Variant report

Variant	rs10515601
Chromosome Location	chr5:147336286-147336287
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10515597	0.85[ASN][1000 genomes]
rs10515599	0.86[ASN][1000 genomes]
rs17774838	0.82[ASN][1000 genomes]
rs34578922	0.82[ASN][1000 genomes]
rs34733654	0.86[ASN][1000 genomes]
rs35020001	0.82[ASN][1000 genomes]
rs35783964	0.82[ASN][1000 genomes]
rs35861469	0.82[ASN][1000 genomes]
rs71580469	0.86[ASN][1000 genomes]
rs71580474	0.80[ASN][1000 genomes]
rs7724336	0.86[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	esv3334831	chr5:147165950-147339765	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv1028477	chr5:147255013-147416217	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	esv16820	chr5:147320290-147337996	Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	esv3692876	chr5:147326902-147337164	Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS Strong transcription ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	esv2760927	chr5:147327342-147343763	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv441968	chr5:147327346-147337913	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv514328	chr5:147329263-147337727	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv818388	chr5:147333945-147337164	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:147326600-147345200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr5:147327000-147343200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr5:147327200-147343400	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr5:147328400-147337600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr5:147328400-147343400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr5:147331800-147343000	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr5:147335200-147338000	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr5:147335400-147336600	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr5:147335400-147336600	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr5:147335400-147337600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr5:147335600-147336400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr5:147335600-147336400	Enhancers	Hela-S3	cervix
13	chr5:147335800-147336400	Genic enhancers	HUES6 Cell Line	embryonic stem cell
14	chr5:147335800-147336600	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr5:147335800-147343200	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr5:147336000-147336400	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr5:147336000-147336800	Flanking Active TSS	NHEK	skin
18	chr5:147336200-147336400	Enhancers	H1 Cell Line	embryonic stem cell
19	chr5:147336200-147336400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr5:147336200-147336600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr5:147336200-147336600	Flanking Active TSS	HMEC	breast
22	chr5:147336200-147336800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links