Variant report

Variant	rs9459669
Chromosome Location	chr6:166844469-166844470
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs16898917	0.86[EUR][1000 genomes]
rs16898924	1.00[EUR][1000 genomes]
rs56171280	0.86[EUR][1000 genomes]
rs56379128	1.00[EUR][1000 genomes]
rs57032504	0.86[EUR][1000 genomes]
rs57106460	0.86[EUR][1000 genomes]
rs58031677	0.86[EUR][1000 genomes]
rs59373594	1.00[EUR][1000 genomes]
rs60789228	1.00[EUR][1000 genomes]
rs6923614	1.00[EUR][1000 genomes]
rs73269236	0.86[EUR][1000 genomes]
rs73269268	1.00[EUR][1000 genomes]
rs73269270	0.86[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	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	nsv886937	chr6:166830696-166922813	Enhancers Weak transcription Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:94 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:166808200-166911800	Weak transcription	Psoas Muscle	Psoas
2	chr6:166824000-166901400	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr6:166824600-166844800	Weak transcription	Colon Smooth Muscle	Colon
4	chr6:166825000-166849200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr6:166825200-166853000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr6:166825200-166875800	Weak transcription	Colonic Mucosa	Colon
7	chr6:166826600-166848800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr6:166827000-166873400	Weak transcription	Placenta Amnion	Placenta Amnion
9	chr6:166827600-166867200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
10	chr6:166829800-166845200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
11	chr6:166829800-166845600	Weak transcription	HSMMtube	muscle
12	chr6:166829800-166847600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
13	chr6:166829800-166851800	Weak transcription	Fetal Brain Male	brain
14	chr6:166830000-166845400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr6:166830000-166866600	Weak transcription	Fetal Intestine Large	intestine
16	chr6:166833200-166864400	Weak transcription	Fetal Kidney	kidney
17	chr6:166833200-166879000	Weak transcription	NH-A	brain
18	chr6:166833400-166854800	Weak transcription	Primary B cells from cord blood	blood
19	chr6:166833400-166879000	Weak transcription	HSMM	muscle
20	chr6:166833600-166845400	Weak transcription	HUES6 Cell Line	embryonic stem cell
21	chr6:166833600-166859600	Weak transcription	HMEC	breast
22	chr6:166834000-166866400	Weak transcription	Rectal Mucosa Donor 31	rectum
23	chr6:166834200-166863800	Weak transcription	HUES64 Cell Line	embryonic stem cell
24	chr6:166834200-166879400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr6:166834600-166862000	Weak transcription	NHDF-Ad	bronchial
26	chr6:166835000-166849000	Weak transcription	Primary T helper cells fromperipheralblood	blood
27	chr6:166835200-166847600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr6:166836400-166853000	Weak transcription	Fetal Lung	lung
29	chr6:166837600-166848200	Weak transcription	Esophagus	oesophagus
30	chr6:166837800-166844800	Weak transcription	NHLF	lung
31	chr6:166837800-166849000	Weak transcription	Primary T cells from cord blood	blood
32	chr6:166838000-166856000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr6:166838200-166849400	Weak transcription	Rectal Mucosa Donor 29	rectum
34	chr6:166838200-166853000	Weak transcription	HUVEC	blood vessel
35	chr6:166838200-166860400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr6:166841000-166846200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
37	chr6:166841200-166849000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
38	chr6:166841400-166846600	Weak transcription	Placenta	Placenta
39	chr6:166842000-166844600	Weak transcription	Primary B cells from peripheral blood	blood
40	chr6:166843000-166846000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr6:166843000-166846000	Strong transcription	Brain Germinal Matrix	brain
42	chr6:166843000-166846000	Strong transcription	Fetal Brain Female	brain
43	chr6:166843000-166846000	Strong transcription	Left Ventricle	heart
44	chr6:166843000-166846200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr6:166843000-166846800	Strong transcription	Primary neutrophils fromperipheralblood	blood
46	chr6:166843000-166847000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr6:166843000-166847000	Strong transcription	Skeletal Muscle Female	skeletal muscle
48	chr6:166843000-166847400	Strong transcription	Fetal Muscle Trunk	muscle
49	chr6:166843000-166847800	Strong transcription	Brain Hippocampus Middle	brain
50	chr6:166843000-166848000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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