Variant report

Variant	rs73507318
Chromosome Location	chr13:67570467-67570468
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 29 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs17082027	1.00[AMR][1000 genomes]
rs181988	1.00[AMR][1000 genomes]
rs195153	0.88[AFR][1000 genomes]
rs260144	1.00[AMR][1000 genomes]
rs260146	1.00[AMR][1000 genomes]
rs28463845	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57098915	0.92[AFR][1000 genomes]
rs58417725	1.00[AMR][1000 genomes]
rs58585764	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60336902	1.00[AMR][1000 genomes]
rs60525328	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73505399	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73505402	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73507308	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73507310	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73507315	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73507326	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73507342	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530605	chr13:67126136-67697306	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1035741	chr13:67212973-68077950	Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv541817	chr13:67212973-68077950	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv900407	chr13:67434161-67603745	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv832640	chr13:67460304-67635966	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv428604	chr13:67480426-67645030	Flanking Active TSS Enhancers Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv900412	chr13:67512877-67572221	Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv900414	chr13:67515590-67701341	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
9	nsv1045093	chr13:67517932-67693875	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
10	nsv541821	chr13:67517932-67693875	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
11	nsv541822	chr13:67550756-67594021	Enhancers Active TSS Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:67566600-67571400	Weak transcription	Gastric	stomach
2	chr13:67568000-67571800	Enhancers	Dnd41	blood
3	chr13:67568800-67571000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr13:67568800-67571600	Enhancers	Brain Cingulate Gyrus	brain
5	chr13:67569000-67571600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr13:67569000-67571600	Enhancers	Muscle Satellite Cultured Cells	--
7	chr13:67569000-67571600	Enhancers	Brain Substantia Nigra	brain
8	chr13:67569200-67571600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr13:67569400-67571600	Enhancers	Brain Anterior Caudate	brain
10	chr13:67569600-67571200	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr13:67569600-67573000	Enhancers	Primary B cells from peripheral blood	blood
12	chr13:67569800-67570800	Weak transcription	Liver	Liver
13	chr13:67569800-67570800	Weak transcription	K562	blood
14	chr13:67569800-67571800	Enhancers	A549	lung
15	chr13:67569800-67572800	Enhancers	Primary B cells from cord blood	blood
16	chr13:67569800-67575600	Weak transcription	Cortex derived primary cultured neurospheres	brain
17	chr13:67569800-67575800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
18	chr13:67569800-67588200	Weak transcription	Brain Angular Gyrus	brain
19	chr13:67570000-67571000	Weak transcription	Brain Hippocampus Middle	brain
20	chr13:67570400-67571200	Weak transcription	Fetal Thymus	thymus
21	chr13:67570400-67571200	Weak transcription	Thymus	Thymus
22	chr13:67570400-67571200	Enhancers	HSMM	muscle

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