EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS180-50218 
Organism
Homo sapiens 
Tissue/cell
Small_intestine 
Coordinate
chr9:130271550-130272420 
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: 1             
ChromosomeStartEnd
chr9130271800130272205
Number: 1             
IDChromosomeStartEnd
GH09I127502chr9130265015130272722
Enhancer Sequence
CCACAAAGGT AAACCCAGGA GGGCCCAGGA CAGAAGCATG AGGCTCTGAA GGCATGGAGG 60
GCGCAGTCCA GTGGCACAGC GCTGTGGAGA GGCAGCCTCG GTGCCGGCAG AAGGCACTCA 120
TCCCTTCTGA GGTGCTGGGT GACCTTGGGC AAGTCATTCA CCCTCTCTGA GCCTCAGTTT 180
CCTCAGCTTC AAAATTGGGA GAGAGCTTTC CTGCTCTCCA AGGTCCTCTC CAGGTCTCAG 240
ATTCTGGGAT TATTATGGTC TGTGGACTCC CCATTTCAGA GTATAAAGGA GGAAACTAAG 300
ATACAGGATA AATTCAATCT GACAACTATG CGGGCTCCGG GCAGCCAGCC CAAGATGGAG 360
ACTGTGGAAG GACGTTCACC CCGAGAGCCA GATAACTGAG GTCAAGTAAG GGCAACGGCT 420
GTCTCCATTT GGAGGGCGCG TGACTTGTGA ATTCTTCCTT ATCAATCTCA TTACTCCACC 480
TGAAGCCCGC CCTTCCCTCT CCCCTCCTCT CCTTCCCTCC TTCCCTCCTC TCCTTCCCTC 540
CTTCCCTCCT CTCCTTCCCT CCTTCCCTCT CCCCTCCTCT CCTTCCCTCC TTCCCTCTCT 600
TCTGTTAAAT TCTTTTCTAT TTTAGCACCA CTCTTGGTTT CTAAAGGCTG GTGGCCGGGA 660
GCTAATGTTC CCTCTTTCCT CAAACTGCAG GCCCCACGAG GACTCCAACA GCCCTGGCCT 720
CACAGCCTCT GCCCCTAGTC CCCAGCAGCC CCTCCCCGTC TACAGGGACG GCCTTGGAGG 780
GGAACGGCTG CCCGGAGTCA CGCAGCCGGG GCCCTCTGGG ACAGACCAGA CCTACTCTCA 840
GGAGACCCCC TCCTAGGGGC GGTGCCGGCC 870