Variant report

Variant	rs576386023
Chromosome Location	chr9:16597218-16597219
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530933	chr9:16251206-16830845	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv530934	chr9:16281246-16779432	Strong transcription Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	nsv1032856	chr9:16465330-16773471	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	nsv540073	chr9:16465330-16773471	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
5	nsv524264	chr9:16596071-16611692	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:16576000-16601600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr9:16576400-16601400	Weak transcription	NHDF-Ad	bronchial
3	chr9:16583000-16606800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr9:16583200-16611200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr9:16586800-16604400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr9:16591400-16598600	Weak transcription	HSMM	muscle
7	chr9:16594800-16601800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr9:16594800-16601800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
9	chr9:16595000-16598000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr9:16595000-16598000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr9:16595000-16611200	Weak transcription	NHLF	lung
12	chr9:16595200-16597600	Enhancers	A549	lung
13	chr9:16595200-16598400	Weak transcription	Osteobl	bone
14	chr9:16595400-16597600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr9:16596000-16598400	Weak transcription	Ovary	ovary
16	chr9:16596400-16597600	Enhancers	Colon Smooth Muscle	Colon
17	chr9:16596600-16597600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr9:16596600-16597800	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr9:16596600-16597800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr9:16596600-16597800	Enhancers	Fetal Lung	lung
21	chr9:16596600-16598800	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr9:16596800-16598400	Weak transcription	Rectal Smooth Muscle	rectum
23	chr9:16597200-16597600	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr9:16597200-16597600	Enhancers	Fetal Stomach	stomach

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