Variant report

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs10508870	0.98[ASN][1000 genomes]
rs10508871	0.98[ASN][1000 genomes]
rs10508872	0.98[ASN][1000 genomes]
rs11238646	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17154164	0.98[ASN][1000 genomes]
rs17154173	0.98[ASN][1000 genomes]
rs17154178	0.98[ASN][1000 genomes]
rs17154182	0.98[ASN][1000 genomes]
rs17154237	0.84[ASN][1000 genomes]
rs17154294	0.81[ASN][1000 genomes]
rs17154300	0.81[ASN][1000 genomes]
rs35542796	0.98[ASN][1000 genomes]
rs4146639	0.97[ASN][1000 genomes]
rs56935737	0.84[ASN][1000 genomes]
rs57137545	0.98[ASN][1000 genomes]
rs57517635	0.98[ASN][1000 genomes]
rs58197647	0.98[ASN][1000 genomes]
rs58967637	0.98[ASN][1000 genomes]
rs59124816	0.98[ASN][1000 genomes]
rs59228864	0.98[ASN][1000 genomes]
rs59235630	0.84[ASN][1000 genomes]
rs59238114	0.98[ASN][1000 genomes]
rs59303606	0.98[ASN][1000 genomes]
rs59968020	0.84[ASN][1000 genomes]
rs60580954	0.98[ASN][1000 genomes]
rs60799950	0.98[ASN][1000 genomes]
rs61185278	0.98[ASN][1000 genomes]
rs61405658	0.98[ASN][1000 genomes]
rs73266552	0.98[ASN][1000 genomes]
rs73266553	0.98[ASN][1000 genomes]
rs73266556	0.97[ASN][1000 genomes]
rs73266557	0.98[ASN][1000 genomes]
rs73266574	0.98[ASN][1000 genomes]
rs73268420	0.84[ASN][1000 genomes]
rs73268460	0.80[ASN][1000 genomes]
rs73268466	0.81[ASN][1000 genomes]
rs7899244	0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3317585	chr10:44202846-44207644	Bivalent Enhancer Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	n/a
2	nsv512160	chr10:44203320-44205904	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	n/a
3	esv3521367	chr10:44203899-44206311	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
4	esv3521366	chr10:44203996-44206694	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
5	esv3521368	chr10:44203996-44206694	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
6	esv3317596	chr10:44204136-44206172	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:44202600-44204200	Enhancers	Adipose Nuclei	Adipose
2	chr10:44202600-44204200	Enhancers	Skeletal Muscle Male	skeletal muscle
3	chr10:44202800-44204400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
4	chr10:44203000-44204200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr10:44203000-44204200	Enhancers	Left Ventricle	heart
6	chr10:44203000-44204200	Enhancers	Lung	lung
7	chr10:44203000-44204200	Enhancers	Pancreas	Pancrea
8	chr10:44203000-44204200	Enhancers	Spleen	Spleen
9	chr10:44203000-44204600	Enhancers	Osteobl	bone
10	chr10:44203200-44204200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr10:44203200-44204200	Enhancers	Fetal Muscle Leg	muscle
12	chr10:44203200-44204200	Enhancers	Ovary	ovary
13	chr10:44203200-44204600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr10:44203200-44204600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr10:44203400-44204200	Enhancers	Fetal Muscle Trunk	muscle
16	chr10:44203400-44207200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr10:44203800-44204200	Enhancers	Fetal Intestine Small	intestine
18	chr10:44203800-44204200	Enhancers	Fetal Kidney	kidney
19	chr10:44203800-44204200	Enhancers	Fetal Lung	lung
20	chr10:44203800-44204200	Enhancers	NHDF-Ad	bronchial

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