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

TagContent
EnhancerAtlas ID
HS010-00106 
Organism
Homo sapiens 
Tissue/cell
B_cell_blood 
Coordinate
chr1:41310550-41311390 
TF binding sites/motifs
Number: 9             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
IRF2MA0051.1chr1:41311001-41311019AAAACAGTTTCGTTTTCC-6.13
ZNF263MA0528.1chr1:41311357-41311378TCCTCCTCCTCCTCCTCCTCT-10.23
ZNF263MA0528.1chr1:41311348-41311369TCTTCCTCTTCCTCCTCCTCC-10.47
ZNF263MA0528.1chr1:41311345-41311366TCCTCTTCCTCTTCCTCCTCC-10.52
ZNF263MA0528.1chr1:41311351-41311372TCCTCTTCCTCCTCCTCCTCC-10.86
ZNF263MA0528.1chr1:41311354-41311375TCTTCCTCCTCCTCCTCCTCC-11.36
ZNF263MA0528.1chr1:41311363-41311384TCCTCCTCCTCCTCTTCTTCT-6.54
ZNF263MA0528.1chr1:41311342-41311363ATCTCCTCTTCCTCTTCCTCC-7.21
ZNF263MA0528.1chr1:41311360-41311381TCCTCCTCCTCCTCCTCTTCT-7.64
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr14131057441311373
Number: 1             
IDChromosomeStartEnd
GH01I040845chr14131087341311272
Enhancer Sequence
TGAACAGCTC TGCTGGTCTC ACCTGGGGTC ACTAATGTGC TTGCAATCAT CTGGCATCAA 60
CAGGGTCTAG ATGGCCCAAG AGGGCCTTCC CCACGTGTCT GCAATCTGGT GTGAGTTGGT 120
CTGCAGGCAA GACGGCTCAT CTCTGTTCTA TGGAGCTTCT CATCCTCCAG TAGATTAGAC 180
TGTACTTCTT CATATGGCAA GAGGGCAAAA GCAGAAGCCA TCAGGCCTCT GGAGGCCCAG 240
GCTCAGAAGC TGTACCAAGG GGCTCAGCTC ACTTTGATGG GTGCTCTGAA TACGTTGCGA 300
TGTTTACACT CTTGTAGATC TAAAAAAACC CATGCAGTTA TTTCTCTATT TAGATAATTT 360
ATTTCATGTA CTTTTGTTTT TTTGAGAGTG CAGAGTGCAG TGGCCACTGC ACTGGGCCAT 420
ATTTCACGTA CTTTTGACAG CTCCAATTGT TAAAACAGTT TCGTTTTCCC TCTGAGAAGC 480
TGAGAGGCAC ATCTTCCCCT ACCACCCACC TCTGTGTATA GCAGGACCGT GATAGCTGCT 540
ACCACGGTGT GTTGGTCTGT GTGGGATGGC ATAGCAAATA TCATGGACTG GAAGGTCTAA 600
ACAACAGAAG TGCATGATCA CACAGTCAAA GTTCTGGAGG CTGGAAATTC AAGACCAAGT 660
TATCAGCAGG GTTGGTTTCA TTCTGAGGCC TCTCTCCTAT GATTGTAGAG GCTGCCTTCT 720
TCTGGTATCT TTGCATGATT ATCTCTTGTT CTCTATGTAC ACAGGTCTGA GGTCTCTCTC 780
TGTGTCCTAA TAATCTCCTC TTCCTCTTCC TCCTCCTCCT CCTCCTCTTC TTCTTTGTGT 840