Variant report

Variant	rs73397334
Chromosome Location	chr15:39749385-39749386
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:39743414..39749749-chr15:39871400..39878085,10	MCF-7	breast:
2	chr15:39745636..39749475-chr15:39752031..39754404,4	K562	blood:

Variant related genes	Relation type
ENSG00000137801	Chromatin interaction

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs58001045	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58836677	1.00[AMR][1000 genomes]
rs59550930	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59611156	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59752089	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60077096	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60658485	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60729119	1.00[AMR][1000 genomes]
rs60772140	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60780722	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61052847	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61140941	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61294562	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61583976	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73393465	1.00[AMR][1000 genomes]
rs73393501	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73395320	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73395324	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73395336	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73395338	1.00[AMR][1000 genomes]
rs73395340	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73397317	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73397367	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8028168	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1049682	chr15:39657279-40027403	Enhancers Flanking Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv542361	chr15:39657279-40027403	Weak transcription Strong transcription Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
3	nsv1042824	chr15:39676039-39757222	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv542362	chr15:39676039-39757222	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	esv3373125	chr15:39691567-40061262	Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
6	nsv1052908	chr15:39692049-39750193	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv1044082	chr15:39693241-39750193	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv1036091	chr15:39699841-39750193	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
9	nsv904094	chr15:39738006-39976057	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 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	chr15:39740000-39759400	Weak transcription	Stomach Smooth Muscle	stomach
2	chr15:39744600-39753400	Weak transcription	Rectal Smooth Muscle	rectum
3	chr15:39745400-39749600	Enhancers	Fetal Lung	lung
4	chr15:39745800-39749400	Enhancers	Adipose Nuclei	Adipose
5	chr15:39745800-39749600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr15:39748200-39753400	Weak transcription	HSMMtube	muscle
7	chr15:39748200-39753800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr15:39748200-39754000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr15:39748400-39749400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr15:39748400-39753200	Weak transcription	K562	blood
11	chr15:39748600-39749600	Enhancers	Fetal Muscle Leg	muscle
12	chr15:39748600-39749600	Enhancers	Fetal Stomach	stomach
13	chr15:39748600-39749600	Enhancers	Pancreas	Pancrea
14	chr15:39748600-39749600	Enhancers	Right Atrium	heart
15	chr15:39748600-39753600	Weak transcription	Muscle Satellite Cultured Cells	--
16	chr15:39748600-39754000	Weak transcription	NHLF	lung
17	chr15:39748800-39752400	Weak transcription	NHDF-Ad	bronchial
18	chr15:39748800-39753600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr15:39748800-39753600	Weak transcription	Osteobl	bone
20	chr15:39749000-39753400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr15:39749200-39749600	Enhancers	Esophagus	oesophagus
22	chr15:39749200-39749600	Enhancers	Fetal Muscle Trunk	muscle

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