Variant report

Variant	rs72950896
Chromosome Location	chr2:113872405-113872406
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr2:113872349-113872545	MCF10A-Er-Src	breast:	n/a	n/a

Variant related genes	Relation type
IL1RN	TF binding region

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs28928277	1.00[AFR][1000 genomes]
rs28928284	1.00[AFR][1000 genomes]
rs28928287	1.00[AFR][1000 genomes]
rs57721277	1.00[AFR][1000 genomes]
rs72952606	1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv997348	chr2:113688093-113986508	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
2	nsv1007254	chr2:113726982-113887782	Enhancers Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
3	nsv535894	chr2:113726982-113887782	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
4	nsv1003928	chr2:113846503-113887782	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv979338	chr2:113869830-113880320	Enhancers Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv874895	chr2:113870663-113875892	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 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	chr2:113868600-113875400	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr2:113869400-113873000	Weak transcription	Stomach Mucosa	stomach
3	chr2:113869800-113873400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr2:113870200-113873000	Weak transcription	Primary hematopoietic stem cells	blood
5	chr2:113870200-113873000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr2:113870200-113873200	Weak transcription	Spleen	Spleen
7	chr2:113870400-113872800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
8	chr2:113870400-113873400	Enhancers	Monocytes-CD14+_RO01746	blood
9	chr2:113870800-113872600	Enhancers	Primary neutrophils fromperipheralblood	blood
10	chr2:113871400-113873600	Enhancers	Placenta	Placenta
11	chr2:113871400-113874800	Enhancers	NHEK	skin
12	chr2:113871400-113875000	Bivalent Enhancer	HepG2	liver
13	chr2:113871400-113875400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr2:113871600-113874600	Weak transcription	Gastric	stomach
15	chr2:113871600-113875400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr2:113871800-113872800	Weak transcription	Primary T cells from cord blood	blood
17	chr2:113871800-113873600	Enhancers	Primary hematopoietic stem cells short term culture	blood
18	chr2:113871800-113873600	Enhancers	HMEC	breast
19	chr2:113871800-113874600	Enhancers	GM12878-XiMat	blood
20	chr2:113871800-113875400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr2:113872200-113873200	Bivalent Enhancer	Primary B cells from cord blood	blood
22	chr2:113872400-113872600	Enhancers	Placenta Amnion	Placenta Amnion
23	chr2:113872400-113872800	Active TSS	Esophagus	oesophagus
24	chr2:113872400-113873000	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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