Variant report

Variant	rs7160749
Chromosome Location	chr14:81106217-81106218
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:81105972..81108126-chr14:81297370..81299564,2	K562	blood:

Extended variants
information (count: 65 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:63)

rs_ID	r²[population]
rs10130406	0.93[ASN][1000 genomes]
rs10130415	0.92[ASN][1000 genomes]
rs10130508	0.98[ASN][1000 genomes]
rs10130522	0.98[ASN][1000 genomes]
rs10131100	0.98[ASN][1000 genomes]
rs10135604	0.81[CEU][hapmap];0.88[EUR][1000 genomes]
rs10136394	0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10139763	0.95[ASN][1000 genomes]
rs10140109	0.95[ASN][1000 genomes]
rs10143228	0.98[ASN][1000 genomes]
rs10145319	0.85[EUR][1000 genomes]
rs10146465	0.92[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10146576	0.98[ASN][1000 genomes]
rs10146659	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10146748	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10147245	0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10150384	0.89[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs10151209	0.98[ASN][1000 genomes]
rs11159468	0.90[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs11159469	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11844906	0.98[ASN][1000 genomes]
rs11847664	0.97[ASN][1000 genomes]
rs12588381	0.95[ASN][1000 genomes]
rs12889844	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1547499	0.90[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs1547500	0.90[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs17110851	0.94[JPT][hapmap]
rs17110854	0.94[JPT][hapmap]
rs17110914	1.00[CHB][hapmap];0.94[JPT][hapmap];0.95[ASN][1000 genomes]
rs17110923	0.87[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs17110926	1.00[CHB][hapmap];0.94[JPT][hapmap];0.95[ASN][1000 genomes]
rs17110955	0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1868546	0.82[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs1972298	0.98[ASN][1000 genomes]
rs2167148	0.98[ASN][1000 genomes]
rs2596116	0.88[CEU][hapmap]
rs2596117	0.83[ASN][1000 genomes]
rs2597083	0.90[CHB][hapmap];0.93[JPT][hapmap];0.98[ASN][1000 genomes]
rs2597085	0.89[ASN][1000 genomes]
rs2619659	1.00[JPT][hapmap]
rs2619667	0.83[ASN][1000 genomes]
rs34481438	0.86[ASN][1000 genomes]
rs56256007	0.83[ASN][1000 genomes]
rs58902662	0.85[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs61429001	0.82[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs61979379	0.95[ASN][1000 genomes]
rs61979380	0.81[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs61979382	0.81[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs6574594	1.00[CHB][hapmap];0.93[JPT][hapmap];0.93[ASN][1000 genomes]
rs6574595	0.95[ASN][1000 genomes]
rs7140355	0.95[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs7140933	0.98[ASN][1000 genomes]
rs7148223	0.98[ASN][1000 genomes]
rs7148754	0.98[ASN][1000 genomes]
rs7148885	0.95[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs7149459	1.00[CHB][hapmap];0.93[JPT][hapmap];0.95[ASN][1000 genomes]
rs7153484	0.90[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs7157843	0.90[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs8007426	0.80[CHB][hapmap]
rs8008043	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs8010347	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8012237	0.98[ASN][1000 genomes]
rs8016151	0.82[CEU][hapmap];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	nsv869348	chr14:80921098-81535754	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv565290	chr14:81085129-81230117	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:81083400-81109400	Weak transcription	Dnd41	blood
2	chr14:81099000-81109600	Weak transcription	Thymus	Thymus
3	chr14:81103200-81106400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr14:81103800-81106400	Enhancers	Hela-S3	cervix
5	chr14:81104800-81106400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr14:81104800-81106600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr14:81105400-81112800	Weak transcription	HSMM	muscle
8	chr14:81105800-81107000	Enhancers	A549	lung
9	chr14:81105800-81107200	Enhancers	HUVEC	blood vessel
10	chr14:81105800-81112000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr14:81106200-81112400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr14:81106200-81135400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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