Variant report

Variant	rs10268869
Chromosome Location	chr7:137362939-137362940
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:137350182..137352785-chr7:137361022..137363744,2	K562	blood:

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10216163	0.83[ASN][1000 genomes]
rs10235994	0.83[ASN][1000 genomes]
rs10248705	0.82[JPT][hapmap];0.94[YRI][hapmap];0.91[ASN][1000 genomes]
rs10267021	0.83[ASN][1000 genomes]
rs10269622	0.82[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs10270098	0.82[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs10273283	0.82[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs10276318	0.83[ASN][1000 genomes]
rs11971088	0.82[JPT][hapmap]
rs11975858	0.82[JPT][hapmap]
rs1424367	0.83[ASN][1000 genomes]
rs1424368	1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs1424369	0.82[JPT][hapmap];0.91[ASN][1000 genomes]
rs28419330	1.00[AMR][1000 genomes]
rs28633970	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs28735762	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs35323708	0.83[ASN][1000 genomes]
rs3778791	0.83[ASN][1000 genomes]
rs3778792	0.83[ASN][1000 genomes]
rs3778793	0.83[ASN][1000 genomes]
rs3778794	0.83[ASN][1000 genomes]
rs3778801	1.00[AMR][1000 genomes]
rs3800621	0.83[ASN][1000 genomes]
rs3800625	1.00[AMR][1000 genomes]
rs56755769	0.83[ASN][1000 genomes]
rs57826418	0.83[ASN][1000 genomes]
rs58290352	1.00[AMR][1000 genomes]
rs58813961	1.00[AMR][1000 genomes]
rs59473559	0.87[ASN][1000 genomes]
rs60053545	0.91[ASN][1000 genomes]
rs60207538	1.00[AMR][1000 genomes]
rs61140981	0.91[ASN][1000 genomes]
rs6946782	0.82[JPT][hapmap]
rs6946901	0.82[JPT][hapmap]
rs73730089	0.91[ASN][1000 genomes]
rs73730092	0.91[ASN][1000 genomes]
rs73730095	1.00[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs73730096	0.96[ASN][1000 genomes]
rs73730098	1.00[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs73731004	1.00[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs7458662	0.82[JPT][hapmap];0.95[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs7459099	0.82[JPT][hapmap];0.95[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs7797609	0.83[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	nsv1022793	chr7:137187383-137619359	Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Active TSS ZNF genes & repeats 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	esv1812888	chr7:137283212-137366467	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv464731	chr7:137356651-137404781	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a
4	nsv608466	chr7:137356651-137404781	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:137355800-137370600	Weak transcription	Aorta	Aorta
2	chr7:137356400-137365800	Weak transcription	HSMM	muscle
3	chr7:137357000-137366400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr7:137357000-137367600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr7:137357400-137365600	Weak transcription	Osteobl	bone
6	chr7:137359200-137365600	Weak transcription	HSMMtube	muscle
7	chr7:137359600-137363200	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr7:137360200-137365800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr7:137360800-137366400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
10	chr7:137361800-137364000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr7:137362600-137363400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr7:137362800-137363000	Genic enhancers	Muscle Satellite Cultured Cells	--

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