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

TagContent
EnhancerAtlas ID
HS048-28951 
Organism
Homo sapiens 
Tissue/cell
Fetal_small_intestine 
Coordinate
chr5:993560-994830 
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ZNF263MA0528.1chr5:994200-994221AGGGGAGAGAGGAGAGGAAAG+6.02
ZNF263MA0528.1chr5:994290-994311GGAGAATGAAGGGGAGAGAGG+6.43
ZNF263MA0528.1chr5:994299-994320AGGGGAGAGAGGAGGGGAGGG+6.46
ZNF263MA0528.1chr5:994273-994294AAAGGAGGGAGGGGAAGGGAG+7.35
ZNF263MA0528.1chr5:994192-994213AGGGGAGGAGGGGAGAGAGGA+7.51
ZNF263MA0528.1chr5:994195-994216GGAGGAGGGGAGAGAGGAGAG+8.74
Number of super-enhancer constituents: 1             
IDCoordinateTissue/cell
SE_61880chr5:989435-1013448Toledo
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr5993600994080
chr5994525994705
Number: 1             
IDChromosomeStartEnd
GH05I000992chr5992428994686
Enhancer Sequence
CAGCCTAGTG ACAGAGCGAG ACTCCGTCTC AAAAAAAAAA AAAAAAAGAA AATGACCCCA 60
GATTGTGAGG CCCGGCTGAG CAGCCGTGAG CAGCTGGATG GGCACAGAGC CACCTCCTAC 120
TCCTCACCCA GGCTGTTCCC GAGGAAACCA TTTCTGGGGT GACTGCAGAG AGGACAGCCC 180
ACCCTCTGCT CTTAGAGAAA CAGCAGGGAG GAGAAGGCTG GAGTTCAACC TCCACCCCCA 240
CTCCCTGACT GTCAGCCAGG ATGATGGAAT CTGTGGTCAT TTCCAGGAGA GCTTGTGCAA 300
GCAGGAAGTA GCCAGACAGC AGCAGCGACC TCTTTAAACC CATTTTTTCA GACTTGGTTG 360
ATAGAGAGTA TCGGAGTCGA GCTAGCCCCA CCTCTCAGTC TGTCGCTCTC AAGTTGCCCA 420
ATGTGGAAGA GATATGGGGT CTGGAGGAGG AACGAGTGAC ACAGGTTCTG CAGGGCCAGT 480
GGGTCAGCGG TGGGACGGGA ATGACAGCCA GGACCCAGCA TGCACTGCCC CCTCACAGGG 540
CTTTTTCACA AAGGCTGAAC TCTGCCTGCA AATTGCACAG AGACCCTTAC ACGGCAAGAA 600
ACTTTTATAA ATGGGAGGTA CCTGCAGGCT CCAGGGGAGG AGGGGAGAGA GGAGAGGAAA 660
GGAGGGAAGA GAGATAGGAG AGTAGGGGAG AGAGGACAGA GAGACCAGGG GAGAAAGGAG 720
GGAGGGGAAG GGAGAATGAA GGGGAGAGAG GAGGGGAGGG GAGCAGGGAG TACCTGGGAG 780
GGCTAATGCC CATTCTCATC CAGGAGCGAG GAAGGACCAG CTCCCAGGCT GGCCTTCTGT 840
TAGGATAGAT CCTGCTCCAT AAGAGGCCAT GGAAGCAGGA CCTGCCACAG AATTTCCAGG 900
ACCCAGGGAA AGATGTCCAT GTAGGACCCC TTGTTCAAAA GTTAAGAATT TCAAGACAGC 960
AACAGCAGAG CATTAAACCA AGCTCAGGGC CCAGGAAGTG GGGCGTGTTA CATGCAGAGG 1020
GCAATGGAGC CCTTGAAAAT GCAAAAGGCA TCTATCCCCG TGCACAGGCT CTGTGTGTGC 1080
TTGTGTGAAC TTGTATATGG GTACATGTGC TGTGTGCATG CATGTGAACG TGTGTGTGCA 1140
TGTTTGGAGG GCAGGTATGC AGAGAAGTGT CATCAGGTAC AACTCTCCTC TACTTCAGTG 1200
GACCCTGGGC TCACCCATGG TGAGGGCCCC CCACATAGAG CGCTTCCACA TCTCAGCCAG 1260
CTGGGAGCCC 1270