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

TagContent
EnhancerAtlas ID
HS148-18634 
Organism
Homo sapiens 
Tissue/cell
NHLF 
Coordinate
chr9:15305700-15307080 
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
TCATCTAGTA GGCAGTGAGC ATAGCTGGGG TGACCATTTG TCAAAGTATC TCCGAAACAG 60
TCCCAGTTTA CACCTATTAT CCCAGTGTTA ATTAATAATA GCACCGCCTC AACAATGCCC 120
TAATCTAGAG AATTACATAG TTCTAAGCAC AGCAAATCTC CTACAAACAG ATCGGGATTC 180
AAATATTTCA TTCTACAGTC TTGGGATCCT CAATGCAAGG GACAGGCTGT AAGCAAGGGT 240
CTGGACAGCC CGGCTTGCCC TCTTGTCTCT CTGTCATGCA GAGGAGCTGT AGTTCAGTTT 300
TTGTTTTTTG TTTATTTTAC GGAGCACATT TAAAGTATAG TCTTCCTTGT CAGGAGATTC 360
CTGGCACTAA AGAGATGGAC GGGAAACTTA ACCGCCTCCT CCAGATCGTC CACTATTGCA 420
TCATTTGAAA CCAAAGCCTT CTAAAGGCAG CGACTCGCAC AATTCAAGTC AGGTAAGATG 480
GCAGGAACAG CAGCTGTGGG TGCTGGCTGC TGCTGGAGCC TCGGTCTCAA CTTCAAGAGC 540
AGGGAGAGCG CTGTCTCTGG AGTTGCCAGG TGCTGAAATG AATAGTCAAT AAATCAACAG 600
GTCCGGCGCG CTAGCCCCTG GGTGCTCAGG CCCGGGCGCG CCACGACTGA AGGAGTGGCT 660
AATTACTCAA ACACAGTTGA AACCAAAGGA GGCCGGAGTC GGTTCTCAAA GTGGTTTCCC 720
TCCGGCCACC ACCGACTCTG AGGACCTGCT AGGGGAAGTG TCCCGGCCCC GTGGAGGGAG 780
AGGGAAGCAC CACAGCCTGG GCTGCGGCTC TAGCCCTCCA GCCCCAGCCC CTGGCAGCCC 840
TGCCCTGCTG TCGCGGCAGG TACCCCTCTA CTCATTGTTC CTCAGGCTGC CCCCTCTTTT 900
CATCAATCGT AAGCCTTTCG GTTCTGCCAC CAGGAAACTT CCATAGAAGG TGAGATTCCC 960
AGGTCGAGGG ATGATTCCAC GAACACCCAG AGAGCCAGTG CCAGGACTTC AGGGTCAGAC 1020
TTCGTAAAGC CCAGGCGTCG CTGGGCCGGC CCGGAACAGC TCAGAGCTGC GGGTCCTATG 1080
GTCCCGCGCC CTCACGCCCA TCCAAGTGCT GGCAGGACGT GGGTCCTCCA TCCCCACGAC 1140
TCGCGGGGCC GGCGCTCCGA ACCTCGGCAC TGCGTCCGCT CCGCGCGCCG CAGGGACCCT 1200
CCTAGCTCCA GCGGGGACAG ACCTACCAAG GCCGGGCGCC CCCACCCGGC GCCCGCCAGC 1260
CCACCCCAGA GAGGGGACCA AGGGGGCGGG GCCTCGGCCG TCCTAGCCGG GCTCACTCTT 1320
CTCTCCCGGA CTCCTGTCCA GGGCTTCAGG GGCCGGGCCC GCAATCCCCA TCGGATCGTA 1380