Variant report

Variant	rs11735317
Chromosome Location	chr4:166120766-166120767
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:166116530..166118783-chr4:166119750..166122677,2	K562	blood:
2	chr4:166119524..166122454-chr4:166247484..166249328,2	MCF-7	breast:
3	chr4:166119224..166120860-chr4:166128330..166130585,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000170088	Chromatin interaction
ENSG00000052802	Chromatin interaction
ENSG00000109466	Chromatin interaction

Extended variants
information (count: 36 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10017705	0.81[CEU][hapmap];0.80[EUR][1000 genomes]
rs10018252	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10023382	0.84[CEU][hapmap]
rs10032366	0.83[ASN][1000 genomes]
rs11724462	0.89[CEU][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs11724504	1.00[ASN][1000 genomes]
rs11731244	0.81[CEU][hapmap];0.80[EUR][1000 genomes]
rs11735290	0.89[CEU][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs12332076	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs17172935	0.83[YRI][hapmap]
rs17585306	0.89[CEU][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs17585333	1.00[CEU][hapmap];1.00[JPT][hapmap];0.84[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs28635044	0.83[ASN][1000 genomes]
rs28875870	0.82[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs4234892	0.82[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs4588419	0.82[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs4605609	1.00[CEU][hapmap];1.00[JPT][hapmap];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4690807	0.81[CEU][hapmap];0.82[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs4690808	0.82[AMR][1000 genomes]
rs4691172	0.89[CEU][hapmap];1.00[JPT][hapmap]
rs4691173	0.83[ASN][1000 genomes]
rs4691176	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4691177	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs58004273	0.81[ASN][1000 genomes]
rs62353271	0.81[EUR][1000 genomes]
rs6834975	0.89[CEU][hapmap];1.00[JPT][hapmap]
rs6846518	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs72993957	0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7686032	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9968334	0.89[CEU][hapmap];1.00[JPT][hapmap]
rs9993501	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1022210	chr4:165792630-166251612	Genic enhancers Enhancers Active TSS Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
2	nsv537337	chr4:165792630-166251612	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
3	nsv1021905	chr4:165852926-166212878	Weak transcription Enhancers Bivalent/Poised TSS Active TSS Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
4	nsv533191	chr4:165879671-166171638	Active TSS Strong transcription Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
5	nsv881168	chr4:165975122-166196438	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:166112800-166120800	Weak transcription	HSMMtube	muscle
2	chr4:166115400-166127400	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr4:166119000-166121200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr4:166119000-166121400	Enhancers	HMEC	breast
5	chr4:166119200-166121000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr4:166119200-166121400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr4:166119200-166121400	Enhancers	Osteobl	bone
8	chr4:166119200-166121600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr4:166119600-166121400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr4:166119800-166127400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr4:166120200-166121400	Enhancers	HSMM	muscle
12	chr4:166120400-166120800	Flanking Active TSS	NHEK	skin
13	chr4:166120400-166121400	Enhancers	Breast Myoepithelial Primary Cells	Breast
14	chr4:166120600-166120800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr4:166120600-166120800	Enhancers	NH-A	brain
16	chr4:166120600-166121000	Enhancers	Pancreas	Pancrea
17	chr4:166120600-166125200	Weak transcription	NHDF-Ad	bronchial

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