Variant report

Variant	rs10795285
Chromosome Location	chr10:5607841-5607842
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:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

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

No.	Distal block	Cell Line	Cell type
1	chr10:5573411..5576339-chr10:5606332..5608916,2	K562	blood:
2	chr10:5590969..5593951-chr10:5606368..5608078,2	K562	blood:
3	chr10:5589141..5591832-chr10:5607489..5609696,2	MCF-7	breast:
4	chr10:5606603..5608938-chr10:5627234..5631685,4	MCF-7	breast:
5	chr10:5593038..5596682-chr10:5605799..5608006,4	MCF-7	breast:
6	chr10:5486761..5489275-chr10:5607037..5608724,2	K562	blood:
7	chr10:5606200..5608461-chr10:5634669..5639030,3	K562	blood:
8	chr10:5604398..5606617-chr10:5607814..5609704,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000173848	Chromatin interaction
ENSG00000242147	Chromatin interaction

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs12218547	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4348801	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4529812	0.93[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:16 , 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	nsv1051283	chr10:5505474-5619941	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
8	nsv1049523	chr10:5542109-5619941	Flanking Active TSS Enhancers Weak transcription Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
9	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
10	nsv1052002	chr10:5544571-5619941	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
11	nsv1038479	chr10:5545773-5619941	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
12	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
13	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
14	nsv894800	chr10:5572893-5621628	Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
15	nsv1044746	chr10:5595343-5619941	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
16	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

No data

Chromatin state (count:51 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:5588400-5608200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr10:5602600-5609400	Weak transcription	A549	lung
3	chr10:5605200-5608800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr10:5605200-5611200	Enhancers	HMEC	breast
5	chr10:5605400-5608200	Enhancers	Placenta	Placenta
6	chr10:5605400-5608200	Enhancers	Placenta Amnion	Placenta Amnion
7	chr10:5605400-5608600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr10:5605400-5608600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr10:5605400-5608600	Bivalent Enhancer	Fetal Muscle Leg	muscle
10	chr10:5605400-5608600	Enhancers	HSMMtube	muscle
11	chr10:5605400-5608800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr10:5605400-5608800	Enhancers	NH-A	brain
13	chr10:5605400-5609000	Enhancers	NHDF-Ad	bronchial
14	chr10:5605400-5609200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr10:5605600-5608000	Enhancers	HSMM	muscle
16	chr10:5605600-5608800	Enhancers	Fetal Thymus	thymus
17	chr10:5605600-5609000	Weak transcription	Right Atrium	heart
18	chr10:5606000-5608000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr10:5606000-5608400	Enhancers	Esophagus	oesophagus
20	chr10:5606000-5609400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr10:5606200-5608000	Enhancers	HepG2	liver
22	chr10:5606200-5608200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr10:5606200-5609000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr10:5606600-5608000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr10:5606600-5608400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr10:5606600-5608800	Enhancers	Osteobl	bone
27	chr10:5606800-5608000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
28	chr10:5606800-5608200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
29	chr10:5606800-5608400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
30	chr10:5606800-5608800	Enhancers	Primary T cells fromperipheralblood	blood
31	chr10:5606800-5608800	Enhancers	Primary T helper cells fromperipheralblood	blood
32	chr10:5607000-5608200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
33	chr10:5607000-5608400	Enhancers	Primary T helper naive cells from peripheral blood	blood
34	chr10:5607000-5608800	Enhancers	Breast Myoepithelial Primary Cells	Breast
35	chr10:5607000-5608800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
36	chr10:5607000-5609200	Weak transcription	Duodenum Mucosa	Duodenum
37	chr10:5607200-5608200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr10:5607200-5609000	Enhancers	Primary T cells from cord blood	blood
39	chr10:5607200-5609200	Enhancers	Primary T helper cells PMA-I stimulated	--
40	chr10:5607200-5611800	Weak transcription	K562	blood
41	chr10:5607400-5608400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
42	chr10:5607400-5612200	Weak transcription	Lung	lung
43	chr10:5607400-5614600	Weak transcription	Rectal Mucosa Donor 31	rectum
44	chr10:5607600-5608000	Enhancers	Fetal Stomach	stomach
45	chr10:5607600-5608200	Enhancers	NHEK	skin
46	chr10:5607600-5608600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
47	chr10:5607600-5608800	Weak transcription	Fetal Intestine Large	intestine
48	chr10:5607600-5609200	Weak transcription	Fetal Intestine Small	intestine
49	chr10:5607800-5608000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
50	chr10:5607800-5608000	Enhancers	NHLF	lung

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links