Variant report

Variant	rs529502307
Chromosome Location	chr8:99847260-99847261
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

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	nsv891218	chr8:99507313-99906221	Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv1027025	chr8:99672977-100115315	Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
3	nsv539690	chr8:99672977-100115315	Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
4	nsv891220	chr8:99681858-99867419	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
5	nsv1031089	chr8:99715785-100399935	Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
6	esv3357563	chr8:99846837-99848644	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:25 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:99837800-99848600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
2	chr8:99838800-99847600	Weak transcription	Fetal Intestine Large	intestine
3	chr8:99838800-99862800	Weak transcription	Ovary	ovary
4	chr8:99844200-99848200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr8:99844600-99847600	Weak transcription	Fetal Intestine Small	intestine
6	chr8:99844600-99848200	Enhancers	HMEC	breast
7	chr8:99844800-99848600	Enhancers	Placenta	Placenta
8	chr8:99845000-99848200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr8:99845400-99847400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr8:99845800-99847400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr8:99846200-99847600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr8:99846600-99847400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr8:99846600-99847600	Enhancers	Hela-S3	cervix
14	chr8:99846600-99847800	Enhancers	Muscle Satellite Cultured Cells	--
15	chr8:99846800-99847800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr8:99847000-99847400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr8:99847000-99847400	Enhancers	NHEK	skin
18	chr8:99847200-99847400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr8:99847200-99847400	Weak transcription	HSMMtube	muscle
20	chr8:99847200-99847400	Weak transcription	NHDF-Ad	bronchial
21	chr8:99847200-99847600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr8:99847200-99847600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr8:99847200-99847600	Flanking Active TSS	A549	lung
24	chr8:99847200-99847800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr8:99847200-99857200	Weak transcription	Placenta Amnion	Placenta Amnion

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