Variant report

Variant	rs2054163
Chromosome Location	chr2:173533188-173533189
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs11895461	0.82[CEU][hapmap]
rs11898565	0.92[CEU][hapmap]
rs11902830	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12615889	0.84[ASN][1000 genomes]
rs12622335	0.82[ASN][1000 genomes]
rs12622834	0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13384307	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs16860794	0.84[ASN][1000 genomes]
rs16860795	0.84[ASN][1000 genomes]
rs16860796	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs16860798	0.84[ASN][1000 genomes]
rs16860809	0.95[CHB][hapmap];0.80[JPT][hapmap];0.82[ASN][1000 genomes]
rs2054162	0.87[ASN][1000 genomes]
rs2084731	0.84[ASN][1000 genomes]
rs2084732	0.95[CHB][hapmap];0.90[JPT][hapmap];0.84[ASN][1000 genomes]
rs3816536	0.92[CEU][hapmap]
rs4313941	0.85[ASN][1000 genomes]
rs4470304	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4972514	0.84[ASN][1000 genomes]
rs4972515	0.86[JPT][hapmap];0.84[ASN][1000 genomes]
rs4972516	1.00[CHB][hapmap];0.95[JPT][hapmap];0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4972849	0.84[ASN][1000 genomes]
rs4972850	0.95[CHB][hapmap];0.84[JPT][hapmap];0.82[ASN][1000 genomes]
rs4972851	0.92[CHB][hapmap];0.86[JPT][hapmap];0.82[ASN][1000 genomes]
rs59103702	0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs61556691	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6716527	0.88[AFR][1000 genomes];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6733953	0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6743273	0.93[YRI][hapmap];0.85[AFR][1000 genomes]
rs6757567	0.80[AFR][1000 genomes]
rs733331	0.96[CHB][hapmap];0.86[JPT][hapmap];0.82[ASN][1000 genomes]
rs7590282	0.88[AFR][1000 genomes];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533927	chr2:173161637-173796894	Active TSS Enhancers Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
2	esv2760591	chr2:173396905-173719520	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription Active TSS 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	29 gene(s)	inside rSNPs	diseases
3	nsv583665	chr2:173460640-173643087	Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:173521400-173536800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr2:173530400-173536400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr2:173530600-173536400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr2:173530800-173536400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr2:173531800-173533400	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr2:173532000-173533400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr2:173532000-173533400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr2:173532000-173533400	Enhancers	NHDF-Ad	bronchial
9	chr2:173532200-173533400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr2:173532200-173533400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr2:173532200-173533400	Enhancers	NHLF	lung
12	chr2:173532400-173533200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr2:173532400-173536400	Weak transcription	Pancreatic Islets	Pancreatic Islet
14	chr2:173532600-173533200	Enhancers	Muscle Satellite Cultured Cells	--
15	chr2:173532800-173533400	Enhancers	Osteobl	bone
16	chr2:173533000-173536800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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