Variant report

Variant	rs17626731
Chromosome Location	chr6:161608292-161608293
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:161590670..161592878-chr6:161605980..161608609,2	MCF-7	breast:
2	chr6:161607404..161608977-chr6:161612196..161613935,2	K562	blood:
3	chr6:161607405..161609725-chr6:161623701..161625620,3	K562	blood:

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs1040724	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs10499315	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs10499316	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs11757882	1.00[YRI][hapmap]
rs11961712	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs11970102	0.85[EUR][1000 genomes]
rs13191415	1.00[CEU][hapmap]
rs13192827	1.00[CEU][hapmap];0.99[EUR][1000 genomes]
rs13193634	1.00[CEU][hapmap];0.80[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs13194692	1.00[CHD][hapmap]
rs13194878	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs13212679	0.93[EUR][1000 genomes]
rs13215186	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs13219494	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs13220357	1.00[CEU][hapmap];0.92[TSI][hapmap];1.00[EUR][1000 genomes]
rs1562026	1.00[CHD][hapmap]
rs16892284	1.00[CEU][hapmap];0.97[EUR][1000 genomes]
rs16892303	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[MEX][hapmap];0.93[TSI][hapmap];0.99[EUR][1000 genomes]
rs17537799	0.83[EUR][1000 genomes]
rs1982291	1.00[CHD][hapmap]
rs34620502	0.99[EUR][1000 genomes]
rs35180185	1.00[EUR][1000 genomes]
rs35267977	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs35505620	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35727114	0.93[EUR][1000 genomes]
rs36030076	0.93[EUR][1000 genomes]
rs4314476	0.83[EUR][1000 genomes]
rs71565796	1.00[EUR][1000 genomes]
rs71565797	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7744842	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs7747618	0.99[EUR][1000 genomes]
rs7751159	1.00[CEU][hapmap];0.99[EUR][1000 genomes]
rs7756321	1.00[CEU][hapmap];0.99[EUR][1000 genomes]
rs7758121	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs7767737	1.00[CEU][hapmap];0.99[EUR][1000 genomes]
rs7770491	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.93[TSI][hapmap];0.99[EUR][1000 genomes]
rs7771961	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs9355867	1.00[CHD][hapmap]
rs9458136	1.00[CHD][hapmap]
rs9458149	1.00[CEU][hapmap];0.99[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv886817	chr6:161371621-161846654	Strong transcription Enhancers Weak transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	esv3381361	chr6:161373617-161864101	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
3	nsv949397	chr6:161592100-161812932	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
4	esv2752091	chr6:161592100-161855785	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
5	esv33824	chr6:161603136-161608905	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv1029727	chr6:161607680-161814295	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:68 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:161585600-161626000	Weak transcription	Right Atrium	heart
2	chr6:161590000-161611600	Weak transcription	HSMMtube	muscle
3	chr6:161591400-161626200	Weak transcription	Stomach Smooth Muscle	stomach
4	chr6:161591600-161615400	Weak transcription	Fetal Heart	heart
5	chr6:161592000-161609600	Weak transcription	Fetal Brain Male	brain
6	chr6:161599800-161647600	Weak transcription	Duodenum Smooth Muscle	Duodenum
7	chr6:161600200-161610000	Weak transcription	Primary T cells from cord blood	blood
8	chr6:161600400-161619400	Weak transcription	Fetal Lung	lung
9	chr6:161600400-161626000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr6:161600600-161613000	Weak transcription	Primary B cells from cord blood	blood
11	chr6:161600600-161613800	Weak transcription	Fetal Brain Female	brain
12	chr6:161600800-161608400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr6:161601400-161610400	Weak transcription	Aorta	Aorta
14	chr6:161601400-161636200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr6:161601800-161609400	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr6:161601800-161609800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr6:161602000-161613800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr6:161602000-161619400	Weak transcription	Brain Germinal Matrix	brain
19	chr6:161602400-161609800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr6:161602400-161613800	Weak transcription	HUES64 Cell Line	embryonic stem cell
21	chr6:161602800-161618600	Weak transcription	Fetal Muscle Leg	muscle
22	chr6:161602800-161626000	Weak transcription	Gastric	stomach
23	chr6:161604000-161609600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
24	chr6:161604000-161610200	Weak transcription	Fetal Muscle Trunk	muscle
25	chr6:161604400-161608800	Weak transcription	Rectal Smooth Muscle	rectum
26	chr6:161604400-161609800	Weak transcription	Brain Hippocampus Middle	brain
27	chr6:161604800-161608600	Strong transcription	Fetal Stomach	stomach
28	chr6:161605000-161608400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr6:161605200-161610200	Weak transcription	Brain Cingulate Gyrus	brain
30	chr6:161605200-161612600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
31	chr6:161605400-161610200	Weak transcription	Brain Substantia Nigra	brain
32	chr6:161606200-161615400	Weak transcription	Fetal Kidney	kidney
33	chr6:161606600-161608400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr6:161606800-161608400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr6:161606800-161608400	Enhancers	Primary hematopoietic stem cells short term culture	blood
36	chr6:161606800-161608400	Enhancers	Muscle Satellite Cultured Cells	--
37	chr6:161606800-161608400	Enhancers	NHDF-Ad	bronchial
38	chr6:161606800-161608400	Enhancers	NHEK	skin
39	chr6:161607000-161608400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr6:161607200-161608400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr6:161607200-161608600	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr6:161607400-161608400	Strong transcription	HUES6 Cell Line	embryonic stem cell
43	chr6:161607400-161608600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr6:161607600-161608400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr6:161607600-161610000	Weak transcription	Brain Anterior Caudate	brain
46	chr6:161607600-161610200	Weak transcription	Esophagus	oesophagus
47	chr6:161607600-161612200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr6:161607600-161621400	Weak transcription	Adipose Nuclei	Adipose
49	chr6:161607800-161610200	Weak transcription	Cortex derived primary cultured neurospheres	brain
50	chr6:161607800-161610200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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