Variant report

Variant	rs565698276
Chromosome Location	chr15:44386507-44386508
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:44384733..44389004-chr15:44397743..44401359,3	K562	blood:

Extended variants
information (count: 9 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv431387	chr15:43929378-44862930	Weak transcription Strong transcription Active TSS ZNF genes & repeats Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	158 gene(s)	inside rSNPs	diseases
2	nsv931051	chr15:43988761-44833518	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	154 gene(s)	inside rSNPs	diseases
3	nsv1044435	chr15:44176103-44507403	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
4	nsv1052511	chr15:44266441-44719023	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
5	nsv542371	chr15:44266441-44719023	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
6	nsv1045362	chr15:44280481-44414443	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	n/a
7	nsv832989	chr15:44306469-44461710	Enhancers Genic enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
8	esv3351630	chr15:44334624-44547841	Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
9	nsv94497	chr15:44385556-44390318	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:44373600-44392800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr15:44379400-44397400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr15:44380800-44387600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
4	chr15:44381200-44389000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr15:44381200-44394200	Weak transcription	HUVEC	blood vessel
6	chr15:44381800-44400800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr15:44383600-44387400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr15:44384600-44388800	Weak transcription	Fetal Heart	heart
9	chr15:44384600-44393400	Weak transcription	HSMMtube	muscle
10	chr15:44384800-44387400	Weak transcription	Brain Angular Gyrus	brain
11	chr15:44384800-44387400	Weak transcription	Brain Hippocampus Middle	brain
12	chr15:44384800-44391800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr15:44384800-44393400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr15:44385000-44386600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr15:44385000-44386800	Weak transcription	Brain Substantia Nigra	brain
16	chr15:44385000-44387600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr15:44385000-44388800	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr15:44385000-44391400	Weak transcription	NHLF	lung
19	chr15:44385000-44392800	Weak transcription	HMEC	breast
20	chr15:44385000-44393400	Weak transcription	A549	lung
21	chr15:44385000-44393400	Weak transcription	HSMM	muscle
22	chr15:44385000-44393600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr15:44385000-44393600	Weak transcription	Muscle Satellite Cultured Cells	--
24	chr15:44385600-44389000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr15:44385800-44393400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr15:44386200-44386600	Enhancers	Brain Cingulate Gyrus	brain
27	chr15:44386200-44386600	Enhancers	Gastric	stomach
28	chr15:44386200-44386800	Enhancers	Brain Anterior Caudate	brain
29	chr15:44386200-44387800	Enhancers	NH-A	brain
30	chr15:44386200-44388200	Enhancers	NHDF-Ad	bronchial
31	chr15:44386400-44386800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr15:44386400-44387400	Enhancers	Osteobl	bone

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