Variant report

Variant	rs76701754
Chromosome Location	chr3:142605990-142605991
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr3:142591058..142593405-chr3:142604358..142606915,2	K562	blood:
2	chr3:142545978..142547931-chr3:142603627..142606168,2	MCF-7	breast:
3	chr3:142605846..142608751-chr3:142718093..142722238,5	K562	blood:

Variant related genes	Relation type
ENSG00000268129	Chromatin interaction
ENSG00000240950	Chromatin interaction
ENSG00000163714	Chromatin interaction

Extended variants
information (count: 2 )
Associated
traits (count: 0)

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	nsv877562	chr3:142573789-142846370	Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Enhancers Weak transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
2	nsv437342	chr3:142605233-142622834	Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Weak transcription Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 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	chr3:142586000-142606600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
2	chr3:142590600-142606000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr3:142601000-142606000	Weak transcription	Right Atrium	heart
4	chr3:142603400-142607000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr3:142603600-142607000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr3:142604000-142606600	Weak transcription	Liver	Liver
7	chr3:142604400-142606600	Weak transcription	HUES64 Cell Line	embryonic stem cell
8	chr3:142604800-142606600	Weak transcription	Right Ventricle	heart
9	chr3:142605000-142606000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr3:142605000-142607000	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr3:142605200-142606800	Enhancers	Muscle Satellite Cultured Cells	--
12	chr3:142605200-142607000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr3:142605400-142606400	Enhancers	Hela-S3	cervix
14	chr3:142605400-142606800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr3:142605400-142606800	Enhancers	Osteobl	bone
16	chr3:142605400-142607200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr3:142605600-142606000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr3:142605600-142606200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr3:142605600-142606200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr3:142605600-142606200	Flanking Active TSS	A549	lung
21	chr3:142605600-142606200	Flanking Active TSS	NH-A	brain
22	chr3:142605600-142607000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
23	chr3:142605600-142607000	Enhancers	NHEK	skin
24	chr3:142605800-142606000	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr3:142605800-142606200	Enhancers	Adipose Nuclei	Adipose
26	chr3:142605800-142606800	Enhancers	Brain Germinal Matrix	brain
27	chr3:142605800-142606800	Weak transcription	K562	blood
28	chr3:142605800-142606800	Enhancers	NHDF-Ad	bronchial
29	chr3:142605800-142607000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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