Variant report

Variant	rs7903412
Chromosome Location	chr10:45382361-45382362
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr10:45358788..45360533-chr10:45380814..45383521,3	MCF-7	breast:
2	chr10:45374438..45376422-chr10:45380219..45382953,2	K562	blood:
3	chr10:45381597..45383969-chr10:45388700..45390361,2	K562	blood:

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs10736831	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10751360	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10751361	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10793562	0.99[ASN][1000 genomes]
rs10793563	1.00[ASN][1000 genomes]
rs10793564	0.82[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10793565	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10900123	0.88[EUR][1000 genomes]
rs10900125	0.99[ASN][1000 genomes]
rs10900126	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10900128	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11239271	0.88[EUR][1000 genomes]
rs12777258	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1332625	0.82[ASN][1000 genomes]
rs1408814	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1977324	0.98[ASN][1000 genomes]
rs2026427	0.94[ASN][1000 genomes]
rs2026428	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2065466	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2183994	0.98[ASN][1000 genomes]
rs2281840	0.88[ASN][1000 genomes]
rs2281841	0.87[EUR][1000 genomes]
rs3900184	0.99[ASN][1000 genomes]
rs4245614	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4268464	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4284362	0.94[ASN][1000 genomes]
rs4439464	1.00[ASN][1000 genomes]
rs4481983	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4506594	1.00[ASN][1000 genomes]
rs4948642	0.99[ASN][1000 genomes]
rs4948643	0.99[ASN][1000 genomes]
rs4948644	0.99[ASN][1000 genomes]
rs4948645	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4948921	0.93[ASN][1000 genomes]
rs4948922	0.99[ASN][1000 genomes]
rs4948924	0.99[ASN][1000 genomes]
rs4948925	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4948926	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4948927	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs5000415	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6593447	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7079573	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7082011	1.00[ASN][1000 genomes]
rs7099692	0.88[ASN][1000 genomes]
rs7894608	0.98[ASN][1000 genomes]
rs7900859	0.84[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs7909074	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs879073	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs879074	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs879343	0.80[ASN][1000 genomes]
rs879344	0.82[ASN][1000 genomes]
rs914699	0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv517161	chr10:45210690-45416256	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv831844	chr10:45228791-45407762	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv831845	chr10:45300268-45460395	Enhancers Genic enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
4	nsv831846	chr10:45322236-45556370	Bivalent Enhancer Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:45375200-45398600	Weak transcription	Right Atrium	heart
2	chr10:45375800-45384200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr10:45376200-45389600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr10:45381200-45382400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr10:45381800-45384800	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr10:45382000-45382800	Enhancers	Rectal Mucosa Donor 31	rectum

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links