Variant report

Variant	rs73074253
Chromosome Location	chr2:213224653-213224654
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:213213790..213216008-chr2:213223245..213225984,2	MCF-7	breast:
2	chr2:213223218..213224821-chr2:213227410..213229033,2	MCF-7	breast:
3	chr2:213217638..213221383-chr2:213223310..213226579,3	MCF-7	breast:

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs16848452	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73056506	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73056514	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73060356	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73060359	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73060360	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73060375	0.85[AFR][1000 genomes]
rs73060377	0.85[AFR][1000 genomes]
rs73060389	0.82[AFR][1000 genomes]
rs73060395	0.82[AFR][1000 genomes]
rs73074259	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1006051	chr2:213052804-213273642	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv584346	chr2:213067749-213258622	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv834526	chr2:213114901-213237146	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
4	nsv834527	chr2:213115966-213334308	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
5	nsv1014680	chr2:213142147-213301614	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
6	nsv1004573	chr2:213186537-213365252	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
7	nsv875811	chr2:213200920-213347104	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
8	nsv3149	chr2:213204282-213248966	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
9	nsv584422	chr2:213214303-213270427	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
10	nsv1003694	chr2:213216431-213290523	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:213219200-213227200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr2:213219200-213233600	Weak transcription	Psoas Muscle	Psoas
3	chr2:213221000-213228600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr2:213223600-213224800	Enhancers	Brain Anterior Caudate	brain
5	chr2:213224000-213225200	Enhancers	Fetal Intestine Small	intestine
6	chr2:213224000-213225400	Enhancers	Fetal Intestine Large	intestine
7	chr2:213224000-213227200	Enhancers	Fetal Heart	heart
8	chr2:213224200-213224800	Active TSS	Brain Cingulate Gyrus	brain
9	chr2:213224200-213225200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr2:213224200-213225200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr2:213224200-213225400	Enhancers	Brain Angular Gyrus	brain
12	chr2:213224200-213225400	Enhancers	Brain Hippocampus Middle	brain
13	chr2:213224200-213225400	Enhancers	Brain Inferior Temporal Lobe	brain
14	chr2:213224200-213226400	Enhancers	Brain Substantia Nigra	brain
15	chr2:213224200-213227400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr2:213224400-213225000	Active TSS	Aorta	Aorta
17	chr2:213224400-213225200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr2:213224400-213225200	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr2:213224600-213225000	Weak transcription	Cortex derived primary cultured neurospheres	brain
20	chr2:213224600-213225200	Enhancers	Fetal Kidney	kidney
21	chr2:213224600-213225200	Flanking Active TSS	HepG2	liver
22	chr2:213224600-213226400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
23	chr2:213224600-213228800	Weak transcription	Brain Germinal Matrix	brain

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