Variant report

Variant	rs502981
Chromosome Location	chr9:18706240-18706241
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	STAT5A	chr9:18706034-18706288	K562	blood:	n/a	n/a
2	STAT1	chr9:18705789-18706634	Hela-S3	cervix:	n/a	chr9:18706401-18706409 chr9:18706138-18706149
3	STAT3	chr9:18705993-18706330	MCF10A-Er-Src	breast:	n/a	chr9:18706138-18706149 chr9:18706159-18706170

Variant related genes	Relation type
ADAMTSL1	TF binding region

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs2507117	0.87[AMR][1000 genomes]
rs2570568	0.84[AMR][1000 genomes]
rs2779124	0.82[AMR][1000 genomes]
rs482009	0.85[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs487882	0.84[AMR][1000 genomes]
rs507556	0.84[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs519115	0.82[AMR][1000 genomes]
rs519878	0.82[AMR][1000 genomes]
rs521546	0.82[AMR][1000 genomes]
rs521911	0.80[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs530120	0.82[AFR][1000 genomes];0.82[AMR][1000 genomes]
rs532101	0.82[AFR][1000 genomes];0.82[AMR][1000 genomes]
rs532543	0.83[ASN][1000 genomes]
rs542956	0.82[AMR][1000 genomes]
rs563805	0.87[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs574090	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs574151	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs776569	0.82[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv491807	chr9:18243672-19009770	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv525659	chr9:18288212-19009041	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	nsv1019127	chr9:18288271-18996288	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
4	nsv1029449	chr9:18414752-18829127	Active TSS Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
5	nsv540077	chr9:18414752-18829127	Enhancers Genic enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
6	nsv1030931	chr9:18414752-18903530	ZNF genes & repeats Flanking Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
7	nsv892691	chr9:18519699-18805483	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
8	nsv892692	chr9:18519699-19045502	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
9	nsv831523	chr9:18592398-18753451	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
10	nsv892694	chr9:18599029-18767830	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
11	nsv613726	chr9:18676163-18709330	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region miRNA target site	1 gene(s)	inside rSNPs	diseases
12	nsv892697	chr9:18700566-18767830	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:38 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:18675800-18710000	Strong transcription	HSMM	muscle
2	chr9:18690000-18714200	Weak transcription	HUVEC	blood vessel
3	chr9:18695400-18706400	Weak transcription	NHLF	lung
4	chr9:18696800-18706600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr9:18701800-18707600	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr9:18702600-18708800	Enhancers	Fetal Lung	lung
7	chr9:18703400-18706800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr9:18703400-18708200	Strong transcription	NH-A	brain
9	chr9:18703600-18707000	Strong transcription	Osteobl	bone
10	chr9:18703800-18706400	Enhancers	Fetal Stomach	stomach
11	chr9:18704000-18707600	Enhancers	Duodenum Smooth Muscle	Duodenum
12	chr9:18704200-18708600	Weak transcription	Fetal Kidney	kidney
13	chr9:18704400-18708600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr9:18704400-18710600	Genic enhancers	NHDF-Ad	bronchial
15	chr9:18704600-18707400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
16	chr9:18704800-18706600	Enhancers	Ovary	ovary
17	chr9:18705000-18706800	Enhancers	Stomach Mucosa	stomach
18	chr9:18705000-18707600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr9:18705000-18708400	Weak transcription	Rectal Smooth Muscle	rectum
20	chr9:18705600-18707800	Enhancers	Colon Smooth Muscle	Colon
21	chr9:18705600-18708600	Enhancers	Fetal Muscle Leg	muscle
22	chr9:18705800-18706600	Enhancers	Right Ventricle	heart
23	chr9:18705800-18706800	Enhancers	HSMMtube	muscle
24	chr9:18705800-18707200	Enhancers	Brain Substantia Nigra	brain
25	chr9:18705800-18707200	Weak transcription	Duodenum Mucosa	Duodenum
26	chr9:18705800-18707200	Enhancers	Fetal Muscle Trunk	muscle
27	chr9:18705800-18707600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr9:18705800-18711200	Strong transcription	Muscle Satellite Cultured Cells	--
29	chr9:18706000-18706600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr9:18706000-18707000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr9:18706000-18707200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr9:18706000-18708200	Enhancers	Adipose Nuclei	Adipose
33	chr9:18706200-18707000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr9:18706200-18707400	Enhancers	Fetal Heart	heart
35	chr9:18706200-18707600	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr9:18706200-18707800	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr9:18706200-18708800	Enhancers	Stomach Smooth Muscle	stomach
38	chr9:18706200-18721200	Weak transcription	Aorta	Aorta

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