Variant report

Variant	rs201127360
Chromosome Location	chr6:35394617-35394618
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:35226026..35228002-chr6:35394504..35397292,2	K562	blood:
2	chr6:35380537..35383478-chr6:35394277..35398227,3	K562	blood:
3	chr6:35388873..35391570-chr6:35394373..35396733,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000065029	Chromatin interaction

Extended variants
information (count: 11 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830641	chr6:35282534-35440603	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	57 gene(s)	inside rSNPs	diseases
2	nsv462907	chr6:35333799-35408959	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv602908	chr6:35333799-35408959	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Active 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
4	nsv602909	chr6:35356640-35423489	Weak transcription Active TSS Enhancers Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	nsv470812	chr6:35374461-35418118	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
6	nsv528351	chr6:35377922-35465786	Flanking Active TSS Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	69 gene(s)	inside rSNPs	diseases
7	nsv885799	chr6:35378778-35442397	Active TSS Strong transcription Weak transcription Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	54 gene(s)	inside rSNPs	diseases
8	nsv462908	chr6:35378778-35457396	Enhancers Weak transcription Bivalent/Poised TSS Genic enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	55 gene(s)	inside rSNPs	diseases
9	nsv602910	chr6:35378778-35457396	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	55 gene(s)	inside rSNPs	diseases
10	nsv519370	chr6:35378778-35537406	Weak transcription Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	72 gene(s)	inside rSNPs	diseases
11	nsv885800	chr6:35394247-35406153	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:118 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:35377800-35395000	Weak transcription	K562	blood
2	chr6:35383000-35396800	Weak transcription	Right Atrium	heart
3	chr6:35383400-35394800	Weak transcription	Fetal Kidney	kidney
4	chr6:35383400-35396600	Weak transcription	Stomach Mucosa	stomach
5	chr6:35383600-35402600	Weak transcription	Fetal Heart	heart
6	chr6:35387400-35395200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr6:35387600-35394800	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
8	chr6:35387600-35395200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr6:35387600-35395200	Strong transcription	Stomach Smooth Muscle	stomach
10	chr6:35387800-35396000	Strong transcription	Fetal Intestine Small	intestine
11	chr6:35388000-35395600	Strong transcription	Primary T cells fromperipheralblood	blood
12	chr6:35388000-35396000	Strong transcription	Fetal Muscle Leg	muscle
13	chr6:35388200-35395200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
14	chr6:35389200-35395200	Strong transcription	Duodenum Mucosa	Duodenum
15	chr6:35389200-35395400	Strong transcription	Fetal Intestine Large	intestine
16	chr6:35389200-35396000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
17	chr6:35389400-35394800	Strong transcription	Primary T helper cells PMA-I stimulated	--
18	chr6:35389400-35394800	Strong transcription	Brain Substantia Nigra	brain
19	chr6:35389400-35395000	Strong transcription	Rectal Smooth Muscle	rectum
20	chr6:35389400-35395200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
21	chr6:35389400-35395200	Strong transcription	Primary T helper cells fromperipheralblood	blood
22	chr6:35389400-35395600	Strong transcription	Primary T cells from cord blood	blood
23	chr6:35389400-35395600	Strong transcription	Brain Cingulate Gyrus	brain
24	chr6:35389400-35395600	Strong transcription	Skeletal Muscle Male	skeletal muscle
25	chr6:35389400-35395800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
26	chr6:35389600-35395200	Strong transcription	Left Ventricle	heart
27	chr6:35389600-35395400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr6:35389600-35395600	Strong transcription	Brain Anterior Caudate	brain
29	chr6:35389600-35395600	Strong transcription	Brain Hippocampus Middle	brain
30	chr6:35389600-35396200	Strong transcription	Gastric	stomach
31	chr6:35390400-35395200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
32	chr6:35390400-35396000	Weak transcription	Pancreatic Islets	Pancreatic Islet
33	chr6:35391400-35395000	Strong transcription	Fetal Brain Female	brain
34	chr6:35391400-35395000	Strong transcription	Pancreas	Pancrea
35	chr6:35391400-35395600	Strong transcription	Colonic Mucosa	Colon
36	chr6:35391400-35396000	Strong transcription	Thymus	Thymus
37	chr6:35391400-35396400	Strong transcription	Right Ventricle	heart
38	chr6:35391600-35394800	Strong transcription	Liver	Liver
39	chr6:35391600-35395000	Strong transcription	Duodenum Smooth Muscle	Duodenum
40	chr6:35391600-35395000	Strong transcription	Rectal Mucosa Donor 31	rectum
41	chr6:35391600-35395200	Strong transcription	Brain Inferior Temporal Lobe	brain
42	chr6:35391600-35395600	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr6:35391800-35395600	Strong transcription	Psoas Muscle	Psoas
44	chr6:35391800-35395800	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
45	chr6:35391800-35396200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr6:35392000-35395800	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr6:35392200-35394800	Genic enhancers	HSMM	muscle
48	chr6:35392400-35395000	Genic enhancers	NHDF-Ad	bronchial
49	chr6:35392400-35395000	Genic enhancers	Osteobl	bone
50	chr6:35392400-35396600	Weak transcription	Small Intestine	intestine

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