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

TagContent
EnhancerAtlas ID
HS092-16033 
Organism
Homo sapiens 
Tissue/cell
HFF 
Coordinate
chr14:55284670-55285940 
Target genes
Number: 8             
NameEnsembl ID
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs7144602chr1455285588hg19
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOSL1MA0477.1chr14:55285575-55285586GATGAGTCACT-6.02
JUNDMA0491.1chr14:55285575-55285586GATGAGTCACT-6.32
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr145528537255285783
chr145528488055285800
chr145528509455285320
Number: 1             
IDChromosomeStartEnd
GH14I054818chr145528477355286138
Enhancer Sequence
AACTCCCTGA CCACGCAGCC GCAGTGTGTT GACTTACTAA ACAGCTAACT GCCAGCACAG 60
CTGTGGAGCT TCAGAAGAGC CACACTGGGC TAGTGACACA CATGCTCAGT CACTATGTTA 120
GTGAACTCAG GGGGCCACAT ACAGCCACTG CCTTACTCGC TGGGGCTGTG CCCCAGGCTC 180
TAATCTTTGT GGGTCCATGA GGAACCAAAC TCTGAAATGG ACACGGATGG CCTGACTGGA 240
AAGAAATGGG AAAATGAAGT CCACTTCCAG GTCTAGCTCA GCTGCCCAAG CATCCTGGGG 300
GCCAGGAGCC CCATTCATGG CTCTAGGACT TTGTTGTAGA AACAGAAAAG CCCCCTAAAG 360
AAAAAAACTG TCCCAAGGAA GAAAATGCCA GGAATGCCGT CATCCCCTGC TGCCCCATAT 420
TCCTAAGAAG CTTCCCAGAT TGAAGCCAGT AGGCACTCAG CTAAAACCGC CTGAGTGCCA 480
TTGGCCAGGC CCCTCCTGGC CCAGGGTCAA GGGGTCCAGG GAGGGCAGGA TGGCTGTCTC 540
TGATCTCCCC CCAACCCCCG CCACTTAGCC ATGAGACCAC AGAGCTCCAA TATGTACCCA 600
TAAACACACA CACCCCTAGC ATCTAGGAAG GGAAATTCTA TCTCTTGCTT ATAACCGAGT 660
TACCCCACTT TCTGACCTTA AAAAAGAACA GCAGGTTTCC TTTGAAGGAT TCAAACCTCA 720
TTAGCCACAG CGGGAAATGA TGCTTTAATG GGCCCGTGAT GGTCTCAGCT TCGGGTGTCT 780
GTGTACGCAG CCATATTACT TAGCAACACC ATAGCCATTT AGGTTTAATT TCCTAGCTTG 840
CCTGATAAGG AGGCTGCAAG TGTAATTTGT GATGCCGCAA GCTGGGCAAA CTCACAGGGC 900
TATTAGATGA GTCACTGTGT GATCCAGGCC ACTGTGCCGA GCTCTGCAGA AGAAGAGAAA 960
TTAACTCTGA TTTGTGGGGC TGATACCGCT CAGGCGGACG CAATTTTCTG TGTCTGGGAG 1020
CTGTGCTTCC GTCTCTCCTG CTTTCTGGTT TGGTGCCATC ATTGATTAAG GGAAGCTTCA 1080
CTCACCTCTC AATCCCTGTT ATGATCATCT TCCAGCTTTC TGAAATCCTC ACACAAACTC 1140
AAAGCCTGGC AAGGTAATAA TAATAACAAT ATCAATAATA ACAGCAATAA CAGTAATAGC 1200
TCACATTTCT GAATGCTATT CGAGTGCTAC TCATAAGTTA TCTCTGTTAA TTCTCCTTAC 1260
AACCCCAGGA 1270