Variant report

Variant	rs10044667
Chromosome Location	chr5:89279260-89279261
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs10068046	0.88[ASN][1000 genomes]
rs10805864	0.86[EUR][1000 genomes]
rs10942581	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11949266	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11958908	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11958926	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12517492	0.92[CEU][hapmap];1.00[CHB][hapmap];0.82[JPT][hapmap];0.86[EUR][1000 genomes]
rs12519494	0.87[EUR][1000 genomes]
rs13362216	0.82[ASN][1000 genomes]
rs154193	0.84[EUR][1000 genomes]
rs1560208	0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs157305	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs157306	0.86[EUR][1000 genomes]
rs157307	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs157308	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs157311	0.86[EUR][1000 genomes]
rs157559	0.84[EUR][1000 genomes]
rs157560	0.84[EUR][1000 genomes]
rs157564	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1596431	0.86[EUR][1000 genomes]
rs1645412	0.87[EUR][1000 genomes]
rs166820	0.86[EUR][1000 genomes]
rs1698138	0.86[EUR][1000 genomes]
rs17589076	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs175965	0.92[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];0.86[EUR][1000 genomes]
rs280671	0.92[CEU][hapmap];1.00[CHB][hapmap];0.86[EUR][1000 genomes]
rs30713	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4019724	0.82[ASN][1000 genomes]
rs60448814	0.81[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs662339	0.92[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];0.86[EUR][1000 genomes]
rs6862722	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6871792	0.87[EUR][1000 genomes]
rs6883728	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs690558	0.92[CEU][hapmap];1.00[CHB][hapmap];0.82[JPT][hapmap];0.86[EUR][1000 genomes]
rs702845	0.92[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];0.85[EUR][1000 genomes]
rs818944	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs818945	0.86[EUR][1000 genomes]
rs818946	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs818947	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs818948	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs889293	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs924627	0.86[EUR][1000 genomes]
rs924628	0.86[EUR][1000 genomes]
rs9293534	0.84[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1021142	chr5:89102893-89897826	Active TSS Weak transcription Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
2	nsv537804	chr5:89102893-89897826	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
3	nsv917025	chr5:89208994-89855436	Enhancers Active TSS Strong transcription Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
4	esv3438759	chr5:89276596-89281994	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	inside rSNPs	n/a
5	esv3446012	chr5:89277896-89281194	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	inside rSNPs	n/a

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:89278600-89279400	Enhancers	ES-I3 Cell Line	embryonic stem cell
2	chr5:89278600-89283200	Weak transcription	NHDF-Ad	bronchial
3	chr5:89278800-89279400	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr5:89278800-89280000	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr5:89279000-89279400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr5:89279000-89279800	Enhancers	iPS-18 Cell Line	embryonic stem cell

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