EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS184-15436 
Organism
Homo sapiens 
Tissue/cell
T47D 
Coordinate
chr19:33764800-33766150 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs10423902chr1933764862hg19
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ZNF263MA0528.1chr19:33765463-33765484TTTTCCTGCTCCACCTCCCTC-6.06
Number of super-enhancer constituents: 11             
IDCoordinateTissue/cell
SE_09601chr19:33763698-33766425CD14
SE_23205chr19:33764413-33767578Colon_Crypt_1
SE_23808chr19:33764326-33767580Colon_Crypt_2
SE_24807chr19:33763936-33767669Colon_Crypt_3
SE_27406chr19:33764404-33766196Esophagus
SE_27669chr19:33764408-33767743Fetal_Intestine
SE_28569chr19:33764450-33767650Fetal_Intestine_Large
SE_31890chr19:33764433-33767612Gastric
SE_35421chr19:33764588-33771627HepG2
SE_43051chr19:33764035-33767549Lung
SE_50571chr19:33764237-33766629Sigmoid_Colon
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr193376488733765213
Number: 1             
IDChromosomeStartEnd
GH19I033273chr193376430833767610
Enhancer Sequence
TGGTCCGGGG CCAACCTCAA GGTGGGTGTC CTCTCCTGCA GCAGGGCCAC GGGCACCTTC 60
CGGCTCCAGC CCCAGCCCAG CCAGGCTCTG AGGGAGCCTG AGGCTGCCTC TCCTCCTCCA 120
GGTTCCTGTT TCCCGGGTGG CCCCAAAGAC AGAAGATGGT GTGAGGTTCA AGGGCTCAGT 180
CCCAGGCTCG GATTTCCTGG GCGTGTCAGA TTTCCTGGGC GCTGTGTGGC TGGTGTCTGC 240
CAGGGAGGCC ACTGAATAAC GTGAAGACCA CTGGGAAAGC ATAGCAGAGT GTGCAGTGGC 300
TGAGTCTGTG TGTGTGTGTG TGTGTGTGTG CGTGCGTGTG TCTGTGTGGG TGTGGGGTGT 360
GACTCACACA GGCCTGGGCT TCATGATGTC TCTTGGGAGC AGGAAGGTCT GTGTGAGTCT 420
GTGTCTGTCT GTGTGTGCAT GTGTGTGTGT ACCCGTGTGA CTACAAGCAT GTGTATGAGT 480
GCACACAGTT GGTGCAGGTG TACCTATGTG TCTGTGCACA TGTGTGTGCA TGTCTGTGAG 540
CGTGTGTGCA TGTGGTTATG AGTGTGTCTG TGGGTACGCA TGTGACTGTA GTGTGTGTGA 600
CTGTGTGTGT GCACGTGTGT GTGTGTGGAC ACAGCCCTCT CTGGCCTGCA CTCCTGGAGC 660
CTGTTTTCCT GCTCCACCTC CCTCCTCGGC AAGTGTTGAC TCAGGGAGGG ATAGGCAGCC 720
TTGGTTCAGG ATTTCCTGGT CAGGCAGAAG TGGTGCCTTG AAAAGGGAAC AATCTCGTGC 780
TAAAGTGGAC GCTGAGGGTC CACACAGTGC AGTGCTCTAG GGTGCCCAAG GCCGAGAGAC 840
CTTGTGCCTT CCTTGCCTGG GTTTACAGTG GGGGTCCCAG AAAGCTTTGC CCCTAGGGTG 900
GCCCATAGGA TGTGCCCTCA GGCTTTTTCT AAATGCTTCC TGATCTGGGC TGCCCGGGGT 960
GGGGGCTCTG GAGCTGGACA CTCCTCTGAC TGCTGTGGAG GCAGGGACAG CACCCCCACA 1020
AGAGGTACCC CAAGAGAAAT GGGGGCCCCC AATGTCCCCA GGCACTAGCT GTCCCAGGTT 1080
CCCTTCCACA GTGGGCAGCT TTACCCCTGC ACCGCCCCAT CCCCCAAAGC CTTAACAAAT 1140
AAAAATGAAG CTCTTTGAGG CTAAGAGTCT ATTCAAGCTC CAAGAGCTCT CTGCCATGTT 1200
GGGAGGAGCC TTCTAGAAGC GCTGCTTCTC TCAGGGGCTG GGAGGGCTGG CCTCACTGGG 1260
TACGCCTGAG AGATGCAGCA TCTTAGTCGG CACCCATCTG CCGCGTCCAC ATCTGGGCTG 1320
TACCAAGGTC CCCCAGAGGC GCCACTGTCC 1350