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

TagContent
EnhancerAtlas ID
HS012-15334 
Organism
Homo sapiens 
Tissue/cell
Caco-2 
Coordinate
chr19:2587930-2589050 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs11672460chr192588423hg19
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
IRF1MA0050.2chr19:2587934-2587955GAAAAGAAAAAGAAAGAAAGA-6.48
Number of super-enhancer constituents: 9             
IDCoordinateTissue/cell
SE_01272chr19:2588004-2589020Adrenal_Gland
SE_31670chr19:2586921-2590048Gastric
SE_40931chr19:2586993-2589097Left_Ventricle
SE_42475chr19:2587037-2589100Lung
SE_47688chr19:2588055-2589023Pancreas
SE_49019chr19:2586964-2589052Right_Atrium
SE_53390chr19:2587822-2589101Spleen
SE_61224chr19:2586887-2637887HBL1
SE_65339chr19:2585603-2590108Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1925880022588286
Number: 1             
IDChromosomeStartEnd
GH19I002586chr1925866292589279
Enhancer Sequence
GAAAGAAAAG AAAAAGAAAG AAAGAACAGG AACAAGATAA GGGTGGCCAC TCTCACTGTT 60
TCTATTCAGT ATTGTTATTG CAAATTCAAG CCAGGGCAAC TGGGCATGAA AAGGAAATGA 120
AAAGCATCCA GATTGGAGCA AGAGAAGAAA AACCATCTCT CTATTTGCAA ACGGCCTGTT 180
GTGGTGTAAA AGGTCCCCGG GTACAATTTG TGCAGCAGAA ATACGGCACT TCACAGGCTG 240
CTTAGAAACC TAGCAAGTCC CTTGAGCACA AACTATTTTC CTAAGCTTGG TGGGGGCGTG 300
AGAGGGTGGC CGGGGACTGG TGACAATGTT GTTTGTGCAC TGGGAGAGTC CGGCTGAATT 360
GCAACTGGCC TTTACATCCT AATCAGCTCC CTGAGGACAA CCCGAAAGAC ATCAGATTAA 420
AAAGTCACAA TGAGATAAAC CAGCACGACG CGGCTCTCTG CAAAGCGACA GGTAGTAAAC 480
AGACCTTAAC GCACGTCATG AGGTTTGTTT TTCTTTTAAA AGTCAACAGC TGGTGAATCG 540
CACAGGGCCG GGCAGGGCGG TCAAAGGGCC CGTTCCCCCG GCTGGGAAAA AAGCAGGAGC 600
CCAGGGCGGC GGCAGCTGGA CGCGGGCCCC GTGGAACTTT CTCCCGTCAG TCAGGGGCCG 660
TATTTCTTAG CCATCCTCCT CTGACCTTCA TTTCAAACCG CCTGCTGACG CATCTAACCT 720
TGGCCCGTTC CGTGGGAACT CCAGACTCAG GGTGACCAAC CCCAGCTGGG TTACCCAGGG 780
TTGTCCTGGT TGGAGTGGCT CCAAGTCCTC AGACCCAGCA AACCCAGGCT TGCTGATCAC 840
ACCGCAGACC CCACCAGGTG GTCATCTTTC TGGGGAAACT GGCTTCTTTT CCTCCCCGAC 900
TCCCTTGCTT TGTCTTCGTG GTGGCACCTC TCTTCCCAGG TGCTCAGGTG TGACATCAGC 960
CGTCCCTTGC TGGCCCTGGT GCCAGCTGAC TCCCAGGTCT CCTTTCTCTT CTTTAAGATG 1020
GAGTCTCCCT CTGTGACCCA GGCTGGAGTG TAATGGCGCG ATCTTGGCTC ACCACAACCT 1080
CCCCCTTCCA GGTTCAAGCG ATTCTCCTGC CTCAGCCTCC 1120