Variant report

Variant	rs6680645
Chromosome Location	chr1:184231798-184231799
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:184207341..184210185-chr1:184231438..184233613,2	K562	blood:

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10158834	0.86[AFR][1000 genomes]
rs10494579	1.00[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs1111087	1.00[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs13375618	1.00[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs13375785	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs16822649	0.88[ASN][1000 genomes]
rs16822650	0.88[ASN][1000 genomes]
rs16822722	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs16822757	1.00[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs16822764	1.00[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs16822766	1.00[AMR][1000 genomes]
rs16822783	1.00[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs16822793	1.00[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs1810915	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs1930289	1.00[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs2161987	0.88[ASN][1000 genomes]
rs4354502	1.00[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs4543760	1.00[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs56797986	1.00[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs59737381	1.00[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs59786945	0.84[ASN][1000 genomes]
rs59949779	0.88[ASN][1000 genomes]
rs6656900	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs6669875	1.00[AMR][1000 genomes]
rs73057576	0.88[ASN][1000 genomes]
rs73057582	0.83[ASN][1000 genomes]
rs73057595	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs73057598	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs73059524	1.00[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs73059529	1.00[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs73059544	1.00[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs7543951	0.88[ASN][1000 genomes]
rs7552391	0.83[ASN][1000 genomes]
rs755483	0.88[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530079	chr1:183797938-184639971	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:184224400-184233000	Weak transcription	Fetal Heart	heart
2	chr1:184225800-184233200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr1:184227800-184239800	Weak transcription	Psoas Muscle	Psoas
4	chr1:184230600-184241600	Weak transcription	NHLF	lung

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links