Variant report

Variant	rs527647981
Chromosome Location	chr6:106982765-106982766
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:106982665..106985601-chr6:106993025..106995759,2	MCF-7	breast:
2	chr6:106982668..106985044-chr6:106987673..106989483,2	K562	blood:

Variant related genes	Relation type
ENSG00000112297	Chromatin interaction

Extended variants
information (count: 5 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv932155	chr6:106281728-107030467	Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
2	nsv532047	chr6:106591482-107143252	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
3	nsv870375	chr6:106696090-107047892	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
4	esv3407164	chr6:106982684-106985232	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
5	esv2481074	chr6:106982686-106984346	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:70 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:106961000-107001400	Weak transcription	Gastric	stomach
2	chr6:106964800-106991000	Weak transcription	Spleen	Spleen
3	chr6:106964800-107029800	Weak transcription	Small Intestine	intestine
4	chr6:106970600-107022400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr6:106973400-106985600	Weak transcription	Stomach Mucosa	stomach
6	chr6:106973600-106985800	Weak transcription	Thymus	Thymus
7	chr6:106973600-106986000	Genic enhancers	Primary T helper memory cells from peripheral blood 1	blood
8	chr6:106973600-106992800	Weak transcription	Duodenum Smooth Muscle	Duodenum
9	chr6:106975000-106983400	Strong transcription	Rectal Mucosa Donor 31	rectum
10	chr6:106975200-106983000	Strong transcription	Adipose Nuclei	Adipose
11	chr6:106976000-106983200	Strong transcription	Duodenum Mucosa	Duodenum
12	chr6:106976200-106982800	Strong transcription	Sigmoid Colon	Sigmoid Colon
13	chr6:106976400-106986200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
14	chr6:106976600-106991400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr6:106977000-106986400	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr6:106978600-106983400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr6:106978800-106984200	Weak transcription	NH-A	brain
18	chr6:106978800-106985600	Weak transcription	Fetal Thymus	thymus
19	chr6:106978800-106993800	Weak transcription	NHLF	lung
20	chr6:106979000-107001400	Weak transcription	Pancreas	Pancrea
21	chr6:106979600-106984200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr6:106979600-106987200	Weak transcription	HepG2	liver
23	chr6:106980200-106983000	Genic enhancers	Primary B cells from peripheral blood	blood
24	chr6:106980200-106984400	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr6:106980400-106982800	Enhancers	Primary neutrophils fromperipheralblood	blood
26	chr6:106980800-106982800	Genic enhancers	Primary T helper naive cells fromperipheralblood	blood
27	chr6:106980800-106982800	Genic enhancers	Primary T helper cells fromperipheralblood	blood
28	chr6:106980800-106982800	Genic enhancers	GM12878-XiMat	blood
29	chr6:106980800-106983200	Genic enhancers	Primary monocytes fromperipheralblood	blood
30	chr6:106980800-106983400	Genic enhancers	Primary T helper 17 cells PMA-I stimulated	--
31	chr6:106980800-106984400	Genic enhancers	HMEC	breast
32	chr6:106980800-106986200	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr6:106980800-106986400	Strong transcription	Liver	Liver
34	chr6:106981000-106982800	Genic enhancers	Primary T cells fromperipheralblood	blood
35	chr6:106981000-106983000	Genic enhancers	Primary T regulatory cells fromperipheralblood	blood
36	chr6:106981200-106984600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr6:106981400-106988000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
38	chr6:106981600-106984600	Genic enhancers	Monocytes-CD14+_RO01746	blood
39	chr6:106981600-106995600	Weak transcription	Colonic Mucosa	Colon
40	chr6:106981800-106983600	Genic enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
41	chr6:106981800-106984000	Weak transcription	Fetal Intestine Small	intestine
42	chr6:106981800-106985200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
43	chr6:106981800-106985600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
44	chr6:106981800-106985600	Weak transcription	Esophagus	oesophagus
45	chr6:106981800-106987800	Weak transcription	Lung	lung
46	chr6:106982000-106983400	Enhancers	Primary T helper naive cells from peripheral blood	blood
47	chr6:106982200-106982800	Enhancers	HUVEC	blood vessel
48	chr6:106982200-106983400	Weak transcription	Dnd41	blood
49	chr6:106982200-106984200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
50	chr6:106982400-106984600	Weak transcription	Primary hematopoietic stem cells	blood

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