Variant report

Variant	rs603214
Chromosome Location	chr2:31509442-31509443
allele	A/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	GATA3	chr2:31509081-31509482	MCF-7	breast:	n/a	n/a

Variant related genes	Relation type
ENSG00000213620	TF binding region

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs12988379	0.96[YRI][hapmap];0.85[AFR][1000 genomes]
rs13405627	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2145036	0.85[AFR][1000 genomes]
rs582594	0.87[AMR][1000 genomes]
rs584875	0.87[AMR][1000 genomes]
rs586195	0.87[AMR][1000 genomes]
rs59281677	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59556133	1.00[EUR][1000 genomes]
rs610240	0.98[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs643137	0.87[AMR][1000 genomes]
rs643577	0.87[AMR][1000 genomes]

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	nsv948552	chr2:31118599-31595424	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv949028	chr2:31502801-31665108	Flanking Active TSS Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	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	chr2:31486600-31510000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr2:31492800-31510600	Weak transcription	Aorta	Aorta
3	chr2:31495800-31509800	Weak transcription	Esophagus	oesophagus
4	chr2:31497000-31510400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr2:31504600-31512800	Enhancers	Placenta	Placenta
6	chr2:31506200-31510000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr2:31507400-31511000	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr2:31507600-31510200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr2:31507800-31510600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr2:31508800-31511200	Enhancers	NHEK	skin
11	chr2:31508800-31511600	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr2:31508800-31511600	Enhancers	HUVEC	blood vessel
13	chr2:31509000-31510200	Enhancers	Fetal Heart	heart
14	chr2:31509000-31510400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr2:31509000-31510600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr2:31509000-31511000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr2:31509000-31511200	Enhancers	HMEC	breast
18	chr2:31509000-31511600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr2:31509200-31511200	Enhancers	Primary hematopoietic stem cells short term culture	blood
20	chr2:31509200-31522000	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr2:31509400-31509600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr2:31509400-31510800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
23	chr2:31509400-31511200	Enhancers	NH-A	brain
24	chr2:31509400-31511400	Enhancers	Primary hematopoietic stem cells	blood
25	chr2:31509400-31511600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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