Variant report

Variant	rs17184412
Chromosome Location	chr4:125863655-125863656
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:125632730..125635851-chr4:125862256..125864898,4	MCF-7	breast:
2	chr4:125631771..125634938-chr4:125861010..125864557,5	MCF-7	breast:
3	chr4:125764608..125767385-chr4:125861503..125863790,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000151458	Chromatin interaction

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs10518454	0.82[CEU][hapmap];1.00[CHB][hapmap];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10518455	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11726687	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11733582	0.82[ASN][1000 genomes]
rs17181767	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17787244	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62323303	0.85[EUR][1000 genomes]
rs6816885	0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1011752	chr4:125708756-125932456	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
2	nsv1001338	chr4:125708756-126103293	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv830050	chr4:125717858-125888563	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:125856200-125866800	Enhancers	Hela-S3	cervix
2	chr4:125858000-125865000	Weak transcription	Ovary	ovary
3	chr4:125858000-125868000	Weak transcription	Pancreas	Pancrea
4	chr4:125858200-125867800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr4:125859400-125870200	Weak transcription	Psoas Muscle	Psoas
6	chr4:125860000-125863800	Enhancers	HUVEC	blood vessel
7	chr4:125861000-125863800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr4:125861200-125866600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr4:125861800-125866600	Weak transcription	Adipose Nuclei	Adipose
10	chr4:125862000-125867800	Weak transcription	Stomach Mucosa	stomach
11	chr4:125862000-125874200	Weak transcription	Fetal Heart	heart
12	chr4:125862400-125866600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr4:125862400-125867800	Weak transcription	Duodenum Smooth Muscle	Duodenum
14	chr4:125862600-125866600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr4:125862600-125866600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr4:125862800-125864400	Weak transcription	Osteobl	bone
17	chr4:125862800-125866200	Weak transcription	A549	lung
18	chr4:125862800-125868600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr4:125862800-125868800	Weak transcription	NH-A	brain
20	chr4:125862800-125869000	Weak transcription	NHLF	lung
21	chr4:125862800-125869200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr4:125862800-125874000	Weak transcription	NHDF-Ad	bronchial
23	chr4:125863000-125864600	Weak transcription	NHEK	skin
24	chr4:125863000-125866600	Weak transcription	HMEC	breast
25	chr4:125863000-125869200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr4:125863600-125865400	Enhancers	Muscle Satellite Cultured Cells	--

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