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

TagContent
EnhancerAtlas ID
HS133-13494 
Organism
Homo sapiens 
Tissue/cell
melanoma 
Coordinate
chr17:76330650-76331530 
Target genes
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
HOXA13MA0650.2chr17:76331426-76331437GTTTTATTGGG-6.62
Number of super-enhancer constituents: 16             
IDCoordinateTissue/cell
SE_02705chr17:76330662-76331532Astrocytes
SE_31461chr17:76330755-76331475Gastric
SE_34704chr17:76330482-76331438HeLa
SE_38941chr17:76330622-76331588IMR90
SE_44143chr17:76330458-76331781NHDF-Ad
SE_44765chr17:76330515-76331617NHLF
SE_45620chr17:76329788-76335520Osteoblasts
SE_47352chr17:76329536-76331972Panc1
SE_51835chr17:76330659-76331357Skeletal_Muscle_Myoblast
SE_55689chr17:76329782-76335716u87
SE_58926chr17:76309354-76389031Ly3
SE_61360chr17:76309626-76357699HBL1
SE_62409chr17:76309367-76385525Tonsil
SE_63627chr17:76330640-76331454HSMM
SE_65603chr17:76330764-76331564Pancreatic_islets
SE_67525chr17:76329782-76335716u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr177633068876331173
Number: 1             
IDChromosomeStartEnd
GH17I078333chr177632986276331667
Enhancer Sequence
TAATTATGTC CTGTCATCTC CCTGCTTGTA GCTACTAAGA TCCCTTAGGA AAGATCCCAT 60
CCTGATTTAA GATTGCATCC CTAATACCTA TAACACAATA ACTTGCACTT ACGGACATGC 120
CATAGATATT TGTTGACTAA GGGCAAGAAT ATATGAATTT GTTTAGTGAT TCACTGCAGT 180
GTTTTGTGGG TGAGTAACAT AGTCGTGAGT TTCTAGTTTC CCCAGTCTAG TTTCTGGCCC 240
ACAGTGGCCT TGTTTGTCAT CTTTCTGTCC CTCTCCTCAT CTCAGGCCAA GGGTGAAAGC 300
CAGCAAGAGT CCGGGGCTGG CATCTACCCA GACAGCGTCT CACTCTGCTG CCCAGCCCAC 360
TTTCAAGTCA ATGTGGAGCT TCCCAGCTCG CCCTCCCCAT CCTGGATTTC AGATCCCTCC 420
TACCCTCACC CTACTTTCTC TCGGAGTTTG ACAGGGGAGC AGGTAGAACC TGGGGCAGAT 480
CTGCATTCCC CTGGGAGATG CTTCAAGCAG TGGCAGGGTC TTAGCCTCTG AGCTGCTCCC 540
TGGTAGGAAG GAAGCAACTG CCCCTGGTCT GTGTTGGGAG ATGGACAGAG CTTTAGGATG 600
GACAGGCGTT GGGGATGCAC CAGTACACAT AGGCGCTCAA TAACGGTGGT CTTTATTCTC 660
TTTCCTCTTC TGTCATCTGA CACGATTCGG TCTTCTCAGC TAAGGACTGG GTCTGTCCTT 720
CGCTCGTCCT TGTAGCCGTG ACTACAACCT TCCAAGCCAT TTTTGTTTTC TTAGAGGTTT 780
TATTGGGAGC TGAGGGTTAA TAGCACCCCA GCCCCTCCCA TCAGGCTCAA GGGGCTCTTT 840
TGCCTTCACT TGTGGTTGAG AGTCCTCCCT CCCTCCTGCC 880