Variant report

Variant	rs73267311
Chromosome Location	chr14:32950095-32950096
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:32942791..32945014-chr14:32949857..32951632,2	MCF-7	breast:
2	chr14:32947699..32950524-chr14:32951801..32954077,2	K562	blood:

Variant related genes	Relation type
ENSG00000151320	Chromatin interaction
ENSG00000259045	Chromatin interaction

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

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

rs_ID	r²[population]
rs73267313	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758352	chr14:32858480-33016442	Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	esv2759978	chr14:32858480-33016442	Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv901595	chr14:32928634-32961434	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	esv1006050	chr14:32950054-32958354	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:25 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:32943200-32950800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr14:32945800-32950200	Enhancers	NHDF-Ad	bronchial
3	chr14:32946800-32951200	Weak transcription	Right Ventricle	heart
4	chr14:32947600-32950600	Weak transcription	Left Ventricle	heart
5	chr14:32947600-32951400	Weak transcription	Fetal Heart	heart
6	chr14:32947600-32962200	Weak transcription	Stomach Smooth Muscle	stomach
7	chr14:32947800-32951000	Weak transcription	Rectal Smooth Muscle	rectum
8	chr14:32947800-32960600	Weak transcription	Fetal Brain Male	brain
9	chr14:32947800-32963400	Weak transcription	Right Atrium	heart
10	chr14:32948000-32950400	Weak transcription	Brain Hippocampus Middle	brain
11	chr14:32948000-32951400	Weak transcription	Colon Smooth Muscle	Colon
12	chr14:32948200-32950600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr14:32948200-32951000	Weak transcription	Brain Angular Gyrus	brain
14	chr14:32948200-32951000	Weak transcription	Brain Inferior Temporal Lobe	brain
15	chr14:32948200-32951000	Weak transcription	Brain Substantia Nigra	brain
16	chr14:32948800-32950200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr14:32948800-32950400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr14:32949200-32950200	Enhancers	Osteobl	bone
19	chr14:32949400-32950200	Enhancers	HSMM	muscle
20	chr14:32949400-32950800	Weak transcription	Brain Cingulate Gyrus	brain
21	chr14:32949600-32951000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr14:32949600-32951200	Weak transcription	Aorta	Aorta
23	chr14:32949800-32950800	Weak transcription	Brain Anterior Caudate	brain
24	chr14:32950000-32950800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr14:32950000-32951400	Weak transcription	HSMMtube	muscle

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