Variant report

Variant	rs57997615
Chromosome Location	chr12:59432620-59432621
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr12:59413167..59414727-chr12:59431190..59432775,2	MCF-7	breast:
2	chr12:59431224..59433433-chr12:59436117..59438900,2	MCF-7	breast:
3	chr12:58926114..58928462-chr12:59432345..59434886,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000244390	Chromatin interaction

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs56962876	0.88[AFR][1000 genomes]
rs57003188	0.96[AFR][1000 genomes]
rs57023637	0.88[AFR][1000 genomes]
rs57954356	1.00[AFR][1000 genomes]
rs58340353	1.00[AFR][1000 genomes]
rs58975592	0.84[AFR][1000 genomes]
rs59734417	0.84[AFR][1000 genomes]
rs60621135	1.00[AFR][1000 genomes]
rs61600019	0.84[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1043385	chr12:59149582-59758952	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
2	nsv1067596	chr12:59167152-59764208	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	nsv492251	chr12:59167152-59764208	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
4	nsv559048	chr12:59336737-59440659	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv559049	chr12:59359937-59436179	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 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	chr12:59425400-59433800	Weak transcription	Pancreas	Pancrea
2	chr12:59428800-59433600	Weak transcription	Esophagus	oesophagus
3	chr12:59430600-59432800	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr12:59431000-59434000	Weak transcription	Osteobl	bone
5	chr12:59431000-59434200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr12:59431000-59434200	Weak transcription	Small Intestine	intestine
7	chr12:59431000-59441800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr12:59431200-59433600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr12:59431200-59437200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr12:59431400-59433800	Weak transcription	HUVEC	blood vessel
11	chr12:59431400-59434000	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr12:59431400-59434200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr12:59431600-59433200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr12:59431600-59433600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr12:59431600-59433600	Weak transcription	NH-A	brain
16	chr12:59431600-59433600	Weak transcription	NHDF-Ad	bronchial
17	chr12:59431800-59433400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr12:59431800-59434200	Weak transcription	Fetal Kidney	kidney
19	chr12:59431800-59434400	Weak transcription	Stomach Mucosa	stomach
20	chr12:59432200-59433600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr12:59432200-59433800	Weak transcription	HSMM	muscle
22	chr12:59432200-59434200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr12:59432400-59433400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr12:59432400-59433600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr12:59432400-59433600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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