Variant report

Variant	rs530853372
Chromosome Location	chr2:85901037-85901038
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:85892613..85895581-chr2:85898917..85901318,2	K562	blood:
2	chr2:85899004..85901888-chr2:85989811..85991933,2	MCF-7	breast:
3	chr2:85900096..85901739-chr2:85904881..85906884,2	K562	blood:

Variant related genes	Relation type
ENSG00000168878	Chromatin interaction

Extended variants
information (count: 7 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv874459	chr2:85828014-85939207	Flanking Active TSS Strong transcription Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
2	nsv874460	chr2:85828014-85941074	Enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Genic enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
3	nsv874461	chr2:85853653-85939207	Flanking Active TSS Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv874462	chr2:85853653-85941074	Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	nsv874463	chr2:85853653-85946708	Strong transcription Bivalent Enhancer Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	nsv874465	chr2:85898898-85939207	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv2812	chr2:85899944-85929267	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 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	chr2:85887000-85905800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr2:85891000-85905800	Weak transcription	Right Atrium	heart
3	chr2:85893000-85903000	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr2:85894000-85905000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
5	chr2:85896200-85901200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr2:85896600-85901200	Weak transcription	Lung	lung
7	chr2:85897200-85905600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
8	chr2:85899200-85902000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
9	chr2:85899600-85902400	Enhancers	Adipose Nuclei	Adipose
10	chr2:85899800-85902200	Enhancers	NHDF-Ad	bronchial
11	chr2:85900200-85901400	Weak transcription	Skeletal Muscle Male	skeletal muscle
12	chr2:85900200-85902000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr2:85900200-85902200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr2:85900400-85901200	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr2:85900400-85905600	Weak transcription	Brain Hippocampus Middle	brain
16	chr2:85900600-85901400	Enhancers	Primary hematopoietic stem cells	blood
17	chr2:85900600-85902200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr2:85900600-85902800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr2:85900600-85906200	Weak transcription	Primary B cells from peripheral blood	blood
20	chr2:85900800-85901200	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr2:85900800-85902600	Enhancers	Primary B cells from cord blood	blood
22	chr2:85901000-85901400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr2:85901000-85901400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
24	chr2:85901000-85901800	Enhancers	H9 Cell Line	embryonic stem cell
25	chr2:85901000-85902200	Enhancers	Placenta	Placenta

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