Variant report

Variant	rs7165052
Chromosome Location	chr15:34064616-34064617
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	chr15:34064205..34066563-chr15:34112300..34114040,2	K562	blood:

Variant related genes	Relation type
ENSG00000198838	Chromatin interaction

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10163114	0.86[EUR][1000 genomes]
rs11072651	0.92[EUR][1000 genomes]
rs11638623	0.96[CEU][hapmap];0.85[JPT][hapmap];0.90[EUR][1000 genomes]
rs11639018	0.92[ASN][1000 genomes]
rs12591565	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12591583	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2115749	0.87[EUR][1000 genomes]
rs2195556	0.82[EUR][1000 genomes]
rs2195557	0.90[JPT][hapmap];0.80[TSI][hapmap];0.83[EUR][1000 genomes]
rs4525460	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4620925	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs57153050	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs59965365	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs62012647	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs62012648	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7164080	1.00[CEU][hapmap];0.94[CHB][hapmap];0.93[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.98[TSI][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7164098	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7165295	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8032500	0.86[EUR][1000 genomes]
rs8035184	0.84[CEU][hapmap];0.85[JPT][hapmap];0.80[TSI][hapmap];0.86[EUR][1000 genomes]
rs8036744	0.87[EUR][1000 genomes]
rs8042401	0.81[CEU][hapmap];0.85[JPT][hapmap];0.87[EUR][1000 genomes]
rs8042647	0.87[EUR][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	nsv1043046	chr15:33714908-34321330	Enhancers Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv456789	chr15:34034421-34426618	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	nsv568920	chr15:34034421-34426618	Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer 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	29 gene(s)	inside rSNPs	diseases
4	nsv471235	chr15:34035529-34421951	Strong transcription Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
5	nsv568921	chr15:34046635-34247622	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:34050400-34074200	Weak transcription	Brain Substantia Nigra	brain
2	chr15:34050800-34072400	Weak transcription	Brain Anterior Caudate	brain
3	chr15:34050800-34080200	Weak transcription	Aorta	Aorta
4	chr15:34051000-34072600	Weak transcription	Skeletal Muscle Male	skeletal muscle
5	chr15:34051000-34089200	Weak transcription	Fetal Muscle Leg	muscle
6	chr15:34051200-34077400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr15:34051600-34072600	Weak transcription	Fetal Muscle Trunk	muscle
8	chr15:34061600-34121000	Weak transcription	Duodenum Smooth Muscle	Duodenum
9	chr15:34063800-34065200	Strong transcription	Stomach Smooth Muscle	stomach
10	chr15:34063800-34068200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
11	chr15:34064200-34069200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
12	chr15:34064400-34072600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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