Variant report

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	GABPA	chr14:70882954-70884580	MCF-7	breast:	n/a	n/a
2	MXI1	chr14:70882610-70884758	SK-N-SH	brain:	n/a	n/a

Variant related genes	Relation type
SYNJ2BP-COX16	TF binding region
SYNJ2BP	TF binding region

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

rs_ID	r²[population]
rs10135431	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs10138530	0.92[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10139883	0.94[ASN][1000 genomes]
rs10139978	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10140251	0.92[ASN][1000 genomes]
rs10143078	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs10143578	1.00[CHB][hapmap];0.89[JPT][hapmap];0.92[ASN][1000 genomes]
rs10146632	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs10147036	0.98[ASN][1000 genomes]
rs10148702	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs10148733	0.86[ASN][1000 genomes]
rs12100666	0.86[ASN][1000 genomes]
rs1892284	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs1892285	0.83[ASN][1000 genomes]
rs28423673	0.98[ASN][1000 genomes]
rs28567569	1.00[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs28600078	0.90[ASN][1000 genomes]
rs28866786	0.98[ASN][1000 genomes]
rs3764181	0.94[ASN][1000 genomes]
rs58601276	0.86[ASN][1000 genomes]
rs59321651	0.98[ASN][1000 genomes]
rs59911766	0.92[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs60455014	0.86[ASN][1000 genomes]
rs7141619	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs7147252	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs73291950	0.98[ASN][1000 genomes]
rs8013640	0.92[AMR][1000 genomes];0.86[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv902075	chr14:70612618-70919016	Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:70884000-70884600	Enhancers	HepG2	liver
2	chr14:70884000-70884800	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr14:70884000-70885000	Flanking Active TSS	Dnd41	blood
4	chr14:70884000-70889000	Weak transcription	Fetal Muscle Leg	muscle
5	chr14:70884200-70884600	Enhancers	Osteobl	bone
6	chr14:70884400-70885800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr14:70884400-70886000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr14:70884400-70886000	Weak transcription	HUES48 Cell Line	embryonic stem cell
9	chr14:70884400-70886400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
10	chr14:70884400-70888600	Weak transcription	HSMM	muscle

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