Variant report

Variant	rs1976191
Chromosome Location	chr15:75475719-75475720
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:75473527..75476578-chr15:75479286..75482209,3	K562	blood:
2	chr15:75473895..75476672-chr15:75480654..75483531,2	MCF-7	breast:
3	chr15:75319716..75322406-chr15:75473522..75476448,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000240366	Chromatin interaction
ENSG00000138621	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs11635338	1.00[AMR][1000 genomes]
rs1466663	1.00[AMR][1000 genomes]
rs4886428	1.00[AMR][1000 genomes]
rs6495165	1.00[AMR][1000 genomes]
rs8027407	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8039284	0.90[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv569993	chr15:75242155-75483752	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	72 gene(s)	inside rSNPs	diseases
2	nsv904383	chr15:75382542-75520378	Weak transcription Genic enhancers Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
3	esv1796196	chr15:75389382-75531124	Weak transcription Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
4	nsv1039713	chr15:75394213-75674389	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
5	nsv1037713	chr15:75401213-75665304	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
6	nsv1053212	chr15:75428467-75534408	Flanking Active TSS Bivalent Enhancer Active TSS Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
7	nsv833056	chr15:75452947-75614590	Enhancers Strong transcription Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:75470200-75475800	Enhancers	Cortex derived primary cultured neurospheres	brain
2	chr15:75471800-75476800	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr15:75473000-75477800	Weak transcription	Right Ventricle	heart
4	chr15:75473000-75478800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr15:75473000-75487600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr15:75473200-75476800	Weak transcription	Spleen	Spleen
7	chr15:75473200-75477800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
8	chr15:75473200-75483200	Weak transcription	Aorta	Aorta
9	chr15:75473200-75483400	Weak transcription	Left Ventricle	heart
10	chr15:75475200-75476000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr15:75475200-75476600	Weak transcription	GM12878-XiMat	blood
12	chr15:75475200-75478000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr15:75475200-75478400	Weak transcription	Thymus	Thymus
14	chr15:75475400-75476600	Weak transcription	Primary monocytes fromperipheralblood	blood
15	chr15:75475400-75476600	Weak transcription	Lung	lung
16	chr15:75475400-75477600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr15:75475400-75477800	Weak transcription	H1 Cell Line	embryonic stem cell
18	chr15:75475400-75477800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
19	chr15:75475400-75487800	Weak transcription	Right Atrium	heart
20	chr15:75475600-75476800	Weak transcription	Primary hematopoietic stem cells	blood
21	chr15:75475600-75476800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
22	chr15:75475600-75476800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
23	chr15:75475600-75477000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr15:75475600-75477600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr15:75475600-75477600	Weak transcription	Fetal Heart	heart
26	chr15:75475600-75477600	Weak transcription	Fetal Thymus	thymus
27	chr15:75475600-75477800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
28	chr15:75475600-75480600	Weak transcription	HepG2	liver
29	chr15:75475600-75481600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr15:75475600-75487600	Weak transcription	Pancreas	Pancrea

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