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

TagContent
EnhancerAtlas ID
HS133-31542 
Organism
Homo sapiens 
Tissue/cell
melanoma 
Coordinate
chr9:15306120-15307080 
Target genes
Number: 1             
NameEnsembl ID
TF binding sites/motifs
Number: 8             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF14MA0740.1chr9:15306979-15306993AAGGGGGCGGGGCC-6.15
KLF16MA0741.1chr9:15306981-15306992GGGGGCGGGGC-6.02
KLF5MA0599.1chr9:15306982-15306992GGGGCGGGGC-6.02
PLAG1MA0163.1chr9:15306972-15306986GGGGACCAAGGGGG+6.59
SP1MA0079.4chr9:15306980-15306995AGGGGGCGGGGCCTC-6.59
SP2MA0516.2chr9:15306979-15306996AAGGGGGCGGGGCCTCG-6.4
SP4MA0685.1chr9:15306978-15306995CAAGGGGGCGGGGCCTC-6.97
ZfxMA0146.2chr9:15306326-15306340CAGGCCCGGGCGCG-6.24
Number of super-enhancer constituents: 5             
IDCoordinateTissue/cell
SE_12243chr9:15305858-15308099CD3
SE_18538chr9:15304122-15312133CD4p_CD25-_Il17-_PMAstim_Th
SE_19786chr9:15305298-15308227CD4p_CD25-_Il17p_PMAstim_Th17
SE_22766chr9:15304870-15308674CD8_primiary
SE_29496chr9:15304336-15309019Fetal_Intestine_Large
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr91530680015307000
Enhancer Sequence
TCATTTGAAA CCAAAGCCTT CTAAAGGCAG CGACTCGCAC AATTCAAGTC AGGTAAGATG 60
GCAGGAACAG CAGCTGTGGG TGCTGGCTGC TGCTGGAGCC TCGGTCTCAA CTTCAAGAGC 120
AGGGAGAGCG CTGTCTCTGG AGTTGCCAGG TGCTGAAATG AATAGTCAAT AAATCAACAG 180
GTCCGGCGCG CTAGCCCCTG GGTGCTCAGG CCCGGGCGCG CCACGACTGA AGGAGTGGCT 240
AATTACTCAA ACACAGTTGA AACCAAAGGA GGCCGGAGTC GGTTCTCAAA GTGGTTTCCC 300
TCCGGCCACC ACCGACTCTG AGGACCTGCT AGGGGAAGTG TCCCGGCCCC GTGGAGGGAG 360
AGGGAAGCAC CACAGCCTGG GCTGCGGCTC TAGCCCTCCA GCCCCAGCCC CTGGCAGCCC 420
TGCCCTGCTG TCGCGGCAGG TACCCCTCTA CTCATTGTTC CTCAGGCTGC CCCCTCTTTT 480
CATCAATCGT AAGCCTTTCG GTTCTGCCAC CAGGAAACTT CCATAGAAGG TGAGATTCCC 540
AGGTCGAGGG ATGATTCCAC GAACACCCAG AGAGCCAGTG CCAGGACTTC AGGGTCAGAC 600
TTCGTAAAGC CCAGGCGTCG CTGGGCCGGC CCGGAACAGC TCAGAGCTGC GGGTCCTATG 660
GTCCCGCGCC CTCACGCCCA TCCAAGTGCT GGCAGGACGT GGGTCCTCCA TCCCCACGAC 720
TCGCGGGGCC GGCGCTCCGA ACCTCGGCAC TGCGTCCGCT CCGCGCGCCG CAGGGACCCT 780
CCTAGCTCCA GCGGGGACAG ACCTACCAAG GCCGGGCGCC CCCACCCGGC GCCCGCCAGC 840
CCACCCCAGA GAGGGGACCA AGGGGGCGGG GCCTCGGCCG TCCTAGCCGG GCTCACTCTT 900
CTCTCCCGGA CTCCTGTCCA GGGCTTCAGG GGCCGGGCCC GCAATCCCCA TCGGATCGTA 960