Variant report

Variant	rs28546523
Chromosome Location	chr15:50168797-50168798
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	CTCF	chr15:50168760-50169765	MCF-7	breast:	n/a	chr15:50169139-50169160 chr15:50169137-50169155

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:49912192..49914242-chr15:50166228..50169006,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000259188	TF binding region
ENSG00000166262	Chromatin interaction
ENSG00000104047	Chromatin interaction

Extended variants
information (count: 8 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs28496735	1.00[AMR][1000 genomes]
rs28565343	1.00[AMR][1000 genomes]
rs28581967	1.00[AMR][1000 genomes]
rs28614053	1.00[AMR][1000 genomes]
rs28739554	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1044277	chr15:49921547-50702386	Enhancers Active TSS Weak transcription Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	107 gene(s)	inside rSNPs	diseases
2	nsv542380	chr15:49921547-50702386	Enhancers Strong transcription Weak transcription Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	107 gene(s)	inside rSNPs	diseases
3	nsv833003	chr15:50100372-50273309	ZNF genes & repeats Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:42 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:50135200-50181400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr15:50135800-50187400	Weak transcription	Liver	Liver
3	chr15:50138200-50189800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
4	chr15:50145600-50200400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr15:50149400-50198000	Strong transcription	Primary neutrophils fromperipheralblood	blood
6	chr15:50158800-50170600	Weak transcription	Placenta	Placenta
7	chr15:50161600-50175600	Strong transcription	Primary monocytes fromperipheralblood	blood
8	chr15:50161800-50179000	Strong transcription	Primary hematopoietic stem cells	blood
9	chr15:50161800-50210600	Strong transcription	Monocytes-CD14+_RO01746	blood
10	chr15:50162400-50172200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr15:50163000-50200400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr15:50166000-50170800	Weak transcription	Left Ventricle	heart
13	chr15:50166600-50170200	Weak transcription	Duodenum Smooth Muscle	Duodenum
14	chr15:50166600-50173000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr15:50167000-50171600	Enhancers	Colon Smooth Muscle	Colon
16	chr15:50167200-50171200	Enhancers	Breast Myoepithelial Primary Cells	Breast
17	chr15:50167600-50200800	Weak transcription	Spleen	Spleen
18	chr15:50167800-50169000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr15:50168200-50171800	Enhancers	Rectal Smooth Muscle	rectum
20	chr15:50168400-50169000	Enhancers	Fetal Intestine Large	intestine
21	chr15:50168400-50169000	Enhancers	HMEC	breast
22	chr15:50168400-50169200	Enhancers	Stomach Smooth Muscle	stomach
23	chr15:50168400-50169600	Enhancers	Pancreas	Pancrea
24	chr15:50168400-50169600	Enhancers	Rectal Mucosa Donor 31	rectum
25	chr15:50168400-50169600	Enhancers	Small Intestine	intestine
26	chr15:50168400-50169800	Enhancers	Skeletal Muscle Female	skeletal muscle
27	chr15:50168400-50170000	Enhancers	Aorta	Aorta
28	chr15:50168400-50170200	Enhancers	Fetal Lung	lung
29	chr15:50168400-50170200	Enhancers	Ovary	ovary
30	chr15:50168400-50170800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr15:50168400-50171200	Enhancers	Fetal Muscle Leg	muscle
32	chr15:50168400-50171400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr15:50168400-50171400	Enhancers	NHDF-Ad	bronchial
34	chr15:50168400-50172600	Enhancers	Fetal Stomach	stomach
35	chr15:50168600-50168800	Flanking Active TSS	Adipose Nuclei	Adipose
36	chr15:50168600-50169600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr15:50168600-50169800	Enhancers	Skeletal Muscle Male	skeletal muscle
38	chr15:50168600-50169800	Enhancers	Hela-S3	cervix
39	chr15:50168600-50171200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr15:50168600-50171200	Enhancers	Fetal Kidney	kidney
41	chr15:50168600-50171200	Enhancers	Right Atrium	heart
42	chr15:50168600-50171200	Enhancers	Osteobl	bone

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