Variant report

Variant	rs150197611
Chromosome Location	chr5:17398929-17398930
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:22 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1029959	chr5:17133214-17455995	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
2	nsv461988	chr5:17296342-17484038	Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
3	nsv597313	chr5:17296342-17484038	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
4	nsv830219	chr5:17325802-17518914	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
5	esv1793466	chr5:17364700-17721569	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
6	esv1801170	chr5:17364700-17721569	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
7	esv1820519	chr5:17364700-17721569	Enhancers Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
8	esv1824831	chr5:17364700-17721569	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
9	esv1827359	chr5:17364700-17721569	Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
10	esv1828062	chr5:17364700-17721569	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
11	nsv427713	chr5:17364700-17721569	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
12	nsv428464	chr5:17364700-17721569	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
13	esv2757986	chr5:17364700-17936404	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
14	esv2759328	chr5:17364700-17936404	Enhancers Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
15	nsv1017469	chr5:17373383-17416643	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	n/a
16	nsv980966	chr5:17379819-17496300	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
17	nsv1023600	chr5:17382604-17418330	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
18	nsv1031214	chr5:17382604-17427825	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
19	nsv881474	chr5:17390145-17509888	Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
20	nsv968881	chr5:17391605-17484624	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
21	esv2757108	chr5:17398090-17804346	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	42 gene(s)	inside rSNPs	diseases
22	nsv1030762	chr5:17398399-17690362	Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	42 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:51 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:17396400-17400000	Weak transcription	Placenta	Placenta
2	chr5:17396600-17400800	Weak transcription	Fetal Kidney	kidney
3	chr5:17396800-17399600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr5:17397200-17401600	Enhancers	Primary B cells from peripheral blood	blood
5	chr5:17397400-17400800	Weak transcription	Ovary	ovary
6	chr5:17397600-17402000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr5:17397800-17399200	Enhancers	NHLF	lung
8	chr5:17397800-17399400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr5:17397800-17399400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr5:17397800-17399400	Enhancers	HMEC	breast
11	chr5:17397800-17399400	Enhancers	Osteobl	bone
12	chr5:17397800-17399600	Enhancers	NH-A	brain
13	chr5:17397800-17401000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr5:17397800-17403000	Enhancers	Primary hematopoietic stem cells short term culture	blood
15	chr5:17398000-17399000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr5:17398000-17399000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr5:17398000-17399000	Enhancers	Hela-S3	cervix
18	chr5:17398000-17399200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr5:17398000-17399200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr5:17398000-17399200	Enhancers	A549	lung
21	chr5:17398000-17399600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr5:17398000-17399600	Enhancers	HSMM	muscle
23	chr5:17398000-17399600	Enhancers	NHDF-Ad	bronchial
24	chr5:17398000-17399600	Enhancers	NHEK	skin
25	chr5:17398000-17400200	Enhancers	Primary hematopoietic stem cells	blood
26	chr5:17398000-17400800	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr5:17398000-17400800	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr5:17398200-17399000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr5:17398200-17399000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr5:17398200-17399200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr5:17398200-17399200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr5:17398200-17399200	Enhancers	Muscle Satellite Cultured Cells	--
33	chr5:17398200-17399400	Enhancers	H1 Cell Line	embryonic stem cell
34	chr5:17398200-17399600	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
35	chr5:17398200-17400600	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr5:17398200-17400800	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr5:17398400-17399200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr5:17398400-17399600	Enhancers	GM12878-XiMat	blood
39	chr5:17398400-17400600	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr5:17398600-17399000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
41	chr5:17398600-17399200	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr5:17398600-17399200	Enhancers	Placenta Amnion	Placenta Amnion
43	chr5:17398600-17399200	Enhancers	Monocytes-CD14+_RO01746	blood
44	chr5:17398600-17403000	Enhancers	Primary monocytes fromperipheralblood	blood
45	chr5:17398800-17399000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr5:17398800-17399000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr5:17398800-17399000	Enhancers	Small Intestine	intestine
48	chr5:17398800-17399200	Weak transcription	HSMMtube	muscle
49	chr5:17398800-17399600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
50	chr5:17398800-17401000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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