Variant report

Variant	rs552065567
Chromosome Location	chr15:59614963-59614964
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv527307	chr15:59103328-60018487	Enhancers Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	145 gene(s)	inside rSNPs	diseases
2	nsv934082	chr15:59608605-59733211	Flanking Active TSS Enhancers Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
3	nsv457175	chr15:59609753-59681214	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
4	nsv569603	chr15:59609753-59681214	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
5	nsv471246	chr15:59610743-59681214	Enhancers Flanking Active TSS Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
6	esv1794268	chr15:59614874-59637355	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:44 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:59600000-59627400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr15:59606600-59621200	Weak transcription	Fetal Kidney	kidney
3	chr15:59606800-59615600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr15:59606800-59621400	Weak transcription	Gastric	stomach
5	chr15:59606800-59623000	Weak transcription	Lung	lung
6	chr15:59606800-59631600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr15:59607000-59620200	Weak transcription	Esophagus	oesophagus
8	chr15:59608600-59615000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr15:59608600-59619000	Weak transcription	Sigmoid Colon	Sigmoid Colon
10	chr15:59608600-59619400	Weak transcription	Rectal Mucosa Donor 29	rectum
11	chr15:59608600-59621400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr15:59608600-59621400	Weak transcription	Ovary	ovary
13	chr15:59608600-59622600	Weak transcription	Brain Inferior Temporal Lobe	brain
14	chr15:59608600-59623200	Weak transcription	Psoas Muscle	Psoas
15	chr15:59608600-59623400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
16	chr15:59608600-59625800	Weak transcription	HMEC	breast
17	chr15:59608800-59621400	Weak transcription	Duodenum Mucosa	Duodenum
18	chr15:59609600-59619000	Weak transcription	Rectal Mucosa Donor 31	rectum
19	chr15:59609800-59620200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr15:59609800-59620400	Weak transcription	HSMM	muscle
21	chr15:59609800-59620800	Weak transcription	NH-A	brain
22	chr15:59609800-59621400	Weak transcription	Pancreas	Pancrea
23	chr15:59610000-59619000	Weak transcription	Stomach Mucosa	stomach
24	chr15:59610200-59617600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr15:59610200-59620400	Weak transcription	Osteobl	bone
26	chr15:59610200-59623000	Weak transcription	Left Ventricle	heart
27	chr15:59610200-59627200	Weak transcription	Cortex derived primary cultured neurospheres	brain
28	chr15:59610400-59617400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr15:59610600-59616200	Weak transcription	NHDF-Ad	bronchial
30	chr15:59610600-59620400	Weak transcription	Fetal Heart	heart
31	chr15:59610600-59623000	Weak transcription	Aorta	Aorta
32	chr15:59611200-59617600	Weak transcription	Hela-S3	cervix
33	chr15:59611200-59617800	Weak transcription	NHEK	skin
34	chr15:59612200-59625800	Weak transcription	HUVEC	blood vessel
35	chr15:59613800-59626000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr15:59614000-59615000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
37	chr15:59614000-59615200	Enhancers	Fetal Intestine Small	intestine
38	chr15:59614000-59616400	Enhancers	GM12878-XiMat	blood
39	chr15:59614000-59620400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr15:59614200-59621600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr15:59614400-59615000	Weak transcription	Fetal Intestine Large	intestine
42	chr15:59614400-59615200	Enhancers	Liver	Liver
43	chr15:59614600-59615000	Enhancers	HepG2	liver
44	chr15:59614600-59615200	Enhancers	A549	lung

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