Variant report

Variant	rs16921744
Chromosome Location	chr10:21633367-21633368
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:21626682..21628254-chr10:21631781..21633550,2	K562	blood:

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10218879	0.96[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10218952	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10218971	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10218986	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11012642	0.89[ASN][1000 genomes]
rs11012644	1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs11012645	0.89[ASN][1000 genomes]
rs11012646	0.89[ASN][1000 genomes]
rs11012648	0.89[ASN][1000 genomes]
rs11012658	0.89[ASN][1000 genomes]
rs11012665	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11012673	0.93[EUR][1000 genomes]
rs12240956	0.89[ASN][1000 genomes]
rs12244309	0.87[CEU][hapmap]
rs12248522	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12250778	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12256314	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12359942	0.89[ASN][1000 genomes]
rs13377089	0.89[ASN][1000 genomes]
rs16921726	1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs2360046	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28476641	0.89[ASN][1000 genomes]
rs34019318	0.91[EUR][1000 genomes]
rs34299719	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55638725	0.89[ASN][1000 genomes]
rs55672286	0.89[ASN][1000 genomes]
rs60875963	0.89[ASN][1000 genomes]
rs61851539	1.00[ASN][1000 genomes]
rs61851542	1.00[ASN][1000 genomes]
rs7080191	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7085637	0.89[ASN][1000 genomes]
rs7090939	0.95[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs7091420	0.95[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7894995	1.00[ASN][1000 genomes]
rs7900321	0.89[ASN][1000 genomes]
rs7907491	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7910000	0.89[ASN][1000 genomes]
rs7913116	1.00[ASN][1000 genomes]
rs7922927	1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs9971139	0.89[ASN][1000 genomes]
rs9971348	0.89[ASN][1000 genomes]
rs9971367	0.89[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	nsv530148	chr10:21065080-21724565	Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
2	nsv831807	chr10:21509185-21688043	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:21626000-21638800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr10:21626000-21638800	Weak transcription	Aorta	Aorta
3	chr10:21626400-21638800	Weak transcription	Right Atrium	heart
4	chr10:21626400-21639200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr10:21627000-21639000	Weak transcription	NHEK	skin
6	chr10:21627800-21638000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr10:21632600-21634400	Weak transcription	A549	lung

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links