Variant report

Variant	rs8007491
Chromosome Location	chr14:104480201-104480202
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ASPG-4	chr14:104479979-104480268	NONHSAT040236

Extended variants
information (count: 60 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs10130042	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10131031	1.00[ASN][1000 genomes]
rs10131231	1.00[ASN][1000 genomes]
rs10133836	0.81[YRI][hapmap]
rs10137517	0.85[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs10137676	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10137889	1.00[ASN][1000 genomes]
rs10139210	1.00[ASN][1000 genomes]
rs10140436	0.87[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs10141374	1.00[ASN][1000 genomes]
rs10142956	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10149898	1.00[ASN][1000 genomes]
rs10151165	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1187452	0.81[YRI][hapmap]
rs1187453	0.81[YRI][hapmap]
rs12436665	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1885596	0.81[YRI][hapmap]
rs1951583	0.86[YRI][hapmap]
rs2295662	1.00[ASN][1000 genomes]
rs2368996	0.91[YRI][hapmap];0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs28416628	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs28439019	1.00[ASN][1000 genomes]
rs28514602	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs28555097	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs28593161	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs28715405	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs28841005	0.87[AMR][1000 genomes]
rs4900606	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4906388	1.00[ASN][1000 genomes]
rs4906393	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4906394	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4906400	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4906403	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4906407	0.87[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs4906412	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4906414	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs55746000	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs55866217	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs56050561	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs56279366	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs56872578	1.00[ASN][1000 genomes]
rs58128911	0.87[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs58220415	1.00[ASN][1000 genomes]
rs59838226	1.00[ASN][1000 genomes]
rs7150795	0.95[YRI][hapmap];0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7161153	0.81[YRI][hapmap]
rs74086783	1.00[ASN][1000 genomes]
rs74086977	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs8004485	1.00[ASN][1000 genomes]
rs8020110	1.00[JPT][hapmap]
rs9324070	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9671924	0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1045162	chr14:104140525-104594841	Flanking Active TSS Strong transcription Bivalent Enhancer Enhancers Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
2	nsv542204	chr14:104140525-104594841	Active TSS Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
3	nsv902319	chr14:104255083-104620077	Weak transcription Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	64 gene(s)	inside rSNPs	diseases
4	nsv1048353	chr14:104361402-104483286	Flanking Active TSS Active TSS Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
5	nsv1049690	chr14:104411621-104575838	Enhancers ZNF genes & repeats Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
6	nsv542208	chr14:104411621-104575838	Enhancers ZNF genes & repeats Genic enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
7	nsv526680	chr14:104427043-104568472	Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
8	nsv1047990	chr14:104460605-104556463	Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:104473600-104495400	Weak transcription	Primary monocytes fromperipheralblood	blood
2	chr14:104474000-104491600	Weak transcription	Primary neutrophils fromperipheralblood	blood
3	chr14:104477200-104481600	Weak transcription	Monocytes-CD14+_RO01746	blood
4	chr14:104478800-104480600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
5	chr14:104478800-104483400	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr14:104478800-104488800	Weak transcription	Left Ventricle	heart
7	chr14:104479800-104481000	Weak transcription	Hela-S3	cervix

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links