Variant report

Variant	rs56792569
Chromosome Location	chr12:120671404-120671405
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr12:120642171..120684465-chr12:120719749..120734210,267	K562	blood:
2	chr12:120628211..120641965-chr12:120660551..120674110,39	K562	blood:
3	chr12:120656223..120689871-chr12:120720394..120738112,311	MCF-7	breast:
4	chr12:120657004..120683911-chr12:120723753..120737731,232	K562	blood:

Variant related genes	Relation type
ENSG00000089154	Chromatin interaction
ENSG00000200795	Chromatin interaction
ENSG00000089157	Chromatin interaction
ENSG00000123009	Chromatin interaction
ENSG00000255857	Chromatin interaction
ENSG00000202538	Chromatin interaction

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs1167257	1.00[EUR][1000 genomes]
rs12301083	1.00[EUR][1000 genomes]
rs13343210	1.00[EUR][1000 genomes]
rs16949884	1.00[EUR][1000 genomes]
rs16949890	1.00[EUR][1000 genomes]
rs16949897	1.00[EUR][1000 genomes]
rs1794740	1.00[EUR][1000 genomes]
rs2522132	1.00[EUR][1000 genomes]
rs25662	1.00[AMR][1000 genomes]
rs35938105	1.00[EUR][1000 genomes]
rs3852590	1.00[EUR][1000 genomes]
rs58733148	1.00[AMR][1000 genomes]
rs59159546	1.00[EUR][1000 genomes]
rs61733796	1.00[EUR][1000 genomes]
rs61753910	1.00[EUR][1000 genomes]
rs7953006	1.00[EUR][1000 genomes]

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	nsv899555	chr12:120519124-120840522	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	499 gene(s)	inside rSNPs	diseases
2	nsv519657	chr12:120533696-120676090	Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	94 gene(s)	inside rSNPs	diseases
3	nsv560433	chr12:120533696-120676090	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	94 gene(s)	inside rSNPs	diseases
4	nsv832530	chr12:120586069-120758175	Flanking Active TSS Strong transcription Enhancers Genic enhancers Weak transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	484 gene(s)	inside rSNPs	diseases
5	nsv1035698	chr12:120645330-120777580	Active TSS Flanking Active TSS Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	436 gene(s)	inside rSNPs	diseases
6	nsv1047447	chr12:120645330-120808621	Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Enhancers Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	436 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:120664400-120675800	Enhancers	Stomach Mucosa	stomach
2	chr12:120665000-120671600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr12:120665200-120692000	Enhancers	Placenta	Placenta
4	chr12:120665400-120673200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr12:120665400-120674200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr12:120665400-120676800	Enhancers	Fetal Heart	heart
7	chr12:120665400-120682200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
8	chr12:120665600-120673800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr12:120665600-120674200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr12:120665600-120674200	Enhancers	Fetal Lung	lung
11	chr12:120665600-120675400	Enhancers	Primary monocytes fromperipheralblood	blood
12	chr12:120665600-120682200	Enhancers	Left Ventricle	heart
13	chr12:120665800-120673600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
14	chr12:120665800-120674000	Enhancers	H1 Cell Line	embryonic stem cell
15	chr12:120665800-120674400	Enhancers	Psoas Muscle	Psoas
16	chr12:120665800-120675400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
17	chr12:120666000-120672800	Enhancers	Right Atrium	heart
18	chr12:120666000-120674200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
19	chr12:120666000-120677200	Enhancers	Lung	lung
20	chr12:120666200-120686000	Enhancers	Placenta Amnion	Placenta Amnion
21	chr12:120666800-120673200	Enhancers	Spleen	Spleen
22	chr12:120666800-120673800	Enhancers	Liver	Liver
23	chr12:120666800-120674000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr12:120666800-120674200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr12:120667000-120672400	Enhancers	Brain Hippocampus Middle	brain
26	chr12:120667400-120672400	Weak transcription	Fetal Brain Male	brain
27	chr12:120667400-120674200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
28	chr12:120667800-120673800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
29	chr12:120668200-120675400	Enhancers	Fetal Intestine Large	intestine
30	chr12:120668800-120671800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
31	chr12:120668800-120674000	Enhancers	H9 Cell Line	embryonic stem cell
32	chr12:120669000-120672400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr12:120669000-120672600	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr12:120669000-120672600	Weak transcription	Fetal Brain Female	brain
35	chr12:120669000-120672800	Enhancers	HepG2	liver
36	chr12:120669000-120674000	Enhancers	Rectal Mucosa Donor 31	rectum
37	chr12:120669000-120674200	Enhancers	Right Ventricle	heart
38	chr12:120669000-120675200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr12:120669000-120675400	Enhancers	HMEC	breast
40	chr12:120669200-120671800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr12:120669200-120674200	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr12:120669200-120674400	Enhancers	Primary T cells fromperipheralblood	blood
43	chr12:120669200-120675400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
44	chr12:120669200-120676200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
45	chr12:120669400-120671600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr12:120669400-120671800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
47	chr12:120669400-120673800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr12:120669400-120677400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
49	chr12:120669400-120677800	Enhancers	Primary T helper naive cells from peripheral blood	blood
50	chr12:120669600-120672400	Enhancers	Adipose Nuclei	Adipose

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