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

TagContent
EnhancerAtlas ID
HS098-34964 
Organism
Homo sapiens 
Tissue/cell
HSMM 
Coordinate
chr20:47493010-47494190 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs34116853chr2047493894hg19
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
IRF1MA0050.2chr20:47493810-47493831AAAAAAAAAAAGAAAGAAAAA-6.59
Nr2f6(var.2)MA0728.1chr20:47493590-47493605GAGGTCAGGAGTTCA+6.22
RREB1MA0073.1chr20:47493047-47493067GGATGGGTGGTGGTTGAGGG-6.22
Number of super-enhancer constituents: 1             
IDCoordinateTissue/cell
SE_59612chr20:47363420-47493230Ly4
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr204749397147494130
Enhancer Sequence
TTTATCTTCC TGATTAATTG CCAGCAAGGG GTCTGTGGGA TGGGTGGTGG TTGAGGGCGA 60
CTCTTGGATG TGTGATCTCG CCTGGGAGGC AGGTAGGTTT CCCAGTCACC CTGGATTTTT 120
AACATTTTCT TGTTGGAAGT CACATCCTCA AGCAAACTCT TAGGCACTAT TTAGGGAGCA 180
CTCCCCAAAC AGCTCCATTA TGGCCTAAAT ATTCTTGGGA AGATGAAAAG GGGAAAAGAC 240
TATCATTGCT CAAAACAAGT CTATAATCTA GATGGAAGCA GGTAAAGAGG CACAATATTT 300
ACCATCTTTT ATTTTTACAG GGTCTTTATC TATTTCCATC ACTTAACCAT GAGCTCTTTG 360
GGAACCAGAA CCCAGTCAGA ACCATTGGGG TATCTGAATC TGGACCCAAG CATGTAGTGG 420
GGCTCAGTCT ACCTGTCACC TCATTCAGGA TTCTTTCAGT TGTAAGTATT AGCAACTCAG 480
CTCAAAAAGG CTTCATTGAA AAGTATGATA TATAGGCCGG GCGCAATGGC TCACACCTGT 540
GATCCCAACA CTTTGGGAGG CTGAGACGGG TGGATCACCT GAGGTCAGGA GTTCAAGACC 600
AGCCTGACCA ACATGGTGAA ACCCCCTCTC TACTAAAAAT ACAAAATTAG CCAGGCGTGG 660
TGATTCACAT GCCTATAATC TCAGCTACTC AGGAGGCTGA GGCAGGAGAA TTGCTTGAAC 720
CCAGAAGGTG GAGGTTGCAG TGAGCCAAGA TCGTGCCATT GCACTCCAGC CTGGTCAACA 780
AGAGCGAAAC TCCATCTCAA AAAAAAAAAA AGAAAGAAAA AAAAGTATGA TATATTAACT 840
CACGGAATAG AGAAATCCAG GTCTAGAATG ACTTCAGGCA TGGATAGATC TAGGAGTCAA 900
AGAACATCAC CAAGATCAGA CTTTCTTTTC CCTCAGCACT TTTTTCTGCA CTCTTTGTGC 960
CAGCCTCAGT TAGATTCTAA CTCAGTGGTG GCTCTCAGTG GCAAAATAGC TTAGCAACAC 1020
CAGTTGGGTT TCTTTTCTCC CAATAGTAAT AGAAATGCTT AAACTGGCTC TAGCTGGATC 1080
AGTGTGGGTC ACATGCTGAT CTCTGATACA ATCACTGGGC AGGGAAATGG GCTACACTGA 1140
TTGGCCTGGT GTAGGCCCCA TGTCCATTTC ATATTTGTTA 1180