Variant report

Variant	rs6911397
Chromosome Location	chr6:5618181-5618182
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:5616037..5618304-chr6:5621666..5623191,2	K562	blood:
2	chr6:5609969..5611663-chr6:5617459..5619947,2	K562	blood:

Variant related genes	Relation type
ENSG00000218574	Chromatin interaction

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs9502312	1.00[YRI][hapmap]

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	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
2	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
3	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
4	nsv600887	chr6:5545046-5694713	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv1016905	chr6:5566364-5639167	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv1015549	chr6:5593965-5630468	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Genic enhancers	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:39 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:5577400-5639800	Weak transcription	Fetal Intestine Small	intestine
2	chr6:5581000-5640400	Weak transcription	Gastric	stomach
3	chr6:5587200-5619400	Weak transcription	Primary B cells from cord blood	blood
4	chr6:5590800-5622000	Weak transcription	Right Atrium	heart
5	chr6:5591200-5619000	Weak transcription	Primary B cells from peripheral blood	blood
6	chr6:5591600-5626400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
7	chr6:5592200-5619200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
8	chr6:5593400-5621000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr6:5605600-5618800	Weak transcription	Primary T cells from cord blood	blood
10	chr6:5605600-5619200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr6:5610400-5620200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
12	chr6:5610600-5641000	Weak transcription	Stomach Smooth Muscle	stomach
13	chr6:5612000-5619200	Weak transcription	Primary T helper cells PMA-I stimulated	--
14	chr6:5612200-5622200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr6:5612400-5628000	Weak transcription	Fetal Intestine Large	intestine
16	chr6:5612600-5640000	Weak transcription	Fetal Stomach	stomach
17	chr6:5612800-5618400	Weak transcription	Primary T helper cells fromperipheralblood	blood
18	chr6:5612800-5626800	Weak transcription	Primary hematopoietic stem cells	blood
19	chr6:5613000-5627200	Weak transcription	Adipose Nuclei	Adipose
20	chr6:5613200-5640400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr6:5613600-5627000	Weak transcription	Dnd41	blood
22	chr6:5613800-5619200	Weak transcription	Primary T cells fromperipheralblood	blood
23	chr6:5614400-5619200	Weak transcription	Fetal Thymus	thymus
24	chr6:5614400-5639000	Weak transcription	Lung	lung
25	chr6:5614600-5619200	Weak transcription	Sigmoid Colon	Sigmoid Colon
26	chr6:5614600-5621200	Weak transcription	Duodenum Smooth Muscle	Duodenum
27	chr6:5614600-5626800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr6:5614600-5628200	Weak transcription	Ovary	ovary
29	chr6:5614600-5636600	Weak transcription	Pancreas	Pancrea
30	chr6:5614600-5640000	Weak transcription	Duodenum Mucosa	Duodenum
31	chr6:5614600-5640400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
32	chr6:5615400-5619000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
33	chr6:5615600-5624200	Weak transcription	Cortex derived primary cultured neurospheres	brain
34	chr6:5616200-5627000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr6:5617000-5619400	Enhancers	Fetal Heart	heart
36	chr6:5617200-5618600	Enhancers	Left Ventricle	heart
37	chr6:5617400-5619600	Weak transcription	Aorta	Aorta
38	chr6:5617800-5625600	Weak transcription	Fetal Muscle Leg	muscle
39	chr6:5618000-5619000	Weak transcription	Primary T helper naive cells from peripheral blood	blood

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