Variant report

Variant	rs7708580
Chromosome Location	chr5:76172149-76172150
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs2227777	1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs2227803	1.00[EUR][1000 genomes]
rs2227810	1.00[EUR][1000 genomes]
rs6864739	1.00[EUR][1000 genomes]
rs6868171	1.00[EUR][1000 genomes]
rs6872686	1.00[EUR][1000 genomes]
rs73131649	1.00[EUR][1000 genomes]
rs73131650	1.00[EUR][1000 genomes]
rs7728753	0.85[YRI][hapmap];0.92[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9918276	1.00[EUR][1000 genomes]
rs9918278	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1019669	chr5:75836365-76477788	Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
2	esv3393424	chr5:76122720-76287744	Enhancers Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Strong transcription Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	esv34133	chr5:76138696-76239330	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
4	nsv524024	chr5:76166018-76187777	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:76153000-76174400	Weak transcription	Primary T cells from cord blood	blood
2	chr5:76169600-76172200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr5:76169600-76172800	Active TSS	Pancreatic Islets	Pancreatic Islet
4	chr5:76169800-76172200	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr5:76170200-76172200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
6	chr5:76170600-76173400	Weak transcription	Primary hematopoietic stem cells	blood
7	chr5:76170600-76174800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr5:76170800-76172200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr5:76171000-76172800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr5:76171000-76182400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
11	chr5:76171200-76175800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr5:76171400-76172200	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr5:76171600-76172200	Enhancers	HUES64 Cell Line	embryonic stem cell
14	chr5:76171600-76172600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr5:76171600-76177400	Strong transcription	Monocytes-CD14+_RO01746	blood
16	chr5:76171600-76192600	Strong transcription	Primary monocytes fromperipheralblood	blood
17	chr5:76171800-76172200	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr5:76171800-76172800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
19	chr5:76172000-76172200	Active TSS	HUES6 Cell Line	embryonic stem cell
20	chr5:76172000-76172400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr5:76172000-76173000	Active TSS	ES-I3 Cell Line	embryonic stem cell

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