Variant report

Variant	rs194634
Chromosome Location	chr6:82521038-82521039
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:82462237..82465542-chr6:82518745..82522401,4	MCF-7	breast:
2	chr6:82519114..82521777-chr6:82521792..82524425,2	MCF-7	breast:
3	chr6:82515412..82518371-chr6:82518489..82521368,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000112773	Chromatin interaction
ENSG00000224995	Chromatin interaction

Extended variants
information (count: 24 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10455133	0.96[CEU][hapmap];0.86[EUR][1000 genomes]
rs10455392	0.81[CEU][hapmap]
rs12189633	0.93[EUR][1000 genomes]
rs12194273	0.81[CEU][hapmap]
rs12196654	0.81[CEU][hapmap]
rs12215262	0.81[CEU][hapmap];0.85[EUR][1000 genomes]
rs12216177	0.92[EUR][1000 genomes]
rs1291466	0.93[EUR][1000 genomes]
rs1931621	0.82[JPT][hapmap]
rs194602	0.93[EUR][1000 genomes]
rs194603	0.93[CEU][hapmap];0.94[EUR][1000 genomes]
rs194623	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs194625	0.92[EUR][1000 genomes]
rs194628	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs194629	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs194630	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs194632	0.94[EUR][1000 genomes]
rs194635	0.92[CEU][hapmap];0.94[EUR][1000 genomes]
rs194636	0.96[CEU][hapmap];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6923136	0.93[EUR][1000 genomes]
rs733415	0.92[EUR][1000 genomes]
rs915123	0.92[CEU][hapmap];0.93[EUR][1000 genomes]
rs926856	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830712	chr6:82491029-82654531	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:82517200-82530600	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr6:82517600-82522400	Weak transcription	HepG2	liver
3	chr6:82518800-82521400	Enhancers	Colon Smooth Muscle	Colon
4	chr6:82518800-82522400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr6:82518800-82524200	Weak transcription	NHLF	lung
6	chr6:82519200-82523000	Weak transcription	Adipose Nuclei	Adipose
7	chr6:82519200-82524200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr6:82519200-82524200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr6:82519200-82524200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr6:82519200-82528800	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr6:82519400-82522400	Weak transcription	Rectal Mucosa Donor 29	rectum
12	chr6:82519400-82524200	Weak transcription	Osteobl	bone
13	chr6:82519600-82522000	Enhancers	Primary monocytes fromperipheralblood	blood
14	chr6:82519600-82522000	Enhancers	Primary hematopoietic stem cells	blood
15	chr6:82519800-82521800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr6:82520000-82521600	Weak transcription	Primary neutrophils fromperipheralblood	blood
17	chr6:82520000-82522000	Enhancers	Primary hematopoietic stem cells short term culture	blood
18	chr6:82520000-82522000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr6:82520400-82521400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
20	chr6:82520400-82521800	Weak transcription	Primary B cells from cord blood	blood
21	chr6:82520600-82521600	Enhancers	Monocytes-CD14+_RO01746	blood
22	chr6:82520600-82522000	Weak transcription	Primary B cells from peripheral blood	blood
23	chr6:82521000-82521400	Enhancers	Ovary	ovary

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