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

TagContent
EnhancerAtlas ID
HS026-16698 
Organism
Homo sapiens 
Tissue/cell
CNCC 
Coordinate
chr2:1770290-1771680 
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
HES2MA0616.2chr2:1771393-1771403GGCACGTGCC+6.02
HES2MA0616.2chr2:1771393-1771403GGCACGTGCC-6.02
Nr5a2MA0505.1chr2:1770515-1770530GTGTTCAAGGTCAGG+6.83
ZNF263MA0528.1chr2:1770875-1770896TGAGGAGGGACGGCAGGGAGA+6.26
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr217708001771620
chr217710921771558
Number: 1             
IDChromosomeStartEnd
GH02I001766chr217703611770550
Enhancer Sequence
GAGGCCTGGC CAGGGGTCTG TGGGATCCCC AGCCACAAGG CCGCTGAAGA GGTCCTGGAG 60
GAAGCATTCT CCCCAGCCTG CAGAGGGAGC AGGGCACGCC CAAGCCCTAC CTTGGACTGC 120
AGGCTTCTGA ACCCTGTAGT TGAAGGCTGT AGTTTGCAGC TCTTTGTTAC AGCAGCCACA 180
GGGAATGCGC CTCCAGCCTG TCTGGAAGTC AGCTCTTCCC ACAGGGTGTT CAAGGTCAGG 240
TGGGCTGCTC CCAGAGGAGC AGGTGCAGGC AGAGACCACA GGCTGCTGGA GGGAAGGGGA 300
TACCCAGCCT TTGCTGAGGC TCTGTCCCAC TTCTGTTTGT CGTATTTTAG CCATTTGGGG 360
TGCACCTAAC CACTGAGCTT ATTCCTTCTC TAGCTCCCTA CCTCCACCAC CCAGACCGTC 420
CCGCTGTGCA GCAGCCAGGC AGCGCCTCTC TTCGGGGCCT CTCCCCCAGT CCCCCTGCTG 480
AGCTCTGGAC ACTCTGGGAT GGACCCCCCG CTCAGATCAG GCAGGGTCTG GGTCAGGCAG 540
GGGCCAGGGG CTTAGCCCGC AGTGGCCTGA GCCCAGGCAG CTCGCTGAGG AGGGACGGCA 600
GGGAGAGACT TGGGTGTCCA CCCTGCCTCA TGGGCTGCTG ACCCTCCCCA CACTCCATCC 660
TGCCCTTCTG CCCTCCTGCC CTGGCTGCCA CCTTGTCCCC TGGACTGGCT CTCAGAACAG 720
CCGAGCACAT GGGGGATGGC CCAGAGGGGT CCCGGCCCCC GACCAGGTAG GCATCTCTGG 780
GTCAGCTGTG CCCCAGGGGG ATGGGTTGAG TCTCAGACCG GCCAGTGCCC CAGGGACCCC 840
TTTCCTTTCA CTTACAGGAG AGTTCCTCTG TCTCACTGCC TGGGGGAAAA ACCAGCTGAG 900
CCCGTCATGC AGATTTTCTA GGGAGCTGGG CCTGCAGGAG GCCTGGCTTT TGCCCTCTGC 960
TCCTGGGAGG TGACCTCTCG GCCGGCCCTC AGAATGTCTT GACTAATAAG AGCGTCTTTC 1020
TTTACCTGGG GCCGTGGGCC ACCCTGGAGA GCCGATGCTT ACAGTGTGAC TTGTGGTGGG 1080
GCCCAGCCTC AGGCGGACCT GCAGGCACGT GCCGCACCGG ATCCCCAGAG TCCGAGCCCG 1140
CCCCACCCCC CACGCCCTCC GTGGGGCTGG TGCGGCCTCC CAGGTGCTGG TCCCCCAGCA 1200
CTTACCACTA AGCCGCCGCA CCTGCTTCCT TCTTATTCAC CCTGGCCCTC CCTCTGCCTC 1260
TCCACACCAC CAGGCTTGAG TTAACTCACA CCTCCTTCCT CTGTATCGTC TCTGCAGTAT 1320
TTCTCAAATG TACTAAAAAA TCGTAAGAAT GACTTTCTGT GGATGTTTGT TAAAAGCATT 1380
TCCCAAGCCC 1390