Variant report

Variant	rs73915427
Chromosome Location	chr2:11700021-11700022
allele	A/G
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	chr2:11698298-11700553	MCF-7	breast:	n/a	n/a
2	POLR2A	chr2:11697332-11700490	MCF-7	breast:	n/a	n/a
3	POLR2A	chr2:11699964-11700546	HepG2	liver:	n/a	n/a
4	ZNF217	chr2:11699390-11700103	MCF-7	breast:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:11698164..11701125-chr2:11728905..11731713,2	K562	blood:
2	chr2:11699009..11701296-chr2:218182757..218185396,2	MCF-7	breast:
3	chr2:11679729..11680386-chr2:11699341..11700025,2	MCF-7	breast:

Variant related genes	Relation type
RNU2-13P	TF binding region
ENSG00000196208	Chromatin interaction

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

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

rs_ID	r²[population]
rs2358038	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55665782	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55721526	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55728517	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55816844	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55927874	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55995663	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56018731	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56198642	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56229595	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56237365	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56700845	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58188623	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58357593	0.85[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58573299	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58849374	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58921396	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58950938	0.95[AFR][1000 genomes]
rs61222790	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61386285	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6432217	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs73915418	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73915421	0.95[AFR][1000 genomes]
rs73915423	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73915426	0.95[AFR][1000 genomes]
rs73915428	0.95[AFR][1000 genomes]
rs73915429	0.95[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:43 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:11678400-11757000	Weak transcription	Right Ventricle	heart
2	chr2:11690000-11711000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr2:11694800-11755200	Weak transcription	Gastric	stomach
4	chr2:11696200-11700400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr2:11696400-11700200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr2:11697000-11702200	Weak transcription	Pancreas	Pancrea
7	chr2:11697000-11706800	Weak transcription	Brain Cingulate Gyrus	brain
8	chr2:11697000-11710800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
9	chr2:11697000-11722600	Weak transcription	Brain Hippocampus Middle	brain
10	chr2:11697000-11723000	Weak transcription	Brain Anterior Caudate	brain
11	chr2:11697000-11723200	Weak transcription	Brain Angular Gyrus	brain
12	chr2:11697600-11700200	Enhancers	Left Ventricle	heart
13	chr2:11697600-11700400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr2:11697600-11700600	Transcr. at gene 5' and 3'	Ovary	ovary
15	chr2:11697800-11706800	Weak transcription	Brain Substantia Nigra	brain
16	chr2:11698600-11713200	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr2:11698600-11713400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr2:11698800-11700400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
19	chr2:11698800-11703600	Weak transcription	Skeletal Muscle Female	skeletal muscle
20	chr2:11698800-11706200	Weak transcription	Fetal Muscle Leg	muscle
21	chr2:11698800-11713400	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr2:11699000-11700400	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr2:11699000-11701000	Strong transcription	HepG2	liver
24	chr2:11699000-11714400	Weak transcription	Skeletal Muscle Male	skeletal muscle
25	chr2:11699400-11700400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr2:11699400-11706600	Weak transcription	Brain Inferior Temporal Lobe	brain
27	chr2:11699400-11706800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr2:11699600-11700200	Genic enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr2:11699600-11700200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
30	chr2:11699600-11700400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr2:11699600-11700400	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr2:11699800-11700200	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr2:11699800-11700200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr2:11699800-11701800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
35	chr2:11699800-11702400	Weak transcription	Fetal Stomach	stomach
36	chr2:11699800-11703400	Weak transcription	Fetal Heart	heart
37	chr2:11699800-11708400	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr2:11699800-11713200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
39	chr2:11699800-11718400	Weak transcription	Pancreatic Islets	Pancreatic Islet
40	chr2:11699800-11723000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr2:11700000-11700200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr2:11700000-11702400	Weak transcription	Fetal Muscle Trunk	muscle
43	chr2:11700000-11767000	Weak transcription	Right Atrium	heart

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