Variant report
Variant | rs61843422 |
---|---|
Chromosome Location | chr10:43427051-43427052 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:1 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr10:43426456..43429844-chr10:43434614..43436862,3 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs1085783 | 1.00[ASN][1000 genomes] |
rs1106646 | 1.00[ASN][1000 genomes] |
rs1106647 | 1.00[ASN][1000 genomes] |
rs12572458 | 1.00[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs12572471 | 1.00[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs1342143 | 1.00[ASN][1000 genomes] |
rs17158193 | 1.00[ASN][1000 genomes] |
rs17158301 | 0.95[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs17158304 | 0.95[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs17159047 | 1.00[ASN][1000 genomes] |
rs17344904 | 1.00[ASN][1000 genomes] |
rs17344997 | 1.00[ASN][1000 genomes] |
rs17345889 | 1.00[ASN][1000 genomes] |
rs17347902 | 1.00[ASN][1000 genomes] |
rs17347944 | 1.00[ASN][1000 genomes] |
rs17429275 | 1.00[ASN][1000 genomes] |
rs17429415 | 1.00[ASN][1000 genomes] |
rs17430796 | 1.00[ASN][1000 genomes] |
rs17431976 | 1.00[ASN][1000 genomes] |
rs17432011 | 1.00[ASN][1000 genomes] |
rs17432429 | 1.00[ASN][1000 genomes] |
rs17432532 | 1.00[ASN][1000 genomes] |
rs17432714 | 1.00[ASN][1000 genomes] |
rs17432763 | 1.00[ASN][1000 genomes] |
rs17432833 | 1.00[ASN][1000 genomes] |
rs1775069 | 1.00[ASN][1000 genomes] |
rs1935644 | 1.00[ASN][1000 genomes] |
rs2051043 | 1.00[ASN][1000 genomes] |
rs2078397 | 1.00[ASN][1000 genomes] |
rs2744082 | 1.00[ASN][1000 genomes] |
rs2795505 | 1.00[ASN][1000 genomes] |
rs2796563 | 1.00[ASN][1000 genomes] |
rs2796565 | 1.00[ASN][1000 genomes] |
rs3026691 | 1.00[ASN][1000 genomes] |
rs3026692 | 1.00[ASN][1000 genomes] |
rs3026695 | 1.00[ASN][1000 genomes] |
rs3026700 | 1.00[ASN][1000 genomes] |
rs41295810 | 1.00[ASN][1000 genomes] |
rs41295811 | 1.00[ASN][1000 genomes] |
rs41295813 | 1.00[ASN][1000 genomes] |
rs515365 | 1.00[ASN][1000 genomes] |
rs58477795 | 1.00[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs61736599 | 1.00[ASN][1000 genomes] |
rs61843172 | 1.00[ASN][1000 genomes] |
rs61843173 | 1.00[ASN][1000 genomes] |
rs61843174 | 1.00[ASN][1000 genomes] |
rs61843175 | 1.00[ASN][1000 genomes] |
rs61843176 | 1.00[ASN][1000 genomes] |
rs61843177 | 1.00[ASN][1000 genomes] |
rs61843178 | 1.00[ASN][1000 genomes] |
rs61843179 | 1.00[ASN][1000 genomes] |
rs61843180 | 1.00[ASN][1000 genomes] |
rs61843181 | 1.00[ASN][1000 genomes] |
rs61843182 | 1.00[ASN][1000 genomes] |
rs61843183 | 1.00[ASN][1000 genomes] |
rs61843184 | 1.00[ASN][1000 genomes] |
rs61843185 | 1.00[ASN][1000 genomes] |
rs61843186 | 1.00[ASN][1000 genomes] |
rs61843187 | 1.00[ASN][1000 genomes] |
rs61843188 | 1.00[ASN][1000 genomes] |
rs61843189 | 1.00[ASN][1000 genomes] |
rs61843190 | 1.00[ASN][1000 genomes] |
rs61843191 | 1.00[ASN][1000 genomes] |
rs61843192 | 1.00[ASN][1000 genomes] |
rs61843196 | 1.00[ASN][1000 genomes] |
rs61843198 | 1.00[ASN][1000 genomes] |
rs61843199 | 1.00[ASN][1000 genomes] |
rs61843201 | 1.00[ASN][1000 genomes] |
rs61843372 | 1.00[ASN][1000 genomes] |
rs61843373 | 1.00[ASN][1000 genomes] |
rs61843374 | 1.00[ASN][1000 genomes] |
rs61843380 | 1.00[ASN][1000 genomes] |
rs61843381 | 1.00[ASN][1000 genomes] |
rs61843382 | 1.00[ASN][1000 genomes] |
rs61843407 | 0.88[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs61843419 | 0.88[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs61843420 | 0.88[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs61843421 | 0.88[EUR][1000 genomes] |
rs61843423 | 0.84[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs61843424 | 0.95[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs61843425 | 0.91[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs61843426 | 0.91[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs61843427 | 0.83[EUR][1000 genomes] |
rs61843428 | 0.84[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs61843429 | 0.82[EUR][1000 genomes] |
rs61843430 | 0.95[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs61843431 | 0.84[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs61843432 | 1.00[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs61843434 | 1.00[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs61843435 | 1.00[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs61843437 | 1.00[ASN][1000 genomes] |
rs61843438 | 0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs61843439 | 0.80[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs61843440 | 0.80[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs61843441 | 0.82[EUR][1000 genomes] |
rs61843457 | 0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs61843459 | 0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs61844763 | 1.00[ASN][1000 genomes] |
rs61844765 | 1.00[ASN][1000 genomes] |
rs61844768 | 1.00[ASN][1000 genomes] |
rs61844770 | 1.00[ASN][1000 genomes] |
rs61844771 | 1.00[ASN][1000 genomes] |
rs61844772 | 1.00[ASN][1000 genomes] |
rs61844774 | 1.00[ASN][1000 genomes] |
rs61844775 | 1.00[ASN][1000 genomes] |
rs61844813 | 1.00[ASN][1000 genomes] |
rs61844815 | 1.00[ASN][1000 genomes] |
rs61844816 | 1.00[ASN][1000 genomes] |
rs61844817 | 1.00[ASN][1000 genomes] |
rs61844821 | 1.00[ASN][1000 genomes] |
rs61844827 | 1.00[ASN][1000 genomes] |
rs61844828 | 1.00[ASN][1000 genomes] |
rs61844829 | 1.00[ASN][1000 genomes] |
rs61844832 | 1.00[ASN][1000 genomes] |
rs61844835 | 1.00[ASN][1000 genomes] |
rs61844837 | 1.00[ASN][1000 genomes] |
rs61844848 | 1.00[ASN][1000 genomes] |
rs61844849 | 1.00[ASN][1000 genomes] |
rs61844854 | 1.00[ASN][1000 genomes] |
rs61845260 | 0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs61845261 | 0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs61845262 | 0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs61845264 | 0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs61845265 | 1.00[ASN][1000 genomes] |
rs61845266 | 1.00[ASN][1000 genomes] |
rs61845268 | 1.00[ASN][1000 genomes] |
rs61845269 | 1.00[ASN][1000 genomes] |
rs61845270 | 1.00[ASN][1000 genomes] |
rs61845271 | 1.00[ASN][1000 genomes] |
rs61845272 | 1.00[ASN][1000 genomes] |
rs61845273 | 1.00[ASN][1000 genomes] |
rs61845274 | 1.00[ASN][1000 genomes] |
rs61845279 | 1.00[ASN][1000 genomes] |
rs61845280 | 1.00[ASN][1000 genomes] |
rs61845281 | 1.00[ASN][1000 genomes] |
rs61845282 | 1.00[ASN][1000 genomes] |
rs61845306 | 1.00[ASN][1000 genomes] |
rs61845307 | 1.00[ASN][1000 genomes] |
rs61845308 | 1.00[ASN][1000 genomes] |
rs61845309 | 1.00[ASN][1000 genomes] |
rs61845310 | 1.00[ASN][1000 genomes] |
rs61845311 | 1.00[ASN][1000 genomes] |
rs61845312 | 1.00[ASN][1000 genomes] |
rs61845314 | 1.00[ASN][1000 genomes] |
rs61845315 | 1.00[ASN][1000 genomes] |
rs61845316 | 1.00[ASN][1000 genomes] |
rs61845317 | 1.00[ASN][1000 genomes] |
rs61845318 | 1.00[ASN][1000 genomes] |
rs61845320 | 1.00[ASN][1000 genomes] |
rs61845321 | 1.00[ASN][1000 genomes] |
rs61845323 | 1.00[ASN][1000 genomes] |
rs61845324 | 1.00[ASN][1000 genomes] |
rs61845325 | 1.00[ASN][1000 genomes] |
rs61845326 | 1.00[ASN][1000 genomes] |
rs61845327 | 1.00[ASN][1000 genomes] |
rs61845328 | 1.00[ASN][1000 genomes] |
rs61845329 | 1.00[ASN][1000 genomes] |
rs61845330 | 1.00[ASN][1000 genomes] |
rs61845331 | 1.00[ASN][1000 genomes] |
rs61845332 | 1.00[ASN][1000 genomes] |
rs61845333 | 1.00[ASN][1000 genomes] |
rs61845335 | 1.00[ASN][1000 genomes] |
rs61845336 | 1.00[ASN][1000 genomes] |
rs61845338 | 1.00[ASN][1000 genomes] |
rs61845339 | 1.00[ASN][1000 genomes] |
rs61845340 | 1.00[ASN][1000 genomes] |
rs61845341 | 1.00[ASN][1000 genomes] |
rs61845342 | 1.00[ASN][1000 genomes] |
rs61845343 | 1.00[ASN][1000 genomes] |
rs61845345 | 1.00[ASN][1000 genomes] |
rs61845346 | 1.00[ASN][1000 genomes] |
rs61845963 | 1.00[ASN][1000 genomes] |
rs61845964 | 1.00[ASN][1000 genomes] |
rs638507 | 1.00[ASN][1000 genomes] |
rs7074380 | 1.00[ASN][1000 genomes] |
rs7089165 | 1.00[ASN][1000 genomes] |
rs7091439 | 1.00[ASN][1000 genomes] |
rs7097557 | 1.00[ASN][1000 genomes] |
rs7100455 | 1.00[ASN][1000 genomes] |
rs74135421 | 0.88[AFR][1000 genomes] |
rs74135422 | 0.84[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs74135423 | 0.87[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs74135424 | 1.00[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs74135429 | 0.87[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs788248 | 1.00[ASN][1000 genomes] |
rs788250 | 1.00[ASN][1000 genomes] |
rs788286 | 1.00[ASN][1000 genomes] |
rs788294 | 1.00[ASN][1000 genomes] |
rs7898367 | 1.00[ASN][1000 genomes] |
rs7899660 | 0.84[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs7900242 | 0.83[EUR][1000 genomes] |
rs7904220 | 1.00[ASN][1000 genomes] |
rs7908539 | 1.00[ASN][1000 genomes] |
rs7915796 | 1.00[ASN][1000 genomes] |
rs7922188 | 0.83[EUR][1000 genomes] |
rs7923121 | 1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv550672 | chr10:42753190-43441729 | Bivalent Enhancer Genic enhancers Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 40 gene(s) | inside rSNPs | diseases |
2 | nsv1042764 | chr10:42846383-43511712 | Flanking Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 50 gene(s) | inside rSNPs | diseases |
3 | nsv1050394 | chr10:42890663-43604956 | Enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 53 gene(s) | inside rSNPs | diseases |
4 | nsv540573 | chr10:42890663-43604956 | Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 53 gene(s) | inside rSNPs | diseases |
5 | nsv534548 | chr10:42890664-43729688 | Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 56 gene(s) | inside rSNPs | diseases |
6 | esv2758216 | chr10:42965131-43510191 | Flanking Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 49 gene(s) | inside rSNPs | diseases |
7 | esv2759746 | chr10:42965131-43510191 | Weak transcription Bivalent Enhancer Bivalent/Poised TSS Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Enhancers Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 49 gene(s) | inside rSNPs | diseases |
8 | nsv430159 | chr10:43291894-43946294 | Flanking Active TSS Enhancers Active TSS Strong transcription Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 92 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr10:43422800-43428200 | Weak transcription | Pancreas | Pancrea |
2 | chr10:43424200-43428200 | Weak transcription | Right Atrium | heart |
3 | chr10:43425400-43427200 | Bivalent Enhancer | Fetal Muscle Leg | muscle |
4 | chr10:43426400-43427400 | Enhancers | iPS DF 19.11 Cell Line | embryonic stem cell |
5 | chr10:43426600-43428400 | Enhancers | ES-UCSF4 Cell Line | embryonic stem cell |
6 | chr10:43427000-43427600 | Bivalent Enhancer | ES-I3 Cell Line | embryonic stem cell |
7 | chr10:43427000-43428000 | Bivalent Enhancer | H1 Cell Line | embryonic stem cell |