Variant report

Variant	rs138957358
Chromosome Location	chr15:72489688-72489689
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:72487407..72489902-chr15:72490450..72492521,2	K562	blood:
2	chr15:72489508..72492052-chr15:72496693..72498858,2	MCF-7	breast:
3	chr15:72488199..72491266-chr15:72491481..72494588,4	MCF-7	breast:
4	chr15:72488604..72491164-chr15:72493836..72495912,3	MCF-7	breast:
5	chr15:72487347..72489902-chr15:72491021..72493729,2	K562	blood:

Variant related genes	Relation type
ENSG00000067225	Chromatin interaction

Extended variants
information (count: 5 )
Associated
traits (count: 0)

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	nsv431395	chr15:72266174-72701777	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	144 gene(s)	inside rSNPs	diseases
2	nsv833051	chr15:72315471-72508429	Weak transcription Strong transcription Bivalent Enhancer ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
3	nsv530817	chr15:72350885-72773374	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	173 gene(s)	inside rSNPs	diseases
4	esv3430860	chr15:72373723-72849907	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	172 gene(s)	inside rSNPs	diseases
5	esv3409471	chr15:72488923-72491471	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:116 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:72485200-72490400	Weak transcription	A549	lung
2	chr15:72485200-72490400	Weak transcription	HSMM	muscle
3	chr15:72487600-72493600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr15:72487800-72490400	Weak transcription	GM12878-XiMat	blood
5	chr15:72488000-72489800	Weak transcription	Gastric	stomach
6	chr15:72488000-72490400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
7	chr15:72488000-72491000	Weak transcription	K562	blood
8	chr15:72488400-72490400	Weak transcription	HSMMtube	muscle
9	chr15:72488800-72489800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr15:72488800-72490600	Weak transcription	Dnd41	blood
11	chr15:72489000-72489800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
12	chr15:72489000-72489800	Flanking Active TSS	Placenta	Placenta
13	chr15:72489000-72489800	Flanking Active TSS	NHEK	skin
14	chr15:72489000-72490000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
15	chr15:72489000-72490000	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
16	chr15:72489000-72490000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr15:72489000-72490000	Active TSS	Duodenum Smooth Muscle	Duodenum
18	chr15:72489000-72490000	Active TSS	Placenta Amnion	Placenta Amnion
19	chr15:72489000-72490200	Active TSS	Lung	lung
20	chr15:72489000-72490600	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
21	chr15:72489000-72490600	Flanking Active TSS	HMEC	breast
22	chr15:72489000-72490800	Active TSS	H9 Cell Line	embryonic stem cell
23	chr15:72489000-72491000	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr15:72489200-72489800	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
25	chr15:72489200-72489800	Bivalent Enhancer	Primary B cells from peripheral blood	blood
26	chr15:72489200-72489800	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
27	chr15:72489200-72489800	Flanking Active TSS	Esophagus	oesophagus
28	chr15:72489200-72489800	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
29	chr15:72489200-72489800	Flanking Active TSS	Hela-S3	cervix
30	chr15:72489200-72489800	Enhancers	NHDF-Ad	bronchial
31	chr15:72489200-72490000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr15:72489200-72490200	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr15:72489200-72490200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr15:72489200-72490200	Weak transcription	NH-A	brain
35	chr15:72489200-72490600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
36	chr15:72489200-72490600	Enhancers	Fetal Heart	heart
37	chr15:72489200-72491600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
38	chr15:72489400-72489800	Bivalent/Poised TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr15:72489400-72489800	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr15:72489400-72489800	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
41	chr15:72489400-72489800	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
42	chr15:72489400-72489800	Bivalent Enhancer	Primary T killer memory cells from peripheral blood	blood
43	chr15:72489400-72489800	Bivalent/Poised TSS	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr15:72489400-72489800	Flanking Bivalent TSS/Enh	Duodenum Mucosa	Duodenum
45	chr15:72489400-72489800	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
46	chr15:72489400-72489800	ZNF genes & repeats	Spleen	Spleen
47	chr15:72489400-72489800	Flanking Bivalent TSS/Enh	HepG2	liver
48	chr15:72489400-72489800	Flanking Active TSS	Osteobl	bone
49	chr15:72489400-72490000	Enhancers	Primary B cells from cord blood	blood
50	chr15:72489400-72490000	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose

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