Variant report

Variant	rs73915418
Chromosome Location	chr2:11696331-11696332
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	SIN3AK20	chr2:11696032-11697143	MCF-7	breast:	n/a	n/a
2	POLR2A	chr2:11695393-11697274	MCF-7	breast:	n/a	n/a

Variant related genes	Relation type
RNU2-13P	TF binding region
GREB1	TF binding region

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs2358038	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55665782	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55721526	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55728517	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55816844	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55927874	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55995663	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56018731	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56198642	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56229595	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56237365	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56700845	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58188623	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58357593	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58573299	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58849374	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58921396	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58950938	0.92[AFR][1000 genomes]
rs61222790	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61386285	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6432217	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs73915421	0.92[AFR][1000 genomes]
rs73915423	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73915426	0.92[AFR][1000 genomes]
rs73915427	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73915428	0.92[AFR][1000 genomes]
rs73915429	0.92[AFR][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	nsv1010506	chr2:11430965-12057286	Enhancers Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
2	nsv535585	chr2:11430965-12057286	Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
3	nsv873663	chr2:11664349-11783775	Genic enhancers Weak transcription ZNF genes & repeats Strong transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
4	esv1814335	chr2:11689048-11718858	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:34 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:11678400-11757000	Weak transcription	Right Ventricle	heart
2	chr2:11683400-11697800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr2:11688600-11696400	Weak transcription	Pancreas	Pancrea
4	chr2:11690000-11711000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr2:11691000-11697600	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr2:11691400-11697600	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr2:11691400-11699800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr2:11694200-11698400	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr2:11694200-11698400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr2:11694600-11698200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr2:11694800-11698000	Strong transcription	HepG2	liver
12	chr2:11694800-11699200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr2:11694800-11699600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr2:11694800-11755200	Weak transcription	Gastric	stomach
15	chr2:11695000-11696400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr2:11695400-11696600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr2:11695600-11696400	Enhancers	Brain Inferior Temporal Lobe	brain
18	chr2:11695800-11696600	Enhancers	Brain Cingulate Gyrus	brain
19	chr2:11696000-11696400	Bivalent Enhancer	Primary hematopoietic stem cells	blood
20	chr2:11696000-11697600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr2:11696000-11699800	Active TSS	Pancreatic Islets	Pancreatic Islet
22	chr2:11696200-11696400	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr2:11696200-11696400	Bivalent Enhancer	Aorta	Aorta
24	chr2:11696200-11696400	Flanking Active TSS	Ovary	ovary
25	chr2:11696200-11696600	Enhancers	Primary hematopoietic stem cells short term culture	blood
26	chr2:11696200-11696600	Active TSS	Brain Angular Gyrus	brain
27	chr2:11696200-11696600	Active TSS	Brain Substantia Nigra	brain
28	chr2:11696200-11696800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr2:11696200-11696800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr2:11696200-11696800	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr2:11696200-11696800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr2:11696200-11696800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr2:11696200-11697400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr2:11696200-11700400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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