Variant report

Variant	rs6905927
Chromosome Location	chr6:53688943-53688944
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	chr6:53657877..53659758-chr6:53688042..53690060,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000228614	Chromatin interaction
ENSG00000137269	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10498795	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1543356	1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes]
rs16884427	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs17748452	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2223617	1.00[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2473599	0.80[EUR][1000 genomes]
rs2473603	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2494087	0.83[AMR][1000 genomes]
rs2820217	1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes]
rs2820218	1.00[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs3000998	0.85[CHB][hapmap]
rs4077760	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.86[EUR][1000 genomes]
rs4131378	0.83[EUR][1000 genomes]
rs4272222	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4276504	1.00[CHB][hapmap];0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4357137	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4380749	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4397225	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4476827	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4580851	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6908101	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6919924	0.86[EUR][1000 genomes]
rs6925165	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs761135	0.86[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap]
rs7752696	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9474672	1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1034955	chr6:53447607-53931055	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	nsv1021506	chr6:53600338-53770482	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:53670800-53693200	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr6:53676200-53697800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr6:53678600-53692200	Weak transcription	Esophagus	oesophagus
4	chr6:53680400-53690000	Weak transcription	Fetal Intestine Small	intestine
5	chr6:53680400-53690200	Weak transcription	Fetal Thymus	thymus
6	chr6:53680400-53691800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr6:53680400-53692400	Weak transcription	Pancreas	Pancrea
8	chr6:53680400-53721600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr6:53680600-53689400	Weak transcription	Fetal Intestine Large	intestine
10	chr6:53680600-53694400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
11	chr6:53680800-53689600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr6:53681200-53689800	Weak transcription	Osteobl	bone
13	chr6:53682600-53689400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr6:53683600-53689800	Weak transcription	Dnd41	blood
15	chr6:53684000-53691400	Weak transcription	Hela-S3	cervix
16	chr6:53684000-53692400	Weak transcription	Left Ventricle	heart
17	chr6:53684000-53694000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr6:53684000-53710200	Weak transcription	Primary T cells from cord blood	blood
19	chr6:53684200-53689400	Weak transcription	Sigmoid Colon	Sigmoid Colon
20	chr6:53684600-53690600	Weak transcription	Muscle Satellite Cultured Cells	--
21	chr6:53684600-53697000	Enhancers	Brain Substantia Nigra	brain
22	chr6:53684800-53689800	Weak transcription	HMEC	breast
23	chr6:53685000-53689600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr6:53685000-53689800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr6:53685000-53690200	Weak transcription	NHEK	skin
26	chr6:53686000-53690400	Weak transcription	Gastric	stomach
27	chr6:53687200-53692400	Weak transcription	Thymus	Thymus
28	chr6:53687400-53689400	Weak transcription	Stomach Mucosa	stomach
29	chr6:53687400-53690400	Weak transcription	Duodenum Smooth Muscle	Duodenum
30	chr6:53687400-53691600	Weak transcription	Right Atrium	heart
31	chr6:53687600-53689200	Weak transcription	Colon Smooth Muscle	Colon
32	chr6:53687600-53692400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr6:53687600-53693000	Weak transcription	Stomach Smooth Muscle	stomach
34	chr6:53687600-53702000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr6:53687800-53689600	Weak transcription	HepG2	liver
36	chr6:53687800-53689800	Weak transcription	Rectal Smooth Muscle	rectum
37	chr6:53687800-53690800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr6:53687800-53691200	Weak transcription	H1 Cell Line	embryonic stem cell
39	chr6:53687800-53692200	Weak transcription	HSMM	muscle
40	chr6:53687800-53692800	Weak transcription	HSMMtube	muscle
41	chr6:53688000-53689200	Weak transcription	Brain Anterior Caudate	brain
42	chr6:53688000-53689600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr6:53688000-53690200	Weak transcription	Brain Inferior Temporal Lobe	brain
44	chr6:53688000-53690400	Weak transcription	Aorta	Aorta
45	chr6:53688000-53692000	Weak transcription	Brain Angular Gyrus	brain
46	chr6:53688000-53692400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr6:53688000-53694600	Weak transcription	Fetal Muscle Leg	muscle
48	chr6:53688200-53689600	Weak transcription	Brain Hippocampus Middle	brain
49	chr6:53688200-53690000	Weak transcription	Brain Cingulate Gyrus	brain
50	chr6:53688400-53689400	Weak transcription	Pancreatic Islets	Pancreatic Islet

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