Variant report

Variant	rs7515770
Chromosome Location	chr1:175095936-175095937
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:175094084..175096187-chr1:175106448..175108286,2	K562	blood:
2	chr1:175050894..175052513-chr1:175093322..175096065,2	MCF-7	breast:
3	chr1:175091685..175094091-chr1:175094460..175097259,2	K562	blood:

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

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs10798333	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10912890	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12087735	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12094153	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6660052	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6670010	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7521981	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv825487	chr1:175031609-175113572	Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv508648	chr1:175056387-175121913	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:175084800-175097000	Weak transcription	Gastric	stomach
2	chr1:175086400-175099600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr1:175091200-175098600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr1:175093800-175096200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr1:175094000-175100000	Enhancers	Liver	Liver
6	chr1:175094400-175098400	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr1:175094400-175098800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr1:175094600-175096800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr1:175094800-175096000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
10	chr1:175094800-175096600	Weak transcription	Primary monocytes fromperipheralblood	blood
11	chr1:175094800-175096800	Weak transcription	Primary neutrophils fromperipheralblood	blood
12	chr1:175095200-175096600	Weak transcription	Monocytes-CD14+_RO01746	blood
13	chr1:175095400-175096000	Enhancers	Adipose Nuclei	Adipose
14	chr1:175095600-175096200	Enhancers	Duodenum Smooth Muscle	Duodenum
15	chr1:175095600-175096200	Enhancers	Spleen	Spleen
16	chr1:175095600-175098200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr1:175095600-175098200	Enhancers	Lung	lung
18	chr1:175095600-175099600	Enhancers	Fetal Lung	lung
19	chr1:175095600-175099800	Enhancers	Placenta	Placenta
20	chr1:175095600-175099800	Enhancers	Right Atrium	heart
21	chr1:175095600-175100400	Enhancers	Fetal Stomach	stomach
22	chr1:175095800-175096000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr1:175095800-175097000	Weak transcription	Left Ventricle	heart
24	chr1:175095800-175102600	Enhancers	Stomach Smooth Muscle	stomach

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links