Variant report

Variant	rs12595120
Chromosome Location	chr15:29695122-29695123
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10519650	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10519651	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11072650	0.94[ASN][1000 genomes]
rs11072655	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11072656	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11853842	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11856277	0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12591108	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12592503	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12592535	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12593061	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12593100	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12593665	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12594856	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4779650	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4780187	0.95[ASN][1000 genomes]
rs4780204	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4780205	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4780210	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4780211	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4780219	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4780223	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs56686951	0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs56755121	0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs59302753	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs60145447	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7162566	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7167288	0.81[ASN][1000 genomes]
rs7171687	0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs73382113	0.98[EUR][1000 genomes];0.95[ASN][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	nsv456736	chr15:29327352-30208654	Weak transcription Active TSS Enhancers ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
2	nsv568675	chr15:29327352-30208654	Flanking Active TSS Strong transcription Active TSS Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
3	nsv903747	chr15:29361126-30008977	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
4	esv3364436	chr15:29459739-29853229	Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:29685800-29696200	Weak transcription	Pancreas	Pancrea
2	chr15:29685800-29696200	Weak transcription	Spleen	Spleen
3	chr15:29691400-29696200	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr15:29693400-29696200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr15:29693400-29696600	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr15:29694200-29695200	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr15:29694200-29695200	Weak transcription	Stomach Smooth Muscle	stomach
8	chr15:29694200-29695800	Weak transcription	HUES48 Cell Line	embryonic stem cell
9	chr15:29694200-29696200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr15:29694200-29701800	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr15:29694200-29702000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr15:29694200-29702000	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr15:29694200-29702000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
14	chr15:29694400-29695400	Enhancers	Primary monocytes fromperipheralblood	blood
15	chr15:29694400-29702000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
16	chr15:29695000-29695200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
17	chr15:29695000-29696000	Enhancers	Colon Smooth Muscle	Colon
18	chr15:29695000-29696000	Enhancers	Fetal Stomach	stomach

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links