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

TagContent
EnhancerAtlas ID
HS061-22916 
Organism
Homo sapiens 
Tissue/cell
GM12892 
Coordinate
chr7:116891160-116892340 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
RORA(var.2)MA0072.1chr7:116891327-116891341TTGACCTAATTAAA-6.69
STAT1MA0137.3chr7:116891352-116891363TTTCCTAGAAA-6.14
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr7116891928116892147
Number: 1             
IDChromosomeStartEnd
GH07I117248chr7116888313116892630
Enhancer Sequence
ATCTTACTAA TCCTTCAAGA AATCCTGATC TCCATTTTCT TCTTCCAAGC CTAAGTTCTC 60
CTTCTATCTG CACTCTTACT GTCTTGGCTC CAATCTGCTC CAAGATCTTA ACACATCCCA 120
TTTTTCGTCT CTTTCTCTAC CATCTCCATG TCCAGGCACC CTTTTCCTTG ACCTAATTAA 180
ATAGTCCAAT GTTTTCCTAG AAACCAGCCC TCTTCAATCT TGCTTCTCCC TTAGCCTGCC 240
ATTCAGCGTC TTCCTACTCA CTCCCTTCTT TAGGGCTTTT GAGCATCATT CTGCCTCTGG 300
TATCTCTTCA CACATTCCTT CTTTAATCCT CCAAACTCTG TTCTGACAGG CCCTAATTCT 360
TGTTGTTGTT ATTATTTTTT TAATACCACC AAGCTTGCTT TTATGGATTT GTTTTTTAAG 420
GGAAAAGGAT GACTGCCCGT GTTCCAGTTC GAATTTGACC ACCAAGCCCT GGGAACTCTC 480
CTCCTTCATC CTCTGCGACA CTCTTTCTTG AGTGTCTGGA GAGGGTTTTC TCCAAGCTCT 540
CTGGTCCGTG TCTTCCTTTG CCACCATAAA TGGAGGCCTC TCTCAAAGTT CTTATGTGGT 600
TCTGGAGGGT CCCTTCACTG TTTCACTCTC TCCCACCCAC CGCCTCCTGA CGCTACCCCC 660
ATCCCTGCTG AGCTGCTGAG CTGCTGAGCT GCTGAGCTAC ATTTTCAACT GCCTATCTGA 720
CATCTTGCTC CAGTTTCAAA CTGAACTCAA TGTCTTTCCC CTAAAAAGCC CCTGTCTGTG 780
TAAATGACAT CACCAACCAG CCATGCACAC AGAAATGTTG GCGGTTGAAT TCCCAAAGTG 840
AATCAGTAGC TCCTAGTGCC AGATGGCCGG AAAGTTCTGC ACCCATTCTG CAATTCAGGG 900
CCTAACTCCC CTCCCTGATC CATGCCTGAT TCATTCCCAT GACCCTCTGC CTGGCTTGTC 960
TGCCTCCAAA CTCCCCTCTT TTCAACCTTA AAACACGGGT TTAGTCCTAA CATTTCCATC 1020
GCCGACTTTG CACTGATTTC TCACCATGTA AAGGGAAAGG CCCTGGCTCC TGGGAGGGGA 1080
CCCAAGGGCT CCATGGTGTC CCTGACACAT CTCCCCCCCC ATACCTCCAA GCCCCTTGGC 1140
TCCTGCCACA GGAGTCTCCC CACTGATCCC TGAACCTGCT 1180