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

TagContent
EnhancerAtlas ID
HS112-06778 
Organism
Homo sapiens 
Tissue/cell
KELLY 
Coordinate
chr18:55869020-55870550 
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOSL1MA0477.1chr18:55869711-55869722GGTGACTCATG+6.62
FOSL2MA0478.1chr18:55869710-55869721GGGTGACTCAT+6.14
JUNBMA0490.1chr18:55869710-55869721GGGTGACTCAT+6.32
JUNDMA0491.1chr18:55869711-55869722GGTGACTCATG+6.02
NR3C2MA0727.1chr18:55869023-55869040TGGTACATACTGTTCTG+6.03
Sox6MA0515.1chr18:55869203-55869213CCATTGTTTT+6.02
Number of super-enhancer constituents: 3             
IDCoordinateTissue/cell
SE_27800chr18:55869040-55870289Fetal_Intestine
SE_28643chr18:55868651-55870453Fetal_Intestine_Large
SE_41571chr18:55869281-55870207LNCaP
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr185586903755869309
chr185586931155869996
Number: 1             
IDChromosomeStartEnd
GH18I058201chr185586892155870489
Enhancer Sequence
ACATGGTACA TACTGTTCTG AGCCCTGGTT TTCTTTTTTT CACTTAGCGT TGTATACTGG 60
AACTCACTCA ATGTCAGTAT ACAGAGAATT CCCTTGTCTT TTTATAACTC TGTGCTATAC 120
GCTGACGGAA GTTCATTCAG TCAGTCCCCT ATTGATGGAC ACTTGAGTTA TTCTCAGACT 180
TGTCCATTGT TTTGCAAAAA TAGCCCTGGG CATATGTCAT TTGGTATTTT TGTCGAGGCA 240
TTCCAATAAA AATAAGTAAA TTCTTCCTCT CTTGCCTTGA AGATGTGCAG CTCCTCAGTA 300
ACCTTTTATT CTCTAAAGCT CTGTCCTCAT CTTTAATCCC TGATTTAAGA GGTGCAGCTC 360
TTCAGGCCAT AAACCTTTCT TCCTGCCTCA AGTTTTTAAA GCTACAAAGG AACCTAAGAG 420
ATCCCTTGTG TTTTACAGCT AAAGGACCTG AGAGCAGGAA ACAAAGGGAG AGCCGGAAGC 480
CCAGGTCTCC TGTTCCCTGC CTGGCAGGTG ATATTCTTTC TGTTAAACTC TCTTTCCCTC 540
TGCCTATTAT TGGCCAGGCT GTCCTCCAGG ACAGTGCTTG CCAAAGTGTG GTCCATGGGC 600
AGCAGCATCC CCGGAGCTCA TCAGCAATGT AAGATGTCAG GCCCTGCCCC AGAGGGGCTG 660
AGATAGAATC TACCAATTAC TGGATTCCCT GGGTGACTCA TGCAGTCAGG TTGGAGAAGC 720
GCTGGACTGG TGGCTTTCTC CAGAGGAGCA TGCAACAGCG GTTTGCAAAC AGGGATGATG 780
CAGTTCCTTT TCAACACGTG GATTTGCACT TCCTCCTGGT GCGCTCCTCC AGCCTGCCTG 840
TCCTGTTCAC ACCAGCCTCC CCCTGGAAGG GGTTCAGACT TGATCCTTTG GGTGGTAGGG 900
TCTTTCTTGG ATAGCGTAGC CATCCATTCC TGCTGCATAC ATTCAACACA GCCTTCATCC 960
TTCGCCATTT GTCTCTGATA CTTCATACTC CTTTTGTTTG ACAAGTGCCC TAGCTTTATT 1020
TATTTTCTCA TCATTGTTGT TAAGGGCCTA TTGTGCTTGC TAGTATACAC ACCACTATGT 1080
AAGTTACTAG TTCAATTTAT TTGTTTTACT GCTGCTGTGA GGTGTGTCCA TGTGTGCACA 1140
TCTACCTGTG TTAATAACTG ATAATATTGG GCCTCAGTAC ATACTTTTTT TTTTTAAGAG 1200
ACAAGGTTTT ACTTCGTCAC CCAGGCTGAA GGACTGAGAC ACACTTGTAG CTCACTGCAG 1260
CCTTGAGCTC CTGGACCCAA GTGATCCTCC CACCTTAACC TCCTGAGTAG CTGGGACTAC 1320
AGGCACACAC CACCACACCA ACTAATTTTT TTATTTTTTG TAGAGACGGA TTCTTACTGT 1380
GTTGCCCAGG CTGGTCTAGA ACTCCTGGCT TCAAGCCATC CTACCACCTC AGCCTTCCAA 1440
AGTGCTGGGA TGATAGGTGT AAGCCGCCGC ACCTGGCCCT CAGTGCATAC TTAGATATAC 1500
TTAAATAAAA ACTTAATTGC AAATTACTTC 1530