Variant report

Variant	rs7860900
Chromosome Location	chr9:117930567-117930568
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10982595	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs10982604	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10982606	0.87[CEU][hapmap];0.81[EUR][1000 genomes]
rs10982609	0.86[CEU][hapmap];0.80[EUR][1000 genomes]
rs1110169	0.91[CEU][hapmap];0.93[CHB][hapmap];0.88[JPT][hapmap];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12379021	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12682693	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13292941	0.81[EUR][1000 genomes]
rs1537732	0.82[CEU][hapmap];0.80[EUR][1000 genomes]
rs17244791	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1888672	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1888673	0.86[CEU][hapmap];0.93[CHB][hapmap];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs34541555	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4147052	0.85[CEU][hapmap];0.81[EUR][1000 genomes]
rs4978628	0.90[CEU][hapmap];0.93[CHB][hapmap];0.88[JPT][hapmap];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6478145	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6478149	0.88[AFR][1000 genomes];0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7866181	1.00[CEU][hapmap];0.93[CHB][hapmap];0.88[JPT][hapmap];0.91[YRI][hapmap];0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][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	nsv615250	chr9:117768021-118012841	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv916912	chr9:117770039-118014140	Flanking Active TSS Enhancers Strong transcription Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv831697	chr9:117860416-118023927	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv6681	chr9:117893926-117938609	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:35 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:117922000-117944600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr9:117926400-117931800	Enhancers	NHEK	skin
3	chr9:117926400-117933600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr9:117926600-117931600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr9:117927200-117931600	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr9:117927200-117931800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr9:117927200-117932200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr9:117927200-117933000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr9:117927200-117933000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr9:117927400-117932000	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr9:117927400-117933000	Weak transcription	A549	lung
12	chr9:117928600-117930600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr9:117928600-117930600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr9:117928600-117930800	Enhancers	NHDF-Ad	bronchial
15	chr9:117929000-117930800	Enhancers	Placenta Amnion	Placenta Amnion
16	chr9:117929200-117930600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr9:117929200-117930600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr9:117929200-117930600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr9:117929200-117930800	Enhancers	HMEC	breast
20	chr9:117929400-117930600	Enhancers	Fetal Muscle Leg	muscle
21	chr9:117929400-117930600	Enhancers	HSMM	muscle
22	chr9:117929400-117930600	Enhancers	HSMMtube	muscle
23	chr9:117929800-117932200	Weak transcription	HUES6 Cell Line	embryonic stem cell
24	chr9:117930000-117932000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chr9:117930000-117932600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr9:117930000-117964400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
27	chr9:117930200-117930800	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr9:117930200-117932800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr9:117930200-117932800	Weak transcription	Muscle Satellite Cultured Cells	--
30	chr9:117930200-117933000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr9:117930200-117933000	Weak transcription	NH-A	brain
32	chr9:117930200-117933000	Weak transcription	Osteobl	bone
33	chr9:117930400-117931600	Enhancers	Colon Smooth Muscle	Colon
34	chr9:117930400-117932800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr9:117930400-117932800	Weak transcription	NHLF	lung

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