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

TagContent
EnhancerAtlas ID
HS080-36563 
Organism
Homo sapiens 
Tissue/cell
H9 
Coordinate
chr9:15305760-15307080 
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
TCCCAGTTTA CACCTATTAT CCCAGTGTTA ATTAATAATA GCACCGCCTC AACAATGCCC 60
TAATCTAGAG AATTACATAG TTCTAAGCAC AGCAAATCTC CTACAAACAG ATCGGGATTC 120
AAATATTTCA TTCTACAGTC TTGGGATCCT CAATGCAAGG GACAGGCTGT AAGCAAGGGT 180
CTGGACAGCC CGGCTTGCCC TCTTGTCTCT CTGTCATGCA GAGGAGCTGT AGTTCAGTTT 240
TTGTTTTTTG TTTATTTTAC GGAGCACATT TAAAGTATAG TCTTCCTTGT CAGGAGATTC 300
CTGGCACTAA AGAGATGGAC GGGAAACTTA ACCGCCTCCT CCAGATCGTC CACTATTGCA 360
TCATTTGAAA CCAAAGCCTT CTAAAGGCAG CGACTCGCAC AATTCAAGTC AGGTAAGATG 420
GCAGGAACAG CAGCTGTGGG TGCTGGCTGC TGCTGGAGCC TCGGTCTCAA CTTCAAGAGC 480
AGGGAGAGCG CTGTCTCTGG AGTTGCCAGG TGCTGAAATG AATAGTCAAT AAATCAACAG 540
GTCCGGCGCG CTAGCCCCTG GGTGCTCAGG CCCGGGCGCG CCACGACTGA AGGAGTGGCT 600
AATTACTCAA ACACAGTTGA AACCAAAGGA GGCCGGAGTC GGTTCTCAAA GTGGTTTCCC 660
TCCGGCCACC ACCGACTCTG AGGACCTGCT AGGGGAAGTG TCCCGGCCCC GTGGAGGGAG 720
AGGGAAGCAC CACAGCCTGG GCTGCGGCTC TAGCCCTCCA GCCCCAGCCC CTGGCAGCCC 780
TGCCCTGCTG TCGCGGCAGG TACCCCTCTA CTCATTGTTC CTCAGGCTGC CCCCTCTTTT 840
CATCAATCGT AAGCCTTTCG GTTCTGCCAC CAGGAAACTT CCATAGAAGG TGAGATTCCC 900
AGGTCGAGGG ATGATTCCAC GAACACCCAG AGAGCCAGTG CCAGGACTTC AGGGTCAGAC 960
TTCGTAAAGC CCAGGCGTCG CTGGGCCGGC CCGGAACAGC TCAGAGCTGC GGGTCCTATG 1020
GTCCCGCGCC CTCACGCCCA TCCAAGTGCT GGCAGGACGT GGGTCCTCCA TCCCCACGAC 1080
TCGCGGGGCC GGCGCTCCGA ACCTCGGCAC TGCGTCCGCT CCGCGCGCCG CAGGGACCCT 1140
CCTAGCTCCA GCGGGGACAG ACCTACCAAG GCCGGGCGCC CCCACCCGGC GCCCGCCAGC 1200
CCACCCCAGA GAGGGGACCA AGGGGGCGGG GCCTCGGCCG TCCTAGCCGG GCTCACTCTT 1260
CTCTCCCGGA CTCCTGTCCA GGGCTTCAGG GGCCGGGCCC GCAATCCCCA TCGGATCGTA 1320