Variant report

Variant	rs28723590
Chromosome Location	chr1:47573834-47573835
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10890458	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10890459	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10890460	0.82[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs1110425	0.80[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs11211450	0.83[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs12564635	0.83[ASN][1000 genomes]
rs12734327	0.82[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs1847222	0.81[AMR][1000 genomes]
rs1847223	0.83[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs1847224	0.82[AMR][1000 genomes]
rs3117713	0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs4314923	0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs4926785	0.80[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs4926786	0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs4926787	0.80[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs4926788	0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs4926789	0.80[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs4926791	0.80[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs4926792	0.80[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs4926793	0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs4926797	0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs4926804	0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs4926809	0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs4926826	0.82[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs6675902	0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs6690005	0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs6693145	0.80[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs6701611	0.80[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs7519903	0.80[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs7526674	0.83[AMR][1000 genomes]
rs7540264	0.81[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2763300	chr1:47358532-47628774	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv916813	chr1:47435635-47666179	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
3	nsv870705	chr1:47533705-47620126	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv871010	chr1:47533705-47637999	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv870899	chr1:47548974-47637999	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	esv13964	chr1:47565590-47574182	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:47572200-47574400	Enhancers	iPS-18 Cell Line	embryonic stem cell
2	chr1:47572200-47574800	Enhancers	HMEC	breast
3	chr1:47573200-47574800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr1:47573200-47578000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr1:47573600-47574000	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr1:47573600-47574400	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr1:47573600-47574400	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr1:47573600-47574600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr1:47573600-47575600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr1:47573600-47575600	Enhancers	Hela-S3	cervix
11	chr1:47573600-47575600	Enhancers	NHEK	skin
12	chr1:47573600-47577200	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr1:47573600-47578600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
14	chr1:47573800-47574200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr1:47573800-47574200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr1:47573800-47574600	Enhancers	HUVEC	blood vessel

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links