Variant report

Variant	rs72965015
Chromosome Location	chr3:119470876-119470877
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	chr3:119464205..119467034-chr3:119468589..119471044,2	K562	blood:

Variant related genes	Relation type
ENSG00000183833	Chromatin interaction

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs57035409	0.91[AFR][1000 genomes]
rs72963200	0.91[AFR][1000 genomes]
rs72965006	1.00[AFR][1000 genomes]
rs72965013	1.00[AFR][1000 genomes]
rs72965014	1.00[AFR][1000 genomes]
rs72965021	1.00[AFR][1000 genomes]
rs72965022	1.00[AFR][1000 genomes]
rs72965033	0.88[AFR][1000 genomes]
rs72965035	0.88[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1011178	chr3:119437192-119589116	Weak transcription Active TSS Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer 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	12 gene(s)	inside rSNPs	diseases
2	nsv536703	chr3:119437192-119589116	Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:119423200-119471600	Weak transcription	Fetal Kidney	kidney
2	chr3:119435400-119478200	Weak transcription	Colon Smooth Muscle	Colon
3	chr3:119450600-119474200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr3:119451000-119473400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr3:119451200-119475200	Weak transcription	Fetal Brain Male	brain
6	chr3:119457600-119472200	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr3:119458800-119471200	Weak transcription	Rectal Smooth Muscle	rectum
8	chr3:119459600-119472200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
9	chr3:119463200-119476000	Weak transcription	Spleen	Spleen
10	chr3:119465600-119474400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr3:119466200-119471200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr3:119468000-119471000	Strong transcription	Brain Inferior Temporal Lobe	brain
13	chr3:119469000-119471000	Strong transcription	Brain Anterior Caudate	brain
14	chr3:119469200-119471400	Strong transcription	Stomach Smooth Muscle	stomach
15	chr3:119469400-119471200	Strong transcription	Brain Hippocampus Middle	brain
16	chr3:119470000-119471000	Strong transcription	Brain Substantia Nigra	brain
17	chr3:119470000-119471200	Strong transcription	Brain Cingulate Gyrus	brain
18	chr3:119470000-119471200	Enhancers	HUVEC	blood vessel
19	chr3:119470000-119474400	Strong transcription	Ovary	ovary
20	chr3:119470200-119471200	Strong transcription	Brain Angular Gyrus	brain
21	chr3:119470200-119472400	Strong transcription	Duodenum Smooth Muscle	Duodenum
22	chr3:119470600-119471200	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
23	chr3:119470600-119471200	ZNF genes & repeats	Left Ventricle	heart
24	chr3:119470600-119474600	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
25	chr3:119470800-119473400	Weak transcription	Pancreas	Pancrea
26	chr3:119470800-119473600	Weak transcription	Aorta	Aorta

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