 | c0005 | t0001 | g0125 | AFR | GWD | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02647 | hp1 | a0002 | c0002 | t0001 | g0153 | AFR | GWD | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02647 | hp2 | a0005 | c0006 | t0002 | g0044 | AFR | GWD | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02683 | hp2 | a0001 | c0004 | t0001 | g0017 | SAS | PJL | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02698 | hp1 | a0001 | c0004 | t0001 | g0023 | SAS | PJL | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02717 | hp1 | a0007 | c0008 | t0001 | g0138 | AFR | GWD | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02717 | hp2 | a0003 | c0003 | t0002 | g0009 | AFR | GWD | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02723 | hp1 | a0008 | c0010 | t0002 | g0028 | AFR | GWD | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02723 | hp2 | a0002 | c0002 | t0001 | g0032 | AFR | GWD | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02735 | hp1 | a0004 | c0005 | t0001 | g0034 | SAS | PJL | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02735 | hp2 | a0002 | c0002 | t0004 | g0018 | SAS | PJL | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02738 | hp1 | a0001 | c0009 | t0007 | g0097 | SAS | PJL | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02738 | hp2 | a0002 | c0002 | t0001 | g0151 | SAS | PJL | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02809 | hp1 | a0008 | c0010 | t0002 | g0028 | AFR | GWD | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02818 | hp1 | a0002 | c0002 | t0001 | g0035 | AFR | GWD | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02886 | hp2 | a0001 | c0001 | t0012 | g0010 | AFR | GWD | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02895 | hp1 | a0003 | c0003 | t0002 | g0009 | AFR | GWD | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02895 | hp2 | a0002 | c0002 | t0001 | g0035 | AFR | GWD | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02896 | hp1 | a0002 | c0002 | t0008 | g0024 | AFR | GWD | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02896 | hp2 | a0002 | c0002 | t0001 | g0143 | AFR | GWD | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02897 | hp1 | a0002 | c0002 | t0001 | g0035 | AFR | GWD | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02897 | hp2 | a0002 | c0002 | t0008 | g0024 | AFR | GWD | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02922 | hp1 | a0003 | c0003 | t0002 | g0038 | AFR | ESN | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02922 | hp2 | a0002 | c0002 | t0004 | g0033 | AFR | ESN | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02965 | hp2 | a0004 | c0005 | t0001 | g0051 | AFR | ESN | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02970 | hp2 | a0003 | c0003 | t0002 | g0171 | AFR | ESN | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02976 | hp2 | a0004 | c0005 | t0001 | g0020 | AFR | ESN | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0015 | AFR | MSL | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG03098 | hp2 | a0002 | c0013 | t0001 | g0139 | AFR | MSL | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG03130 | hp1 | a0003 | c0003 | t0002 | g0021 | AFR | ESN | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG03130 | hp2 | a0004 | c0005 | t0001 | g0050 | AFR | ESN | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG03139 | hp2 | a0002 | c0002 | t0001 | g0015 | AFR | ESN | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG03195 | hp1 | a0004 | c0005 | t0001 | g0050 | AFR | ESN | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG03195 | hp2 | a0004 | c0005 | t0001 | g0020 | AFR | ESN | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | MSL | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG03209 | hp2 | a0007 | c0008 | t0001 | g0137 | AFR | MSL | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG03225 | hp1 | a0008 | c0010 | t0002 | g0006 | AFR | MSL | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG03239 | hp1 | a0002 | c0002 | t0004 | g0018 | SAS | PJL | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG03453 | hp1 | a0003 | c0003 | t0002 | g0038 | AFR | MSL | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG03453 | hp2 | a0005 | c0006 | t0002 | g0044 | AFR | MSL | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG03486 | hp1 | a0002 | c0002 | t0001 | g0147 | AFR | MSL | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG03486 | hp2 | a0004 | c0005 | t0001 | g0020 | AFR | MSL | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG03490 | hp1 | a0001 | c0004 | t0001 | g0023 | SAS | PJL | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG03490 | hp2 | a0001 | c0004 | t0001 | g0046 | SAS | PJL | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0024 | SAS | PJL | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0142 | SAS | PJL | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG03492 | hp2 | a0001 | c0004 | t0001 | g0046 | SAS | PJL | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG03540 | hp1 | a0003 | c0003 | t0002 | g0038 | AFR | GWD | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG03540 | hp2 | a0002 | c0002 | t0001 | g0140 | AFR | GWD | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG03579 | hp1 | a0003 | c0011 | t0002 | g0172 | AFR | MSL | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG03579 | hp2 | a0001 | c0009 | t0007 | g0093 | AFR | MSL | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0024 | SAS | PJL | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG03669 | hp1 | a0001 | c0004 | t0001 | g0104 | SAS | PJL | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0149 | SAS | STU | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | STU | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG03704 | hp1 | a0005 | c0006 | t0002 | g0014 | SAS | PJL | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG03704 | hp2 | a0003 | c0003 | t0002 | g0109 | SAS | PJL | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0005 | SAS | PJL | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG03831 | hp2 | a0001 | c0004 | t0001 | g0017 | SAS | BEB | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | BEB | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG03834 | hp2 | a0003 | c0003 | t0006 | g0021 | SAS | BEB | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | BEB | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG04115 | hp1 | a0001 | c0004 | t0001 | g0023 | SAS | STU | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG04115 | hp2 | a0005 | c0006 | t0002 | g0014 | SAS | STU | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG04184 | hp1 | a0005 | c0006 | t0002 | g0014 | SAS | BEB | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG04184 | hp2 | a0002 | c0002 | t0004 | g0018 | SAS | BEB | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG04199 | hp1 | a0003 | c0003 | t0002 | g0063 | SAS | STU | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG04199 | hp2 | a0004 | c0005 | t0001 | g0034 | SAS | STU | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG04204 | hp1 | a0001 | c0004 | t0001 | g0102 | SAS | STU | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG04204 | hp2 | a0002 | c0002 | t0004 | g0018 | SAS | STU | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG04228 | hp1 | a0002 | c0002 | t0004 | g0018 | SAS | STU | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG04228 | hp2 | a0003 | c0003 | t0002 | g0063 | SAS | STU | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18522 | hp1 | a0002 | c0002 | t0001 | g0130 | AFR | YRI | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18522 | hp2 | a0004 | c0005 | t0001 | g0127 | AFR | YRI | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18612 | hp1 | a0003 | c0003 | t0006 | g0021 | EAS | CHB | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18612 | hp2 | a0005 | c0006 | t0002 | g0043 | EAS | CHB | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18747 | hp2 | a0003 | c0003 | t0002 | g0009 | EAS | CHB | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18906 | hp2 | a0004 | c0005 | t0001 | g0020 | AFR | YRI | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18940 | hp2 | a0001 | c0004 | t0001 | g0003 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18941 | hp2 | a0003 | c0003 | t0002 | g0106 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18946 | hp1 | a0003 | c0003 | t0002 | g0009 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18946 | hp2 | a0001 | c0004 | t0001 | g0003 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18948 | hp1 | a0003 | c0003 | t0002 | g0009 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18949 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18949 | hp2 | a0003 | c0003 | t0002 | g0006 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18950 | hp1 | a0001 | c0004 | t0001 | g0003 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18950 | hp2 | a0003 | c0003 | t0002 | g0006 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18952 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18952 | hp2 | a0003 | c0003 | t0002 | g0006 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18953 | hp2 | a0003 | c0003 | t0002 | g0178 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18954 | hp1 | a0007 | c0008 | t0001 | g0049 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18954 | hp2 | a0001 | c0004 | t0001 | g0003 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18956 | hp1 | a0001 | c0004 | t0001 | g0003 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18957 | hp1 | a0001 | c0004 | t0001 | g0017 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18957 | hp2 | a0001 | c0004 | t0001 | g0100 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18961 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18962 | hp1 | a0001 | c0004 | t0001 | g0003 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18962 | hp2 | a0003 | c0003 | t0002 | g0028 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18963 | hp2 | a0002 | c0002 | t0001 | g0055 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18965 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18967 | hp1 | a0003 | c0003 | t0002 | g0177 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18967 | hp2 | a0002 | c0002 | t0001 | g0155 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18968 | hp2 | a0001 | c0004 | t0001 | g0047 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18969 | hp1 | a0001 | c0004 | t0001 | g0003 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18969 | hp2 | a0006 | c0007 | t0002 | g0030 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18970 | hp2 | a0003 | c0003 | t0002 | g0064 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0128 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18971 | hp2 | a0009 | c0014 | t0001 | g0134 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18972 | hp2 | a0002 | c0002 | t0001 | g0055 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18974 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18975 | hp2 | a0003 | c0003 | t0002 | g0006 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18977 | hp2 | a0003 | c0003 | t0002 | g0061 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18979 | hp1 | a0001 | c0004 | t0001 | g0017 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18980 | hp1 | a0003 | c0003 | t0002 | g0062 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18980 | hp2 | a0007 | c0008 | t0001 | g0049 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18981 | hp1 | a0001 | c0004 | t0001 | g0047 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18981 | hp2 | a0001 | c0004 | t0001 | g0103 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18982 | hp1 | a0001 | c0004 | t0001 | g0003 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18984 | hp2 | a0001 | c0004 | t0001 | g0003 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18985 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18987 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18988 | hp1 | a0007 | c0008 | t0001 | g0116 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18988 | hp2 | a0003 | c0003 | t0002 | g0009 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18989 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18990 | hp2 | a0002 | c0002 | t0001 | g0054 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18991 | hp2 | a0001 | c0004 | t0001 | g0003 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18992 | hp2 | a0001 | c0004 | t0001 | g0003 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18994 | hp1 | a0003 | c0003 | t0002 | g0006 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18994 | hp2 | a0002 | c0002 | t0001 | g0150 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18998 | hp1 | a0001 | c0004 | t0001 | g0003 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18999 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19000 | hp1 | a0003 | c0003 | t0002 | g0006 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19001 | hp1 | a0001 | c0004 | t0001 | g0003 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19001 | hp2 | a0003 | c0003 | t0002 | g0006 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19002 | hp2 | a0003 | c0003 | t0006 | g0021 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19003 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19004 | hp1 | a0003 | c0003 | t0002 | g0061 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19004 | hp2 | a0001 | c0004 | t0001 | g0003 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19005 | hp1 | a0004 | c0005 | t0001 | g0123 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19009 | hp2 | a0001 | c0004 | t0001 | g0003 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19011 | hp2 | a0003 | c0003 | t0002 | g0006 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | LWK | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19030 | hp2 | a0002 | c0002 | t0004 | g0120 | AFR | LWK | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19057 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19060 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19060 | hp2 | a0001 | c0004 | t0001 | g0099 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19064 | hp1 | a0003 | c0003 | t0002 | g0064 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19065 | hp2 | a0001 | c0004 | t0001 | g0098 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19066 | hp2 | a0001 | c0004 | t0001 | g0017 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19070 | hp1 | a0001 | c0004 | t0001 | g0003 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19072 | hp1 | a0004 | c0005 | t0001 | g0111 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19074 | hp1 | a0001 | c0004 | t0001 | g0003 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0129 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19077 | hp1 | a0010 | c0016 | t0006 | g0166 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19079 | hp2 | a0006 | c0007 | t0002 | g0088 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19080 | hp1 | a0004 | c0005 | t0001 | g0126 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19080 | hp2 | a0006 | c0007 | t0002 | g0086 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19081 | hp2 | a0001 | c0004 | t0001 | g0003 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19082 | hp1 | a0002 | c0002 | t0001 | g0133 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19082 | hp2 | a0002 | c0002 | t0001 | g0132 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19083 | hp1 | a0001 | c0001 | t0015 | g0158 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19085 | hp2 | a0001 | c0004 | t0001 | g0003 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19086 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19086 | hp2 | a0003 | c0003 | t0002 | g0006 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19087 | hp2 | a0001 | c0001 | t0011 | g0002 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | YRI | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA19240 | hp2 | a0003 | c0003 | t0002 | g0174 | AFR | YRI | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA20129 | hp1 | a0011 | c0015 | t0001 | g0161 | AFR | ASW | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA20129 | hp2 | a0006 | c0007 | t0002 | g0085 | AFR | ASW | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA20752 | hp1 | a0001 | c0004 | t0001 | g0101 | EUR | TSI | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0029 | EUR | TSI | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA20805 | hp1 | a0001 | c0001 | t0005 | g0025 | EUR | TSI | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA20805 | hp2 | a0003 | c0003 | t0002 | g0179 | EUR | TSI | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | GIH | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0146 | SAS | GIH | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0056 | AMR | CLM | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG01123 | hp2 | a0002 | c0002 | t0001 | g0135 | AMR | CLM | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0157 | AFR | ACB | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02109 | hp2 | a0002 | c0002 | t0004 | g0122 | AFR | ACB | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02486 | hp1 | a0002 | c0002 | t0001 | g0015 | AFR | ACB | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02486 | hp2 | a0002 | c0002 | t0001 | g0057 | AFR | ACB | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02559 | hp1 | a0002 | c0002 | t0001 | g0005 | AFR | ACB | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG03471 | hp1 | a0002 | c0002 | t0001 | g0015 | AFR | MSL | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG03471 | hp2 | a0002 | c0002 | t0001 | g0032 | AFR | MSL | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG06807 | hp1 | a0005 | c0006 | t0016 | g0089 | AFR | USA | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | USA | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA18955 | hp2 | a0006 | c0007 | t0002 | g0091 | EAS | JPT | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0015 | AFR | USA | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | USA | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA21309 | hp1 | a0005 | c0006 | t0002 | g0014 | AFR | LWK | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| NA21309 | hp2 | a0004 | c0005 | t0001 | g0112 | AFR | LWK | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0131 | REF | REF | MICB_chr6_31493145_31516124 | MICB | chr6 | 31493145 | 31516124 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:31505635 | A | C | 1 | a0010 | 1 | NA19077.hp1 | missense_variant | MODERATE | c.89A>C | p.Tyr30Ser | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 2/6 | 138/2416 | 89/1152 | 30/383 | chr6 | 31505635 | |||
| chr6:31505636 | C | A | 1 | a0010 | 1 | NA19077.hp1 | stop_gained | HIGH | c.90C>A | p.Tyr30* | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 2/6 | 139/2416 | 90/1152 | 30/383 | chr6 | 31505636 | |||
| chr6:31505637 | A | C | 1 | a0010 | 1 | NA19077.hp1 | missense_variant | MODERATE | c.91A>C | p.Asn31His | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 2/6 | 140/2416 | 91/1152 | 31/383 | chr6 | 31505637 | |||
| chr6:31505701 | A | C | 1 | a0011 | 1 | NA20129.hp1 | missense_variant | MODERATE | c.155A>C | p.Asp52Ala | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 2/6 | 204/2416 | 155/1152 | 52/383 | chr6 | 31505701 | |||
| chr6:31505709 | C | T | 1 | a0008 | 4 | HG01884.hp1 HG02723.hp1 HG02809.hp1 others(1): Show |
missense_variant | MODERATE | c.163C>T | p.Pro55Ser | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 2/6 | 212/2416 | 163/1152 | 55/383 | chr6 | 31505709 | |||
| chr6:31505769 | A | G | 8 | a0001 a0002 a0004 others(5): Show |
399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
missense_variant | MODERATE | c.223A>G | p.Asn75Asp | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 2/6 | 272/2416 | 223/1152 | 75/383 | chr6 | 31505769 | |||
| chr6:31505784 | A | G | 4 | a0002 a0004 a0007 others(1): Show |
124 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(121): Show |
missense_variant | MODERATE | c.238A>G | p.Lys80Glu | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 2/6 | 287/2416 | 238/1152 | 80/383 | chr6 | 31505784 | |||
| chr6:31506180 | C | G | 1 | a0004 | 27 | HG00099.hp2 HG00280.hp1 HG00738.hp2 others(24): Show |
missense_variant | MODERATE | c.363C>G | p.Ile121Met | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 3/6 | 412/2416 | 363/1152 | 121/383 | chr6 | 31506180 | |||
| chr6:31506223 | G | A | 3 | a0002 a0004 a0007 |
123 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(120): Show |
missense_variant | MODERATE | c.406G>A | p.Asp136Asn | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 3/6 | 455/2416 | 406/1152 | 136/383 | chr6 | 31506223 | |||
| chr6:31506394 | C | T | 1 | a0006 | 9 | HG00673.hp2 HG01167.hp2 HG02056.hp2 others(6): Show |
stop_gained | HIGH | c.577C>T | p.Arg193* | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 3/6 | 626/2416 | 577/1152 | 193/383 | chr6 | 31506394 | |||
| chr6:31507043 | C | T | 2 | a0005 a0006 |
22 | HG00140.hp1 HG00673.hp2 HG01167.hp2 others(19): Show |
missense_variant | MODERATE | c.635C>T | p.Thr212Ile | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 4/6 | 684/2416 | 635/1152 | 212/383 | chr6 | 31507043 | |||
| chr6:31507279 | G | A | 1 | a0007 | 8 | HG00323.hp1 HG02083.hp1 HG02155.hp1 others(5): Show |
missense_variant | MODERATE | c.871G>A | p.Gly291Ser | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 4/6 | 920/2416 | 871/1152 | 291/383 | chr6 | 31507279 | |||
| chr6:31509904 | A | G | 6 | a0001 a0002 a0004 others(3): Show |
377 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(374): Show |
missense_variant | MODERATE | c.1147A>G | p.Thr383Ala | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 6/6 | 1196/2416 | 1147/1152 | 383/383 | chr6 | 31509904 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:31498226 | C | T | 1 | a0002c0017 | 1 | HG00597.hp1 | synonymous_variant | LOW | c.33C>T | p.Ala11Ala | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/6 | 82/2416 | 33/1152 | 11/383 | chr6 | 31498226 | |||
| chr6:31506159 | G | A | 1 | a0003c0011 | 1 | HG03579.hp1 | synonymous_variant | LOW | c.342G>A | p.Gln114Gln | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 3/6 | 391/2416 | 342/1152 | 114/383 | chr6 | 31506159 | |||
| chr6:31507107 | G | A | 1 | a0001c0004 | 40 | HG00673.hp1 HG02602.hp1 HG02683.hp2 others(37): Show |
synonymous_variant | LOW | c.699G>A | p.Arg233Arg | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 4/6 | 748/2416 | 699/1152 | 233/383 | chr6 | 31507107 | |||
| chr6:31507170 | G | T | 1 | a0001c0009 | 4 | HG01074.hp1 HG02145.hp1 HG02738.hp1 others(1): Show |
synonymous_variant | LOW | c.762G>T | p.Gly254Gly | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 4/6 | 811/2416 | 762/1152 | 254/383 | chr6 | 31507170 | |||
| chr6:31507278 | C | T | 1 | a0001c0012 | 1 | HG00733.hp2 | synonymous_variant | LOW | c.870C>T | p.His290His | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 4/6 | 919/2416 | 870/1152 | 290/383 | chr6 | 31507278 | |||
| chr6:31509795 | G | A | 1 | a0002c0013 | 1 | HG03098.hp2 | synonymous_variant | LOW | c.1038G>A | p.Leu346Leu | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 6/6 | 1087/2416 | 1038/1152 | 346/383 | chr6 | 31509795 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:31509925 | G | A | 1 | a0001c0001t0009 | 1 | HG02074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*16G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 6/6 | 16 | chr6 | 31509925 | ||||||
| chr6:31509990 | CAG | C | 22 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(19): Show |
377 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(374): Show |
3_prime_UTR_variant | MODIFIER | c.*85_*86delGA | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 6/6 | 85 | INFO_REALIGN_3_PRIME | chr6 | 31509990 | |||||
| chr6:31510003 | A | G | 1 | a0001c0001t0015 | 1 | NA19083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*94A>G | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 6/6 | 94 | chr6 | 31510003 | ||||||
| chr6:31510262 | T | C | 1 | a0005c0006t0016 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*353T>C | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 6/6 | 353 | chr6 | 31510262 | ||||||
| chr6:31510325 | CT | C | 1 | a0002c0002t0004 | 11 | HG00735.hp1 HG01167.hp1 HG01169.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*417delT | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 6/6 | 417 | chr6 | 31510325 | ||||||
| chr6:31510459 | C | T | 2 | a0003c0003t0006 a0010c0016t0006 |
5 | HG00558.hp2 HG03834.hp2 NA18612.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*550C>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 6/6 | 550 | chr6 | 31510459 | ||||||
| chr6:31510491 | G | A | 1 | a0001c0009t0007 | 4 | HG01074.hp1 HG02145.hp1 HG02738.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*582G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 6/6 | 582 | chr6 | 31510491 | ||||||
| chr6:31510531 | GTTGTTT | G | 3 | a0001c0001t0003 a0001c0001t0005 a0001c0012t0003 |
18 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*650_*655delTTTTTG | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 6/6 | 650 | INFO_REALIGN_3_PRIME | chr6 | 31510531 | |||||
| chr6:31510531 | GTTGTTTT others(5): Show |
G | 1 | a0001c0001t0010 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*644_*655delTTTTTG others(6): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 6/6 | 644 | INFO_REALIGN_3_PRIME | chr6 | 31510531 | |||||
| chr6:31510552 | G | A | 1 | a0002c0002t0008 | 2 | HG02896.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*643G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 6/6 | 643 | chr6 | 31510552 | ||||||
| chr6:31510653 | C | G | 1 | a0001c0001t0014 | 1 | HG02273.hp2 | 3_prime_UTR_variant | MODIFIER | c.*744C>G | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 6/6 | 744 | chr6 | 31510653 | ||||||
| chr6:31510738 | G | A | 1 | a0001c0001t0005 | 6 | HG00642.hp1 HG00733.hp1 HG01257.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*829G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 6/6 | 829 | chr6 | 31510738 | ||||||
| chr6:31511046 | G | A | 1 | a0001c0001t0011 | 1 | NA19087.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1137G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 6/6 | 1137 | chr6 | 31511046 | ||||||
| chr6:31511054 | G | A | 1 | a0001c0001t0012 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1145G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 6/6 | 1145 | chr6 | 31511054 | ||||||
| chr6:31511069 | G | A | 1 | a0001c0001t0013 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1160G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 6/6 | 1160 | chr6 | 31511069 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:31498274 | T | A | 43 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(40): Show |
94 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.70+11T>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31498274 | |||||||
| chr6:31498280 | G | A | 21 | a0001c0001t0001g0012 a0001c0001t0001g0022 a0001c0001t0001g0031 others(18): Show |
61 | HG00408.hp2 HG00558.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.70+17G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31498280 | |||||||
| chr6:31498306 | G | A | 4 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0065 others(1): Show |
12 | HG02145.hp2 HG02559.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.70+43G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31498306 | |||||||
| chr6:31498371 | T | C | 1 | a0003c0003t0002g0048 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.70+108T>C | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31498371 | |||||||
| chr6:31498440 | C | T | 43 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(40): Show |
94 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.70+177C>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31498440 | |||||||
| chr6:31498446 | C | CT | 7 | a0003c0003t0002g0006 a0003c0003t0002g0048 a0003c0003t0002g0063 others(4): Show |
22 | HG00140.hp2 HG00438.hp1 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.70+220dupT | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 31498446 | ||||||
| chr6:31498446 | CT | C | 5 | a0003c0003t0002g0028 a0003c0003t0002g0173 a0003c0003t0002g0174 others(2): Show |
7 | HG01106.hp2 HG01884.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.70+220delT | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 31498446 | ||||||
| chr6:31498446 | CTTTTTTT others(3): Show |
C | 7 | a0001c0001t0001g0031 a0001c0004t0001g0017 a0001c0004t0001g0047 others(4): Show |
14 | HG00741.hp2 HG02683.hp2 HG02970.hp2 others(11): Show |
intron_variant | MODIFIER | c.70+211_70+220delTT others(8): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 31498446 | ||||||
| chr6:31498446 | CTTTTTTT others(4): Show |
C | 22 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0060 others(19): Show |
57 | HG00423.hp1 HG00558.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.70+210_70+220delTT others(9): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 31498446 | ||||||
| chr6:31498446 | CTTTTTTT others(5): Show |
C | 23 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(20): Show |
104 | HG00280.hp2 HG00408.hp2 HG00597.hp2 others(101): Show |
intron_variant | MODIFIER | c.70+209_70+220delTT others(10): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 31498446 | ||||||
| chr6:31498446 | CTTTTTTT others(6): Show |
C | 5 | a0001c0001t0001g0156 a0001c0001t0005g0157 a0001c0001t0015g0158 others(2): Show |
5 | HG01981.hp1 HG02027.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.70+208_70+220delTT others(11): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 31498446 | ||||||
| chr6:31498446 | CTTTTTTT others(7): Show |
C | 7 | a0002c0002t0001g0057 a0002c0002t0001g0149 a0002c0002t0001g0150 others(4): Show |
8 | HG00597.hp1 HG01346.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.70+207_70+220delTT others(12): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 31498446 | ||||||
| chr6:31498446 | CTTTTTTT others(8): Show |
C | 49 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0015 others(46): Show |
105 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.70+206_70+220delTT others(13): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 31498446 | ||||||
| chr6:31498446 | CTTTTTTT others(9): Show |
C | 8 | a0002c0002t0001g0113 a0004c0005t0001g0110 a0004c0005t0001g0111 others(5): Show |
9 | HG01070.hp2 HG01168.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.70+205_70+220delTT others(14): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 31498446 | ||||||
| chr6:31498446 | CTTTTTTT others(12): Show |
C | 1 | a0003c0003t0002g0109 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.70+202_70+220delTT others(17): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 31498446 | ||||||
| chr6:31498446 | CTTTTTTT others(13): Show |
C | 3 | a0001c0001t0003g0011 a0001c0001t0003g0107 a0001c0001t0003g0108 |
10 | HG00099.hp1 HG00639.hp1 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.70+201_70+220delTT others(18): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 31498446 | ||||||
| chr6:31498446 | CTTTTTTT others(14): Show |
C | 1 | a0003c0003t0002g0106 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.70+200_70+220delTT others(19): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 31498446 | ||||||
| chr6:31498446 | CTTTTTTT others(18): Show |
C | 1 | a0001c0001t0010g0072 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.70+196_70+220delTT others(23): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 31498446 | ||||||
| chr6:31498446 | CTTTTTTT others(19): Show |
C | 12 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0029 others(9): Show |
26 | HG00423.hp2 HG01074.hp2 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.70+195_70+220delTT others(24): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 31498446 | ||||||
| chr6:31498455 | T | TTTCTTTC others(146): Show |
3 | a0005c0006t0002g0014 a0005c0006t0002g0044 a0006c0007t0002g0087 |
3 | HG00673.hp2 HG02083.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.70+194_70+195insCT others(151): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 31498455 | ||||||
| chr6:31498456 | T | TTCTTTCT others(145): Show |
4 | a0005c0006t0002g0014 a0005c0006t0002g0043 a0005c0006t0002g0090 others(1): Show |
9 | HG00140.hp1 HG01934.hp2 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.70+194_70+195insCT others(150): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 31498456 | ||||||
| chr6:31498457 | T | TCTTTCTG others(143): Show |
1 | a0006c0007t0002g0091 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.70+194_70+195insCT others(148): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31498457 | |||||||
| chr6:31498457 | T | TCTTTCTG others(144): Show |
7 | a0005c0006t0002g0044 a0005c0006t0002g0092 a0005c0006t0016g0089 others(4): Show |
9 | HG01167.hp2 HG02129.hp2 HG02300.hp2 others(6): Show |
intron_variant | MODIFIER | c.70+194_70+195insCT others(149): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31498457 | |||||||
| chr6:31498458 | T | A | 1 | a0006c0007t0002g0091 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.70+195T>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31498458 | |||||||
| chr6:31498458 | T | C | 17 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0041 others(14): Show |
45 | HG00438.hp2 HG01192.hp2 HG01346.hp1 others(42): Show |
intron_variant | MODIFIER | c.70+195T>C | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31498458 | |||||||
| chr6:31498460 | T | C | 1 | a0001c0001t0001g0105 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.70+197T>C | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31498460 | |||||||
| chr6:31498462 | T | C | 17 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0041 others(14): Show |
45 | HG00438.hp2 HG01192.hp2 HG01346.hp1 others(42): Show |
intron_variant | MODIFIER | c.70+199T>C | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31498462 | |||||||
| chr6:31498463 | T | TGAGACGG others(134): Show |
12 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0041 others(9): Show |
40 | HG01192.hp2 HG01346.hp1 HG01358.hp2 others(37): Show |
intron_variant | MODIFIER | c.70+200_70+201insGA others(139): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31498463 | |||||||
| chr6:31498463 | T | TGAGACGG others(135): Show |
4 | a0001c0001t0001g0042 a0001c0001t0001g0081 a0001c0001t0001g0082 others(1): Show |
4 | HG00438.hp2 HG02273.hp2 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.70+200_70+201insGA others(140): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31498463 | |||||||
| chr6:31498463 | T | TGAGACGG others(138): Show |
1 | a0001c0001t0001g0083 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.70+200_70+201insGA others(143): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31498463 | |||||||
| chr6:31498464 | T | C | 12 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0041 others(9): Show |
40 | HG01192.hp2 HG01346.hp1 HG01358.hp2 others(37): Show |
intron_variant | MODIFIER | c.70+201T>C | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31498464 | |||||||
| chr6:31498465 | T | A | 4 | a0001c0001t0001g0042 a0001c0001t0001g0081 a0001c0001t0001g0082 others(1): Show |
4 | HG00438.hp2 HG02273.hp2 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.70+202T>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31498465 | |||||||
| chr6:31498466 | T | A | 16 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0041 others(13): Show |
44 | HG00438.hp2 HG01192.hp2 HG01346.hp1 others(41): Show |
intron_variant | MODIFIER | c.70+203T>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31498466 | |||||||
| chr6:31498467 | T | A | 12 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0041 others(9): Show |
40 | HG01192.hp2 HG01346.hp1 HG01358.hp2 others(37): Show |
intron_variant | MODIFIER | c.70+204T>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31498467 | |||||||
| chr6:31498484 | C | T | 29 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0041 others(26): Show |
66 | HG00140.hp1 HG00438.hp2 HG00673.hp2 others(63): Show |
intron_variant | MODIFIER | c.70+221C>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31498484 | |||||||
| chr6:31498488 | C | T | 29 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0041 others(26): Show |
66 | HG00140.hp1 HG00438.hp2 HG00673.hp2 others(63): Show |
intron_variant | MODIFIER | c.70+225C>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31498488 | |||||||
| chr6:31498499 | T | TCTCG | 30 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0041 others(27): Show |
67 | HG00140.hp1 HG00438.hp2 HG00673.hp2 others(64): Show |
intron_variant | MODIFIER | c.70+239_70+240insGC others(2): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 31498499 | ||||||
| chr6:31498506 | C | T | 54 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(51): Show |
181 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.70+243C>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31498506 | |||||||
| chr6:31498510 | T | C | 84 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(81): Show |
248 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.70+247T>C | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31498510 | |||||||
| chr6:31498514 | C | CCGGACTG | 30 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0041 others(27): Show |
67 | HG00140.hp1 HG00438.hp2 HG00673.hp2 others(64): Show |
intron_variant | MODIFIER | c.70+251_70+252insCG others(5): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31498514 | |||||||
| chr6:31498515 | T | C | 30 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0041 others(27): Show |
67 | HG00140.hp1 HG00438.hp2 HG00673.hp2 others(64): Show |
intron_variant | MODIFIER | c.70+252T>C | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31498515 | |||||||
| chr6:31498517 | T | G | 85 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(82): Show |
249 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.70+254T>G | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31498517 | |||||||
| chr6:31498519 | G | C | 30 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0041 others(27): Show |
67 | HG00140.hp1 HG00438.hp2 HG00673.hp2 others(64): Show |
intron_variant | MODIFIER | c.70+256G>C | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31498519 | |||||||
| chr6:31498523 | A | C | 12 | a0001c0004t0001g0003 a0001c0004t0001g0017 a0001c0004t0001g0023 others(9): Show |
40 | HG00673.hp1 HG02602.hp1 HG02683.hp2 others(37): Show |
intron_variant | MODIFIER | c.70+260A>C | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31498523 | |||||||
| chr6:31498531 | G | A | 30 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0041 others(27): Show |
67 | HG00140.hp1 HG00438.hp2 HG00673.hp2 others(64): Show |
intron_variant | MODIFIER | c.70+268G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31498531 | |||||||
| chr6:31498534 | C | A | 66 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0015 others(63): Show |
124 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.70+271C>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31498534 | |||||||
| chr6:31498536 | T | C | 30 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0041 others(27): Show |
67 | HG00140.hp1 HG00438.hp2 HG00673.hp2 others(64): Show |
intron_variant | MODIFIER | c.70+273T>C | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31498536 | |||||||
| chr6:31498551 | G | T | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(160): Show |
399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.70+288G>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31498551 | |||||||
| chr6:31498553 | C | T | 30 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0041 others(27): Show |
67 | HG00140.hp1 HG00438.hp2 HG00673.hp2 others(64): Show |
intron_variant | MODIFIER | c.70+290C>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31498553 | |||||||
| chr6:31498556 | C | T | 30 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0041 others(27): Show |
67 | HG00140.hp1 HG00438.hp2 HG00673.hp2 others(64): Show |
intron_variant | MODIFIER | c.70+293C>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31498556 | |||||||
| chr6:31498593 | T | G | 30 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0041 others(27): Show |
67 | HG00140.hp1 HG00438.hp2 HG00673.hp2 others(64): Show |
intron_variant | MODIFIER | c.70+330T>G | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31498593 | |||||||
| chr6:31498593 | T | TAGTAGCT others(166): Show |
1 | a0001c0001t0001g0066 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.70+347_70+348insAC others(171): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 31498593 | ||||||
| chr6:31498593 | T | TAGTAGCT others(167): Show |
10 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0039 others(7): Show |
22 | HG00423.hp2 HG01074.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.70+347_70+348insAC others(172): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 31498593 | ||||||
| chr6:31498593 | T | TAGTAGCT others(168): Show |
2 | a0001c0001t0001g0029 a0001c0001t0010g0072 |
4 | HG02622.hp1 HG03834.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.70+347_70+348insAC others(173): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 31498593 | ||||||
| chr6:31498623 | A | G | 43 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(40): Show |
94 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.70+360A>G | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31498623 | |||||||
| chr6:31498745 | G | A | 33 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(30): Show |
120 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.70+482G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31498745 | |||||||
| chr6:31498746 | C | G | 54 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(51): Show |
181 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.70+483C>G | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31498746 | |||||||
| chr6:31498759 | G | C | 43 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(40): Show |
94 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.70+496G>C | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31498759 | |||||||
| chr6:31498770 | T | C | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(160): Show |
399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.70+507T>C | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31498770 | |||||||
| chr6:31498818 | G | T | 25 | a0002c0002t0001g0015 a0002c0002t0001g0024 a0002c0002t0001g0035 others(22): Show |
37 | HG00323.hp1 HG00323.hp2 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.70+555G>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31498818 | |||||||
| chr6:31498821 | T | TC | 120 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(117): Show |
305 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.70+559dupC | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 31498821 | ||||||
| chr6:31498988 | TCAGGTCC others(50): Show |
T | 1 | a0001c0001t0003g0159 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.70+729_70+785delGT others(55): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 31498988 | ||||||
| chr6:31498992 | G | C | 53 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(50): Show |
180 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.70+729G>C | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31498992 | |||||||
| chr6:31499083 | G | A | 43 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(40): Show |
94 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.70+820G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31499083 | |||||||
| chr6:31499102 | G | A | 66 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0015 others(63): Show |
124 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.70+839G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31499102 | |||||||
| chr6:31499108 | G | A | 66 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0015 others(63): Show |
124 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.70+845G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31499108 | |||||||
| chr6:31499121 | G | A | 12 | a0001c0004t0001g0003 a0001c0004t0001g0017 a0001c0004t0001g0023 others(9): Show |
40 | HG00673.hp1 HG02602.hp1 HG02683.hp2 others(37): Show |
intron_variant | MODIFIER | c.70+858G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31499121 | |||||||
| chr6:31499191 | C | G | 1 | a0003c0003t0002g0064 | 2 | NA18970.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.70+928C>G | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31499191 | |||||||
| chr6:31499227 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.70+964G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31499227 | |||||||
| chr6:31499275 | T | TATGACCA others(6): Show |
1 | a0005c0006t0002g0092 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.70+1013_70+1014ins others(13): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 31499275 | ||||||
| chr6:31499278 | G | T | 1 | a0005c0006t0002g0092 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.70+1015G>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31499278 | |||||||
| chr6:31499329 | G | T | 1 | a0003c0003t0002g0175 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.70+1066G>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31499329 | |||||||
| chr6:31499334 | G | T | 66 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0015 others(63): Show |
124 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.70+1071G>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31499334 | |||||||
| chr6:31499338 | C | T | 54 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(51): Show |
181 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.70+1075C>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31499338 | |||||||
| chr6:31499388 | T | C | 3 | a0006c0007t0002g0030 a0006c0007t0002g0084 a0006c0007t0002g0085 |
5 | HG01167.hp2 HG02056.hp2 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.70+1125T>C | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31499388 | |||||||
| chr6:31499393 | G | A | 66 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0015 others(63): Show |
124 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.70+1130G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31499393 | |||||||
| chr6:31499410 | T | G | 21 | a0001c0001t0001g0012 a0001c0001t0001g0022 a0001c0001t0001g0031 others(18): Show |
61 | HG00408.hp2 HG00558.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.70+1147T>G | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31499410 | |||||||
| chr6:31499505 | C | G | 4 | a0001c0004t0001g0003 a0001c0004t0001g0017 a0001c0004t0001g0102 others(1): Show |
27 | HG02602.hp1 HG02683.hp2 HG03669.hp1 others(24): Show |
intron_variant | MODIFIER | c.70+1242C>G | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31499505 | |||||||
| chr6:31499548 | C | CG | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(92): Show |
273 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(270): Show |
intron_variant | MODIFIER | c.70+1292dupG | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 31499548 | ||||||
| chr6:31499588 | C | T | 66 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0015 others(63): Show |
124 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.70+1325C>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31499588 | |||||||
| chr6:31499634 | C | G | 1 | a0002c0002t0001g0135 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.70+1371C>G | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31499634 | |||||||
| chr6:31499688 | G | A | 2 | a0001c0004t0001g0098 a0001c0004t0001g0103 |
2 | NA18981.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.70+1425G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31499688 | |||||||
| chr6:31499744 | C | G | 30 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(27): Show |
72 | HG00423.hp2 HG00438.hp2 HG01074.hp2 others(69): Show |
intron_variant | MODIFIER | c.70+1481C>G | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31499744 | |||||||
| chr6:31499763 | G | A | 54 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(51): Show |
181 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.70+1500G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31499763 | |||||||
| chr6:31499826 | A | G | 54 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(51): Show |
181 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.70+1563A>G | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31499826 | |||||||
| chr6:31500078 | G | A | 1 | a0001c0001t0001g0073 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.70+1815G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31500078 | |||||||
| chr6:31500215 | A | C | 23 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(20): Show |
100 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.70+1952A>C | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31500215 | |||||||
| chr6:31500244 | C | T | 43 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(40): Show |
94 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.70+1981C>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31500244 | |||||||
| chr6:31500247 | T | C | 54 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(51): Show |
181 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.70+1984T>C | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31500247 | |||||||
| chr6:31500282 | C | T | 20 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0052 others(17): Show |
46 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.70+2019C>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31500282 | |||||||
| chr6:31500314 | T | G | 54 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(51): Show |
181 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.70+2051T>G | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31500314 | |||||||
| chr6:31500322 | G | A | 43 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(40): Show |
94 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.70+2059G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31500322 | |||||||
| chr6:31500368 | G | C | 43 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(40): Show |
94 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.70+2105G>C | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31500368 | |||||||
| chr6:31500375 | G | C | 1 | a0003c0003t0002g0109 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.70+2112G>C | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31500375 | |||||||
| chr6:31500582 | G | A | 1 | a0003c0003t0002g0061 | 2 | NA18977.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.70+2319G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31500582 | |||||||
| chr6:31500622 | G | A | 120 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(117): Show |
305 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.70+2359G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31500622 | |||||||
| chr6:31500622 | G | T | 43 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(40): Show |
94 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.70+2359G>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31500622 | |||||||
| chr6:31500627 | C | A | 13 | a0005c0006t0002g0014 a0005c0006t0002g0043 a0005c0006t0002g0044 others(10): Show |
22 | HG00140.hp1 HG00673.hp2 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.70+2364C>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31500627 | |||||||
| chr6:31500697 | G | A | 54 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(51): Show |
181 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.70+2434G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31500697 | |||||||
| chr6:31500708 | C | G | 54 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(51): Show |
181 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.70+2445C>G | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31500708 | |||||||
| chr6:31500769 | A | G | 120 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(117): Show |
305 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.70+2506A>G | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31500769 | |||||||
| chr6:31500822 | C | T | 21 | a0001c0001t0001g0012 a0001c0001t0001g0022 a0001c0001t0001g0031 others(18): Show |
61 | HG00408.hp2 HG00558.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.70+2559C>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31500822 | |||||||
| chr6:31500845 | C | G | 21 | a0001c0001t0001g0012 a0001c0001t0001g0022 a0001c0001t0001g0031 others(18): Show |
61 | HG00408.hp2 HG00558.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.70+2582C>G | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31500845 | |||||||
| chr6:31500977 | A | G | 54 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(51): Show |
181 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.70+2714A>G | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31500977 | |||||||
| chr6:31501041 | T | C | 7 | a0007c0008t0001g0049 a0007c0008t0001g0114 a0007c0008t0001g0115 others(4): Show |
8 | HG00323.hp1 HG02083.hp1 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.70+2778T>C | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31501041 | |||||||
| chr6:31501082 | TC | T | 21 | a0001c0001t0001g0012 a0001c0001t0001g0022 a0001c0001t0001g0031 others(18): Show |
61 | HG00408.hp2 HG00558.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.70+2820delC | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31501082 | |||||||
| chr6:31501084 | G | A | 43 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(40): Show |
94 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.70+2821G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31501084 | |||||||
| chr6:31501263 | C | T | 1 | a0011c0015t0001g0161 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.70+3000C>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31501263 | |||||||
| chr6:31501451 | A | G | 43 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(40): Show |
94 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.70+3188A>G | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31501451 | |||||||
| chr6:31501474 | C | G | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(160): Show |
399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.70+3211C>G | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31501474 | |||||||
| chr6:31501546 | C | T | 120 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(117): Show |
305 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.70+3283C>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31501546 | |||||||
| chr6:31501549 | A | G | 2 | a0007c0008t0001g0137 a0007c0008t0001g0138 |
2 | HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.70+3286A>G | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31501549 | |||||||
| chr6:31501588 | C | A | 54 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(51): Show |
181 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.70+3325C>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31501588 | |||||||
| chr6:31501589 | C | T | 21 | a0001c0001t0001g0012 a0001c0001t0001g0022 a0001c0001t0001g0031 others(18): Show |
61 | HG00408.hp2 HG00558.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.70+3326C>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31501589 | |||||||
| chr6:31501624 | G | T | 54 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(51): Show |
181 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.70+3361G>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31501624 | |||||||
| chr6:31501691 | C | T | 3 | a0001c0001t0003g0011 a0001c0001t0003g0107 a0001c0001t0003g0108 |
10 | HG00099.hp1 HG00639.hp1 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.70+3428C>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31501691 | |||||||
| chr6:31501714 | G | C | 43 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(40): Show |
94 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.70+3451G>C | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31501714 | |||||||
| chr6:31501812 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.70+3549C>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31501812 | |||||||
| chr6:31501814 | G | A | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(92): Show |
271 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(268): Show |
intron_variant | MODIFIER | c.70+3551G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31501814 | |||||||
| chr6:31501872 | G | T | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(160): Show |
399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.70+3609G>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31501872 | |||||||
| chr6:31501891 | C | T | 66 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0015 others(63): Show |
124 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.70+3628C>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31501891 | |||||||
| chr6:31501989 | G | A | 1 | a0002c0002t0001g0032 | 3 | HG02280.hp2 HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.71-3628G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31501989 | |||||||
| chr6:31501990 | C | A | 1 | a0002c0002t0001g0032 | 3 | HG02280.hp2 HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.71-3627C>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31501990 | |||||||
| chr6:31501997 | A | G | 13 | a0004c0005t0001g0019 a0004c0005t0001g0020 a0004c0005t0001g0034 others(10): Show |
25 | HG00099.hp2 HG00280.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.71-3620A>G | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31501997 | |||||||
| chr6:31502102 | G | C | 1 | a0003c0003t0002g0176 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.71-3515G>C | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31502102 | |||||||
| chr6:31502124 | T | A | 2 | a0001c0001t0001g0067 a0001c0001t0001g0068 |
2 | HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.71-3493T>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31502124 | |||||||
| chr6:31502156 | G | A | 120 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(117): Show |
305 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.71-3461G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31502156 | |||||||
| chr6:31502164 | C | G | 1 | a0006c0007t0002g0091 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.71-3453C>G | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31502164 | |||||||
| chr6:31502165 | G | C | 1 | a0006c0007t0002g0091 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.71-3452G>C | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31502165 | |||||||
| chr6:31502243 | G | A | 2 | a0004c0005t0001g0118 a0004c0005t0001g0119 |
2 | HG02040.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.71-3374G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31502243 | |||||||
| chr6:31502251 | G | T | 3 | a0001c0009t0007g0045 a0001c0009t0007g0093 a0001c0009t0007g0097 |
4 | HG01074.hp1 HG02145.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.71-3366G>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31502251 | |||||||
| chr6:31502330 | C | T | 2 | a0001c0001t0001g0022 a0001c0001t0001g0096 |
5 | HG00408.hp2 HG00597.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.71-3287C>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31502330 | |||||||
| chr6:31502371 | G | A | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(160): Show |
399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.71-3246G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31502371 | |||||||
| chr6:31502494 | T | G | 55 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(52): Show |
182 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(179): Show |
intron_variant | MODIFIER | c.71-3123T>G | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31502494 | |||||||
| chr6:31502501 | A | T | 1 | a0001c0001t0001g0068 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.71-3116A>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31502501 | |||||||
| chr6:31502521 | G | A | 1 | a0003c0003t0002g0173 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.71-3096G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31502521 | |||||||
| chr6:31502566 | G | A | 162 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(159): Show |
398 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(395): Show |
intron_variant | MODIFIER | c.71-3051G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31502566 | |||||||
| chr6:31502566 | G | T | 1 | a0006c0007t0002g0091 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.71-3051G>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31502566 | |||||||
| chr6:31502575 | T | A | 120 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(117): Show |
305 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.71-3042T>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31502575 | |||||||
| chr6:31502583 | AT | A | 5 | a0002c0002t0004g0018 a0002c0002t0004g0033 a0002c0002t0004g0120 others(2): Show |
11 | HG00735.hp1 HG01167.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.71-3033delT | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31502583 | |||||||
| chr6:31502678 | T | C | 1 | a0001c0001t0001g0036 | 3 | HG01106.hp1 HG01261.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.71-2939T>C | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31502678 | |||||||
| chr6:31502684 | G | A | 2 | a0001c0001t0001g0022 a0001c0001t0001g0096 |
5 | HG00408.hp2 HG00597.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.71-2933G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31502684 | |||||||
| chr6:31502768 | T | G | 54 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(51): Show |
181 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.71-2849T>G | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31502768 | |||||||
| chr6:31502779 | G | A | 2 | a0001c0001t0001g0022 a0001c0001t0001g0096 |
5 | HG00408.hp2 HG00597.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.71-2838G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31502779 | |||||||
| chr6:31502799 | G | A | 2 | a0001c0001t0001g0022 a0001c0001t0001g0096 |
5 | HG00408.hp2 HG00597.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.71-2818G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31502799 | |||||||
| chr6:31502896 | G | A | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(160): Show |
399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.71-2721G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31502896 | |||||||
| chr6:31503073 | C | T | 43 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(40): Show |
94 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.71-2544C>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31503073 | |||||||
| chr6:31503098 | T | A | 54 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(51): Show |
181 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.71-2519T>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31503098 | |||||||
| chr6:31503199 | G | A | 1 | a0002c0002t0001g0128 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.71-2418G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31503199 | |||||||
| chr6:31503352 | C | A | 120 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(117): Show |
305 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.71-2265C>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31503352 | |||||||
| chr6:31503370 | G | A | 57 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(54): Show |
184 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.71-2247G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31503370 | |||||||
| chr6:31503428 | C | T | 4 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0094 others(1): Show |
12 | HG00558.hp1 HG00741.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.71-2189C>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31503428 | |||||||
| chr6:31503445 | A | G | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(160): Show |
399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.71-2172A>G | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31503445 | |||||||
| chr6:31503490 | T | C | 1 | a0001c0001t0001g0162 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.71-2127T>C | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31503490 | |||||||
| chr6:31503547 | G | A | 1 | a0003c0003t0002g0174 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.71-2070G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31503547 | |||||||
| chr6:31503671 | A | G | 33 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(30): Show |
120 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.71-1946A>G | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31503671 | |||||||
| chr6:31503677 | T | C | 66 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0015 others(63): Show |
124 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.71-1940T>C | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31503677 | |||||||
| chr6:31503696 | A | G | 54 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(51): Show |
181 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.71-1921A>G | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31503696 | |||||||
| chr6:31503763 | A | G | 1 | a0001c0001t0015g0158 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.71-1854A>G | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31503763 | |||||||
| chr6:31503780 | G | A | 43 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(40): Show |
94 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.71-1837G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31503780 | |||||||
| chr6:31503813 | T | C | 2 | a0001c0009t0007g0045 a0001c0009t0007g0097 |
3 | HG01074.hp1 HG02145.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.71-1804T>C | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31503813 | |||||||
| chr6:31503949 | C | CTG | 2 | a0003c0003t0002g0062 a0003c0003t0002g0181 |
3 | HG01257.hp1 HG01258.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.71-1631_71-1630dup others(2): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 31503949 | ||||||
| chr6:31503949 | C | CTGTG | 4 | a0003c0003t0002g0048 a0003c0003t0002g0171 a0003c0003t0002g0178 others(1): Show |
5 | HG00140.hp2 HG01070.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-1633_71-1630dup others(4): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 31503949 | ||||||
| chr6:31503949 | C | CTGTGTG | 4 | a0003c0003t0002g0021 a0003c0003t0002g0106 a0003c0003t0002g0179 others(1): Show |
7 | HG00558.hp2 HG03130.hp1 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.71-1635_71-1630dup others(6): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 31503949 | ||||||
| chr6:31503949 | C | CTGTGTGT others(1): Show |
4 | a0003c0003t0002g0038 a0003c0003t0002g0064 a0003c0011t0002g0172 others(1): Show |
7 | HG02922.hp1 HG03453.hp1 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.71-1637_71-1630dup others(8): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 31503949 | ||||||
| chr6:31503949 | C | CTGTTGTG others(6): Show |
3 | a0002c0002t0001g0129 a0002c0002t0001g0135 a0002c0002t0001g0142 |
3 | HG01123.hp2 HG03492.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.71-1665_71-1664ins others(13): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 31503949 | ||||||
| chr6:31503949 | C | CTGTTGTG others(8): Show |
2 | a0002c0013t0001g0139 a0004c0005t0001g0123 |
2 | HG03098.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.71-1665_71-1664ins others(15): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 31503949 | ||||||
| chr6:31503949 | C | CTGTTTG | 10 | a0002c0002t0001g0052 a0002c0002t0001g0113 a0005c0006t0002g0092 others(7): Show |
13 | HG00673.hp2 HG01167.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.71-1665_71-1664ins others(6): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 31503949 | ||||||
| chr6:31503949 | C | CTGTTTGT others(1): Show |
9 | a0002c0002t0001g0005 a0002c0002t0001g0053 a0002c0002t0001g0056 others(6): Show |
25 | HG00323.hp2 HG00597.hp1 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.71-1665_71-1664ins others(8): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 31503949 | ||||||
| chr6:31503949 | C | CTGTTTGT others(3): Show |
5 | a0002c0002t0001g0054 a0002c0002t0004g0018 a0005c0006t0002g0014 others(2): Show |
17 | HG00140.hp1 HG00408.hp1 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.71-1665_71-1664ins others(10): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 31503949 | ||||||
| chr6:31503949 | C | CTGTTTGT others(5): Show |
6 | a0002c0002t0001g0024 a0002c0002t0001g0132 a0002c0002t0001g0151 others(3): Show |
8 | HG00735.hp1 HG01934.hp2 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.71-1665_71-1664ins others(12): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 31503949 | ||||||
| chr6:31503949 | C | CTGTTTGT others(7): Show |
19 | a0002c0002t0001g0007 a0002c0002t0001g0015 a0002c0002t0001g0035 others(16): Show |
42 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.71-1665_71-1664ins others(14): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 31503949 | ||||||
| chr6:31503949 | C | CTGTTTGT others(9): Show |
11 | a0002c0002t0001g0032 a0002c0002t0001g0055 a0002c0002t0001g0057 others(8): Show |
21 | HG01243.hp1 HG01346.hp2 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.71-1665_71-1664ins others(16): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 31503949 | ||||||
| chr6:31503949 | C | CTGTTTGT others(11): Show |
9 | a0002c0002t0001g0141 a0002c0002t0001g0147 a0002c0002t0001g0153 others(6): Show |
10 | HG02109.hp2 HG02155.hp1 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.71-1665_71-1664ins others(18): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 31503949 | ||||||
| chr6:31503949 | C | CTGTTTGT others(13): Show |
3 | a0004c0005t0001g0119 a0007c0008t0001g0116 a0007c0008t0001g0138 |
3 | HG02040.hp1 HG02717.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.71-1665_71-1664ins others(20): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 31503949 | ||||||
| chr6:31503949 | CTG | C | 7 | a0001c0001t0001g0022 a0001c0001t0001g0096 a0001c0001t0003g0107 others(4): Show |
11 | HG00408.hp2 HG00597.hp2 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.71-1631_71-1630del others(2): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 31503949 | ||||||
| chr6:31503949 | CTGTG | C | 17 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0031 others(14): Show |
67 | HG00099.hp1 HG00558.hp1 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.71-1633_71-1630del others(4): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 31503949 | ||||||
| chr6:31503949 | CTGTGTG | C | 30 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(27): Show |
103 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(100): Show |
intron_variant | MODIFIER | c.71-1635_71-1630del others(6): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 31503949 | ||||||
| chr6:31503951 | G | GTT | 11 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(8): Show |
24 | HG00423.hp2 HG01074.hp2 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.71-1665_71-1664ins others(2): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 31503951 | ||||||
| chr6:31503953 | G | T | 19 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0041 others(16): Show |
45 | HG00438.hp2 HG01192.hp2 HG01346.hp1 others(42): Show |
intron_variant | MODIFIER | c.71-1664G>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31503953 | |||||||
| chr6:31503955 | G | T | 7 | a0001c0001t0001g0022 a0001c0001t0001g0096 a0001c0001t0003g0107 others(4): Show |
11 | HG00408.hp2 HG00597.hp2 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.71-1662G>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31503955 | |||||||
| chr6:31503957 | G | T | 17 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0031 others(14): Show |
67 | HG00099.hp1 HG00558.hp1 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.71-1660G>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31503957 | |||||||
| chr6:31503959 | G | T | 30 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(27): Show |
103 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(100): Show |
intron_variant | MODIFIER | c.71-1658G>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31503959 | |||||||
| chr6:31503961 | G | T | 1 | a0011c0015t0001g0161 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.71-1656G>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31503961 | |||||||
| chr6:31503985 | G | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(52): Show |
182 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(179): Show |
intron_variant | MODIFIER | c.71-1632G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31503985 | |||||||
| chr6:31503986 | T | A | 9 | a0002c0002t0001g0032 a0005c0006t0002g0092 a0006c0007t0002g0030 others(6): Show |
13 | HG00673.hp2 HG01167.hp2 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.71-1631T>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31503986 | |||||||
| chr6:31503986 | T | TGTGTGTG others(4): Show |
2 | a0003c0003t0002g0173 a0003c0003t0002g0174 |
2 | HG01106.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.71-1630_71-1629ins others(11): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 31503986 | ||||||
| chr6:31503990 | A | C | 1 | a0003c0003t0002g0174 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.71-1627A>C | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31503990 | |||||||
| chr6:31503992 | T | C | 1 | a0002c0002t0001g0133 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.71-1625T>C | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31503992 | |||||||
| chr6:31504024 | A | G | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(146): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.71-1593A>G | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31504024 | |||||||
| chr6:31504053 | G | A | 54 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(51): Show |
181 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.71-1564G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31504053 | |||||||
| chr6:31504066 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.71-1551G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31504066 | |||||||
| chr6:31504161 | C | T | 1 | a0003c0003t0002g0175 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.71-1456C>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31504161 | |||||||
| chr6:31504242 | C | G | 1 | a0001c0001t0001g0156 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.71-1375C>G | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31504242 | |||||||
| chr6:31504246 | C | CTTTCTTT others(6): Show |
1 | a0006c0007t0002g0030 | 3 | HG01167.hp2 HG02300.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.71-1370_71-1369ins others(13): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 31504246 | ||||||
| chr6:31504246 | C | CTTTCTTT others(7): Show |
3 | a0006c0007t0002g0084 a0006c0007t0002g0086 a0006c0007t0002g0091 |
3 | HG02056.hp2 NA18955.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.71-1370_71-1369ins others(14): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 31504246 | ||||||
| chr6:31504246 | C | CTTTCTTT others(8): Show |
2 | a0005c0006t0002g0092 a0006c0007t0002g0087 |
2 | HG00673.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.71-1370_71-1369ins others(15): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 31504246 | ||||||
| chr6:31504246 | C | CTTTCTTT others(9): Show |
1 | a0006c0007t0002g0085 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.71-1370_71-1369ins others(16): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 31504246 | ||||||
| chr6:31504246 | C | CTTTCTTT others(10): Show |
2 | a0005c0006t0002g0043 a0006c0007t0002g0088 |
3 | HG00140.hp1 NA18612.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.71-1370_71-1369ins others(17): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 31504246 | ||||||
| chr6:31504246 | C | CTTTCTTT others(11): Show |
2 | a0005c0006t0002g0014 a0005c0006t0002g0090 |
7 | HG01934.hp2 HG02080.hp2 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.71-1370_71-1369ins others(18): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 31504246 | ||||||
| chr6:31504246 | C | CTTTCTTT others(17): Show |
1 | a0005c0006t0016g0089 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.71-1370_71-1369ins others(24): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 31504246 | ||||||
| chr6:31504248 | C | CTCTTTTT others(8): Show |
1 | a0001c0001t0010g0072 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.71-1368_71-1367ins others(15): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 31504248 | ||||||
| chr6:31504248 | C | CTT | 12 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0042 others(9): Show |
39 | HG01192.hp2 HG01346.hp1 HG01358.hp2 others(36): Show |
intron_variant | MODIFIER | c.71-1365_71-1364dup others(2): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 31504248 | ||||||
| chr6:31504248 | C | CTTT | 4 | a0001c0001t0001g0041 a0001c0001t0001g0079 a0001c0001t0001g0080 others(1): Show |
5 | HG00438.hp2 NA18965.hp1 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-1366_71-1364dup others(3): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 31504248 | ||||||
| chr6:31504248 | C | CTTTTTTT others(5): Show |
1 | a0001c0001t0001g0070 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.71-1364_71-1363ins others(12): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 31504248 | ||||||
| chr6:31504248 | C | CTTTTTTT others(6): Show |
1 | a0001c0001t0001g0071 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.71-1364_71-1363ins others(13): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 31504248 | ||||||
| chr6:31504248 | C | CTTTTTTT others(7): Show |
1 | a0001c0001t0001g0013 | 6 | HG00423.hp2 HG01099.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.71-1364_71-1363ins others(14): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 31504248 | ||||||
| chr6:31504248 | C | T | 13 | a0005c0006t0002g0014 a0005c0006t0002g0043 a0005c0006t0002g0044 others(10): Show |
22 | HG00140.hp1 HG00673.hp2 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.71-1369C>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31504248 | |||||||
| chr6:31504248 | CTTTTTCT others(9): Show |
C | 5 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0039 others(2): Show |
14 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.71-1363_71-1348del others(16): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 31504248 | ||||||
| chr6:31504254 | C | CT | 35 | a0001c0001t0001g0059 a0001c0004t0001g0003 a0002c0002t0001g0005 others(32): Show |
65 | HG00140.hp2 HG00408.hp1 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.71-1340dupT | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 31504254 | ||||||
| chr6:31504254 | C | CTT | 70 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0012 others(67): Show |
175 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.71-1341_71-1340dup others(2): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 31504254 | ||||||
| chr6:31504254 | C | CTTT | 42 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(39): Show |
80 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.71-1342_71-1340dup others(3): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 31504254 | ||||||
| chr6:31504254 | C | CTTTT | 6 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0156 others(3): Show |
9 | HG00597.hp2 HG01123.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.71-1343_71-1340dup others(4): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 31504254 | ||||||
| chr6:31504254 | C | T | 35 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0040 others(32): Show |
77 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.71-1363C>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31504254 | |||||||
| chr6:31504323 | G | A | 1 | a0002c0002t0004g0018 | 5 | HG02735.hp2 HG03239.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.71-1294G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31504323 | |||||||
| chr6:31504338 | C | T | 32 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(29): Show |
119 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.71-1279C>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31504338 | |||||||
| chr6:31504346 | G | A | 74 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0015 others(71): Show |
134 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.71-1271G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31504346 | |||||||
| chr6:31504372 | G | A | 120 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(117): Show |
305 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.71-1245G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31504372 | |||||||
| chr6:31504385 | G | T | 66 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0015 others(63): Show |
124 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.71-1232G>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31504385 | |||||||
| chr6:31504416 | C | T | 54 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(51): Show |
181 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.71-1201C>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31504416 | |||||||
| chr6:31504421 | G | A | 11 | a0001c0004t0001g0003 a0001c0004t0001g0017 a0001c0004t0001g0046 others(8): Show |
36 | HG02602.hp1 HG02683.hp2 HG03490.hp2 others(33): Show |
intron_variant | MODIFIER | c.71-1196G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31504421 | |||||||
| chr6:31504438 | T | C | 2 | a0002c0002t0001g0015 a0002c0002t0001g0147 |
7 | HG01891.hp2 HG02486.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.71-1179T>C | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31504438 | |||||||
| chr6:31504506 | G | A | 1 | a0005c0006t0016g0089 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.71-1111G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31504506 | |||||||
| chr6:31504527 | G | A | 1 | a0001c0001t0001g0081 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.71-1090G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31504527 | |||||||
| chr6:31504531 | C | T | 120 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(117): Show |
305 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.71-1086C>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31504531 | |||||||
| chr6:31504538 | C | T | 4 | a0001c0001t0001g0040 a0001c0001t0001g0075 a0001c0001t0001g0080 others(1): Show |
5 | NA18951.hp1 NA18953.hp1 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-1079C>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31504538 | |||||||
| chr6:31504550 | C | T | 2 | a0004c0005t0001g0118 a0004c0005t0001g0119 |
2 | HG02040.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.71-1067C>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31504550 | |||||||
| chr6:31504561 | CTGGAAAC others(1): Show |
C | 4 | a0005c0006t0002g0014 a0005c0006t0002g0043 a0005c0006t0002g0044 others(1): Show |
11 | HG00140.hp1 HG01934.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.71-1055_71-1048del others(8): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31504561 | |||||||
| chr6:31504567 | A | G | 20 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0052 others(17): Show |
46 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.71-1050A>G | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31504567 | |||||||
| chr6:31504572 | T | C | 4 | a0005c0006t0002g0014 a0005c0006t0002g0043 a0005c0006t0002g0044 others(1): Show |
11 | HG00140.hp1 HG01934.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.71-1045T>C | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31504572 | |||||||
| chr6:31504635 | CTGAT | C | 43 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(40): Show |
94 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.71-979_71-976delAT others(2): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 31504635 | ||||||
| chr6:31504664 | T | C | 1 | a0003c0003t0002g0177 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.71-953T>C | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31504664 | |||||||
| chr6:31504665 | T | A | 1 | a0003c0003t0002g0177 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.71-952T>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31504665 | |||||||
| chr6:31504666 | G | C | 1 | a0003c0003t0002g0177 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.71-951G>C | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31504666 | |||||||
| chr6:31504667 | A | T | 1 | a0003c0003t0002g0177 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.71-950A>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31504667 | |||||||
| chr6:31504669 | T | G | 1 | a0003c0003t0002g0177 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.71-948T>G | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31504669 | |||||||
| chr6:31504670 | T | A | 1 | a0003c0003t0002g0177 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.71-947T>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31504670 | |||||||
| chr6:31504672 | T | C | 1 | a0003c0003t0002g0177 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.71-945T>C | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31504672 | |||||||
| chr6:31504673 | T | G | 1 | a0003c0003t0002g0177 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.71-944T>G | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31504673 | |||||||
| chr6:31504675 | A | G | 1 | a0003c0003t0002g0177 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.71-942A>G | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31504675 | |||||||
| chr6:31504678 | A | T | 1 | a0003c0003t0002g0177 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.71-939A>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31504678 | |||||||
| chr6:31504679 | G | T | 1 | a0003c0003t0002g0177 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.71-938G>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31504679 | |||||||
| chr6:31504682 | C | T | 43 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(40): Show |
94 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.71-935C>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31504682 | |||||||
| chr6:31504800 | T | A | 1 | a0003c0003t0002g0177 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.71-817T>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31504800 | |||||||
| chr6:31504927 | T | C | 1 | a0003c0003t0002g0174 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.71-690T>C | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31504927 | |||||||
| chr6:31504943 | G | T | 41 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0032 others(38): Show |
87 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.71-674G>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31504943 | |||||||
| chr6:31504980 | G | T | 54 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(51): Show |
181 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.71-637G>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31504980 | |||||||
| chr6:31504983 | C | T | 1 | a0002c0002t0001g0035 | 3 | HG02818.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.71-634C>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31504983 | |||||||
| chr6:31505004 | C | T | 1 | a0007c0008t0001g0136 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.71-613C>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31505004 | |||||||
| chr6:31505015 | T | C | 133 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(130): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.71-602T>C | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31505015 | |||||||
| chr6:31505030 | G | A | 101 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0022 others(98): Show |
245 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.71-587G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31505030 | |||||||
| chr6:31505044 | T | C | 54 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(51): Show |
181 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.71-573T>C | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31505044 | |||||||
| chr6:31505046 | A | G | 46 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0022 others(43): Show |
142 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.71-571A>G | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31505046 | |||||||
| chr6:31505085 | A | T | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(126): Show |
316 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.71-532A>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31505085 | |||||||
| chr6:31505088 | G | A | 99 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(96): Show |
244 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.71-529G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31505088 | |||||||
| chr6:31505101 | T | C | 1 | a0003c0003t0002g0063 | 2 | HG04199.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.71-516T>C | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31505101 | |||||||
| chr6:31505143 | A | G | 1 | a0001c0001t0001g0016 | 6 | HG00280.hp2 HG00735.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.71-474A>G | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31505143 | |||||||
| chr6:31505163 | T | C | 1 | a0001c0001t0001g0016 | 6 | HG00280.hp2 HG00735.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.71-454T>C | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31505163 | |||||||
| chr6:31505169 | A | G | 44 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(41): Show |
100 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.71-448A>G | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31505169 | |||||||
| chr6:31505179 | G | C | 33 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(30): Show |
120 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.71-438G>C | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31505179 | |||||||
| chr6:31505201 | A | AG | 1 | a0001c0001t0001g0016 | 6 | HG00280.hp2 HG00735.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.71-416_71-415insG | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31505201 | |||||||
| chr6:31505205 | G | A | 1 | a0001c0001t0001g0016 | 6 | HG00280.hp2 HG00735.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.71-412G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31505205 | |||||||
| chr6:31505213 | C | T | 1 | a0001c0012t0003g0180 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.71-404C>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31505213 | |||||||
| chr6:31505265 | T | C | 30 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(27): Show |
72 | HG00423.hp2 HG00438.hp2 HG01074.hp2 others(69): Show |
intron_variant | MODIFIER | c.71-352T>C | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31505265 | |||||||
| chr6:31505293 | A | C | 34 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(31): Show |
121 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.71-324A>C | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31505293 | |||||||
| chr6:31505294 | C | T | 1 | a0001c0001t0001g0164 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.71-323C>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31505294 | |||||||
| chr6:31505316 | T | C | 30 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(27): Show |
72 | HG00423.hp2 HG00438.hp2 HG01074.hp2 others(69): Show |
intron_variant | MODIFIER | c.71-301T>C | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31505316 | |||||||
| chr6:31505387 | C | A | 1 | a0001c0001t0001g0076 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.71-230C>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31505387 | |||||||
| chr6:31505470 | C | T | 7 | a0007c0008t0001g0049 a0007c0008t0001g0114 a0007c0008t0001g0115 others(4): Show |
8 | HG00323.hp1 HG02083.hp1 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.71-147C>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31505470 | |||||||
| chr6:31505491 | C | G | 1 | a0001c0004t0001g0101 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.71-126C>G | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31505491 | |||||||
| chr6:31505506 | A | G | 1 | a0001c0001t0001g0059 | 2 | HG02074.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.71-111A>G | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31505506 | |||||||
| chr6:31505509 | C | T | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(160): Show |
399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.71-108C>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31505509 | |||||||
| chr6:31505576 | T | C | 1 | a0001c0001t0003g0159 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.71-41T>C | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 1/5 | chr6 | 31505576 | |||||||
| chr6:31505930 | A | G | 1 | a0003c0003t0002g0173 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.325+59A>G | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 2/5 | chr6 | 31505930 | |||||||
| chr6:31505953 | G | A | 18 | a0002c0002t0001g0015 a0002c0002t0001g0024 a0002c0002t0001g0035 others(15): Show |
29 | HG00323.hp2 HG01123.hp1 HG01346.hp2 others(26): Show |
intron_variant | MODIFIER | c.325+82G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 2/5 | chr6 | 31505953 | |||||||
| chr6:31505969 | G | A | 13 | a0004c0005t0001g0019 a0004c0005t0001g0020 a0004c0005t0001g0034 others(10): Show |
25 | HG00099.hp2 HG00280.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.325+98G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 2/5 | chr6 | 31505969 | |||||||
| chr6:31506008 | T | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0168 |
5 | HG03239.hp2 HG03669.hp2 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.326-135T>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 2/5 | chr6 | 31506008 | |||||||
| chr6:31506067 | T | C | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(160): Show |
399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.326-76T>C | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 2/5 | chr6 | 31506067 | |||||||
| chr6:31506503 | G | A | 26 | a0001c0001t0003g0108 a0002c0002t0001g0005 a0002c0002t0001g0007 others(23): Show |
60 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.613+73G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 3/5 | chr6 | 31506503 | |||||||
| chr6:31506517 | T | C | 1 | a0010c0016t0006g0166 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.613+87T>C | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 3/5 | chr6 | 31506517 | |||||||
| chr6:31506518 | G | T | 1 | a0010c0016t0006g0166 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.613+88G>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 3/5 | chr6 | 31506518 | |||||||
| chr6:31506672 | T | G | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(160): Show |
399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.613+242T>G | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 3/5 | chr6 | 31506672 | |||||||
| chr6:31506690 | G | A | 1 | a0010c0016t0006g0166 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.613+260G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 3/5 | chr6 | 31506690 | |||||||
| chr6:31506691 | A | G | 1 | a0010c0016t0006g0166 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.613+261A>G | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 3/5 | chr6 | 31506691 | |||||||
| chr6:31506693 | G | A | 1 | a0010c0016t0006g0166 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.613+263G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 3/5 | chr6 | 31506693 | |||||||
| chr6:31506730 | G | A | 1 | a0002c0002t0001g0005 | 3 | HG00639.hp2 HG01099.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.614-292G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 3/5 | chr6 | 31506730 | |||||||
| chr6:31506843 | A | T | 1 | a0003c0003t0002g0174 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.614-179A>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 3/5 | chr6 | 31506843 | |||||||
| chr6:31506861 | G | A | 2 | a0007c0008t0001g0137 a0007c0008t0001g0138 |
2 | HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.614-161G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 3/5 | chr6 | 31506861 | |||||||
| chr6:31506908 | C | T | 19 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0052 others(16): Show |
45 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.614-114C>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 3/5 | chr6 | 31506908 | |||||||
| chr6:31506911 | T | G | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(160): Show |
399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.614-111T>G | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 3/5 | chr6 | 31506911 | |||||||
| chr6:31507307 | C | CTGGGGTG others(1): Show |
18 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0041 others(15): Show |
46 | HG00438.hp2 HG01192.hp2 HG01346.hp1 others(43): Show |
intron_variant | MODIFIER | c.892+8_892+15dupTGG others(5): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr6 | 31507307 | ||||||
| chr6:31507350 | A | G | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(160): Show |
399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.892+50A>G | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 4/5 | chr6 | 31507350 | |||||||
| chr6:31507568 | T | G | 2 | a0002c0002t0001g0145 a0002c0002t0001g0152 |
2 | HG01346.hp2 HG02015.hp1 |
intron_variant | MODIFIER | c.1024+37T>G | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 5/5 | chr6 | 31507568 | |||||||
| chr6:31507597 | G | T | 2 | a0001c0004t0001g0102 a0001c0004t0001g0104 |
2 | HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1024+66G>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 5/5 | chr6 | 31507597 | |||||||
| chr6:31507636 | G | A | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(147): Show |
377 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(374): Show |
intron_variant | MODIFIER | c.1024+105G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 5/5 | chr6 | 31507636 | |||||||
| chr6:31507709 | C | T | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(147): Show |
377 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(374): Show |
intron_variant | MODIFIER | c.1024+178C>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 5/5 | chr6 | 31507709 | |||||||
| chr6:31507718 | G | A | 9 | a0002c0002t0001g0007 a0002c0002t0001g0054 a0002c0002t0001g0055 others(6): Show |
19 | HG00408.hp1 HG01952.hp1 NA18949.hp1 others(16): Show |
intron_variant | MODIFIER | c.1024+187G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 5/5 | chr6 | 31507718 | |||||||
| chr6:31507736 | G | A | 18 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0041 others(15): Show |
46 | HG00438.hp2 HG01192.hp2 HG01346.hp1 others(43): Show |
intron_variant | MODIFIER | c.1024+205G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 5/5 | chr6 | 31507736 | |||||||
| chr6:31507786 | G | A | 9 | a0001c0001t0001g0012 a0001c0001t0001g0022 a0001c0001t0001g0031 others(6): Show |
21 | HG00408.hp2 HG00558.hp1 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.1024+255G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 5/5 | chr6 | 31507786 | |||||||
| chr6:31507842 | CTAGG | C | 8 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0016 others(5): Show |
39 | HG00280.hp2 HG00735.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.1024+312_1024+315d others(6): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 5/5 | chr6 | 31507842 | |||||||
| chr6:31507847 | G | C | 8 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0016 others(5): Show |
39 | HG00280.hp2 HG00735.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.1024+316G>C | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 5/5 | chr6 | 31507847 | |||||||
| chr6:31507851 | G | A | 13 | a0005c0006t0002g0014 a0005c0006t0002g0043 a0005c0006t0002g0044 others(10): Show |
22 | HG00140.hp1 HG00673.hp2 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.1024+320G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 5/5 | chr6 | 31507851 | |||||||
| chr6:31507876 | A | G | 2 | a0004c0005t0001g0050 a0004c0005t0001g0051 |
4 | HG01109.hp2 HG02965.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1024+345A>G | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 5/5 | chr6 | 31507876 | |||||||
| chr6:31507878 | G | A | 25 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(22): Show |
103 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(100): Show |
intron_variant | MODIFIER | c.1024+347G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 5/5 | chr6 | 31507878 | |||||||
| chr6:31507894 | G | A | 1 | a0001c0001t0001g0079 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1024+363G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 5/5 | chr6 | 31507894 | |||||||
| chr6:31507986 | G | A | 5 | a0003c0003t0002g0021 a0003c0003t0002g0171 a0003c0003t0006g0021 others(2): Show |
8 | HG00558.hp2 HG02970.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.1024+455G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 5/5 | chr6 | 31507986 | |||||||
| chr6:31507987 | A | G | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(147): Show |
377 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(374): Show |
intron_variant | MODIFIER | c.1024+456A>G | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 5/5 | chr6 | 31507987 | |||||||
| chr6:31507987 | A | T | 1 | a0010c0016t0006g0166 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1024+456A>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 5/5 | chr6 | 31507987 | |||||||
| chr6:31507997 | G | C | 3 | a0001c0009t0007g0045 a0001c0009t0007g0093 a0001c0009t0007g0097 |
4 | HG01074.hp1 HG02145.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.1024+466G>C | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 5/5 | chr6 | 31507997 | |||||||
| chr6:31508034 | T | C | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(147): Show |
377 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(374): Show |
intron_variant | MODIFIER | c.1024+503T>C | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 5/5 | chr6 | 31508034 | |||||||
| chr6:31508111 | G | A | 1 | a0011c0015t0001g0161 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1024+580G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 5/5 | chr6 | 31508111 | |||||||
| chr6:31508136 | A | T | 65 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0015 others(62): Show |
123 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.1024+605A>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 5/5 | chr6 | 31508136 | |||||||
| chr6:31508316 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1024+785C>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 5/5 | chr6 | 31508316 | |||||||
| chr6:31508317 | A | G | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(147): Show |
377 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(374): Show |
intron_variant | MODIFIER | c.1024+786A>G | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 5/5 | chr6 | 31508317 | |||||||
| chr6:31508357 | A | G | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(147): Show |
377 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(374): Show |
intron_variant | MODIFIER | c.1024+826A>G | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 5/5 | chr6 | 31508357 | |||||||
| chr6:31508488 | G | A | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(160): Show |
399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.1024+957G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 5/5 | chr6 | 31508488 | |||||||
| chr6:31508494 | C | G | 1 | a0003c0003t0002g0061 | 2 | NA18977.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.1024+963C>G | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 5/5 | chr6 | 31508494 | |||||||
| chr6:31508520 | C | A | 8 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0016 others(5): Show |
39 | HG00280.hp2 HG00735.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.1024+989C>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 5/5 | chr6 | 31508520 | |||||||
| chr6:31508522 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1024+991G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 5/5 | chr6 | 31508522 | |||||||
| chr6:31508562 | C | T | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(147): Show |
377 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(374): Show |
intron_variant | MODIFIER | c.1024+1031C>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 5/5 | chr6 | 31508562 | |||||||
| chr6:31508563 | A | G | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(160): Show |
399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.1024+1032A>G | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 5/5 | chr6 | 31508563 | |||||||
| chr6:31508586 | G | A | 6 | a0001c0001t0003g0011 a0001c0001t0003g0107 a0001c0001t0003g0108 others(3): Show |
16 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(13): Show |
intron_variant | MODIFIER | c.1024+1055G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 5/5 | chr6 | 31508586 | |||||||
| chr6:31508642 | A | G | 1 | a0010c0016t0006g0166 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1024+1111A>G | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 5/5 | chr6 | 31508642 | |||||||
| chr6:31508643 | T | A | 1 | a0010c0016t0006g0166 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1024+1112T>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 5/5 | chr6 | 31508643 | |||||||
| chr6:31508681 | T | A | 3 | a0004c0005t0001g0019 a0004c0005t0001g0110 a0004c0005t0001g0112 |
7 | HG00099.hp2 HG00280.hp1 HG00738.hp2 others(4): Show |
intron_variant | MODIFIER | c.1025-1101T>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 5/5 | chr6 | 31508681 | |||||||
| chr6:31508737 | C | A | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(147): Show |
377 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(374): Show |
intron_variant | MODIFIER | c.1025-1045C>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 5/5 | chr6 | 31508737 | |||||||
| chr6:31508843 | A | T | 1 | a0001c0001t0001g0078 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1025-939A>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 5/5 | chr6 | 31508843 | |||||||
| chr6:31508917 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1025-865A>G | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 5/5 | chr6 | 31508917 | |||||||
| chr6:31509016 | C | T | 2 | a0001c0001t0003g0159 a0011c0015t0001g0161 |
2 | HG01361.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1025-766C>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 5/5 | chr6 | 31509016 | |||||||
| chr6:31509056 | A | G | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(160): Show |
399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.1025-726A>G | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 5/5 | chr6 | 31509056 | |||||||
| chr6:31509077 | C | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(83): Show |
255 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(252): Show |
intron_variant | MODIFIER | c.1025-705C>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 5/5 | chr6 | 31509077 | |||||||
| chr6:31509218 | G | T | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(160): Show |
399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.1025-564G>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 5/5 | chr6 | 31509218 | |||||||
| chr6:31509245 | C | T | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(161): Show |
400 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(397): Show |
intron_variant | MODIFIER | c.1025-537C>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 5/5 | chr6 | 31509245 | |||||||
| chr6:31509291 | G | T | 1 | a0001c0001t0001g0077 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1025-491G>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 5/5 | chr6 | 31509291 | |||||||
| chr6:31509351 | A | G | 1 | a0001c0001t0001g0163 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1025-431A>G | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 5/5 | chr6 | 31509351 | |||||||
| chr6:31509376 | G | A | 1 | a0001c0001t0001g0058 | 2 | HG02135.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.1025-406G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 5/5 | chr6 | 31509376 | |||||||
| chr6:31509389 | G | A | 1 | a0007c0008t0001g0138 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1025-393G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 5/5 | chr6 | 31509389 | |||||||
| chr6:31509407 | G | C | 1 | a0001c0001t0001g0169 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1025-375G>C | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 5/5 | chr6 | 31509407 | |||||||
| chr6:31509412 | A | G | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(147): Show |
377 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(374): Show |
intron_variant | MODIFIER | c.1025-370A>G | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 5/5 | chr6 | 31509412 | |||||||
| chr6:31509547 | A | C | 7 | a0001c0001t0003g0159 a0003c0003t0002g0021 a0003c0003t0002g0171 others(4): Show |
10 | HG00558.hp2 HG01361.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.1025-235A>C | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 5/5 | chr6 | 31509547 | |||||||
| chr6:31509559 | G | T | 1 | a0007c0008t0001g0115 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1025-223G>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 5/5 | chr6 | 31509559 | |||||||
| chr6:31509566 | G | T | 1 | a0003c0003t0002g0109 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1025-216G>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 5/5 | chr6 | 31509566 | |||||||
| chr6:31509616 | CAG | C | 13 | a0005c0006t0002g0014 a0005c0006t0002g0043 a0005c0006t0002g0044 others(10): Show |
22 | HG00140.hp1 HG00673.hp2 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.1025-165_1025-164d others(4): Show |
MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 5/5 | chr6 | 31509616 | |||||||
| chr6:31509652 | A | G | 3 | a0004c0005t0001g0020 a0004c0005t0001g0125 a0004c0005t0001g0127 |
7 | HG01243.hp1 HG02622.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1025-130A>G | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 5/5 | chr6 | 31509652 | |||||||
| chr6:31509658 | G | A | 4 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0094 others(1): Show |
12 | HG00558.hp1 HG00741.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.1025-124G>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 5/5 | chr6 | 31509658 | |||||||
| chr6:31509684 | C | T | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(160): Show |
399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.1025-98C>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 5/5 | chr6 | 31509684 | |||||||
| chr6:31509689 | C | A | 1 | a0004c0005t0001g0050 | 2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1025-93C>A | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 5/5 | chr6 | 31509689 | |||||||
| chr6:31509738 | A | T | 1 | a0001c0001t0010g0072 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1025-44A>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 5/5 | chr6 | 31509738 | |||||||
| chr6:31509747 | C | T | 6 | a0001c0001t0001g0012 a0001c0001t0001g0022 a0001c0001t0001g0031 others(3): Show |
17 | HG00408.hp2 HG00558.hp1 HG00597.hp2 others(14): Show |
intron_variant | MODIFIER | c.1025-35C>T | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 5/5 | chr6 | 31509747 | |||||||
| chr6:31509754 | A | G | 34 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(31): Show |
121 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.1025-28A>G | MICB | ENSG00000204516.10 | transcript | ENST00000252229.7 | protein_coding | 5/5 | chr6 | 31509754 |