Variant report

Variant	rs10105316
Chromosome Location	chr8:124601844-124601845
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs17253999	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2385455	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2385456	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs28445658	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs28484830	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs28490211	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28613586	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28825116	0.86[ASN][1000 genomes]
rs35066700	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4871390	0.85[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs4871392	0.88[ASN][1000 genomes]
rs4871394	0.85[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs55987314	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62520905	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72711208	0.93[ASN][1000 genomes]
rs72711214	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7814093	0.82[AMR][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	nsv831450	chr8:124471741-124661359	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:124598400-124602200	Weak transcription	Fetal Muscle Leg	muscle
2	chr8:124599000-124602000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr8:124599200-124602400	Enhancers	Skeletal Muscle Female	skeletal muscle
4	chr8:124599200-124604400	Weak transcription	HSMMtube	muscle
5	chr8:124599400-124604400	Weak transcription	HSMM	muscle
6	chr8:124599400-124604600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr8:124599400-124604800	Enhancers	Stomach Smooth Muscle	stomach
8	chr8:124599400-124605000	Enhancers	Colon Smooth Muscle	Colon
9	chr8:124599600-124606200	Enhancers	Skeletal Muscle Male	skeletal muscle
10	chr8:124600200-124602400	Enhancers	Right Atrium	heart
11	chr8:124600400-124602000	Weak transcription	Rectal Smooth Muscle	rectum
12	chr8:124600400-124602200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr8:124600400-124602200	Weak transcription	Left Ventricle	heart
14	chr8:124600400-124604400	Weak transcription	Psoas Muscle	Psoas
15	chr8:124600400-124604600	Weak transcription	Adipose Nuclei	Adipose
16	chr8:124600600-124602000	Weak transcription	Fetal Heart	heart
17	chr8:124600600-124602400	Enhancers	Right Ventricle	heart
18	chr8:124600800-124602200	Weak transcription	Duodenum Smooth Muscle	Duodenum
19	chr8:124601000-124602800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
20	chr8:124601200-124602400	Enhancers	HMEC	breast
21	chr8:124601200-124603800	Enhancers	K562	blood
22	chr8:124601200-124605000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr8:124601400-124602400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr8:124601400-124602600	Enhancers	NHLF	lung
25	chr8:124601400-124603400	Weak transcription	Aorta	Aorta
26	chr8:124601400-124605400	Enhancers	NHDF-Ad	bronchial
27	chr8:124601400-124607200	Enhancers	Osteobl	bone
28	chr8:124601800-124603200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr8:124601800-124604600	Weak transcription	Pancreas	Pancrea

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