Variant report

Variant	rs141446514
Chromosome Location	chr6:28763047-28763048
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:28762168..28764957-chr6:28971752..28974125,2	K562	blood:
2	chr6:28691994..28695396-chr6:28761030..28763739,3	K562	blood:
3	chr6:28761882..28764605-chr6:28861705..28864953,3	K562	blood:

Variant related genes	Relation type
ENSG00000197935	Chromatin interaction
ENSG00000224157	Chromatin interaction

Extended variants
information (count: 4 )
Associated
traits (count: 0)

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	nsv534089	chr6:28636972-28841640	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
2	nsv883517	chr6:28751727-28802149	Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	esv3384463	chr6:28759027-28776259	Bivalent Enhancer Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	esv2621756	chr6:28762692-28779791	Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS Enhancers Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:28759600-28763600	Weak transcription	Hela-S3	cervix
2	chr6:28761600-28763800	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
3	chr6:28761600-28764600	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
4	chr6:28761800-28763600	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
5	chr6:28761800-28763600	Flanking Active TSS	K562	blood
6	chr6:28761800-28764200	Flanking Active TSS	HepG2	liver
7	chr6:28762400-28763200	Flanking Bivalent TSS/Enh	GM12878-XiMat	blood
8	chr6:28762800-28763200	Bivalent Enhancer	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr6:28762800-28763200	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 2	blood
10	chr6:28762800-28763400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr6:28762800-28763400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
12	chr6:28762800-28763400	Enhancers	HMEC	breast
13	chr6:28762800-28763400	Bivalent Enhancer	Osteobl	bone
14	chr6:28762800-28763600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
15	chr6:28762800-28763800	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr6:28763000-28763200	Flanking Bivalent TSS/Enh	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr6:28763000-28763200	Flanking Bivalent TSS/Enh	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr6:28763000-28763400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
19	chr6:28763000-28763400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr6:28763000-28763400	Flanking Active TSS	A549	lung
21	chr6:28763000-28763400	Bivalent Enhancer	NHEK	skin

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