Variant report

Variant	rs370805134
Chromosome Location	chr2:11294313-11294314
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:11293490..11296297-chr2:11680693..11684323,3	MCF-7	breast:
2	chr2:11273055..11275301-chr2:11293268..11296881,3	MCF-7	breast:
3	chr2:11292941..11297094-chr2:11480820..11486254,6	MCF-7	breast:
4	chr2:11273067..11276077-chr2:11294167..11297061,3	K562	blood:
5	chr2:11292794..11295094-chr2:11339407..11341727,2	MCF-7	breast:
6	chr2:11294308..11297184-chr2:11482767..11485221,3	K562	blood:
7	chr2:11271098..11275692-chr2:11293512..11297101,4	MCF-7	breast:
8	chr2:11292916..11295580-chr2:11604494..11607840,3	MCF-7	breast:
9	chr2:11284657..11286652-chr2:11293189..11295227,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000134318	Chromatin interaction
ENSG00000264010	Chromatin interaction
ENSG00000145063	Chromatin interaction
ENSG00000196208	Chromatin interaction
ENSG00000150873	Chromatin interaction
ENSG00000169016	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	nsv520789	chr2:11259067-11312224	Weak transcription Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
2	esv3392188	chr2:11294026-11296874	Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:11273600-11294400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
2	chr2:11274000-11294600	Weak transcription	Right Atrium	heart
3	chr2:11284600-11294600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr2:11288200-11294400	Weak transcription	Monocytes-CD14+_RO01746	blood
5	chr2:11288200-11294600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr2:11289600-11294600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr2:11289800-11294400	Weak transcription	Pancreas	Pancrea
8	chr2:11291600-11294400	Weak transcription	Adipose Nuclei	Adipose
9	chr2:11291800-11294800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr2:11292800-11294600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr2:11294200-11294400	Enhancers	Primary monocytes fromperipheralblood	blood
12	chr2:11294200-11294400	Active TSS	Primary T helper cells fromperipheralblood	blood
13	chr2:11294200-11294400	Bivalent Enhancer	Stomach Smooth Muscle	stomach
14	chr2:11294200-11294400	Flanking Active TSS	Spleen	Spleen
15	chr2:11294200-11294400	Enhancers	Hela-S3	cervix
16	chr2:11294200-11294600	Enhancers	Primary B cells from cord blood	blood
17	chr2:11294200-11294600	Enhancers	Primary B cells from peripheral blood	blood
18	chr2:11294200-11294600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
19	chr2:11294200-11294600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr2:11294200-11294600	Bivalent Enhancer	Fetal Intestine Small	intestine
21	chr2:11294200-11294600	Bivalent Enhancer	Fetal Muscle Leg	muscle
22	chr2:11294200-11294600	Enhancers	Placenta	Placenta
23	chr2:11294200-11294600	Enhancers	Rectal Mucosa Donor 29	rectum
24	chr2:11294200-11294800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin

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