Variant report

Variant	rs6917139
Chromosome Location	chr6:166974388-166974389
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	chr6:166974194..166976909-chr6:166977553..166980494,3	K562	blood:
2	chr6:166970917..166973753-chr6:166974346..166977201,2	K562	blood:

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

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs11969174	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs11970618	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs16899148	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs16899153	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs58032331	1.00[ASN][1000 genomes]
rs73257231	1.00[ASN][1000 genomes]
rs73257242	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3490076	chr6:166727901-167306743	Strong transcription Weak transcription Flanking Active TSS Genic enhancers Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	25 gene(s)	inside rSNPs	diseases
2	esv3490077	chr6:166727901-167306743	Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	25 gene(s)	inside rSNPs	diseases
3	nsv886941	chr6:166907173-166996991	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA	5 gene(s)	inside rSNPs	diseases
4	nsv5592	chr6:166958317-167002951	Weak transcription Flanking Active TSS Active TSS Enhancers ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:56 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:166966200-166978000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr6:166968400-166985800	Weak transcription	Fetal Kidney	kidney
3	chr6:166969400-166978800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr6:166970200-166976200	Weak transcription	Right Ventricle	heart
5	chr6:166970800-166979800	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr6:166970800-166986200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr6:166971000-166974800	Weak transcription	Psoas Muscle	Psoas
8	chr6:166971000-166974800	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr6:166971000-166975600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr6:166971000-166976600	Weak transcription	H1 Cell Line	embryonic stem cell
11	chr6:166971000-166986000	Weak transcription	Pancreas	Pancrea
12	chr6:166971400-166980200	Weak transcription	Brain Anterior Caudate	brain
13	chr6:166972200-166976200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr6:166972200-166976200	Weak transcription	Right Atrium	heart
15	chr6:166972200-166979600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr6:166972200-166986000	Weak transcription	Gastric	stomach
17	chr6:166972400-166974600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr6:166972400-166974600	Weak transcription	Fetal Stomach	stomach
19	chr6:166972400-166974600	Weak transcription	Skeletal Muscle Female	skeletal muscle
20	chr6:166972400-166974800	Weak transcription	Left Ventricle	heart
21	chr6:166972400-166974800	Weak transcription	NHLF	lung
22	chr6:166972400-166979200	Weak transcription	NHEK	skin
23	chr6:166972600-166976400	Weak transcription	HUVEC	blood vessel
24	chr6:166973000-166974800	Weak transcription	Lung	lung
25	chr6:166973000-166979200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr6:166973200-166975800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr6:166973400-166974400	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr6:166973400-166984600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr6:166973600-166974400	Enhancers	H9 Cell Line	embryonic stem cell
30	chr6:166973600-166974800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr6:166973600-166978000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr6:166973800-166974600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr6:166973800-166974600	Weak transcription	NHDF-Ad	bronchial
34	chr6:166973800-166974800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr6:166973800-166975000	Weak transcription	HSMM	muscle
36	chr6:166973800-166975200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr6:166973800-166975600	Weak transcription	HSMMtube	muscle
38	chr6:166973800-166976000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr6:166973800-166977400	Weak transcription	Primary neutrophils fromperipheralblood	blood
40	chr6:166973800-166977400	Weak transcription	Fetal Brain Female	brain
41	chr6:166973800-166979000	Weak transcription	HMEC	breast
42	chr6:166973800-166979200	Weak transcription	Brain Inferior Temporal Lobe	brain
43	chr6:166973800-166986000	Weak transcription	Fetal Intestine Small	intestine
44	chr6:166974000-166974400	Weak transcription	Brain Cingulate Gyrus	brain
45	chr6:166974000-166974600	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr6:166974000-166974600	Enhancers	Muscle Satellite Cultured Cells	--
47	chr6:166974000-166974800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
48	chr6:166974000-166975200	Weak transcription	Osteobl	bone
49	chr6:166974000-166975400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr6:166974000-166975400	Weak transcription	Brain Germinal Matrix	brain

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