Variant report

Variant	rs2029682
Chromosome Location	chr1:76341619-76341620
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	chr1:76256252..76258786-chr1:76340738..76342721,2	K562	blood:

Variant related genes	Relation type
ENSG00000137955	Chromatin interaction

Extended variants
information (count: 77 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:68)

rs_ID	r²[population]
rs1001160	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap]
rs10873797	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs11161699	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11161848	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs11161887	0.84[CEU][hapmap]
rs11161902	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11163967	1.00[JPT][hapmap]
rs1146631	1.00[JPT][hapmap]
rs1146634	1.00[JPT][hapmap]
rs1146636	1.00[JPT][hapmap]
rs1146644	1.00[JPT][hapmap]
rs11578480	0.92[CEU][hapmap];1.00[JPT][hapmap]
rs11584577	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11588643	1.00[CEU][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1159215	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11810154	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12043473	1.00[JPT][hapmap]
rs12118229	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12118306	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12130832	0.96[CEU][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes]
rs12138898	0.87[ASN][1000 genomes]
rs12142247	0.96[CEU][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes]
rs1250876	0.84[CEU][hapmap]
rs1250880	0.81[CEU][hapmap]
rs1251533	0.81[ASN][1000 genomes]
rs1251584	0.81[ASN][1000 genomes]
rs1303870	0.84[CEU][hapmap]
rs1463812	1.00[JPT][hapmap]
rs1498311	1.00[CEU][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1628063	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap]
rs1630302	0.87[ASN][1000 genomes]
rs1630587	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap]
rs1689270	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17647178	0.92[CEU][hapmap];1.00[JPT][hapmap];0.80[EUR][1000 genomes]
rs17647711	0.88[EUR][1000 genomes]
rs1770889	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap]
rs1796795	0.87[ASN][1000 genomes]
rs1796810	0.87[ASN][1000 genomes]
rs1796813	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1796815	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1796827	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap]
rs1846233	0.88[CEU][hapmap]
rs1856791	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs1908089	0.85[CEU][hapmap]
rs2307077	0.89[YRI][hapmap]
rs4638068	0.88[CEU][hapmap];1.00[JPT][hapmap]
rs4646960	0.80[EUR][1000 genomes]
rs5745323	1.00[JPT][hapmap]
rs5745325	0.96[CEU][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs5745331	1.00[CEU][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs5745347	1.00[CEU][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs5745383	1.00[CEU][hapmap];1.00[JPT][hapmap];0.80[YRI][hapmap];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs5745394	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs5745430	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs5745523	0.85[CEU][hapmap]
rs5745543	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap]
rs5745545	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap];0.87[ASN][1000 genomes]
rs5745546	0.85[CEU][hapmap]
rs5745547	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap]
rs6593520	1.00[JPT][hapmap]
rs6593521	1.00[JPT][hapmap]
rs6656501	1.00[CEU][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6664254	0.85[EUR][1000 genomes]
rs6675212	0.85[EUR][1000 genomes]
rs721204	1.00[JPT][hapmap]
rs72979226	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7516477	0.84[CEU][hapmap]
rs879268	1.00[JPT][hapmap];0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv519329	chr1:75830438-76358591	Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	nsv1014072	chr1:76200531-76460726	Genic enhancers Enhancers Strong transcription Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
3	nsv535005	chr1:76200531-76460726	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
4	esv1795237	chr1:76268573-76383565	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	esv1800125	chr1:76269439-76379497	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	esv1799260	chr1:76269439-76383297	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
7	esv1847721	chr1:76269439-76383565	Weak transcription ZNF genes & repeats Enhancers Strong transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
8	nsv1004669	chr1:76301198-76409451	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
9	nsv871671	chr1:76304215-76391646	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	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