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

TagContent
EnhancerAtlas ID
HS129-36955 
Organism
Homo sapiens 
Tissue/cell
MCF10A 
Coordinate
chr9:33133190-33134340 
Target genes
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
RORAMA0071.1chr9:33134226-33134236TGACCTTGAT-6.02
Number of super-enhancer constituents: 9             
IDCoordinateTissue/cell
SE_10912chr9:33119344-33169982CD20
SE_27770chr9:33133434-33136209Fetal_Intestine
SE_28724chr9:33133427-33136185Fetal_Intestine_Large
SE_31534chr9:33133555-33134361Gastric
SE_42236chr9:33133177-33134351Lung
SE_48426chr9:33133123-33134192Psoas_Muscle
SE_58985chr9:33124740-33168862Ly3
SE_62118chr9:33106994-33169093Toledo
SE_62346chr9:33106942-33169226Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr93313328033133507
chr93313373033133860
chr93313415033134329
Number: 1             
IDChromosomeStartEnd
GH09I033133chr93313369733146567
Enhancer Sequence
GCGCCTAGGC CCAAATATAT ATTTTAACCT ACCTATATGG CACCCAGACC ACAGCTGTCT 60
GTCTTCTACT CAGGCAGATT TGTGGGATGC TATCAGATGC CCTGCTGAAT AAGATATGAC 120
AGCATTGTAT CCACAGTACA TCCCTCATCT ACTGGCATAG CAACTGTCAA GAGAGAAACG 180
AGATGCAGCT GGCACGGCTT ATTAGTCATC CCTGCTGGCT CCTGGTGATG GTGGCCGCCT 240
CTTCCAGGTG CTCGCTGCCA CTGCTTTAAT AACAGGCTCC TGAATCTTGC CGTCATTGGT 300
ATGTGCTAAC TGGCATCAGA CAAATGTTTC TCAATCACAG AGCTTTTCTT AAATGAATAT 360
GTGTTGGGTT AAAGTGACCC GCATTTTGCA GGACATTTAC CTGTTCTCTC TTGCATTCTC 420
CAATATTCTT CCAAGGTGAC CCACAACTGC GTGGCTGTCT TGCTTGCAGG TGTTCATAGG 480
GCCCTGGTCT GTACCTCACT TGGCCGAAGA ATTCAAACAG CCTCAAGGGG TTTGCCCACC 540
ACCTGCTCTC CTGCTTCAGT TTCCTTGTAA CAGGGCTTGT TCTGCTCTCT CCTGCCTCAC 600
AGGCTTAACT CTGACACCTG GTCCCAGAGC TTCTGGTGCT TTCCTACCCC AGTGGGCATC 660
TCAATTTCCA GGAACATGCA AGGCTCCTTT CTGCCTTAAG GTCCCTGCTC ACTGGCCCCA 720
GCTGAGAAGC CCATCTCCCT GCAGACTTTA GAACCTAGTT TATATCCTGG TTCTTCCAAG 780
CCATTGCTCT CTCTCCTTCC TCTGAGCTTC CAAAGCATTT GGCAGCCACC ATCCAATCAC 840
AGGATATTTG GGTCTGTTAA CAAATTGTTC CCTGGGAAGG TCCCACTTGC CAGAAGTGGG 900
TTGGAGGCTT CGGGACAGGG CAGGACTGAG ACCTTACACT TCTTCAGAAT CTCCCTGCAG 960
CAAGTGATGC AGCACAATGC CACAGCAGTC CTCGAGTGCT TCCCCTGGGG TCATAGGGAA 1020
GGTGCACAGA GTTCCTTGAC CTTGATGGAA GCCGTAAACT GCCAACAATC CTCCTACCTA 1080
AAGCAGAGTT TATCTCGAAA TGAAATGGAC ATTGGGCCTT GTAGAAATGG GCGTACTCAG 1140
ACTCTTCAAA 1150