Variant report

Variant	rs808813
Chromosome Location	chr6:5316152-5316153
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:5314865..5316963-chr6:5319263..5320833,2	K562	blood:

Extended variants
information (count: 67 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs11752747	1.00[JPT][hapmap]
rs1807139	1.00[JPT][hapmap]
rs2081359	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2224393	1.00[JPT][hapmap]
rs6926122	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs708037	0.85[CEU][hapmap];0.82[ASN][1000 genomes]
rs7751332	1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs7765867	1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs7769327	1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs7771926	1.00[JPT][hapmap]
rs797123	1.00[CEU][hapmap];0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs797130	1.00[CEU][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs797135	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs797136	0.85[CEU][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs797137	1.00[CEU][hapmap];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs797138	0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs797141	0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs797144	1.00[CEU][hapmap];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs797145	0.85[CEU][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs797147	0.82[ASN][1000 genomes]
rs797148	1.00[CEU][hapmap];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs797151	0.82[ASN][1000 genomes]
rs808812	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs808814	0.85[CEU][hapmap];0.82[ASN][1000 genomes]
rs809490	0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs811274	0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs811275	0.85[CEU][hapmap];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs811611	0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs812177	0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs812757	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9328291	1.00[JPT][hapmap]
rs9502286	1.00[JPT][hapmap]
rs9502289	1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs9502291	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9504375	1.00[JPT][hapmap]
rs9504376	1.00[JPT][hapmap]
rs9504381	0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9504382	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs965720	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:28 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1023527	chr6:4729592-5387176	Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
2	nsv600872	chr6:4975313-5342190	Weak transcription Active TSS Strong transcription Flanking Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
3	nsv1031837	chr6:4996667-5418726	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	23 gene(s)	inside rSNPs	diseases
4	nsv1034681	chr6:5070351-5387176	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	15 gene(s)	inside rSNPs	diseases
5	nsv538113	chr6:5070351-5387176	Enhancers Genic enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	15 gene(s)	inside rSNPs	diseases
6	nsv1018152	chr6:5077025-5387176	Flanking Active TSS Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
7	nsv600873	chr6:5089278-5400658	Enhancers Active TSS Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	12 gene(s)	inside rSNPs	diseases
8	nsv1030254	chr6:5132261-5431585	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases
9	nsv1034463	chr6:5137959-5345678	Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases
10	nsv1021646	chr6:5157795-5367254	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
11	nsv538115	chr6:5157795-5367254	Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
12	nsv1029609	chr6:5187633-5397254	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
13	nsv1035080	chr6:5206533-5396019	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
14	nsv538116	chr6:5206533-5396019	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
15	nsv1019428	chr6:5216835-5627839	Enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
16	nsv538118	chr6:5216835-5627839	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
17	nsv1028185	chr6:5247624-5340163	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
18	nsv830578	chr6:5264086-5455570	ZNF genes & repeats Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
19	nsv1022911	chr6:5286297-5322133	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
20	nsv538119	chr6:5286297-5322133	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
21	nsv1022738	chr6:5298362-5411645	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
22	nsv600883	chr6:5302619-5400658	Enhancers Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
23	nsv883417	chr6:5307432-5431340	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
24	nsv883418	chr6:5307432-5501389	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
25	nsv1015643	chr6:5311590-5452427	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
26	nsv1034607	chr6:5311590-5573514	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
27	nsv538120	chr6:5311590-5573514	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
28	nsv916361	chr6:5315853-5695486	Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers 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:56 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:5288000-5316200	Weak transcription	Fetal Stomach	stomach
2	chr6:5288400-5324000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr6:5288400-5331000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr6:5292800-5334400	Weak transcription	Rectal Smooth Muscle	rectum
5	chr6:5295400-5325000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr6:5301800-5322200	Weak transcription	Ovary	ovary
7	chr6:5302800-5319200	Weak transcription	Aorta	Aorta
8	chr6:5303200-5368800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr6:5303600-5317400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr6:5303600-5319000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
11	chr6:5303600-5332400	Weak transcription	Gastric	stomach
12	chr6:5303800-5316200	Weak transcription	Left Ventricle	heart
13	chr6:5304000-5320400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
14	chr6:5304000-5325400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
15	chr6:5304000-5326000	Weak transcription	Primary T cells fromperipheralblood	blood
16	chr6:5304000-5337600	Weak transcription	Primary T helper cells fromperipheralblood	blood
17	chr6:5304200-5322800	Weak transcription	Pancreas	Pancrea
18	chr6:5306800-5321400	Weak transcription	Sigmoid Colon	Sigmoid Colon
19	chr6:5307000-5320400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
20	chr6:5307000-5323800	Weak transcription	HepG2	liver
21	chr6:5307800-5318800	Weak transcription	Fetal Intestine Large	intestine
22	chr6:5308800-5318000	Weak transcription	Primary B cells from cord blood	blood
23	chr6:5308800-5325000	Weak transcription	Primary T cells from cord blood	blood
24	chr6:5308800-5325000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr6:5309000-5317200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr6:5309200-5333400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr6:5309200-5334000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr6:5312800-5317400	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr6:5313000-5316400	Enhancers	H1 Cell Line	embryonic stem cell
30	chr6:5313800-5322800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr6:5314800-5323800	Weak transcription	GM12878-XiMat	blood
32	chr6:5315000-5326400	Weak transcription	Primary B cells from peripheral blood	blood
33	chr6:5315400-5316400	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr6:5315400-5316400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr6:5315400-5316800	Enhancers	Cortex derived primary cultured neurospheres	brain
36	chr6:5315400-5316800	Enhancers	Pancreatic Islets	Pancreatic Islet
37	chr6:5315600-5317400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr6:5315800-5316400	Enhancers	Duodenum Smooth Muscle	Duodenum
39	chr6:5316000-5316200	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr6:5316000-5316200	Enhancers	Right Atrium	heart
41	chr6:5316000-5316200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
42	chr6:5316000-5316200	Flanking Active TSS	Stomach Smooth Muscle	stomach
43	chr6:5316000-5316400	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr6:5316000-5316400	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr6:5316000-5316400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr6:5316000-5316400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr6:5316000-5316400	Enhancers	Brain Inferior Temporal Lobe	brain
48	chr6:5316000-5316400	Enhancers	Brain Substantia Nigra	brain
49	chr6:5316000-5316400	Enhancers	Fetal Muscle Leg	muscle
50	chr6:5316000-5316400	Enhancers	Lung	lung

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