Variant report

Variant	rs557708137
Chromosome Location	chr4:7634198-7634199
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916610	chr4:7238883-7731946	Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
2	nsv1011547	chr4:7318232-7637410	Active TSS ZNF genes & repeats Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
3	nsv537017	chr4:7318232-7637410	Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
4	esv34156	chr4:7526515-7750588	Active TSS Flanking Active TSS Strong transcription Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
5	nsv878570	chr4:7534603-7836835	Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
6	nsv491712	chr4:7582506-8155069	Enhancers Bivalent Enhancer Genic enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
7	nsv461213	chr4:7584560-7637297	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv593618	chr4:7584560-7637297	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
9	nsv508272	chr4:7591967-7722112	Strong transcription Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
10	nsv517503	chr4:7632330-7639906	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
11	esv3371702	chr4:7633552-7637750	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:7631200-7635000	Enhancers	Fetal Brain Male	brain
2	chr4:7631600-7634600	Enhancers	Brain Hippocampus Middle	brain
3	chr4:7631600-7635200	Enhancers	Right Ventricle	heart
4	chr4:7631800-7634600	Enhancers	Brain Cingulate Gyrus	brain
5	chr4:7631800-7634600	Enhancers	Brain Substantia Nigra	brain
6	chr4:7631800-7634600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
7	chr4:7631800-7634600	Enhancers	Left Ventricle	heart
8	chr4:7631800-7634800	Enhancers	Brain Inferior Temporal Lobe	brain
9	chr4:7631800-7635200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
10	chr4:7632200-7634600	Enhancers	Right Atrium	heart
11	chr4:7632400-7634200	Enhancers	Fetal Brain Female	brain
12	chr4:7632400-7634400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr4:7633000-7634600	Bivalent Enhancer	Fetal Muscle Leg	muscle
14	chr4:7633000-7636400	Weak transcription	Spleen	Spleen
15	chr4:7633200-7634200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr4:7633200-7634200	Enhancers	HepG2	liver
17	chr4:7633200-7634800	Enhancers	Fetal Heart	heart
18	chr4:7633200-7635400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr4:7633200-7635400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr4:7633200-7636600	Weak transcription	Esophagus	oesophagus
21	chr4:7633200-7643800	Weak transcription	Brain Anterior Caudate	brain
22	chr4:7633400-7635000	Enhancers	Brain Germinal Matrix	brain
23	chr4:7633400-7636400	Weak transcription	HSMM	muscle
24	chr4:7633400-7644400	Weak transcription	Ovary	ovary
25	chr4:7633600-7634400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr4:7633600-7635000	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
27	chr4:7633800-7634800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr4:7633800-7635000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr4:7633800-7635600	Enhancers	NH-A	brain
30	chr4:7633800-7646000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr4:7634000-7634400	Weak transcription	Brain Angular Gyrus	brain
32	chr4:7634000-7634800	Weak transcription	NHLF	lung

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