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

TagContent
EnhancerAtlas ID
HS053-32970 
Organism
Homo sapiens 
Tissue/cell
Foreskin_keratinocyte 
Coordinate
chr5:159720070-159721490 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Nr2f6(var.2)MA0728.1chr5:159720209-159720224GAGGTCAGGAGTTCA+6.22
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr5159720972159721325
Number: 1             
IDChromosomeStartEnd
GH05I160293chr5159720530159722098
Enhancer Sequence
CAAAACACTG TGTTCTAACC CTCCATGTGA TAGTTTAGGT TTGTTTGTAT TTTCCTTTCA 60
AAATAATGTT TTAGGCTGGG CATGGTGGCT CACACCTGTA ATCCCAGCAC TTTGGGAGGC 120
CGAGGCAGGC AGATTACCTG AGGTCAGGAG TTCAAGACCA GCCTGGCCAA CATGGTGAAA 180
CCCCGTCTCT ACTACAAATA CAAAAGGATT AGCTGGGCGT GGTGGTGCAC GCCTGTAACC 240
TCAGCCTCAG CTACTTGGGA GGCTGAAATA AGAGAATTGC TTGAACCCGG GAGGTGGAGG 300
TTGCAGTGGG CTGCATTCCA GCCTGGGTGA CAGAGCGAGA CTCCATCTCA GAAAATGATA 360
ATAATAATAA TGTTTTATTT AACTGATTAT AAAATACTTA ATCACTATAG GAATTTTAGA 420
AAATACAGAG GAGCACAAAG AGAACTAAAG TCTCCAGCAA TTCCATCAGC ACGTAAATAC 480
TCGGAGAATG TACACATGTC GGCATGCGCA TGTCCGGTCC TGTTTCTCTG TGCGCACGCA 540
TGTCCACTTC TCTCTCTCTC ATGGGACTAT CTCCTCCCTT ACAACTAGAA CGTAAATGCT 600
ATGTGCATTT GCTATCTCCC CACACCCACC CTCCGAGGTG GAACCAGCAC TAGCCCTAGT 660
AGCCAGGAAA CTGAGGCACA GAAGTATAAC TGCCAAGGCC ACACTGCAGG TGAGTGGTAA 720
ATCTTGGGCT TGGACATCAG AGGAGCGGGC CAGGGCTTGG GGTATGACAA TACTTGGAGG 780
GCGACAACCA CTTCGTAAAC AGCTCAAGGT GCAGTAAAGC AGGGCTGAGC TGCTCTCAAA 840
CACCAGCCAC CAAGAGAAAC CACTCTGCTT TCCTCCTCCA ATCTCCCTAC CATGCCTATC 900
CCTACTGCTG CCAACAAGAG CCCGGGAATC CACGCCCTGG GTTGAGACAA CAGCTAGAGG 960
GGTCTTGTCT AAGAACAAAG AACCGCAGAG AGGTGAAGAA ACACCATGTG TAACCAAGGT 1020
GACCAACAGG AAGTGGAGAC TTGCAAATGT AAAGTGGCAA AGAAAGGGGG AGAAAGGCTG 1080
GCTCTTCAGA GGCCTCAGTA CACAGCACGA CCTGGGAGGC CCAGCAAGGC AGGAGGCTCA 1140
CCCTCCTTCC TCTCTCTGCC CCGATTGCTT CATAAGGCCC AAGGAAGCAT TTTCCGTAAA 1200
GCATCAACAC CTCTGTGGGA ACACTATTTC AACATTCTTG AGAGGGTGGC CCGTGTCACA 1260
TAAGGCCAAC AATGCCCGTA ACGTCCCCTC CTGCTGAAGT CCAGCCTGTA GCTTCCTTCC 1320
AGCAGAGTGA AAGGTAACCC AGGCACCACA TCCGCAGCCG GCGTCTGTAC TACTCCTGGG 1380
CAGATGGCAG GCAGGCCAGC TCCAAGCACA CCTCCTCATT 1420