Variant report

Variant	rs7702283
Chromosome Location	chr5:114974122-114974123
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr5:114971626..114974342-chr5:115178110..115179917,2	K562	blood:
2	chr5:114970607..114974645-chr5:114975238..114977621,3	K562	blood:
3	chr5:114972992..114975914-chr5:115155123..115157177,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000177879	Chromatin interaction

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs10055677	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13164545	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs13186296	0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs171774	0.92[EUR][1000 genomes]
rs2303747	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs256941	0.97[ASN][1000 genomes]
rs256942	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs256944	0.92[EUR][1000 genomes]
rs256945	0.92[EUR][1000 genomes]
rs256947	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs256948	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs256949	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs256950	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs256951	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs256952	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs256953	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs256954	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs256962	0.94[ASN][1000 genomes]
rs256964	0.94[EUR][1000 genomes]
rs256967	0.92[EUR][1000 genomes]
rs256969	0.92[EUR][1000 genomes]
rs256988	0.91[EUR][1000 genomes]
rs256991	0.91[EUR][1000 genomes]
rs256993	0.91[EUR][1000 genomes]
rs256997	0.90[EUR][1000 genomes]
rs256998	0.92[EUR][1000 genomes]
rs377290	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3822579	0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs400570	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs413059	0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs415577	0.92[EUR][1000 genomes]
rs416234	0.94[ASN][1000 genomes]
rs424434	0.94[ASN][1000 genomes]
rs428191	0.92[ASN][1000 genomes]
rs4920967	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4920969	0.89[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs62371215	0.81[ASN][1000 genomes]
rs698366	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs698367	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs712550	0.94[ASN][1000 genomes]
rs712551	0.95[ASN][1000 genomes]
rs7702869	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7702881	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs790824	0.94[ASN][1000 genomes]
rs790825	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9326969	0.95[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	nsv916273	chr5:114656592-115089901	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
2	nsv868915	chr5:114723371-115252527	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:114970600-114974400	Weak transcription	Liver	Liver
2	chr5:114971600-114975400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr5:114971800-114976800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr5:114972000-114975600	Enhancers	Cortex derived primary cultured neurospheres	brain
5	chr5:114972800-114974400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr5:114972800-114976800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr5:114972800-114977000	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr5:114973000-114974200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr5:114973400-114974200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr5:114973400-114974200	Enhancers	NHDF-Ad	bronchial
11	chr5:114973600-114974600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr5:114973800-114974800	Enhancers	GM12878-XiMat	blood
13	chr5:114974000-114974200	Enhancers	H9 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links