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

TagContent
EnhancerAtlas ID
HS180-00147 
Organism
Homo sapiens 
Tissue/cell
Small_intestine 
Coordinate
chr1:6411580-6412700 
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF5MA0599.1chr1:6412510-6412520GCCCCGCCCC+6.02
ZNF263MA0528.1chr1:6412412-6412433CTTCCCCTCCCCACCTCCCTC-6.02
ZNF263MA0528.1chr1:6412416-6412437CCCTCCCCACCTCCCTCATTC-6.68
ZNF263MA0528.1chr1:6412404-6412425CCCTCCCTCTTCCCCTCCCCA-6.82
Number of super-enhancer constituents: 5             
IDCoordinateTissue/cell
SE_23464chr1:6411485-6412692Colon_Crypt_1
SE_24052chr1:6411536-6412670Colon_Crypt_2
SE_37032chr1:6406618-6415653HSMMtube
SE_50714chr1:6411474-6412754Sigmoid_Colon
SE_53099chr1:6411468-6412739Small_Intestine
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr164119306412623
chr164120006412692
Number: 2             
IDChromosomeStartEnd
GH01I006351chr164117606411944
GH01I006353chr164123216412530
Enhancer Sequence
GTAGGAAGGG CCTTCCCCGC ACCAGCTGCA GCGGGCAGAG GGTCACTTTC CACACAGGCC 60
TGTCCTGGGG GCACTAGCCA AGGCTGTGGG TGGGTGCGGA GAGCAGGGCC CAGCTCCTGG 120
TTCTAGAGCA GTGAGGAAAC ATCAGCCCAG CATTTCCCAG GAGCAGCAGA GCCAGCCTCC 180
AGAGCAGCCT GAATGACTGC TGCAGGCCTC ACTTTGCCTG TCTGTGAAGT GGAGCCACAC 240
ACAGCAGGCT GGCCCCCAGG AATGACACAA GGCCAGGGAG AGAAGACGCG GGCCAAGGGC 300
TGCAGAGCAG CGGAGGAAGT GCTTTCATGC GGTGGGCACT GAAGACAGGA CAGATATGTG 360
GGTAGCCTTT AAGACAGAAG ACCAGGGACA GTGCCTGAGG CCCCGAGGAA GAGCCTGGAG 420
CCACCTGGCA ACAAAGTGAG GACTCGGCAC TTGGCGCTGT GCCATCAGGA GTACATGCCA 480
GGAACTGCAG ACCGCACGCC AGCTGGCTAC CACGGGCCTG GCCGCCTTTC TTCGGCACCT 540
TGGGTCCTGC ACCAAGGACC ATCCTAACTC CCCAACTGAC CACCCAGGAA GCCAGCCCCT 600
GCCCTCAAGG TCAGACACAA CCCTCTCCCC TACAGGACCT GACTCCTGCC TGGGGACTGT 660
GCTGTCACCT CCAATGCACA AGGCTCAAAG CCCAACTCAC TTACCCCTTC TCCCTTTCCC 720
CAAATCAGAC ACCTTCCCTC CAAGCCAGGG CAGCCAGTGA GTCCCAGCCT CAGCTGGGAT 780
TCCTTCCCAT CCTGCATACC ACCACCAGCT GCTCCACACC TGGCCCCTCC CTCTTCCCCT 840
CCCCACCTCC CTCATTCCTT CCAAACAGCT CAGGAACCGC TGGATCCAGC CAGCCTCCAG 900
GACCCATAAA CAGCTCTGTC ACTCTCTCAG GCCCCGCCCC ATGGCCTGGC CAAGGCCAAC 960
CGTGTCCATC CCAGGACAGG GTCATGACTG CCTCTGTCTA AAGGCAGGCA GGGGTGAGAG 1020
CCAGGGAGCC AGGGAAGCTG CTGCGTCTCA CTGGAGACTT CGTTTTCCCA TTTCTTTTTT 1080
TTTTTTTTTG AGACGGCGTC TCGCTCTGTC TCCCAGGCTG 1120