Variant report

Variant	rs288079
Chromosome Location	chr2:210435476-210435477
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 98 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:98)

rs_ID	r²[population]
rs10172200	0.80[JPT][hapmap]
rs10196314	0.80[JPT][hapmap]
rs10196600	0.80[JPT][hapmap]
rs10198751	0.85[JPT][hapmap]
rs10204207	0.93[ASN][1000 genomes]
rs10206817	0.85[JPT][hapmap]
rs10207186	0.80[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10490021	0.80[JPT][hapmap]
rs10932305	0.80[JPT][hapmap]
rs11692075	0.80[JPT][hapmap]
rs12614031	0.80[JPT][hapmap]
rs12615372	0.93[JPT][hapmap]
rs12616589	0.87[JPT][hapmap]
rs12618080	0.80[JPT][hapmap]
rs12620654	0.82[CHB][hapmap];0.93[JPT][hapmap];0.88[ASN][1000 genomes]
rs12623006	0.82[EUR][1000 genomes]
rs12992342	0.84[EUR][1000 genomes]
rs13385585	0.80[JPT][hapmap]
rs13419929	1.00[CEU][hapmap];0.83[CHB][hapmap];0.93[JPT][hapmap];0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1396779	0.93[AFR][1000 genomes];0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1509465	1.00[CEU][hapmap];0.93[JPT][hapmap];0.84[EUR][1000 genomes]
rs1509468	0.82[JPT][hapmap]
rs1509469	0.87[JPT][hapmap]
rs16843022	0.82[CEU][hapmap]
rs16843351	0.86[JPT][hapmap]
rs16843354	0.80[JPT][hapmap]
rs16843360	0.86[JPT][hapmap]
rs16843382	0.80[JPT][hapmap]
rs16843453	0.80[JPT][hapmap]
rs16843614	0.80[JPT][hapmap]
rs16843618	0.80[JPT][hapmap]
rs169636	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2048250	1.00[CEU][hapmap];0.93[JPT][hapmap];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2191910	0.80[JPT][hapmap]
rs2239552	0.80[JPT][hapmap]
rs2239553	0.80[JPT][hapmap]
rs2239672	0.80[JPT][hapmap]
rs2268042	0.80[JPT][hapmap]
rs2268044	0.80[JPT][hapmap]
rs2271252	0.80[JPT][hapmap]
rs2286850	0.80[JPT][hapmap]
rs2300154	0.80[JPT][hapmap]
rs2366112	0.93[JPT][hapmap]
rs2663648	1.00[CEU][hapmap];0.93[JPT][hapmap];0.84[EUR][1000 genomes]
rs2663659	0.91[CEU][hapmap];0.93[JPT][hapmap]
rs2710477	0.92[JPT][hapmap]
rs2710482	0.80[JPT][hapmap]
rs2710486	1.00[CEU][hapmap];0.93[JPT][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs288070	1.00[CEU][hapmap];0.92[CHB][hapmap];0.80[JPT][hapmap];0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs288071	1.00[CEU][hapmap];0.92[CHB][hapmap];0.80[JPT][hapmap];0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs288081	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs288084	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs288087	1.00[CEU][hapmap];0.84[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs288088	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs288089	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs288091	0.82[AFR][1000 genomes];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs288094	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs288096	1.00[CEU][hapmap];0.92[CHB][hapmap];0.80[JPT][hapmap];0.86[AMR][1000 genomes];0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs3754597	0.80[JPT][hapmap]
rs3768810	0.80[JPT][hapmap]
rs3768813	0.80[JPT][hapmap]
rs3768814	0.80[JPT][hapmap]
rs3768815	0.80[JPT][hapmap]
rs3768816	0.80[JPT][hapmap]
rs3768822	0.80[JPT][hapmap]
rs3768826	0.80[JPT][hapmap]
rs3768832	0.80[JPT][hapmap]
rs3768833	0.80[JPT][hapmap]
rs3768834	0.80[JPT][hapmap]
rs3768835	0.80[JPT][hapmap]
rs3820746	0.83[JPT][hapmap]
rs3820748	0.80[JPT][hapmap]
rs4673486	0.80[JPT][hapmap]
rs55703768	0.81[EUR][1000 genomes]
rs56023260	0.86[ASN][1000 genomes]
rs56164239	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs56677957	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs57781584	0.82[ASN][1000 genomes]
rs60120123	0.82[EUR][1000 genomes]
rs60497472	0.82[ASN][1000 genomes]
rs6709925	0.80[JPT][hapmap]
rs6717554	0.80[JPT][hapmap]
rs6720659	0.80[JPT][hapmap]
rs6722585	0.84[ASN][1000 genomes]
rs6724834	0.80[JPT][hapmap]
rs6726061	1.00[CEU][hapmap];0.84[CHB][hapmap];0.93[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6733319	0.84[CHB][hapmap];0.93[JPT][hapmap]
rs6746029	0.80[JPT][hapmap]
rs723683	0.80[JPT][hapmap]
rs73071034	0.83[ASN][1000 genomes]
rs741006	0.80[JPT][hapmap]
rs7568260	0.83[ASN][1000 genomes]
rs7593381	0.92[CHB][hapmap];0.84[ASN][1000 genomes]
rs7594601	0.80[JPT][hapmap]
rs7594825	0.84[CHB][hapmap]
rs906831	1.00[CEU][hapmap];0.93[JPT][hapmap]
rs9288410	1.00[CEU][hapmap];0.93[JPT][hapmap];0.82[EUR][1000 genomes]
rs994862	0.80[JPT][hapmap]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:210431600-210441200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr2:210432800-210440400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr2:210434400-210441200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr2:210435200-210442200	Weak transcription	Pancreatic Islets	Pancreatic Islet

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links