Variant report

Variant	rs17075465
Chromosome Location	chr6:146226889-146226890
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	chr6:146225888..146227710-chr6:146240517..146242939,2	K562	blood:
2	chr6:146082619..146083392-chr6:146226555..146227506,3	MCF-7	breast:

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs17054153	1.00[CHB][hapmap];0.94[ASN][1000 genomes]
rs17075370	1.00[CHB][hapmap];0.94[ASN][1000 genomes]
rs17075385	1.00[CHB][hapmap];0.94[ASN][1000 genomes]
rs17075389	0.94[ASN][1000 genomes]
rs17075400	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.94[ASN][1000 genomes]
rs17075404	1.00[CHB][hapmap];0.94[ASN][1000 genomes]
rs17075411	0.94[ASN][1000 genomes]
rs17075414	1.00[CHB][hapmap];0.94[ASN][1000 genomes]
rs17075446	1.00[CHB][hapmap];1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs17075499	1.00[CHB][hapmap];1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs17075501	1.00[CHB][hapmap];1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs17075511	1.00[CHB][hapmap];1.00[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs17075515	1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs17075527	1.00[CHB][hapmap];1.00[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs17075530	1.00[CHB][hapmap];1.00[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs17075544	1.00[CHB][hapmap];1.00[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs17075546	1.00[CHB][hapmap];1.00[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs17075548	1.00[CHB][hapmap];1.00[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs17075552	1.00[CHB][hapmap];0.88[ASN][1000 genomes]
rs17075584	0.82[ASN][1000 genomes]
rs17075588	1.00[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs17075604	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[AFR][1000 genomes]
rs17075636	1.00[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs17075661	1.00[AFR][1000 genomes]
rs17075663	1.00[AFR][1000 genomes]
rs17075666	1.00[AFR][1000 genomes]
rs17725112	0.83[ASN][1000 genomes]
rs17725154	0.83[ASN][1000 genomes]
rs17798183	0.88[ASN][1000 genomes]
rs17798189	0.88[ASN][1000 genomes]
rs17798207	0.88[ASN][1000 genomes]
rs1970304	1.00[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs6570721	1.00[CHB][hapmap];0.90[CHD][hapmap];0.88[ASN][1000 genomes]
rs7739858	0.82[ASN][1000 genomes]
rs9497449	0.82[ASN][1000 genomes]
rs999859	0.94[ASN][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	nsv1034226	chr6:146071068-146306942	Weak transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
2	nsv830835	chr6:146145148-146287473	Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv437525	chr6:146212285-146230454	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:146200400-146228600	Weak transcription	Pancreas	Pancrea
2	chr6:146201200-146230400	Weak transcription	NHEK	skin
3	chr6:146207800-146240200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr6:146208800-146230000	Weak transcription	Colonic Mucosa	Colon
5	chr6:146210200-146231000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr6:146210400-146230400	Weak transcription	NH-A	brain
7	chr6:146210400-146282000	Weak transcription	Spleen	Spleen
8	chr6:146211600-146236000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
9	chr6:146213800-146230400	Weak transcription	HUVEC	blood vessel
10	chr6:146215000-146242200	Weak transcription	Hela-S3	cervix
11	chr6:146219000-146228000	Weak transcription	Rectal Mucosa Donor 29	rectum
12	chr6:146219000-146228000	Weak transcription	Stomach Smooth Muscle	stomach
13	chr6:146219200-146227800	Weak transcription	Brain Cingulate Gyrus	brain
14	chr6:146219200-146249200	Strong transcription	HUES6 Cell Line	embryonic stem cell
15	chr6:146219200-146276600	Strong transcription	HUES64 Cell Line	embryonic stem cell
16	chr6:146219600-146250600	Strong transcription	Dnd41	blood
17	chr6:146219800-146227800	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr6:146219800-146271400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr6:146220000-146227000	Weak transcription	Fetal Muscle Trunk	muscle
20	chr6:146220000-146227200	Weak transcription	Duodenum Mucosa	Duodenum
21	chr6:146220000-146227400	Weak transcription	Fetal Kidney	kidney
22	chr6:146220000-146228600	Weak transcription	Fetal Intestine Large	intestine
23	chr6:146220000-146228600	Weak transcription	Fetal Thymus	thymus
24	chr6:146220000-146229000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
25	chr6:146220000-146231400	Weak transcription	Aorta	Aorta
26	chr6:146220000-146249400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr6:146220000-146255200	Weak transcription	Gastric	stomach
28	chr6:146220000-146259400	Weak transcription	Esophagus	oesophagus
29	chr6:146220000-146276800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr6:146220000-146283200	Weak transcription	Small Intestine	intestine
31	chr6:146220200-146228000	Weak transcription	Lung	lung
32	chr6:146220200-146228800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr6:146220200-146228800	Weak transcription	HMEC	breast
34	chr6:146220200-146230200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr6:146220200-146231400	Weak transcription	Thymus	Thymus
36	chr6:146220200-146231600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr6:146220200-146268400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr6:146220400-146227200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
39	chr6:146220400-146255200	Weak transcription	Fetal Intestine Small	intestine
40	chr6:146221000-146228600	Weak transcription	Primary T helper cells fromperipheralblood	blood
41	chr6:146221000-146229400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
42	chr6:146221000-146230200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
43	chr6:146221200-146228400	Weak transcription	Duodenum Smooth Muscle	Duodenum
44	chr6:146221600-146230200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
45	chr6:146221800-146228000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr6:146221800-146228000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr6:146221800-146229000	Weak transcription	Primary T helper cells PMA-I stimulated	--
48	chr6:146221800-146230400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
49	chr6:146222400-146227200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
50	chr6:146222800-146229400	Weak transcription	Placenta Amnion	Placenta Amnion

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