Variant report

Variant	rs72621302
Chromosome Location	chr13:40129220-40129221
allele	A/C
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:33)

rs_ID	r²[population]
rs10459367	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11841092	0.85[EUR][1000 genomes]
rs12585456	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs17060245	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs58418761	0.84[EUR][1000 genomes]
rs58662524	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs58918104	0.84[EUR][1000 genomes]
rs59531868	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs72621301	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72623303	0.95[EUR][1000 genomes]
rs72623305	0.84[EUR][1000 genomes]
rs7332354	0.82[EUR][1000 genomes]
rs9315708	0.94[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9566452	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9566455	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9566456	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9576839	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9576844	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9576845	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9576846	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9576847	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9576849	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9576850	0.82[EUR][1000 genomes]
rs9576853	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9576855	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9576856	0.97[EUR][1000 genomes]
rs9576857	0.96[EUR][1000 genomes]
rs9576858	0.97[EUR][1000 genomes]
rs9576860	0.96[EUR][1000 genomes]
rs9576863	0.87[EUR][1000 genomes]
rs9576864	0.84[EUR][1000 genomes]
rs9576867	0.84[EUR][1000 genomes]
rs9576868	0.84[EUR][1000 genomes]

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	esv2754118	chr13:39347702-40222644	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
2	nsv1054600	chr13:39801283-40545027	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:39 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:40107800-40140200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr13:40111200-40133200	Weak transcription	Aorta	Aorta
3	chr13:40114000-40131200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr13:40114400-40136000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr13:40115400-40133200	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr13:40115600-40133600	Weak transcription	Osteobl	bone
7	chr13:40117000-40130000	Weak transcription	Fetal Muscle Leg	muscle
8	chr13:40117000-40130400	Weak transcription	HSMMtube	muscle
9	chr13:40117800-40131200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr13:40119800-40130200	Weak transcription	Fetal Heart	heart
11	chr13:40120000-40131600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr13:40121400-40136200	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chr13:40123000-40131800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr13:40125000-40131600	Weak transcription	Fetal Lung	lung
15	chr13:40125400-40133400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr13:40125600-40131400	Weak transcription	HSMM	muscle
17	chr13:40125600-40133000	Weak transcription	Lung	lung
18	chr13:40125800-40130000	Weak transcription	Adipose Nuclei	Adipose
19	chr13:40126400-40137200	Weak transcription	NHLF	lung
20	chr13:40126600-40130200	Weak transcription	Right Ventricle	heart
21	chr13:40126800-40130600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr13:40127000-40131200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr13:40127000-40133400	Weak transcription	Brain Angular Gyrus	brain
24	chr13:40127000-40136200	Weak transcription	NHDF-Ad	bronchial
25	chr13:40128600-40129600	Enhancers	Ovary	ovary
26	chr13:40128800-40129400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr13:40128800-40130400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr13:40128800-40137600	Weak transcription	Colon Smooth Muscle	Colon
29	chr13:40129000-40130000	Weak transcription	Right Atrium	heart
30	chr13:40129000-40131400	Weak transcription	Left Ventricle	heart
31	chr13:40129000-40131800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr13:40129000-40133000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
33	chr13:40129000-40133200	Weak transcription	Brain Cingulate Gyrus	brain
34	chr13:40129000-40145600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr13:40129000-40152800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr13:40129200-40133200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
37	chr13:40129200-40133200	Weak transcription	Brain Substantia Nigra	brain
38	chr13:40129200-40135800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr13:40129200-40135800	Weak transcription	HMEC	breast

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