Variant report

Variant	rs4917043
Chromosome Location	chr7:48339977-48339978
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10280046	0.91[CEU][hapmap];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10499676	0.80[CEU][hapmap];1.00[ASN][1000 genomes]
rs13233225	0.88[CEU][hapmap];1.00[ASN][1000 genomes]
rs13244649	0.85[CEU][hapmap];1.00[ASN][1000 genomes]
rs1526096	0.88[CEU][hapmap];1.00[ASN][1000 genomes]
rs1526097	0.85[CEU][hapmap];1.00[ASN][1000 genomes]
rs1526100	0.85[CEU][hapmap];1.00[ASN][1000 genomes]
rs1608951	0.88[CEU][hapmap];1.00[ASN][1000 genomes]
rs17547830	0.88[CEU][hapmap];1.00[ASN][1000 genomes]
rs17629765	0.88[CEU][hapmap];1.00[ASN][1000 genomes]
rs1852266	1.00[ASN][1000 genomes]
rs1880736	0.92[CEU][hapmap];1.00[ASN][1000 genomes]
rs1949895	0.87[CEU][hapmap];1.00[ASN][1000 genomes]
rs2091345	0.92[CEU][hapmap];1.00[ASN][1000 genomes]
rs2222648	1.00[ASN][1000 genomes]
rs2222649	0.88[CEU][hapmap];1.00[ASN][1000 genomes]
rs35060898	1.00[ASN][1000 genomes]
rs35688896	1.00[ASN][1000 genomes]
rs60189113	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6583478	0.85[CEU][hapmap]
rs6583546	0.88[CEU][hapmap];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6949467	0.83[CEU][hapmap];1.00[ASN][1000 genomes]
rs6957283	1.00[ASN][1000 genomes]
rs7779867	0.85[CEU][hapmap];1.00[ASN][1000 genomes]
rs7785405	1.00[ASN][1000 genomes]
rs7789281	1.00[ASN][1000 genomes]
rs7797546	0.85[CEU][hapmap];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv470221	chr7:47917495-48354363	Strong transcription Flanking Active TSS Enhancers Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
2	nsv464442	chr7:47917495-48354820	Genic enhancers Flanking Active TSS Weak transcription Enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
3	nsv606893	chr7:47917495-48354820	Flanking Active TSS Strong transcription Genic enhancers Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
4	nsv1027414	chr7:48117684-48438543	Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	nsv1033738	chr7:48143988-48349357	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
6	nsv817336	chr7:48238233-48563988	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv1022980	chr7:48243227-48567060	Weak transcription Enhancers Genic enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv538833	chr7:48243227-48567060	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv1022578	chr7:48244414-48584664	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
10	nsv1023575	chr7:48244414-48586685	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
11	nsv1015183	chr7:48244414-48588598	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
12	nsv1032135	chr7:48293104-48414154	Genic enhancers Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
13	nsv1032221	chr7:48302789-48546684	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
14	nsv533811	chr7:48313757-48482470	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
15	nsv1015399	chr7:48321542-48544359	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:48319800-48382200	Strong transcription	Primary neutrophils fromperipheralblood	blood
2	chr7:48336400-48341400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr7:48338000-48340000	Enhancers	HMEC	breast
4	chr7:48338200-48341400	Weak transcription	Primary hematopoietic stem cells	blood
5	chr7:48338400-48341400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr7:48339000-48340600	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr7:48339000-48341400	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr7:48339000-48341800	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr7:48339200-48341600	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr7:48339200-48346000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr7:48339400-48340200	Enhancers	H1 Cell Line	embryonic stem cell
12	chr7:48339400-48340200	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr7:48339400-48340200	Enhancers	Brain Germinal Matrix	brain
14	chr7:48339400-48340600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr7:48339400-48340800	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr7:48339400-48341400	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr7:48339600-48340600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr7:48339600-48341200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr7:48339800-48340800	Enhancers	H9 Cell Line	embryonic stem cell
20	chr7:48339800-48343800	Weak transcription	Breast Myoepithelial Primary Cells	Breast

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links