Variant report

Variant	rs45444494
Chromosome Location	chr2:113955923-113955924
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ZEB1	chr2:113955475-113957329	HepG2	liver:	n/a	n/a
2	POLR2A	chr2:113955822-113956122	HepG2	liver:	n/a	n/a

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:113931492..113932996-chr2:113955583..113957836,2	MCF-7	breast:
2	chr2:113949542..113953586-chr2:113955251..113958622,5	MCF-7	breast:
3	chr2:113954862..113956783-chr2:113998620..114001129,2	MCF-7	breast:
4	chr2:113955248..113957880-chr2:113994557..113996875,2	MCF-7	breast:
5	chr2:113912322..113918193-chr2:113953978..113958305,10	MCF-7	breast:
6	chr2:113913769..113918338-chr2:113954843..113958220,11	MCF-7	breast:
7	chr2:113950663..113952350-chr2:113953925..113956890,2	K562	blood:
8	chr2:113941477..113944460-chr2:113951684..113956081,4	K562	blood:

No data

Variant related genes	Relation type
PSD4	TF binding region
ENSG00000234174	Chromatin interaction
ENSG00000189223	Chromatin interaction
ENSG00000125637	Chromatin interaction
ENSG00000125618	Chromatin interaction

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs17043030	1.00[EUR][1000 genomes]
rs45522233	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs45578731	1.00[EUR][1000 genomes]
rs73955173	1.00[EUR][1000 genomes]

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	nsv997348	chr2:113688093-113986508	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
2	nsv582711	chr2:113895516-113984503	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
3	nsv582712	chr2:113932431-113985170	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS 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	14 gene(s)	inside rSNPs	diseases
4	nsv874899	chr2:113935407-113962071	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	nsv874900	chr2:113948378-113967990	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:69 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:113923000-113956000	Weak transcription	HMEC	breast
2	chr2:113934200-113956200	Weak transcription	Rectal Smooth Muscle	rectum
3	chr2:113939400-113956000	Weak transcription	Brain Cingulate Gyrus	brain
4	chr2:113939400-113956400	Weak transcription	Small Intestine	intestine
5	chr2:113939600-113956200	Weak transcription	Fetal Lung	lung
6	chr2:113940000-113961000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
7	chr2:113942800-113956600	Strong transcription	Fetal Thymus	thymus
8	chr2:113942800-113961000	Strong transcription	Dnd41	blood
9	chr2:113943000-113956200	Weak transcription	Brain Substantia Nigra	brain
10	chr2:113943600-113956200	Weak transcription	Adipose Nuclei	Adipose
11	chr2:113943800-113956000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr2:113947400-113961000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
13	chr2:113947800-113956200	Strong transcription	GM12878-XiMat	blood
14	chr2:113947800-113959600	Strong transcription	Primary T helper naive cells from peripheral blood	blood
15	chr2:113947800-113960600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
16	chr2:113948600-113961000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
17	chr2:113949000-113956000	Strong transcription	Primary monocytes fromperipheralblood	blood
18	chr2:113949000-113956000	Strong transcription	Primary B cells from peripheral blood	blood
19	chr2:113949000-113961200	Strong transcription	Primary neutrophils fromperipheralblood	blood
20	chr2:113950000-113961000	Strong transcription	Primary T cells from cord blood	blood
21	chr2:113951000-113956200	Weak transcription	Fetal Kidney	kidney
22	chr2:113951000-113956400	Strong transcription	Primary T helper cells PMA-I stimulated	--
23	chr2:113951400-113956200	Weak transcription	Skeletal Muscle Female	skeletal muscle
24	chr2:113952400-113956000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr2:113952600-113957800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
26	chr2:113952800-113956200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
27	chr2:113953400-113956000	Weak transcription	Duodenum Smooth Muscle	Duodenum
28	chr2:113954000-113956400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
29	chr2:113954000-113957000	Strong transcription	Primary T helper memory cells from peripheral blood 2	blood
30	chr2:113954200-113956000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
31	chr2:113954200-113956000	Weak transcription	Colonic Mucosa	Colon
32	chr2:113954200-113956200	Strong transcription	Primary T cells fromperipheralblood	blood
33	chr2:113954200-113956200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
34	chr2:113954200-113956200	Weak transcription	Placenta Amnion	Placenta Amnion
35	chr2:113954400-113956000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
36	chr2:113954400-113956400	Strong transcription	Primary T helper cells fromperipheralblood	blood
37	chr2:113954800-113956200	Weak transcription	Gastric	stomach
38	chr2:113954800-113956200	Weak transcription	NHEK	skin
39	chr2:113955000-113956000	Enhancers	Pancreas	Pancrea
40	chr2:113955200-113956400	ZNF genes & repeats	Thymus	Thymus
41	chr2:113955400-113956000	Enhancers	Liver	Liver
42	chr2:113955400-113956000	Weak transcription	Rectal Mucosa Donor 31	rectum
43	chr2:113955400-113956400	Genic enhancers	Spleen	Spleen
44	chr2:113955600-113956000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr2:113955600-113956000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr2:113955600-113956000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
47	chr2:113955600-113956000	Weak transcription	Placenta	Placenta
48	chr2:113955600-113956200	Weak transcription	Esophagus	oesophagus
49	chr2:113955600-113956200	Enhancers	NH-A	brain
50	chr2:113955800-113956000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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