Variant report

Variant	rs34395849
Chromosome Location	chr7:137160933-137160934
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:137159775..137161658-chr7:137173667..137176568,2	K562	blood:

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs10228926	0.95[EUR][1000 genomes]
rs10235650	0.85[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10236626	0.97[EUR][1000 genomes]
rs10236885	0.94[EUR][1000 genomes]
rs10249961	0.94[EUR][1000 genomes]
rs10250999	0.98[EUR][1000 genomes]
rs10257221	0.86[AFR][1000 genomes];0.97[EUR][1000 genomes]
rs10264765	0.97[EUR][1000 genomes]
rs10268873	0.97[EUR][1000 genomes]
rs10268889	0.97[EUR][1000 genomes]
rs10276002	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10480523	0.95[EUR][1000 genomes]
rs12707360	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13242243	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1406088	0.95[EUR][1000 genomes]
rs1528099	0.94[EUR][1000 genomes]
rs1528100	0.95[EUR][1000 genomes]
rs1852641	0.97[EUR][1000 genomes]
rs2293546	0.88[ASN][1000 genomes]
rs28434741	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs28491569	0.95[EUR][1000 genomes]
rs28573283	0.98[EUR][1000 genomes]
rs35080869	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs35470018	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs35481034	0.95[EUR][1000 genomes]
rs36125942	0.97[EUR][1000 genomes]
rs57998109	0.93[ASN][1000 genomes]
rs6467704	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6467705	0.97[EUR][1000 genomes]
rs6467706	0.92[EUR][1000 genomes]
rs6467707	0.95[EUR][1000 genomes]
rs67112765	0.97[EUR][1000 genomes]
rs68124742	0.98[EUR][1000 genomes]
rs6950579	0.95[EUR][1000 genomes]
rs6951059	0.95[EUR][1000 genomes]
rs6971080	0.95[EUR][1000 genomes]
rs7341469	0.95[EUR][1000 genomes]
rs7341533	0.97[EUR][1000 genomes]
rs73730628	0.88[ASN][1000 genomes]
rs7779526	0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7788161	0.94[EUR][1000 genomes]
rs7802865	0.95[EUR][1000 genomes]
rs7807425	0.97[EUR][1000 genomes]
rs9655902	0.92[EUR][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	nsv869820	chr7:136990386-137347718	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv1027868	chr7:137004690-137311653	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	nsv539134	chr7:137004690-137311653	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
4	nsv520950	chr7:137154572-137167984	Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:137139800-137165000	Weak transcription	Fetal Brain Female	brain
2	chr7:137148200-137161800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr7:137148600-137206400	Weak transcription	Aorta	Aorta
4	chr7:137149600-137161600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr7:137152000-137179400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr7:137159400-137162400	Enhancers	Breast Myoepithelial Primary Cells	Breast
7	chr7:137160400-137162000	Enhancers	HSMMtube	muscle
8	chr7:137160600-137162000	Enhancers	NH-A	brain
9	chr7:137160600-137162200	Enhancers	Muscle Satellite Cultured Cells	--
10	chr7:137160600-137162200	Enhancers	Osteobl	bone
11	chr7:137160800-137162000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr7:137160800-137162000	Enhancers	HMEC	breast
13	chr7:137160800-137162000	Enhancers	HSMM	muscle

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