Variant report

Variant	rs3845344
Chromosome Location	chr1:75001480-75001481
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs10218727	0.85[EUR][1000 genomes]
rs1040070	0.85[CEU][hapmap]
rs10493544	0.85[CEU][hapmap]
rs10890130	0.96[CEU][hapmap];0.80[GIH][hapmap];0.89[TSI][hapmap];0.89[EUR][1000 genomes]
rs11210477	0.92[CEU][hapmap];0.80[GIH][hapmap];0.80[MEX][hapmap];0.91[TSI][hapmap];0.89[EUR][1000 genomes]
rs11210478	0.96[CEU][hapmap];0.81[TSI][hapmap];0.86[EUR][1000 genomes]
rs12036473	0.96[CEU][hapmap];0.89[CHB][hapmap];0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12041852	0.89[CEU][hapmap]
rs12041912	0.89[CEU][hapmap]
rs12042908	0.89[CEU][hapmap]
rs12142020	0.96[CEU][hapmap]
rs12566985	0.89[CEU][hapmap]
rs12568287	0.89[EUR][1000 genomes]
rs1514173	0.96[CEU][hapmap];0.90[EUR][1000 genomes]
rs1514174	0.85[CEU][hapmap]
rs1514175	0.83[EUR][1000 genomes]
rs1514176	0.88[CEU][hapmap];0.83[EUR][1000 genomes]
rs1514177	0.88[CEU][hapmap];0.82[TSI][hapmap];0.83[EUR][1000 genomes]
rs2344508	0.89[CEU][hapmap]
rs34062471	0.86[EUR][1000 genomes]
rs3765680	0.96[CEU][hapmap];0.87[EUR][1000 genomes]
rs3765681	0.86[EUR][1000 genomes]
rs3843262	0.84[EUR][1000 genomes]
rs3845345	0.96[CEU][hapmap];0.80[GIH][hapmap];0.89[TSI][hapmap];0.89[EUR][1000 genomes]
rs3845347	0.89[CEU][hapmap]
rs3894212	0.96[CEU][hapmap];0.89[EUR][1000 genomes]
rs3895907	0.89[CEU][hapmap]
rs3911350	0.80[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs6604866	0.84[CEU][hapmap]
rs6604867	0.85[CEU][hapmap]
rs6604871	0.96[CEU][hapmap];0.84[TSI][hapmap];0.87[EUR][1000 genomes]
rs6604872	0.89[CEU][hapmap]
rs6656785	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6690871	0.84[CEU][hapmap]
rs6695685	0.87[EUR][1000 genomes]
rs6698622	0.96[CEU][hapmap];0.89[EUR][1000 genomes]
rs6698760	0.88[EUR][1000 genomes]
rs6703637	0.96[CEU][hapmap];0.88[EUR][1000 genomes]
rs7514705	0.89[CEU][hapmap]
rs7520945	0.89[CEU][hapmap]
rs7526762	0.88[CEU][hapmap]
rs7541513	0.94[ASN][1000 genomes]
rs7551507	0.89[CEU][hapmap]
rs7553158	0.89[CEU][hapmap]
rs7553348	0.89[CEU][hapmap]
rs953567	0.91[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1003171	chr1:74407468-75122270	Strong transcription Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
2	nsv535000	chr1:74407468-75122270	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
3	nsv1011745	chr1:74730942-75477618	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
4	nsv535003	chr1:74730942-75477618	Flanking Active TSS Active TSS Weak transcription Enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
5	nsv1010042	chr1:74798856-75001977	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
6	nsv830248	chr1:74962391-75144458	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
7	nsv1003356	chr1:74983681-75024938	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	nsv871900	chr1:74983835-75014195	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	esv2752695	chr1:74995225-75008411	Weak transcription Enhancers	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
10	esv2755299	chr1:74995225-75008411	Weak transcription Enhancers	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
11	nsv432387	chr1:74995225-75008411	Weak transcription Enhancers	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:74990200-75006600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr1:74990200-75017200	Weak transcription	Left Ventricle	heart
3	chr1:75000000-75001600	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr1:75000800-75012400	Weak transcription	Fetal Heart	heart

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