Variant report

Variant	rs1367697
Chromosome Location	chr7:18399925-18399926
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs6461377	0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs73307426	0.81[AMR][1000 genomes]
rs7788359	0.86[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1024398	chr7:17630148-18545073	Strong transcription Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases
2	nsv538764	chr7:17630148-18545073	Strong transcription Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases
3	nsv1030201	chr7:17898410-18491985	Enhancers Strong transcription Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
4	nsv606358	chr7:18084843-18416097	Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
5	nsv830916	chr7:18254299-18433349	Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Weak transcription Genic enhancers Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	esv2755157	chr7:18337660-18805860	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:18385600-18401600	Weak transcription	Aorta	Aorta
2	chr7:18387400-18409800	Weak transcription	Primary B cells from cord blood	blood
3	chr7:18392800-18401200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr7:18394400-18402800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr7:18396200-18401200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr7:18396200-18401400	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr7:18396200-18401400	Weak transcription	Adipose Nuclei	Adipose
8	chr7:18396200-18403600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr7:18396200-18406200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr7:18396400-18401200	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr7:18396400-18401200	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr7:18396400-18401200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
13	chr7:18396400-18401400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
14	chr7:18396400-18410200	Weak transcription	Monocytes-CD14+_RO01746	blood
15	chr7:18396400-18413800	Weak transcription	Primary monocytes fromperipheralblood	blood
16	chr7:18396400-18416800	Weak transcription	Primary B cells from peripheral blood	blood
17	chr7:18399800-18401600	Weak transcription	Esophagus	oesophagus

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dbSNP/dbVar ID: rs12345 /nsv7879
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