Variant report

Variant	rs10110021
Chromosome Location	chr8:125883275-125883276
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:125876735..125880494-chr8:125880552..125885100,4	K562	blood:
2	chr8:125882022..125884684-chr8:125903554..125905435,2	K562	blood:
3	chr8:125877925..125881102-chr8:125882727..125885100,3	K562	blood:
4	chr8:125882022..125884684-chr8:125903554..125906736,3	K562	blood:
5	chr8:125870078..125872946-chr8:125880944..125883376,2	K562	blood:

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10956220	0.82[CEU][hapmap]
rs11774426	0.85[CEU][hapmap]
rs11784930	0.89[CEU][hapmap];0.90[EUR][1000 genomes]
rs11987239	0.86[CEU][hapmap];0.91[EUR][1000 genomes]
rs11988572	0.83[EUR][1000 genomes]
rs11990757	0.96[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap]
rs12542397	0.83[CEU][hapmap];0.91[JPT][hapmap]
rs12547431	0.85[CEU][hapmap]
rs12549299	0.91[CEU][hapmap]
rs13272895	0.86[CEU][hapmap];0.90[EUR][1000 genomes]
rs28513649	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4871560	0.86[CEU][hapmap]
rs4871562	0.89[CEU][hapmap];0.91[EUR][1000 genomes]
rs4871564	0.91[EUR][1000 genomes]
rs4871565	0.91[EUR][1000 genomes]
rs62529062	0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs62529063	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs62530623	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6470289	0.85[CEU][hapmap]
rs6470290	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6470296	0.86[CEU][hapmap];0.90[EUR][1000 genomes]
rs6470313	0.96[CEU][hapmap];0.87[EUR][1000 genomes]
rs6985287	0.91[EUR][1000 genomes]
rs6987095	0.89[CEU][hapmap];0.91[JPT][hapmap];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6992468	0.82[CEU][hapmap]
rs7461829	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7464057	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7819144	0.90[EUR][1000 genomes]
rs7835994	0.85[CEU][hapmap]
rs7845282	0.96[CEU][hapmap];1.00[CHB][hapmap];0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9694326	0.86[CEU][hapmap];0.92[JPT][hapmap];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv891434	chr8:125630655-126324432	Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
2	nsv1030803	chr8:125868684-125969635	Weak transcription Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
3	nsv1024405	chr8:125868684-125971035	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
4	nsv1020502	chr8:125868684-125972572	Active TSS Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:125871000-125885200	Weak transcription	Esophagus	oesophagus
2	chr8:125874400-125884800	Weak transcription	Right Atrium	heart
3	chr8:125879400-125884600	Weak transcription	HSMMtube	muscle
4	chr8:125879600-125884400	Weak transcription	HSMM	muscle
5	chr8:125879600-125884400	Weak transcription	Osteobl	bone
6	chr8:125879600-125884600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr8:125879800-125884400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr8:125879800-125884400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr8:125879800-125884400	Weak transcription	NHDF-Ad	bronchial
10	chr8:125879800-125884400	Weak transcription	NHEK	skin
11	chr8:125879800-125884600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr8:125879800-125884600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr8:125879800-125884600	Weak transcription	Muscle Satellite Cultured Cells	--
14	chr8:125880000-125884400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr8:125880600-125884600	Weak transcription	NHLF	lung
16	chr8:125880800-125884400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr8:125880800-125885000	Weak transcription	Left Ventricle	heart
18	chr8:125882600-125886400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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