Variant report

Variant	rs558358341
Chromosome Location	chr6:5303615-5303616
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	chr6:5302902..5305704-chr6:5324020..5325616,2	K562	blood:
2	chr6:5295225..5299115-chr6:5300154..5305822,5	K562	blood:

Extended variants
information (count: 24 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:24 , 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	nsv1016456	chr6:5216835-5315913	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats 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
16	nsv538117	chr6:5216835-5315913	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
17	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
18	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
19	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
20	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
21	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
22	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
23	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
24	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

No data

Chromatin state (count:75 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:5280800-5308200	Weak transcription	Primary T cells from cord blood	blood
2	chr6:5287800-5313600	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr6:5288000-5316200	Weak transcription	Fetal Stomach	stomach
4	chr6:5288400-5324000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr6:5288400-5331000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr6:5292800-5334400	Weak transcription	Rectal Smooth Muscle	rectum
7	chr6:5293800-5306200	Weak transcription	HUES64 Cell Line	embryonic stem cell
8	chr6:5295200-5306000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr6:5295200-5311600	Weak transcription	Small Intestine	intestine
10	chr6:5295400-5305800	Weak transcription	Fetal Intestine Large	intestine
11	chr6:5295400-5325000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr6:5296200-5316000	Weak transcription	Lung	lung
13	chr6:5296400-5306000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr6:5298600-5305000	Weak transcription	Fetal Intestine Small	intestine
15	chr6:5300600-5303800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
16	chr6:5301000-5315400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr6:5301600-5303800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
18	chr6:5301600-5304200	Enhancers	Breast Myoepithelial Primary Cells	Breast
19	chr6:5301800-5322200	Weak transcription	Ovary	ovary
20	chr6:5302000-5304000	Enhancers	Primary T helper cells fromperipheralblood	blood
21	chr6:5302000-5313000	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr6:5302200-5304000	Enhancers	Primary B cells from peripheral blood	blood
23	chr6:5302200-5304000	Enhancers	Primary T cells fromperipheralblood	blood
24	chr6:5302200-5304000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
25	chr6:5302200-5304000	Flanking Active TSS	GM12878-XiMat	blood
26	chr6:5302400-5303800	Enhancers	Placenta	Placenta
27	chr6:5302400-5304000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
28	chr6:5302400-5304200	Enhancers	Fetal Muscle Leg	muscle
29	chr6:5302400-5304200	Enhancers	Pancreas	Pancrea
30	chr6:5302600-5303800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr6:5302600-5303800	Enhancers	Left Ventricle	heart
32	chr6:5302600-5303800	Enhancers	Spleen	Spleen
33	chr6:5302600-5316000	Weak transcription	Brain Inferior Temporal Lobe	brain
34	chr6:5302800-5303800	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
35	chr6:5302800-5303800	Enhancers	Esophagus	oesophagus
36	chr6:5302800-5303800	Enhancers	Sigmoid Colon	Sigmoid Colon
37	chr6:5302800-5303800	Enhancers	Stomach Smooth Muscle	stomach
38	chr6:5302800-5303800	Enhancers	HSMMtube	muscle
39	chr6:5302800-5304200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr6:5302800-5319200	Weak transcription	Aorta	Aorta
41	chr6:5303000-5303800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr6:5303000-5303800	Enhancers	Primary hematopoietic stem cells short term culture	blood
43	chr6:5303000-5303800	Enhancers	Right Atrium	heart
44	chr6:5303000-5304000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr6:5303000-5304200	Enhancers	Liver	Liver
46	chr6:5303000-5306200	Weak transcription	Fetal Lung	lung
47	chr6:5303000-5308400	Weak transcription	Cortex derived primary cultured neurospheres	brain
48	chr6:5303200-5303800	Enhancers	Primary monocytes fromperipheralblood	blood
49	chr6:5303200-5303800	Weak transcription	Pancreatic Islets	Pancreatic Islet
50	chr6:5303200-5304000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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