Variant report

Variant	rs2421455
Chromosome Location	chr18:29939659-29939660
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs10502585	1.00[JPT][hapmap]
rs10502588	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs10502589	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap]
rs10502590	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.86[AFR][1000 genomes];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11877702	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1458860	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16959889	1.00[JPT][hapmap]
rs16963135	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap]
rs16963169	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap]
rs16963196	0.88[EUR][1000 genomes]
rs16963205	0.92[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.91[LWK][hapmap];0.86[MKK][hapmap];0.96[YRI][hapmap];0.95[AFR][1000 genomes];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16963218	0.94[AFR][1000 genomes];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16963225	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16963230	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16963239	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16963245	0.95[AFR][1000 genomes];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16963272	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16963275	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16963279	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16963339	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs16963367	1.00[JPT][hapmap]
rs16963370	1.00[CHD][hapmap];1.00[JPT][hapmap]
rs16963374	1.00[CHD][hapmap];1.00[JPT][hapmap]
rs35779665	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4485446	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4499310	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55866517	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56945883	1.00[EUR][1000 genomes]
rs57478295	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57613491	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59676860	0.88[EUR][1000 genomes]
rs7228337	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7236432	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap]
rs7237501	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[GIH][hapmap]
rs7240587	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[GIH][hapmap]
rs7240755	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs73956901	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73956902	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73958403	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73958404	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73958405	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73958411	1.00[ASN][1000 genomes]
rs902950	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs902951	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs931494	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

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	nsv833616	chr18:29792336-29964212	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:34 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:29926800-29951000	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr18:29930000-29947600	Weak transcription	Esophagus	oesophagus
3	chr18:29930200-29945400	Weak transcription	Fetal Intestine Small	intestine
4	chr18:29930200-29945600	Weak transcription	Fetal Intestine Large	intestine
5	chr18:29930200-29953600	Weak transcription	Fetal Muscle Leg	muscle
6	chr18:29931200-29948000	Weak transcription	Brain Angular Gyrus	brain
7	chr18:29931400-29940400	Weak transcription	Brain Substantia Nigra	brain
8	chr18:29931600-29942000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr18:29932600-29943600	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr18:29932800-29954000	Weak transcription	Ovary	ovary
11	chr18:29933000-29948000	Weak transcription	Brain Hippocampus Middle	brain
12	chr18:29934800-29945600	Weak transcription	Aorta	Aorta
13	chr18:29935600-29939800	Enhancers	Fetal Heart	heart
14	chr18:29936200-29942000	Weak transcription	HSMM	muscle
15	chr18:29936400-29940600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr18:29936400-29942000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr18:29936800-29940000	Enhancers	Pancreas	Pancrea
18	chr18:29936800-29942400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr18:29937000-29946200	Weak transcription	Duodenum Smooth Muscle	Duodenum
20	chr18:29937600-29952600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr18:29938000-29941800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr18:29938200-29948000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr18:29938400-29945600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr18:29938400-29947600	Weak transcription	Gastric	stomach
25	chr18:29939000-29942600	Weak transcription	HUES6 Cell Line	embryonic stem cell
26	chr18:29939000-29942600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
27	chr18:29939000-29945600	Weak transcription	Lung	lung
28	chr18:29939000-29947600	Weak transcription	Left Ventricle	heart
29	chr18:29939000-29948000	Weak transcription	Right Atrium	heart
30	chr18:29939000-29951000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr18:29939000-29952800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr18:29939400-29939800	Enhancers	Stomach Mucosa	stomach
33	chr18:29939400-29940000	Weak transcription	Liver	Liver
34	chr18:29939600-29939800	ZNF genes & repeats	Fetal Stomach	stomach

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