Variant report

Variant	rs10106983
Chromosome Location	chr8:99004384-99004385
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:98994950..98998234-chr8:99001793..99004607,3	K562	blood:

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs10955140	0.87[CHB][hapmap];0.82[JPT][hapmap];0.95[ASN][1000 genomes]
rs10955143	0.87[CHB][hapmap];0.90[JPT][hapmap];0.96[ASN][1000 genomes]
rs10955144	0.96[ASN][1000 genomes]
rs12549307	0.94[ASN][1000 genomes]
rs12676252	0.94[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];0.81[YRI][hapmap];0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13270713	0.87[CHB][hapmap];0.91[JPT][hapmap];0.96[ASN][1000 genomes]
rs2034780	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs36191777	0.83[ASN][1000 genomes]
rs4735521	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6985434	0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1032904	chr8:98756076-99476925	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
2	nsv539687	chr8:98756076-99476925	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
3	nsv528695	chr8:98960813-99022009	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	esv1801513	chr8:98996645-99009024	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:31 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:98988000-99011800	Weak transcription	Aorta	Aorta
2	chr8:98992600-99019400	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr8:98994200-99014800	Weak transcription	Duodenum Mucosa	Duodenum
4	chr8:98994600-99008200	Weak transcription	Fetal Muscle Trunk	muscle
5	chr8:98994600-99008400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
6	chr8:98994600-99014200	Weak transcription	Ovary	ovary
7	chr8:98995200-99008000	Weak transcription	Fetal Stomach	stomach
8	chr8:98996400-99006000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr8:98996600-99006800	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr8:98998200-99006600	Weak transcription	NHLF	lung
11	chr8:99002200-99004400	Weak transcription	NHDF-Ad	bronchial
12	chr8:99002800-99008200	Weak transcription	Right Atrium	heart
13	chr8:99003000-99007200	Weak transcription	NH-A	brain
14	chr8:99003200-99006800	Weak transcription	Muscle Satellite Cultured Cells	--
15	chr8:99003200-99007200	Weak transcription	NHEK	skin
16	chr8:99003400-99006400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr8:99003400-99007200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr8:99003400-99007200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr8:99003400-99007600	Weak transcription	HMEC	breast
20	chr8:99003400-99008400	Weak transcription	Adipose Nuclei	Adipose
21	chr8:99003600-99005800	Weak transcription	Osteobl	bone
22	chr8:99003600-99006000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr8:99003600-99006000	Weak transcription	Brain Substantia Nigra	brain
24	chr8:99003600-99006400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr8:99003600-99006600	Weak transcription	Brain Cingulate Gyrus	brain
26	chr8:99003600-99006600	Weak transcription	Brain Inferior Temporal Lobe	brain
27	chr8:99003600-99007600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr8:99003600-99013200	Weak transcription	Brain Anterior Caudate	brain
29	chr8:99003800-99006400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
30	chr8:99003800-99006400	Weak transcription	Brain Hippocampus Middle	brain
31	chr8:99003800-99007000	Weak transcription	Fetal Muscle Leg	muscle

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