Variant report

Variant	rs61733504
Chromosome Location	chr13:52484385-52484386
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs11148231	0.80[AFR][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	nsv530718	chr13:52291802-52832752	Enhancers ZNF genes & repeats Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
2	nsv933424	chr13:52293482-52507732	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
3	nsv1044310	chr13:52321564-52643924	Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
4	nsv1050117	chr13:52325116-52643924	Enhancers Genic enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription 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 target site	33 gene(s)	inside rSNPs	diseases
5	nsv934070	chr13:52362588-53174923	Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Active TSS Enhancers Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
6	nsv976115	chr13:52480923-52484571	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:52464600-52494400	Weak transcription	Aorta	Aorta
2	chr13:52475600-52493800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr13:52476200-52493800	Weak transcription	K562	blood
4	chr13:52476400-52496600	Weak transcription	Duodenum Mucosa	Duodenum
5	chr13:52479400-52491000	Weak transcription	Fetal Intestine Large	intestine
6	chr13:52480000-52486200	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr13:52480200-52497200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr13:52481200-52484800	Weak transcription	Esophagus	oesophagus
9	chr13:52481200-52485800	Weak transcription	Brain Anterior Caudate	brain
10	chr13:52481200-52485800	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr13:52481200-52496400	Weak transcription	Stomach Smooth Muscle	stomach
12	chr13:52481200-52496600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr13:52481400-52484800	Enhancers	GM12878-XiMat	blood
14	chr13:52481400-52486000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr13:52481400-52486000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
16	chr13:52481400-52486200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr13:52481400-52491000	Weak transcription	Lung	lung
18	chr13:52481600-52486000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr13:52481600-52486000	Weak transcription	Brain Cingulate Gyrus	brain
20	chr13:52481600-52486000	Weak transcription	Pancreas	Pancrea
21	chr13:52481600-52486200	Weak transcription	Fetal Lung	lung
22	chr13:52481600-52502000	Weak transcription	Right Atrium	heart
23	chr13:52481800-52484600	Weak transcription	Fetal Intestine Small	intestine
24	chr13:52481800-52485600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr13:52481800-52486200	Weak transcription	Fetal Heart	heart
26	chr13:52481800-52487600	Weak transcription	Spleen	Spleen
27	chr13:52481800-52487800	Weak transcription	HepG2	liver
28	chr13:52481800-52506000	Weak transcription	Ovary	ovary
29	chr13:52482000-52491000	Weak transcription	Liver	Liver
30	chr13:52483200-52484400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood

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