Variant report

Variant	rs559881599
Chromosome Location	chr5:111688925-111688926
allele	-/TGTTGGCATGCTTG
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1015302	chr5:111339022-111802947	Enhancers Active TSS Strong transcription Weak transcription Bivalent/Poised TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
2	nsv537861	chr5:111339022-111802947	Strong transcription Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
3	nsv599368	chr5:111399885-112032675	Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
4	nsv948869	chr5:111476404-111695183	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
5	nsv531291	chr5:111497440-111756788	Enhancers Flanking Active TSS Genic enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
6	nsv882714	chr5:111655382-111807579	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv462386	chr5:111667572-111699317	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
8	nsv599372	chr5:111667572-111699317	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
9	nsv437471	chr5:111682654-111691924	Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
10	esv274937	chr5:111688750-111691016	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:28 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:111676200-111689000	Weak transcription	Lung	lung
2	chr5:111678400-111689000	Weak transcription	Gastric	stomach
3	chr5:111678600-111695600	Weak transcription	Pancreas	Pancrea
4	chr5:111683800-111689000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr5:111683800-111689400	Weak transcription	Spleen	Spleen
6	chr5:111684000-111702600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr5:111684800-111689000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr5:111684800-111689600	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr5:111684800-111689600	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr5:111685000-111689000	Weak transcription	H1 Cell Line	embryonic stem cell
11	chr5:111685000-111689400	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr5:111685000-111689600	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr5:111685000-111689800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr5:111685200-111689800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
15	chr5:111685200-111689800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
16	chr5:111685200-111689800	Weak transcription	Brain Anterior Caudate	brain
17	chr5:111685200-111690600	Weak transcription	GM12878-XiMat	blood
18	chr5:111685200-111707000	Weak transcription	Ovary	ovary
19	chr5:111685200-111709800	Weak transcription	Aorta	Aorta
20	chr5:111685600-111689400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
21	chr5:111685800-111693600	Weak transcription	Right Atrium	heart
22	chr5:111686400-111692000	Weak transcription	Right Ventricle	heart
23	chr5:111687200-111693600	Weak transcription	Sigmoid Colon	Sigmoid Colon
24	chr5:111687600-111690400	Weak transcription	HUVEC	blood vessel
25	chr5:111688200-111689200	Enhancers	Fetal Heart	heart
26	chr5:111688800-111689400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr5:111688800-111689600	Enhancers	Left Ventricle	heart
28	chr5:111688800-111690400	Enhancers	ES-I3 Cell Line	embryonic stem cell

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