Variant report

Variant	rs73107814
Chromosome Location	chr4:22240338-22240339
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs10013755	0.84[EUR][1000 genomes]
rs10461102	0.92[EUR][1000 genomes]
rs11931969	0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11933715	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16872470	0.92[EUR][1000 genomes]
rs2323302	0.92[EUR][1000 genomes]
rs59722857	0.92[EUR][1000 genomes]
rs73105789	0.92[EUR][1000 genomes]
rs73801078	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	nsv817467	chr4:21602921-22422816	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv829881	chr4:22084704-22254679	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv593822	chr4:22165174-22246276	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv997783	chr4:22223503-22338543	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
5	nsv428756	chr4:22239826-22406106	Weak transcription Strong transcription Active TSS Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:22238800-22240400	Enhancers	Brain Hippocampus Middle	brain
2	chr4:22239000-22240400	Active TSS	Colonic Mucosa	Colon
3	chr4:22239000-22240800	Active TSS	Rectal Mucosa Donor 29	rectum
4	chr4:22239400-22240600	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr4:22239600-22240400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr4:22239600-22240400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr4:22239600-22240400	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr4:22239600-22240400	Enhancers	Cortex derived primary cultured neurospheres	brain
9	chr4:22239600-22240400	Flanking Active TSS	Liver	Liver
10	chr4:22239600-22240400	Active TSS	Brain Anterior Caudate	brain
11	chr4:22239600-22240400	Enhancers	Brain Germinal Matrix	brain
12	chr4:22239600-22240600	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr4:22239600-22240600	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr4:22239800-22240400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr4:22239800-22240400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr4:22239800-22240600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr4:22240000-22240400	Enhancers	Pancreatic Islets	Pancreatic Islet
18	chr4:22240000-22240600	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
19	chr4:22240200-22240400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr4:22240200-22240400	Flanking Active TSS	Fetal Intestine Large	intestine
21	chr4:22240200-22240400	Flanking Active TSS	Fetal Intestine Small	intestine
22	chr4:22240200-22240400	Enhancers	Ovary	ovary
23	chr4:22240200-22240400	Flanking Active TSS	Stomach Mucosa	stomach
24	chr4:22240200-22240600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
25	chr4:22240200-22240600	Flanking Active TSS	Duodenum Mucosa	Duodenum
26	chr4:22240200-22240600	Flanking Active TSS	HepG2	liver

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