Variant report

Variant	rs375584413
Chromosome Location	chr6:160550144-160550145
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr6:160550129-160550205	GM12878	blood:	n/a	n/a
2	MYC	chr6:160550141-160550299	H1-hESC	embryonic stem cell:	n/a	n/a
3	CTCF	chr6:160550020-160550170	GM12865	blood:	n/a	n/a

Variant related genes	Relation type
SLC22A1	TF binding region

Extended variants
information (count: 7 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758089	chr6:160372244-161234665	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
2	esv2759484	chr6:160372244-161234665	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
3	esv35098	chr6:160422589-161070870	Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
4	esv2757197	chr6:160432331-161070870	Weak transcription Genic enhancers Active TSS Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
5	nsv818463	chr6:160435569-161025547	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
6	esv13999	chr6:160545917-160553013	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv886807	chr6:160549080-160559234	Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:36 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:160529400-160559200	Weak transcription	Skeletal Muscle Female	skeletal muscle
2	chr6:160530800-160553400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr6:160533400-160552800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr6:160538800-160557600	Weak transcription	Skeletal Muscle Male	skeletal muscle
5	chr6:160539000-160553000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr6:160539400-160554200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr6:160539400-160554800	Weak transcription	Spleen	Spleen
8	chr6:160539400-160558000	Weak transcription	Gastric	stomach
9	chr6:160539400-160559400	Weak transcription	Brain Angular Gyrus	brain
10	chr6:160539400-160559400	Weak transcription	HSMMtube	muscle
11	chr6:160539400-160559600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr6:160539400-160580400	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr6:160539600-160553400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr6:160539600-160574600	Weak transcription	Adipose Nuclei	Adipose
15	chr6:160539800-160553400	Weak transcription	Ovary	ovary
16	chr6:160540200-160576200	Weak transcription	Right Ventricle	heart
17	chr6:160540400-160568800	Weak transcription	Esophagus	oesophagus
18	chr6:160541600-160553200	Weak transcription	Muscle Satellite Cultured Cells	--
19	chr6:160543200-160561400	Weak transcription	Right Atrium	heart
20	chr6:160543400-160558600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr6:160543800-160551200	Weak transcription	Fetal Stomach	stomach
22	chr6:160544200-160552200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr6:160544200-160553000	Weak transcription	Fetal Muscle Trunk	muscle
24	chr6:160545000-160555200	Weak transcription	Fetal Muscle Leg	muscle
25	chr6:160545000-160559000	Weak transcription	Stomach Smooth Muscle	stomach
26	chr6:160545200-160552200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr6:160545200-160553000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr6:160546000-160557000	Weak transcription	Pancreas	Pancrea
29	chr6:160546000-160559200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr6:160546400-160560200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr6:160546800-160550200	Weak transcription	Fetal Intestine Large	intestine
32	chr6:160548200-160550600	Enhancers	HepG2	liver
33	chr6:160548200-160560000	Weak transcription	Aorta	Aorta
34	chr6:160549200-160550600	Enhancers	Fetal Intestine Small	intestine
35	chr6:160549600-160559600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr6:160549800-160558400	Genic enhancers	Liver	Liver

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