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

TagContent
EnhancerAtlas ID
HS141-07069 
Organism
Homo sapiens 
Tissue/cell
NB4 
Coordinate
chr16:23874720-23875870 
Target genes
Number: 3             
NameEnsembl ID
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
IRF8MA0652.1chr16:23874937-23874951AGTTTCATTTTCGT-6.01
IRF9MA0653.1chr16:23874937-23874952AGTTTCATTTTCGTA-6.02
SPI1MA0080.4chr16:23875259-23875273TAAAAGAGGAAGTT+6.83
SPICMA0687.1chr16:23875259-23875273TAAAAGAGGAAGTT+6.34
Number of super-enhancer constituents: 6             
IDCoordinateTissue/cell
SE_10067chr16:23863461-23878484CD14
SE_10888chr16:23856132-23883188CD20
SE_32644chr16:23868998-23876906GM12878
SE_60111chr16:23838010-23894131Ly4
SE_63093chr16:23837102-23894105Tonsil
SE_67999chr16:23846983-23921777TC32
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr162387486323875389
Number: 1             
IDChromosomeStartEnd
GH16I023855chr162386692223876752
Enhancer Sequence
TTTGCACTGT GGACTCACCC TGAATTCTTT CTTGTGCAAG ATCCAAGAAC CCTTTCTTGG 60
GGTCTGGATC AGGACTCCTT TCCTGTAATA CAATGTCACA GAGCTCTTAA GTGGCAGAGC 120
TTGGGGCCAA ACTTAGGCTG CTGCACCCGA TGTCCCAGCT CCTCTGCCCT ATCTAGCTGT 180
GGATTTGTGC CTCGAAATAG AATTGCATTT TGAATGCAGT TTCATTTTCG TATGGAAAGT 240
GTCTATCCTG TAAATGTAAC TGTAGCAGCC CCAAAGCTGA GCTGGGCAGT TTTATGGCAG 300
CCTGGAGTCA GTCTTGTCCG CTTCCAATCA GGGTTCCTGG ACTGGCTCCT ATATTAAAAT 360
TGGTATTAGT AGACAATGTT CCAGGCAGAG TTTTGGATAG AAACTATCCA TCAGCACCAA 420
GAATGTGCCT GATTTGGTAA TCTTTTTACC AAAGTAAAAG TCAGTAGTAA GTTGTGGTTA 480
AAAGAGAGGA AGTTCAGAGT TCAGTACGTT ATTTCTCTCT CTCTCTCTCT TTGTTTAAAT 540
AAAAGAGGAA GTTACTGCTC TTATTTTTGT ACCAGCCCGT CAGTAATGGG TACAGAGTAA 600
AATCTTAGCT AAGCTGAGGT CAAACTTCAA AACTTAGTAA TAAGGATCTC CCTTGTTCCT 660
TTGTAGGGCG ACTAACATGA AGGTTCTGAC TCTTAACCCA TAGAGCCACA AAAAATAGTC 720
CTAGGAAAAT CATATGATTT TATTTATTTT AGGAACAGAA ATGGTCCCTT CCGAAGTAGA 780
GGCATTTCTA CTTCTTTCCT AAACACCATC TCTGCTCAGT GAGCTCTCCC ACCCTCAGGT 840
ACTGTGTTTC AGGCTTATTG CTGTATTGCT AGAAGTATCC TCACCTTCGA GATTAAGAAA 900
AGATATTTAT TGCCGGGCAC AGTGGCTCAC GCCTGCAATC CCAGTCTTTT GGGAAGCTGA 960
GACGGGAGGA TCACTTGAGC CCAGGATCTT GAGACCAGCC AGGGCAGTAT AGTGAGAACT 1020
CATCTTGAAA AGAAAAATTT ATTGAGCTCC TACTGTATAC TGGGGATACA GCAATAGGCA 1080
AGATAGCCCT TGCTCCTCAT GTAACCTACA GATAATAAAC AAGATTACAA ACAAACAAAA 1140
TAAGAGGTCG 1150