Variant report

Variant	rs10022194
Chromosome Location	chr4:125863974-125863975
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

Variant related genes	Relation type
ENSG00000151458	Chromatin interaction

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10023830	0.93[ASN][1000 genomes]
rs1021628	0.84[YRI][hapmap]
rs1120767	0.93[ASN][1000 genomes]
rs11722357	0.89[AFR][1000 genomes]
rs11729566	1.00[YRI][hapmap];0.91[AFR][1000 genomes]
rs11732928	0.91[AFR][1000 genomes]
rs11945096	0.93[AFR][1000 genomes]
rs12644910	0.93[ASN][1000 genomes]
rs1483592	0.84[ASW][hapmap];0.84[GIH][hapmap];0.89[LWK][hapmap];0.89[MEX][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes]
rs1483601	0.84[GIH][hapmap]
rs1506548	0.93[ASN][1000 genomes]
rs1553093	0.84[GIH][hapmap]
rs1553095	0.91[AFR][1000 genomes]
rs1564721	1.00[YRI][hapmap];0.96[AFR][1000 genomes]
rs17184111	0.91[AFR][1000 genomes]
rs17788496	0.93[AFR][1000 genomes]
rs2390741	0.93[ASN][1000 genomes]
rs2390766	0.93[ASN][1000 genomes]
rs28477204	0.81[AMR][1000 genomes]
rs28607791	0.81[AMR][1000 genomes]
rs4834009	0.93[ASN][1000 genomes]
rs6824446	0.91[AFR][1000 genomes]
rs6831229	0.82[ASN][1000 genomes]
rs72920861	0.93[AFR][1000 genomes]
rs7656356	0.93[ASN][1000 genomes]
rs7657807	1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs7657969	0.93[ASN][1000 genomes]
rs7658320	0.93[ASN][1000 genomes]
rs7662742	0.93[ASN][1000 genomes]
rs7664577	0.93[ASN][1000 genomes]
rs7686429	0.93[ASN][1000 genomes]
rs7698052	0.93[ASN][1000 genomes]
rs9307556	1.00[CHB][hapmap];1.00[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs9685726	0.93[ASN][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	chr4:125861200-125866600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr4:125861800-125866600	Weak transcription	Adipose Nuclei	Adipose
8	chr4:125862000-125867800	Weak transcription	Stomach Mucosa	stomach
9	chr4:125862000-125874200	Weak transcription	Fetal Heart	heart
10	chr4:125862400-125866600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr4:125862400-125867800	Weak transcription	Duodenum Smooth Muscle	Duodenum
12	chr4:125862600-125866600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr4:125862600-125866600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr4:125862800-125864400	Weak transcription	Osteobl	bone
15	chr4:125862800-125866200	Weak transcription	A549	lung
16	chr4:125862800-125868600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr4:125862800-125868800	Weak transcription	NH-A	brain
18	chr4:125862800-125869000	Weak transcription	NHLF	lung
19	chr4:125862800-125869200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr4:125862800-125874000	Weak transcription	NHDF-Ad	bronchial
21	chr4:125863000-125864600	Weak transcription	NHEK	skin
22	chr4:125863000-125866600	Weak transcription	HMEC	breast
23	chr4:125863000-125869200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr4:125863600-125865400	Enhancers	Muscle Satellite Cultured Cells	--
25	chr4:125863800-125865400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr4:125863800-125866400	Weak transcription	HUVEC	blood vessel

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