Variant report

Variant	rs6492905
Chromosome Location	chr15:39892402-39892403
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	chr15:39886322..39888433-chr15:39891587..39894545,2	K562	blood:

Variant related genes	Relation type
ENSG00000259279	Chromatin interaction

Extended variants
information (count: 89 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:82)

rs_ID	r²[population]
rs10152903	1.00[CHB][hapmap]
rs10152951	1.00[CHB][hapmap]
rs1038097	0.93[EUR][1000 genomes]
rs1051442	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[GIH][hapmap];0.92[MEX][hapmap];0.96[TSI][hapmap];0.85[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10520139	1.00[CHD][hapmap]
rs10520141	1.00[CEU][hapmap];1.00[CHB][hapmap];0.84[MEX][hapmap];0.89[TSI][hapmap];0.94[EUR][1000 genomes]
rs10520143	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[EUR][1000 genomes]
rs10520146	0.91[CEU][hapmap];1.00[CHB][hapmap];0.82[EUR][1000 genomes]
rs10520147	1.00[CHB][hapmap]
rs10520148	1.00[CHB][hapmap]
rs1073675	1.00[CHB][hapmap]
rs1382443	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[MEX][hapmap];0.89[TSI][hapmap];0.93[EUR][1000 genomes]
rs1382444	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[TSI][hapmap];0.93[EUR][1000 genomes]
rs1551946	1.00[CHD][hapmap]
rs16969167	1.00[CHB][hapmap]
rs16969487	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[EUR][1000 genomes]
rs16969491	0.86[CEU][hapmap];1.00[CHB][hapmap];0.93[EUR][1000 genomes]
rs16969546	1.00[CHD][hapmap]
rs16969547	1.00[CHB][hapmap];0.85[TSI][hapmap];0.83[EUR][1000 genomes]
rs16969559	1.00[CHD][hapmap]
rs16969560	1.00[CHD][hapmap]
rs16969663	1.00[CHB][hapmap]
rs16969664	1.00[CHB][hapmap]
rs16969666	1.00[CHB][hapmap]
rs16969672	1.00[CHB][hapmap]
rs16969679	1.00[CHB][hapmap]
rs16969680	1.00[CHB][hapmap]
rs16969688	1.00[CHB][hapmap]
rs17632916	1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs17633107	1.00[CEU][hapmap];1.00[CHB][hapmap];0.85[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs17633210	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[GIH][hapmap];0.84[MEX][hapmap];0.93[TSI][hapmap];0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs17705806	1.00[CEU][hapmap];1.00[CHB][hapmap];0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs17706083	1.00[CEU][hapmap];1.00[CHB][hapmap];0.84[MEX][hapmap];0.93[TSI][hapmap];0.81[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs17706179	1.00[CEU][hapmap];1.00[CHB][hapmap];0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1813493	0.93[EUR][1000 genomes]
rs1988082	0.84[EUR][1000 genomes]
rs1988555	0.87[EUR][1000 genomes]
rs1994380	1.00[CHB][hapmap]
rs2129457	1.00[CHB][hapmap]
rs2228262	1.00[CHB][hapmap]
rs2228263	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[GIH][hapmap];0.92[LWK][hapmap];0.92[MEX][hapmap];1.00[TSI][hapmap];0.81[YRI][hapmap];0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2411316	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[EUR][1000 genomes]
rs2618156	0.93[EUR][1000 genomes]
rs2618160	0.94[EUR][1000 genomes]
rs2618161	1.00[CEU][hapmap];1.00[CHB][hapmap];0.83[GIH][hapmap];0.93[TSI][hapmap];0.93[EUR][1000 genomes]
rs2618164	1.00[CEU][hapmap];0.83[GIH][hapmap];0.93[TSI][hapmap];0.95[EUR][1000 genomes]
rs2618165	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs2618167	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[EUR][1000 genomes]
rs2664123	0.94[EUR][1000 genomes]
rs2664136	0.93[EUR][1000 genomes]
rs2664137	0.93[EUR][1000 genomes]
rs2664138	0.92[CEU][hapmap];1.00[CHB][hapmap];0.93[EUR][1000 genomes]
rs2664140	0.94[EUR][1000 genomes]
rs2664142	0.94[EUR][1000 genomes]
rs28377784	0.94[EUR][1000 genomes]
rs28549326	0.94[EUR][1000 genomes]
rs28619289	0.94[EUR][1000 genomes]
rs28653011	0.94[EUR][1000 genomes]
rs34878675	0.89[EUR][1000 genomes]
rs41315060	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4319740	0.83[CEU][hapmap]
rs4415979	1.00[CEU][hapmap];1.00[CHB][hapmap];0.84[MEX][hapmap];0.96[TSI][hapmap];0.81[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4503768	1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[EUR][1000 genomes]
rs45461294	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs4923835	0.92[CEU][hapmap];1.00[CHB][hapmap];0.87[EUR][1000 genomes]
rs58188999	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs59578395	0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs59628570	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7172155	1.00[CHB][hapmap]
rs7173948	1.00[CHB][hapmap]
rs7179604	1.00[CHB][hapmap]
rs7181354	1.00[CHB][hapmap]
rs7182423	1.00[CHB][hapmap]
rs74008647	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs74008648	0.94[EUR][1000 genomes]
rs8024038	1.00[CHD][hapmap]
rs8041266	1.00[CHB][hapmap]
rs880270	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[EUR][1000 genomes]
rs937961	1.00[CHB][hapmap]
rs937962	1.00[CHB][hapmap]
rs954152	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9972350	1.00[CEU][hapmap];1.00[CHB][hapmap];0.84[MEX][hapmap];0.93[TSI][hapmap];0.94[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1049682	chr15:39657279-40027403	Enhancers Flanking Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv542361	chr15:39657279-40027403	Weak transcription Strong transcription Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
3	esv3373125	chr15:39691567-40061262	Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
4	nsv904094	chr15:39738006-39976057	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
5	nsv832977	chr15:39817512-39981520	Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
6	nsv1048628	chr15:39877498-39940104	Enhancers Genic enhancers Strong transcription ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
7	nsv1502	chr15:39884314-39928968	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs6492905	C15orf57	cis	parietal	SCAN

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:39888400-39899200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr15:39888400-39899200	Weak transcription	Esophagus	oesophagus
3	chr15:39888400-39899200	Weak transcription	Left Ventricle	heart
4	chr15:39888400-39900600	Weak transcription	Fetal Brain Female	brain
5	chr15:39888400-39901000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr15:39888400-39901000	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr15:39888800-39894400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
8	chr15:39889200-39901200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr15:39889800-39893200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr15:39890200-39900800	Weak transcription	HMEC	breast
11	chr15:39890600-39897000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr15:39891400-39892600	Enhancers	HUVEC	blood vessel
13	chr15:39891800-39892600	Enhancers	Osteobl	bone
14	chr15:39891800-39893200	Enhancers	Muscle Satellite Cultured Cells	--
15	chr15:39892000-39892600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr15:39892200-39892600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr15:39892200-39899200	Weak transcription	Rectal Mucosa Donor 31	rectum
18	chr15:39892400-39892800	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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