Variant report

Variant	rs10786156
Chromosome Location	chr10:96014622-96014623
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10882416	0.86[MKK][hapmap]
rs11187830	0.84[ASW][hapmap]
rs11187838	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12263737	0.86[MKK][hapmap]
rs17109869	0.84[ASW][hapmap]
rs1830890	1.00[ASW][hapmap];0.83[GIH][hapmap]
rs2274224	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3765524	0.86[MKK][hapmap]
rs3891783	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4918188	0.83[GIH][hapmap];0.82[LWK][hapmap];0.85[MKK][hapmap];0.83[AFR][1000 genomes]
rs55753709	0.83[AFR][1000 genomes]
rs57866767	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7080472	0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7084339	0.86[MKK][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1036676	chr10:95851376-96103876	Strong transcription Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	esv2761616	chr10:95966768-96303701	Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs10786156	SFRP5	cis	cerebellum	SCAN

Chromatin state (count:42 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:95974200-96034000	Weak transcription	Colon Smooth Muscle	Colon
2	chr10:95984800-96023800	Weak transcription	Pancreas	Pancrea
3	chr10:95985800-96033800	Weak transcription	Left Ventricle	heart
4	chr10:95994600-96045400	Weak transcription	Lung	lung
5	chr10:95995800-96051800	Weak transcription	Fetal Kidney	kidney
6	chr10:96004200-96015200	Weak transcription	Brain Substantia Nigra	brain
7	chr10:96004200-96022600	Strong transcription	Fetal Muscle Trunk	muscle
8	chr10:96004400-96034000	Weak transcription	Fetal Brain Male	brain
9	chr10:96005000-96016400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr10:96005000-96031200	Weak transcription	Brain Germinal Matrix	brain
11	chr10:96005600-96019000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr10:96006600-96030200	Weak transcription	Gastric	stomach
13	chr10:96006600-96030200	Weak transcription	Ovary	ovary
14	chr10:96006600-96033600	Weak transcription	Duodenum Smooth Muscle	Duodenum
15	chr10:96008600-96022600	Strong transcription	Fetal Muscle Leg	muscle
16	chr10:96009400-96024000	Weak transcription	Small Intestine	intestine
17	chr10:96009600-96018800	Weak transcription	Duodenum Mucosa	Duodenum
18	chr10:96010600-96014800	Strong transcription	Cortex derived primary cultured neurospheres	brain
19	chr10:96010600-96014800	Strong transcription	Rectal Mucosa Donor 29	rectum
20	chr10:96010800-96017200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr10:96011200-96016800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
22	chr10:96011400-96015000	Strong transcription	Fetal Stomach	stomach
23	chr10:96011800-96015200	Strong transcription	Stomach Smooth Muscle	stomach
24	chr10:96012000-96016000	Strong transcription	Fetal Intestine Small	intestine
25	chr10:96012000-96016800	Strong transcription	Fetal Intestine Large	intestine
26	chr10:96012000-96016800	Strong transcription	Rectal Mucosa Donor 31	rectum
27	chr10:96012200-96015000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr10:96012400-96014800	Strong transcription	Sigmoid Colon	Sigmoid Colon
29	chr10:96012400-96015000	Strong transcription	Fetal Brain Female	brain
30	chr10:96012600-96020600	Weak transcription	Fetal Lung	lung
31	chr10:96012600-96030600	Weak transcription	Stomach Mucosa	stomach
32	chr10:96012800-96019800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr10:96012800-96030600	Weak transcription	Spleen	Spleen
34	chr10:96013000-96014800	Strong transcription	Colonic Mucosa	Colon
35	chr10:96013200-96034000	Weak transcription	Adipose Nuclei	Adipose
36	chr10:96013400-96019800	Weak transcription	Aorta	Aorta
37	chr10:96013600-96034000	Weak transcription	Rectal Smooth Muscle	rectum
38	chr10:96014000-96014800	Strong transcription	A549	lung
39	chr10:96014000-96030000	Weak transcription	Skeletal Muscle Female	skeletal muscle
40	chr10:96014000-96034000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr10:96014200-96016600	Weak transcription	HSMMtube	muscle
42	chr10:96014400-96030800	Weak transcription	Placenta	Placenta

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