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

TagContent
EnhancerAtlas ID
HS066-03498 
Organism
Homo sapiens 
Tissue/cell
GM18516 
Coordinate
chr20:36050380-36051360 
TF binding sites/motifs
Number: 12             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
RREB1MA0073.1chr20:36050539-36050559TGTGTGTGTGTGGTGTGTGT-6.16
RREB1MA0073.1chr20:36051081-36051101TGTGTGTGTGTGTGGGGGGG-6.17
RREB1MA0073.1chr20:36050580-36050600TGTGTGTGTGTGGTGGGTGG-6.38
RREB1MA0073.1chr20:36051083-36051103TGTGTGTGTGTGGGGGGGGG-6.38
RREB1MA0073.1chr20:36050576-36050596GGGTTGTGTGTGTGTGGTGG-6.51
RREB1MA0073.1chr20:36051079-36051099TGTGTGTGTGTGTGTGGGGG-6.95
ZNF263MA0528.1chr20:36050435-36050456CTCTCCTTCCTCCTCTTCTCC-6.08
ZNF263MA0528.1chr20:36050438-36050459TCCTTCCTCCTCTTCTCCACC-6.09
ZNF263MA0528.1chr20:36051164-36051185GCCCTTCCTCCCTCCTCCTTC-6.63
ZNF263MA0528.1chr20:36051168-36051189TTCCTCCCTCCTCCTTCCTCC-6.77
ZNF263MA0528.1chr20:36051171-36051192CTCCCTCCTCCTTCCTCCTCT-7.33
ZNF740MA0753.2chr20:36051092-36051105GTGGGGGGGGGGA-6.3
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr203605040136050632
Number: 1             
IDChromosomeStartEnd
GH20I037421chr203605024536050646
Enhancer Sequence
GCGGGGGTGA GTGAGTGTGT CTGTCTGTCC TTCCACCTCC AGGCTTCCTG GCTGCCTCTC 60
CTTCCTCCTC TTCTCCACCC TTTTTCCTGG AGATTTCTGG AATTTCACTC TCGCCGCTCC 120
TGCTGTGAGC CTGAAGAAGG GGCTGTGTGT GTGTGTGTGT GTGTGTGTGT GGTGTGTGTG 180
TGAGTGTGGG CGCTGAGGGT TGTGTGTGTG TGGTGGGTGG GTGTGAGCCA GGCTGCATGT 240
ACTCCCGCCT TCCCTCACCG CCTCTGCAGC CCTGCCAGCT TTTGTTCCCC TCTGCGAACA 300
TTTCCTTTCT TTCAGAAATG ACATTTATTG TTTTCCTTTG GTTTCAGATG TCATATGTGT 360
TCCCTGTAGA AAAGGTGGAA AATACCAAAA AGAATGTGCA GAGGAAGACA AATAAAAATC 420
CCTGTGCTCC CAACTCCCAG GGAGAGAGGA GCCGTCGCCG ACATTTTGGG GAGCTTTTCA 480
TTATCTTTGC CTTGTGTCTG TGCACTGTTT TTCTCGCTTT TTCTTTGCAG ATTCTACCCC 540
ACTCTCTACT CTCTTATTCA TTCCTTCAGA AACATTTGGG GGTCCCCACT TGGGGCACCC 600
CTGTGTGTCT TCGTCAGCCC ATCTGAATGT CTTTGTTGGG AAGGTCCGTC TGTTTGAGGG 660
TCTCCTACCT CTCTCCCTTC GTGTGGGTGT GAGTGCGTGT GTGTGTGTGT GTGTGGGGGG 720
GGGGAAGCAG CTAGAAAGAA ATAGTTGGGG GGAGAGAGAG ACAGAAAGAG ACCCTGCGTC 780
CTCCGCCCTT CCTCCCTCCT CCTTCCTCCT CTGCCCGCTT CGGGATGCAG GGATAACTGT 840
GCTAGGTGCC TGCCTGTGGC CCCCAGTCCC TTTTCCTGTC CCCATCCCTT TGTCTTTGGG 900
TTCCTAAAGG ATGGCACAGA GCCTCCAGGA GCGGAGTGGG GCGGTGTAGG CAGAGGACAC 960
AGCTCCTAGC AGCAAGTGGA 980