Variant report

Variant	rs28704681
Chromosome Location	chr9:71350437-71350438
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:71341357..71343787-chr9:71348342..71350761,2	K562	blood:

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs12340186	0.84[ASN][1000 genomes]
rs12379662	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12380573	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs45501692	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1026962	chr9:71130848-71357605	Bivalent/Poised TSS Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv1032210	chr9:71130848-71511987	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
3	esv2422258	chr9:71234845-71663340	Enhancers Flanking Active TSS Strong transcription Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
4	nsv1017903	chr9:71276951-71690579	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
5	esv2757339	chr9:71291107-71353743	Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	esv2759693	chr9:71291107-71353743	Bivalent Enhancer Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv893415	chr9:71347988-71364351	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:34 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:71337000-71350600	Weak transcription	Gastric	stomach
2	chr9:71342600-71354600	Enhancers	Fetal Intestine Large	intestine
3	chr9:71343400-71363000	Weak transcription	GM12878-XiMat	blood
4	chr9:71343800-71357200	Weak transcription	Primary B cells from peripheral blood	blood
5	chr9:71344600-71354000	Weak transcription	Primary hematopoietic stem cells	blood
6	chr9:71345400-71350800	Weak transcription	Colonic Mucosa	Colon
7	chr9:71345600-71352800	Enhancers	Fetal Heart	heart
8	chr9:71346600-71352200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr9:71346600-71353400	Weak transcription	Psoas Muscle	Psoas
10	chr9:71346800-71350600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr9:71346800-71350600	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr9:71346800-71350800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr9:71347000-71352200	Enhancers	Duodenum Mucosa	Duodenum
14	chr9:71347200-71350600	Weak transcription	HUES48 Cell Line	embryonic stem cell
15	chr9:71347200-71354600	Weak transcription	K562	blood
16	chr9:71347400-71357800	Weak transcription	Primary B cells from cord blood	blood
17	chr9:71348000-71354400	Weak transcription	Pancreas	Pancrea
18	chr9:71348200-71350800	Weak transcription	Small Intestine	intestine
19	chr9:71348200-71350800	Enhancers	HepG2	liver
20	chr9:71348200-71359000	Weak transcription	Lung	lung
21	chr9:71348400-71350600	Weak transcription	Right Atrium	heart
22	chr9:71348400-71354600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr9:71349400-71353600	Weak transcription	Placenta Amnion	Placenta Amnion
24	chr9:71350000-71351600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr9:71350000-71353400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr9:71350000-71353400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr9:71350000-71356600	Weak transcription	Aorta	Aorta
28	chr9:71350200-71350600	Weak transcription	Stomach Mucosa	stomach
29	chr9:71350400-71351000	Enhancers	Left Ventricle	heart
30	chr9:71350400-71351200	Genic enhancers	Fetal Intestine Small	intestine
31	chr9:71350400-71351200	Enhancers	Rectal Mucosa Donor 29	rectum
32	chr9:71350400-71351200	Enhancers	Right Ventricle	heart
33	chr9:71350400-71351600	Enhancers	Sigmoid Colon	Sigmoid Colon
34	chr9:71350400-71354600	Enhancers	Rectal Mucosa Donor 31	rectum

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