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

TagContent
EnhancerAtlas ID
HS047-20254 
Organism
Homo sapiens 
Tissue/cell
Fetal_placenta 
Coordinate
chr2:208395260-208396100 
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
MEF2AMA0052.3chr2:208396061-208396073ACTAAAAATAGA+6.27
MEF2BMA0660.1chr2:208396061-208396073ACTAAAAATAGA+6.32
MEF2CMA0497.1chr2:208396059-208396074CTACTAAAAATAGAC+6.03
Number of super-enhancer constituents: 12             
IDCoordinateTissue/cell
SE_00665chr2:208392218-208400855Adipose_Nuclei
SE_10550chr2:208391325-208397011CD19_Primary
SE_11014chr2:208386866-208401144CD20
SE_12233chr2:208394646-208397091CD3
SE_15280chr2:208392331-208400476CD4_Memory_Primary_7pool
SE_17182chr2:208392318-208397118CD4p_CD225int_CD127p_Tmem
SE_17739chr2:208389400-208400532CD4p_CD25-_CD45RAp_Naive
SE_19611chr2:208392077-208397765CD4p_CD25-_Il17p_PMAstim_Th17
SE_23046chr2:208392136-208400583CD8_primiary
SE_36190chr2:208393267-208397115HMEC
SE_55904chr2:208393387-208396862u87
SE_64432chr2:208395219-208396945NHEK
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr2208395422208395980
Enhancer Sequence
GCCGCCCGCT CGGCCCGGCG CTGCCCCCCG CGCCGCTCGC TCGTCCGGCC CCCGCCGCCC 60
GCCTCGCCCC CGGCCCGACC CGGCCGGGCC TCCGGGGCAG CCGCCGCCTA GGTGCCGGTG 120
GGGGATGGAG GAGGAAGAAG GCGACAGTTG AGGGCAGAGG AGGTGAAGGT GCCTGCTGCC 180
TTCCCGGTGG CTTCGGTGCC TGCCATGCCC GCTTCGCAAG GGGAAGAGCT GCAACGTCTG 240
ACCTACTCTT CTCTCCACTC TTTGTGCAAT AAAGTTCGAA ACCCAAGGTT TCCTCTCGTG 300
CTGTATTTTA TTCGTGCCCT TTCCCCCCCG CTCCTACACC GTTGAGGAAA TGCTGCTTTC 360
TGCCCTGTGT TGCTTAGTTG AGAGATGAGA GCTTGTGCTT TTGGGGGGAA TTTTTGACTC 420
CCTCACCCCT TTGCTTTTTT TTTTTTTTTA AAGTCAGTCA TGGAAATGCA TGCTTTTTGG 480
GAGAAAGGGT GCTAAGAAAA ACATTTATAA TAACTTTTTA AACTGTTGGG ATCTTATAAA 540
AGGGAAGCTG GTGTTTGAAA ACAGTTTCGG TTTTAACCCT TTTTAATAAG GTAATCATCA 600
CTTGAGATCT ATCATTCTGA AACACTTCGT TGGAACGAGT ATCAGCCGAT GTACTCTTGT 660
TTTACATCAT TTCGCGGGGT GCAACCTTGC CAACCGCGTT TGGGTCATCT GGATCTCCCC 720
TCACCCTCCG TCCCACTCCC CCTACCATAT TTCCCACGAA TTTCTGTGTG AACTTTAATG 780
AGAGATTGAT TTAATACTAC TACTAAAAAT AGACATTAAA GTATCCATTA TTTGTCTCAT 840