Variant report

Variant	rs556940876
Chromosome Location	chr8:91691945-91691946
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:91659065..91661571-chr8:91690814..91693630,2	K562	blood:
2	chr8:91657079..91658654-chr8:91690664..91693571,2	MCF-7	breast:
3	chr8:91655723..91658520-chr8:91691444..91693877,2	K562	blood:
4	chr8:91657324..91660204-chr8:91691658..91693612,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000246792	Chromatin interaction
ENSG00000180694	Chromatin interaction

Extended variants
information (count: 3 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1028628	chr8:91680968-92418954	Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
2	nsv539672	chr8:91680968-92418954	Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
3	esv3326233	chr8:91690825-91708859	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:91688800-91693400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr8:91688800-91694000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr8:91689000-91693400	Weak transcription	Brain Cingulate Gyrus	brain
4	chr8:91689000-91693600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr8:91689400-91694000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr8:91690800-91692000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr8:91691000-91692400	Enhancers	Placenta	Placenta
8	chr8:91691200-91692000	Enhancers	Placenta Amnion	Placenta Amnion
9	chr8:91691200-91692200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr8:91691200-91694600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr8:91691200-91694600	Enhancers	Fetal Lung	lung
12	chr8:91691400-91692200	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr8:91691400-91692400	Flanking Active TSS	HepG2	liver
14	chr8:91691600-91692200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr8:91691600-91692200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr8:91691600-91692400	Enhancers	H1 Cell Line	embryonic stem cell
17	chr8:91691600-91692400	Enhancers	H9 Cell Line	embryonic stem cell
18	chr8:91691600-91695000	Enhancers	K562	blood
19	chr8:91691600-91695600	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr8:91691600-91696000	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr8:91691600-91696400	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr8:91691600-91696400	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr8:91691600-91696400	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr8:91691800-91692000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr8:91691800-91692000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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