Variant report

Variant	rs3115915
Chromosome Location	chr8:94952727-94952728
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CDH17-4	chr8:94952330-94952920	NONHSAT127761

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs3115905	1.00[CHB][hapmap]
rs3115906	1.00[CHB][hapmap]
rs3115909	1.00[CHB][hapmap]
rs3115910	1.00[CHB][hapmap]
rs3115913	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs3115914	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs3115916	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs3115917	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs3115918	0.96[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs3115919	0.96[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs3115920	0.87[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs3115921	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs3115941	0.85[JPT][hapmap]
rs3133978	1.00[CHB][hapmap]
rs3133980	1.00[CHB][hapmap]
rs3133983	1.00[CHB][hapmap]
rs3133985	1.00[CHB][hapmap]
rs3133986	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs3134000	0.85[JPT][hapmap]
rs3134001	0.85[JPT][hapmap]
rs3134003	0.85[JPT][hapmap]
rs3134004	0.85[JPT][hapmap]
rs3134007	0.85[JPT][hapmap]
rs3134008	0.85[JPT][hapmap]
rs3134011	0.85[JPT][hapmap]
rs3134013	0.85[JPT][hapmap]
rs6983462	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6997830	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7006289	1.00[CEU][hapmap]
rs723039	1.00[CHB][hapmap]
rs7836063	0.85[JPT][hapmap]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2754970	chr8:94675324-94991724	Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:28 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:94948200-94956600	Weak transcription	Stomach Smooth Muscle	stomach
2	chr8:94948400-94956400	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr8:94948800-94952800	Weak transcription	HSMMtube	muscle
4	chr8:94948800-94955800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr8:94948800-94955800	Weak transcription	Ovary	ovary
6	chr8:94948800-94956200	Weak transcription	NHLF	lung
7	chr8:94949000-94954200	Weak transcription	Right Ventricle	heart
8	chr8:94950800-94953800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr8:94950800-94954000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
10	chr8:94951000-94955600	Weak transcription	Psoas Muscle	Psoas
11	chr8:94951200-94955800	Weak transcription	Fetal Heart	heart
12	chr8:94951400-94954000	Weak transcription	Right Atrium	heart
13	chr8:94951400-94954800	Weak transcription	Skeletal Muscle Female	skeletal muscle
14	chr8:94951400-94955400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr8:94951400-94955400	Weak transcription	Left Ventricle	heart
16	chr8:94951400-94956000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr8:94951600-94955400	Weak transcription	Skeletal Muscle Male	skeletal muscle
18	chr8:94951800-94952800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr8:94951800-94955800	Weak transcription	Osteobl	bone
20	chr8:94951800-94956000	Weak transcription	NHDF-Ad	bronchial
21	chr8:94952000-94954200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
22	chr8:94952200-94956000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr8:94952400-94953600	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr8:94952400-94953600	ZNF genes & repeats	Fetal Adrenal Gland	Adrenal Gland
25	chr8:94952600-94952800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr8:94952600-94953000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr8:94952600-94953400	ZNF genes & repeats	Fetal Intestine Small	intestine
28	chr8:94952600-94953600	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin

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