Variant report

Variant	rs11206922
Chromosome Location	chr1:57282933-57282934
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs10889019	0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11206923	0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11206924	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11206927	0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12084638	0.92[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12137176	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72668400	0.89[EUR][1000 genomes];0.97[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	nsv869295	chr1:56894955-57656562	Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:57278400-57283000	Weak transcription	Fetal Heart	heart
2	chr1:57278800-57283000	Weak transcription	Skeletal Muscle Male	skeletal muscle
3	chr1:57278800-57284400	Weak transcription	Right Ventricle	heart
4	chr1:57279000-57283400	Weak transcription	Fetal Kidney	kidney
5	chr1:57280000-57283400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr1:57280000-57283800	Weak transcription	Gastric	stomach
7	chr1:57280200-57283400	Weak transcription	Esophagus	oesophagus
8	chr1:57280400-57285000	Weak transcription	Lung	lung
9	chr1:57280800-57284200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr1:57281400-57283000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr1:57281400-57283400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr1:57281400-57284000	Enhancers	Fetal Intestine Large	intestine
13	chr1:57281400-57284600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr1:57281800-57283600	Weak transcription	Osteobl	bone
15	chr1:57281800-57287600	Enhancers	Fetal Intestine Small	intestine
16	chr1:57282000-57283800	Enhancers	HepG2	liver
17	chr1:57282000-57285600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr1:57282200-57283400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr1:57282400-57283400	Enhancers	Psoas Muscle	Psoas
20	chr1:57282400-57283800	Enhancers	Skeletal Muscle Female	skeletal muscle
21	chr1:57282600-57283000	Enhancers	Hela-S3	cervix
22	chr1:57282600-57283200	Weak transcription	Pancreatic Islets	Pancreatic Islet
23	chr1:57282600-57283200	Enhancers	HMEC	breast
24	chr1:57282600-57283400	Active TSS	Liver	Liver
25	chr1:57282800-57283000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr1:57282800-57283000	Enhancers	Left Ventricle	heart
27	chr1:57282800-57283200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr1:57282800-57283200	Enhancers	GM12878-XiMat	blood
29	chr1:57282800-57283800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr1:57282800-57285800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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