Variant report

Variant	rs7803925
Chromosome Location	chr7:127101187-127101188
allele	A/C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10238301	0.89[AFR][1000 genomes]
rs10267540	0.93[AFR][1000 genomes]
rs10267624	0.93[AFR][1000 genomes]
rs11971040	0.95[AFR][1000 genomes]
rs11971083	0.95[AFR][1000 genomes]
rs11977840	0.95[AFR][1000 genomes]
rs12706812	0.89[YRI][hapmap]
rs13223469	0.86[YRI][hapmap]
rs13242010	0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13309123	1.00[YRI][hapmap];0.90[AFR][1000 genomes]
rs1361946	0.81[YRI][hapmap]
rs1419411	0.89[AFR][1000 genomes]
rs1582251	0.93[AFR][1000 genomes]
rs1582252	0.95[AFR][1000 genomes]
rs17133014	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1894722	0.90[YRI][hapmap];0.87[AFR][1000 genomes]
rs2213966	0.93[AFR][1000 genomes]
rs2213967	0.93[AFR][1000 genomes]
rs2301561	0.89[AFR][1000 genomes]
rs6467128	0.93[AFR][1000 genomes]
rs6942509	0.95[AFR][1000 genomes]
rs6946059	0.90[AFR][1000 genomes]
rs6949560	0.84[AFR][1000 genomes]
rs6958074	0.89[AFR][1000 genomes]
rs6958391	0.92[AFR][1000 genomes]
rs6961001	0.95[AFR][1000 genomes]
rs6961344	0.95[AFR][1000 genomes]
rs6962782	0.90[YRI][hapmap];0.84[AFR][1000 genomes]
rs6963011	0.87[AFR][1000 genomes]
rs6963346	0.95[AFR][1000 genomes]
rs6964250	0.95[AFR][1000 genomes]
rs6964923	0.95[AFR][1000 genomes]
rs6965471	0.93[AFR][1000 genomes]
rs6966790	0.90[YRI][hapmap];0.84[AFR][1000 genomes]
rs6968152	0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6976096	0.93[AFR][1000 genomes]
rs6976225	0.95[AFR][1000 genomes]
rs6976434	0.91[AFR][1000 genomes]
rs6977367	0.95[AFR][1000 genomes]
rs7784526	0.89[AFR][1000 genomes]
rs7786742	0.95[AFR][1000 genomes]
rs7789682	0.84[AFR][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	esv1820283	chr7:127101187-127110765	Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:127097400-127116000	Weak transcription	Pancreas	Pancrea

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links