Variant report

Variant	rs1981161
Chromosome Location	chr9:73563097-73563098
allele	A/C
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:12)

rs_ID	r²[population]
rs10780983	0.80[AMR][1000 genomes]
rs10868929	0.82[AMR][1000 genomes]
rs10868930	0.85[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs11142648	0.82[AMR][1000 genomes]
rs1337017	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1415219	0.82[AMR][1000 genomes]
rs1890019	0.96[ASN][1000 genomes]
rs1981160	0.94[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1981162	0.99[AFR][1000 genomes];0.93[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2992995	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2993022	0.96[ASN][1000 genomes]
rs3010419	1.00[CHB][hapmap];0.91[JPT][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	nsv893441	chr9:73486034-73594114	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	nsv430072	chr9:73509677-73640530	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:73561400-73563800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr9:73561800-73563800	Enhancers	NHEK	skin
3	chr9:73562000-73563600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr9:73562000-73563800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr9:73562000-73563800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr9:73562200-73563600	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr9:73562200-73564000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr9:73562400-73563800	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr9:73562400-73566800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr9:73562600-73563600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr9:73562600-73563800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr9:73562600-73563800	Enhancers	HMEC	breast
13	chr9:73562800-73565400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr9:73562800-73565400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr9:73562800-73565600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr9:73562800-73566400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr9:73562800-73566600	Weak transcription	Osteobl	bone
18	chr9:73562800-73568200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr9:73563000-73563400	Weak transcription	Placenta Amnion	Placenta Amnion
20	chr9:73563000-73567200	Weak transcription	Muscle Satellite Cultured Cells	--
21	chr9:73563000-73569000	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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