EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS155-14478 
Organism
Homo sapiens 
Tissue/cell
Ovary 
Coordinate
chr9:130271410-130272420 
Target genes
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs2244843chr9130271666hg19
TF binding sites/motifs
Number: 31             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr9:130272064-130272082CCCTCCTTCCCTCCTCTC-6.33
EWSR1-FLI1MA0149.1chr9:130272085-130272103CCCTCCTTCCCTCCTCTC-6.33
EWSR1-FLI1MA0149.1chr9:130272102-130272120CCTTCCCTCCTTCCCTCT-6.55
EWSR1-FLI1MA0149.1chr9:130272130-130272148CCTTCCCTCCTTCCCTCT-6.55
EWSR1-FLI1MA0149.1chr9:130272056-130272074CTCTCCTTCCCTCCTTCC-7.66
EWSR1-FLI1MA0149.1chr9:130272077-130272095CTCTCCTTCCCTCCTTCC-7.66
EWSR1-FLI1MA0149.1chr9:130272098-130272116CTCTCCTTCCCTCCTTCC-7.66
EWSR1-FLI1MA0149.1chr9:130272126-130272144CTCTCCTTCCCTCCTTCC-7.66
EWSR1-FLI1MA0149.1chr9:130272060-130272078CCTTCCCTCCTTCCCTCC-7.85
EWSR1-FLI1MA0149.1chr9:130272081-130272099CCTTCCCTCCTTCCCTCC-7.85
ZNF263MA0528.1chr9:130272069-130272090CTTCCCTCCTCTCCTTCCCTC-6.57
ZNF263MA0528.1chr9:130272090-130272111CTTCCCTCCTCTCCTTCCCTC-6.57
ZNF263MA0528.1chr9:130272056-130272077CTCTCCTTCCCTCCTTCCCTC-6.62
ZNF263MA0528.1chr9:130272077-130272098CTCTCCTTCCCTCCTTCCCTC-6.62
ZNF263MA0528.1chr9:130272098-130272119CTCTCCTTCCCTCCTTCCCTC-6.62
ZNF263MA0528.1chr9:130272126-130272147CTCTCCTTCCCTCCTTCCCTC-6.62
ZNF263MA0528.1chr9:130272065-130272086CCTCCTTCCCTCCTCTCCTTC-6.84
ZNF263MA0528.1chr9:130272086-130272107CCTCCTTCCCTCCTCTCCTTC-6.84
ZNF263MA0528.1chr9:130272048-130272069CTCCCCTCCTCTCCTTCCCTC-6.85
ZNF263MA0528.1chr9:130272118-130272139CTCCCCTCCTCTCCTTCCCTC-6.85
ZNF263MA0528.1chr9:130272052-130272073CCTCCTCTCCTTCCCTCCTTC-7.04
ZNF263MA0528.1chr9:130272073-130272094CCTCCTCTCCTTCCCTCCTTC-7.04
ZNF263MA0528.1chr9:130272094-130272115CCTCCTCTCCTTCCCTCCTTC-7.04
ZNF263MA0528.1chr9:130272122-130272143CCTCCTCTCCTTCCCTCCTTC-7.04
ZNF263MA0528.1chr9:130272044-130272065CCCTCTCCCCTCCTCTCCTTC-7.05
ZNF263MA0528.1chr9:130272114-130272135CCCTCTCCCCTCCTCTCCTTC-7.05
ZNF263MA0528.1chr9:130272039-130272060CCCTTCCCTCTCCCCTCCTCT-7.15
ZNF263MA0528.1chr9:130272109-130272130TCCTTCCCTCTCCCCTCCTCT-7.25
ZNF263MA0528.1chr9:130272060-130272081CCTTCCCTCCTTCCCTCCTCT-7.37
ZNF263MA0528.1chr9:130272081-130272102CCTTCCCTCCTTCCCTCCTCT-7.37
ZNF410MA0752.1chr9:130271797-130271814GATTATTATGGTCTGTG-6.18
Number of super-enhancer constituents: 15             
IDCoordinateTissue/cell
SE_00872chr9:130266016-130272828Adrenal_Gland
SE_01693chr9:130271139-130272839Aorta
SE_02928chr9:130272182-130272691Bladder
SE_26528chr9:130271711-130272711Esophagus
SE_31422chr9:130271416-130271938Gastric
SE_31422chr9:130272012-130272710Gastric
SE_42140chr9:130271269-130272735Lung
SE_44773chr9:130271769-130272503NHLF
SE_46654chr9:130271839-130272710Ovary
SE_48868chr9:130271216-130272794Right_Atrium
SE_52507chr9:130270909-130272733Small_Intestine
SE_53712chr9:130271567-130272743Spleen
SE_54748chr9:130271667-130272732Stomach_Smooth_Muscle
SE_65259chr9:130271508-130272912Pancreatic_islets
SE_68760chr9:130272100-130272837H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr9130271800130272205
chr9130271490130271701
Number: 1             
IDChromosomeStartEnd
GH09I127502chr9130265015130272722
Enhancer Sequence
CTGCAGGGGC CGGGGCCGCG GGGGCTGAGC AGGGCCGCCC TGTGGCCAGG CAGCACCCCC 60
CACACACTTT GCCTGGGTCC TCGAAGTCCA GGCCCTGGGG CTGGCGCCTG CTACCAGGGA 120
TGGCCACCTG GTGCTCATGG CCACAAAGGT AAACCCAGGA GGGCCCAGGA CAGAAGCATG 180
AGGCTCTGAA GGCATGGAGG GCGCAGTCCA GTGGCACAGC GCTGTGGAGA GGCAGCCTCG 240
GTGCCGGCAG AAGGCACTCA TCCCTTCTGA GGTGCTGGGT GACCTTGGGC AAGTCATTCA 300
CCCTCTCTGA GCCTCAGTTT CCTCAGCTTC AAAATTGGGA GAGAGCTTTC CTGCTCTCCA 360
AGGTCCTCTC CAGGTCTCAG ATTCTGGGAT TATTATGGTC TGTGGACTCC CCATTTCAGA 420
GTATAAAGGA GGAAACTAAG ATACAGGATA AATTCAATCT GACAACTATG CGGGCTCCGG 480
GCAGCCAGCC CAAGATGGAG ACTGTGGAAG GACGTTCACC CCGAGAGCCA GATAACTGAG 540
GTCAAGTAAG GGCAACGGCT GTCTCCATTT GGAGGGCGCG TGACTTGTGA ATTCTTCCTT 600
ATCAATCTCA TTACTCCACC TGAAGCCCGC CCTTCCCTCT CCCCTCCTCT CCTTCCCTCC 660
TTCCCTCCTC TCCTTCCCTC CTTCCCTCCT CTCCTTCCCT CCTTCCCTCT CCCCTCCTCT 720
CCTTCCCTCC TTCCCTCTCT TCTGTTAAAT TCTTTTCTAT TTTAGCACCA CTCTTGGTTT 780
CTAAAGGCTG GTGGCCGGGA GCTAATGTTC CCTCTTTCCT CAAACTGCAG GCCCCACGAG 840
GACTCCAACA GCCCTGGCCT CACAGCCTCT GCCCCTAGTC CCCAGCAGCC CCTCCCCGTC 900
TACAGGGACG GCCTTGGAGG GGAACGGCTG CCCGGAGTCA CGCAGCCGGG GCCCTCTGGG 960
ACAGACCAGA CCTACTCTCA GGAGACCCCC TCCTAGGGGC GGTGCCGGCC 1010