Variant report

Variant	rs7898549
Chromosome Location	chr10:5629111-5629112
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:5612030..5614229-chr10:5627783..5630248,2	MCF-7	breast:
2	chr10:5606603..5608938-chr10:5627234..5631685,4	MCF-7	breast:
3	chr10:5624309..5631245-chr10:5648674..5654250,8	MCF-7	breast:
4	chr10:5623673..5635207-chr10:5656121..5669428,27	MCF-7	breast:
5	chr10:5558645..5561778-chr10:5628008..5630881,3	MCF-7	breast:
6	chr10:5527980..5531416-chr10:5628213..5631359,3	MCF-7	breast:
7	chr10:5599218..5601467-chr10:5626638..5630611,4	MCF-7	breast:
8	chr10:5624590..5636573-chr10:5652742..5661113,15	MCF-7	breast:
9	chr10:5584975..5598212-chr10:5621607..5634806,86	MCF-7	breast:
10	chr10:5486586..5497147-chr10:5622068..5633259,25	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000231483	Chromatin interaction
ENSG00000228685	Chromatin interaction
ENSG00000228951	Chromatin interaction
ENSG00000173848	Chromatin interaction

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs11597288	0.89[CEU][hapmap]
rs55794432	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs55915230	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs56019774	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs56052209	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs56113508	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs56172763	0.97[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs56197874	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs56280752	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs56870093	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs58411480	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs58589352	0.83[AMR][1000 genomes]
rs61628927	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv534685	chr10:4914018-5853324	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	68 gene(s)	inside rSNPs	diseases
2	nsv932104	chr10:5203626-5641023	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
3	nsv549886	chr10:5205437-5632060	Strong transcription Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
4	nsv1054865	chr10:5225305-5638119	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
5	nsv831774	chr10:5463556-5657421	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
6	nsv894798	chr10:5503610-5670275	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
7	nsv523491	chr10:5542109-5720067	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
8	esv2757364	chr10:5557024-5720512	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
9	esv2759729	chr10:5557024-5804780	Flanking Active TSS Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
10	nsv894801	chr10:5600202-5631737	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
11	nsv894802	chr10:5608202-5631737	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Active TSS	Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
12	nsv549889	chr10:5610349-5630131	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:72 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:5624200-5630400	Enhancers	HUES6 Cell Line	embryonic stem cell
2	chr10:5624400-5629400	Weak transcription	Colonic Mucosa	Colon
3	chr10:5624400-5629600	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr10:5625000-5631800	Weak transcription	K562	blood
5	chr10:5625000-5632400	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr10:5625200-5634400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr10:5625600-5629800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr10:5626000-5629800	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr10:5626000-5634600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr10:5626200-5629200	Enhancers	HMEC	breast
11	chr10:5626200-5636200	Weak transcription	Primary B cells from cord blood	blood
12	chr10:5626400-5633600	Enhancers	Fetal Thymus	thymus
13	chr10:5626600-5629400	Enhancers	A549	lung
14	chr10:5626600-5631800	Enhancers	Fetal Heart	heart
15	chr10:5627000-5629600	Enhancers	HSMMtube	muscle
16	chr10:5627200-5629800	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr10:5627200-5629800	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr10:5627400-5639400	Enhancers	Fetal Muscle Leg	muscle
19	chr10:5627600-5629200	Weak transcription	Duodenum Mucosa	Duodenum
20	chr10:5627600-5629200	Weak transcription	Placenta Amnion	Placenta Amnion
21	chr10:5627600-5629200	Enhancers	Rectal Mucosa Donor 31	rectum
22	chr10:5627600-5631400	Weak transcription	Osteobl	bone
23	chr10:5627800-5629200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr10:5627800-5629200	Weak transcription	Esophagus	oesophagus
25	chr10:5627800-5629400	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr10:5627800-5629400	Weak transcription	Placenta	Placenta
27	chr10:5627800-5629400	Weak transcription	Right Ventricle	heart
28	chr10:5627800-5631000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr10:5628000-5629200	Enhancers	H9 Cell Line	embryonic stem cell
30	chr10:5628000-5629200	Weak transcription	Colon Smooth Muscle	Colon
31	chr10:5628000-5629800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr10:5628000-5629800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr10:5628200-5629200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr10:5628200-5629200	Weak transcription	Fetal Lung	lung
35	chr10:5628200-5629400	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr10:5628200-5629400	Weak transcription	Brain Germinal Matrix	brain
37	chr10:5628200-5629800	Enhancers	HepG2	liver
38	chr10:5628200-5630000	Enhancers	H1 Cell Line	embryonic stem cell
39	chr10:5628200-5630000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr10:5628200-5631600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr10:5628200-5631800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr10:5628200-5631800	Weak transcription	HSMM	muscle
43	chr10:5628400-5629800	Enhancers	Fetal Intestine Large	intestine
44	chr10:5628400-5629800	Enhancers	Fetal Intestine Small	intestine
45	chr10:5628400-5630000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr10:5628400-5631400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr10:5628400-5631800	Weak transcription	NHDF-Ad	bronchial
48	chr10:5628600-5630800	Weak transcription	NHEK	skin
49	chr10:5628600-5631200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr10:5628600-5633200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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