Variant report

Variant	rs989774
Chromosome Location	chr8:113984662-113984663
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	chr8:113982822..113985286-chr8:113988301..113991083,2	K562	blood:

Extended variants
information (count: 164 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:145)

rs_ID	r²[population]
rs10092868	1.00[JPT][hapmap]
rs10094069	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10094486	0.81[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs10108312	1.00[JPT][hapmap]
rs10111703	1.00[JPT][hapmap]
rs1014321	1.00[JPT][hapmap]
rs1021875	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1021876	1.00[JPT][hapmap]
rs1021877	1.00[JPT][hapmap]
rs1021878	1.00[JPT][hapmap]
rs1034511	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1038192	1.00[JPT][hapmap]
rs10505199	1.00[CEU][hapmap];0.82[CHB][hapmap]
rs1073350	0.93[YRI][hapmap]
rs10808453	0.91[YRI][hapmap]
rs10955642	0.81[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs10955646	1.00[JPT][hapmap]
rs1156075	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1156076	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs1159225	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11985196	0.80[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs11990304	1.00[JPT][hapmap]
rs11995656	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs12541577	1.00[JPT][hapmap]
rs12550692	1.00[JPT][hapmap]
rs12675949	1.00[JPT][hapmap]
rs1351387	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1351388	1.00[JPT][hapmap]
rs1351392	1.00[JPT][hapmap]
rs1351393	0.92[YRI][hapmap]
rs1354446	1.00[JPT][hapmap]
rs1383293	1.00[JPT][hapmap]
rs1383294	1.00[JPT][hapmap]
rs1383296	1.00[JPT][hapmap]
rs1383298	1.00[JPT][hapmap];0.80[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs1383299	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1383300	1.00[JPT][hapmap]
rs1394269	1.00[JPT][hapmap]
rs1394270	1.00[JPT][hapmap]
rs1394271	1.00[JPT][hapmap]
rs1472724	1.00[JPT][hapmap]
rs1480443	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs1480446	1.00[JPT][hapmap]
rs1480448	1.00[JPT][hapmap]
rs1480455	1.00[JPT][hapmap]
rs1480463	1.00[JPT][hapmap]
rs1504336	0.93[YRI][hapmap];0.83[AFR][1000 genomes]
rs1504337	0.84[ASN][1000 genomes]
rs1504338	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1504339	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1504340	0.84[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs1504341	1.00[JPT][hapmap]
rs1504342	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs1504343	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1504346	1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap]
rs1504347	1.00[JPT][hapmap]
rs1522057	1.00[JPT][hapmap]
rs1522064	1.00[JPT][hapmap]
rs1532797	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs1532798	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1532799	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1566835	1.00[JPT][hapmap]
rs1600574	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17602288	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17602393	1.00[JPT][hapmap]
rs17602529	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17605667	1.00[JPT][hapmap]
rs17659540	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1817453	1.00[JPT][hapmap]
rs1857717	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1857718	1.00[JPT][hapmap]
rs1948845	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1969112	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1969113	1.00[JPT][hapmap]
rs2030506	1.00[JPT][hapmap]
rs2045539	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2125550	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2127689	1.00[JPT][hapmap]
rs2134838	1.00[JPT][hapmap]
rs2134839	1.00[JPT][hapmap]
rs2134840	1.00[JPT][hapmap]
rs2134842	1.00[JPT][hapmap]
rs2883836	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2883875	1.00[JPT][hapmap]
rs3853260	1.00[JPT][hapmap]
rs3853261	1.00[JPT][hapmap]
rs3912243	1.00[JPT][hapmap]
rs4242551	1.00[JPT][hapmap]
rs4437684	1.00[JPT][hapmap]
rs4509361	1.00[JPT][hapmap]
rs4876299	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4876300	1.00[JPT][hapmap]
rs4876502	1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap]
rs4876507	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs58021089	0.81[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs6982602	1.00[JPT][hapmap]
rs6993468	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6995484	1.00[JPT][hapmap]
rs6997105	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6999773	0.81[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs6999828	1.00[JPT][hapmap]
rs7004426	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7007093	1.00[JPT][hapmap]
rs7007990	1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs7013894	1.00[JPT][hapmap]
rs7014643	1.00[JPT][hapmap]
rs7015519	1.00[JPT][hapmap]
rs7015794	1.00[JPT][hapmap]
rs7015938	1.00[JPT][hapmap]
rs7812581	1.00[JPT][hapmap]
rs7812971	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs7817385	1.00[JPT][hapmap];0.80[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs7817505	1.00[JPT][hapmap];0.80[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs7820383	1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs7821294	1.00[JPT][hapmap]
rs7824314	1.00[JPT][hapmap];0.80[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs7824563	0.80[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs7824652	1.00[JPT][hapmap]
rs7828518	1.00[JPT][hapmap]
rs7829709	1.00[JPT][hapmap]
rs7829954	1.00[JPT][hapmap]
rs7834106	1.00[JPT][hapmap]
rs7835368	1.00[JPT][hapmap]
rs7836578	1.00[JPT][hapmap]
rs7840572	1.00[JPT][hapmap]
rs7840573	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7840935	1.00[JPT][hapmap]
rs899831	1.00[JPT][hapmap]
rs9283946	1.00[JPT][hapmap]
rs9297481	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9297482	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9297486	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9297487	0.92[YRI][hapmap]
rs9297488	1.00[JPT][hapmap]
rs9642818	1.00[JPT][hapmap]
rs964763	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs964764	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs971124	1.00[JPT][hapmap]
rs972149	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs974760	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs979895	1.00[JPT][hapmap]
rs979896	1.00[JPT][hapmap]
rs990220	1.00[JPT][hapmap]
rs990745	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs996252	1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2753595	chr8:113283214-114190390	Enhancers Weak transcription Active TSS Strong transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
2	esv2754315	chr8:113736824-114048824	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv891326	chr8:113777669-114091732	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv891327	chr8:113828980-114109342	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	esv2756439	chr8:113920441-114060648	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv2753160	chr8:113920441-114190390	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv891328	chr8:113929201-113994873	Enhancers Weak transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a
8	nsv891329	chr8:113929201-114021484	Enhancers Weak transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
9	nsv534557	chr8:113929740-114131155	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
10	esv2756532	chr8:113931884-114120265	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
11	nsv1030305	chr8:113942232-113992360	Enhancers Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a
12	nsv891330	chr8:113942738-114009227	Enhancers Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
13	nsv891331	chr8:113951265-114108147	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
14	nsv1017791	chr8:113953316-114017477	Enhancers Weak transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
15	nsv1020528	chr8:113955730-113999858	Enhancers Weak transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a
16	nsv1015797	chr8:113958358-113999858	Enhancers Weak transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a
17	nsv465766	chr8:113959206-114025705	Enhancers Weak transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
18	nsv611908	chr8:113959206-114025705	Enhancers Weak transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
19	esv2752734	chr8:113972011-114113977	Enhancers Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

Quick Search:

Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links