Variant report

Variant	rs73091242
Chromosome Location	chr3:56151364-56151365
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 88 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:86)

rs_ID	r²[population]
rs10461036	0.89[EUR][1000 genomes]
rs10510779	0.90[EUR][1000 genomes]
rs10510780	0.90[EUR][1000 genomes]
rs10510781	0.91[EUR][1000 genomes]
rs11428238	0.90[EUR][1000 genomes]
rs13315826	0.85[EUR][1000 genomes]
rs13326476	0.85[EUR][1000 genomes]
rs13326628	0.85[EUR][1000 genomes]
rs17056469	0.87[EUR][1000 genomes]
rs17056472	0.88[EUR][1000 genomes]
rs17235263	0.92[EUR][1000 genomes]
rs17235291	0.92[EUR][1000 genomes]
rs17235305	0.92[EUR][1000 genomes]
rs17235368	0.85[EUR][1000 genomes]
rs17235375	0.92[EUR][1000 genomes]
rs17235382	0.85[EUR][1000 genomes]
rs17235389	0.85[EUR][1000 genomes]
rs17235396	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs17825183	0.92[EUR][1000 genomes]
rs17825189	0.92[EUR][1000 genomes]
rs17825201	0.85[EUR][1000 genomes]
rs17825207	0.92[EUR][1000 genomes]
rs17825213	0.92[EUR][1000 genomes]
rs17825219	0.85[EUR][1000 genomes]
rs17825278	0.92[EUR][1000 genomes]
rs28464790	0.85[EUR][1000 genomes]
rs35563958	0.90[EUR][1000 genomes]
rs58375176	0.90[EUR][1000 genomes]
rs61401343	0.90[EUR][1000 genomes]
rs6800841	0.80[EUR][1000 genomes]
rs6807938	0.83[EUR][1000 genomes]
rs73089299	0.85[EUR][1000 genomes]
rs73091008	0.85[EUR][1000 genomes]
rs73091011	0.89[EUR][1000 genomes]
rs73091012	0.89[EUR][1000 genomes]
rs73091207	0.92[EUR][1000 genomes]
rs73091213	0.84[EUR][1000 genomes]
rs73091231	0.85[EUR][1000 genomes]
rs73091236	0.91[EUR][1000 genomes]
rs73091241	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7625220	0.87[EUR][1000 genomes]
rs7625230	0.86[EUR][1000 genomes]
rs7625422	0.87[EUR][1000 genomes]
rs7629639	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7629769	0.88[EUR][1000 genomes]
rs7632887	0.87[EUR][1000 genomes]
rs7632901	0.87[EUR][1000 genomes]
rs7651932	0.88[EUR][1000 genomes]
rs9311594	0.84[EUR][1000 genomes]
rs9311595	0.85[EUR][1000 genomes]
rs9311596	0.84[EUR][1000 genomes]
rs9810107	0.85[EUR][1000 genomes]
rs9811060	0.85[EUR][1000 genomes]
rs9811789	0.85[EUR][1000 genomes]
rs9811790	0.85[EUR][1000 genomes]
rs9814900	0.85[EUR][1000 genomes]
rs9815611	0.85[EUR][1000 genomes]
rs9817492	0.85[EUR][1000 genomes]
rs9817542	0.85[EUR][1000 genomes]
rs9819890	0.80[EUR][1000 genomes]
rs9820348	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs9820493	0.88[EUR][1000 genomes]
rs9827514	0.85[EUR][1000 genomes]
rs9828337	0.85[EUR][1000 genomes]
rs9830503	0.88[EUR][1000 genomes]
rs9831925	0.84[EUR][1000 genomes]
rs9837290	0.85[EUR][1000 genomes]
rs9842617	0.80[EUR][1000 genomes]
rs9844291	0.85[EUR][1000 genomes]
rs9855148	0.85[EUR][1000 genomes]
rs9855836	0.85[EUR][1000 genomes]
rs9857687	0.80[EUR][1000 genomes]
rs9860909	0.85[EUR][1000 genomes]
rs9861486	0.85[EUR][1000 genomes]
rs9862215	0.85[EUR][1000 genomes]
rs9866951	0.85[EUR][1000 genomes]
rs9869654	0.85[EUR][1000 genomes]
rs9870248	0.83[EUR][1000 genomes]
rs9870989	0.85[EUR][1000 genomes]
rs9871223	0.85[EUR][1000 genomes]
rs9874507	0.86[EUR][1000 genomes]
rs9874662	0.84[EUR][1000 genomes]
rs9880824	0.85[EUR][1000 genomes]
rs9881126	0.85[EUR][1000 genomes]
rs9882373	0.85[EUR][1000 genomes]
rs9883636	0.85[EUR][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	nsv1013063	chr3:55835413-56173713	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1009709	chr3:56000827-56294945	Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:56144600-56152200	Enhancers	HUES64 Cell Line	embryonic stem cell
2	chr3:56144800-56152400	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr3:56147200-56152400	Enhancers	iPS-20b Cell Line	embryonic stem cell
4	chr3:56147400-56152000	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr3:56147600-56152400	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr3:56147800-56152400	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr3:56148000-56152200	Enhancers	H9 Cell Line	embryonic stem cell
8	chr3:56149000-56152000	Enhancers	H1 Cell Line	embryonic stem cell
9	chr3:56150000-56152600	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr3:56150400-56152200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
11	chr3:56150400-56152200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr3:56150600-56151400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr3:56150600-56152400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr3:56151000-56151800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links