Variant report

Variant	rs2071
Chromosome Location	chr15:57814129-57814130
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 1 )

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

rs_ID	r²[population]
rs11071331	0.83[CEU][hapmap];0.92[CHB][hapmap];0.83[CHD][hapmap];0.88[JPT][hapmap]
rs1995990	0.92[CHB][hapmap];0.82[JPT][hapmap];0.82[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs4774952	0.83[MEX][hapmap]
rs7183994	0.83[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	nsv1045611	chr15:57350965-58070807	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
2	nsv1054547	chr15:57600488-57977659	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
3	nsv833022	chr15:57657412-57830112	Weak transcription Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv904255	chr15:57790436-57907574	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs2071	WDR72	cis	cerebellum	SCAN

Chromatin state (count:47 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:57797000-57827200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr15:57801800-57819000	Weak transcription	Esophagus	oesophagus
3	chr15:57802000-57819600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr15:57802600-57846600	Weak transcription	Duodenum Smooth Muscle	Duodenum
5	chr15:57802800-57822600	Weak transcription	Brain Hippocampus Middle	brain
6	chr15:57803000-57818800	Weak transcription	Fetal Intestine Large	intestine
7	chr15:57803200-57819400	Weak transcription	Ovary	ovary
8	chr15:57803200-57842800	Weak transcription	Aorta	Aorta
9	chr15:57805400-57814200	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr15:57807000-57816200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr15:57807000-57818400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr15:57807400-57814200	Strong transcription	Liver	Liver
13	chr15:57808400-57817200	Strong transcription	H1 Cell Line	embryonic stem cell
14	chr15:57808600-57817200	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr15:57808600-57817800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
16	chr15:57808800-57818000	Strong transcription	HUES48 Cell Line	embryonic stem cell
17	chr15:57808800-57818000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
18	chr15:57808800-57818200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr15:57809000-57814200	Weak transcription	Stomach Mucosa	stomach
20	chr15:57809000-57817200	Strong transcription	HUES6 Cell Line	embryonic stem cell
21	chr15:57809400-57814200	Weak transcription	Brain Anterior Caudate	brain
22	chr15:57809400-57816600	Weak transcription	Fetal Muscle Leg	muscle
23	chr15:57809800-57815600	Weak transcription	Lung	lung
24	chr15:57810000-57814400	Weak transcription	Fetal Lung	lung
25	chr15:57810400-57814400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
26	chr15:57811000-57814400	Weak transcription	H9 Cell Line	embryonic stem cell
27	chr15:57811000-57816400	Weak transcription	Placenta	Placenta
28	chr15:57811000-57827800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr15:57811200-57815400	Weak transcription	HepG2	liver
30	chr15:57811200-57819400	Weak transcription	Fetal Intestine Small	intestine
31	chr15:57811600-57817200	Weak transcription	HUVEC	blood vessel
32	chr15:57812400-57819400	Weak transcription	Brain Inferior Temporal Lobe	brain
33	chr15:57812600-57815200	Weak transcription	HUES64 Cell Line	embryonic stem cell
34	chr15:57813200-57816000	Enhancers	Fetal Heart	heart
35	chr15:57813600-57814800	Enhancers	Pancreas	Pancrea
36	chr15:57813800-57814200	Enhancers	Breast Myoepithelial Primary Cells	Breast
37	chr15:57813800-57814200	Enhancers	Gastric	stomach
38	chr15:57813800-57814600	Enhancers	Brain Cingulate Gyrus	brain
39	chr15:57813800-57814600	Enhancers	Brain Substantia Nigra	brain
40	chr15:57813800-57814800	Enhancers	Left Ventricle	heart
41	chr15:57813800-57815200	Enhancers	Colon Smooth Muscle	Colon
42	chr15:57813800-57816400	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr15:57813800-57817200	Strong transcription	Fetal Stomach	stomach
44	chr15:57814000-57814400	Enhancers	Rectal Smooth Muscle	rectum
45	chr15:57814000-57814800	Enhancers	Brain Angular Gyrus	brain
46	chr15:57814000-57815200	Enhancers	Stomach Smooth Muscle	stomach
47	chr15:57814000-57815400	Enhancers	Fetal Kidney	kidney

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