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

TagContent
EnhancerAtlas ID
HS044-09636 
Organism
Homo sapiens 
Tissue/cell
Fetal_kidney 
Coordinate
chr4:23932190-23933500 
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr4:23932951-23932969GGAAGGAAGGAGGAAAAA+6.18
EWSR1-FLI1MA0149.1chr4:23932947-23932965GGCAGGAAGGAAGGAGGA+7.18
SPI1MA0080.4chr4:23933145-23933159AAAAAGAGGAAGAA+6.14
SPICMA0687.1chr4:23933145-23933159AAAAAGAGGAAGAA+7.01
ZNF263MA0528.1chr4:23932956-23932977GAAGGAGGAAAAAAAAAGGAA+6.34
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr42393235423933012
Number: 1             
IDChromosomeStartEnd
GH04I023930chr42393194523933702
Enhancer Sequence
TGATTTCTTT CTTTTTAGGC CAAAAGAGCA TATATCATTC AAGCTATGGG GACAAAAATA 60
AATTGTTGCC AGAGGCTGTT CAAATGGAAA CCAGTAGCAC CCTTCAGGGT TCAATGTACT 120
TTTTTGTTTC TTTTTTCCTA CCCAGACTCT CAAAGGGACA AACACATGCA GGAAAGTGAT 180
CCTGGAAAGA AGGGGTTAAT ATAAGCTGCA CAGTGCACTC AGTGATGCCT TAAATAATTG 240
TCACATGTCC CCTATAATCT GTCCCATGCT GTCAGCACTG AGTTAGTCAT AATAATATCA 300
GATAAGAGCT GTTCAAAGTG ACACACTAAC CAACATGGGA GCCACATGAC TTTCTGGCTT 360
GGCTACTGCC CTTCAGCTGA ACTTTGGCTT AGAACACAAG GCTCCCAGAG GCAGCCTGGC 420
ACATGCCGCC GCGTGGAGTG TCCGGTGGCA TTTTCCGTTG CTAGGGCCTC TGTTGCTTCA 480
CAGTCTAGTG AGGGGCAGCT GGGGATCAGT GACAGGGAGT CACCTGCTCA CCCCACCTCT 540
GGGGACAGGG AAAGGAATTG GCTGCTGTGG TGGCCGCTGC CTTTCTGAGC TTGTGCTGGG 600
ACTCCCTGTC CCCTCCACAG TTGATTAGTT TTGCAAATGT GTGTGTCACG CGTTATGCCA 660
AGAACCACAG CAGGGAAACT CGGACCCCCA AAGGGAGTTT GTGCTGGAAG AGGTAGAGAA 720
GGAATGTGAC TCTTGGCTAA GAGGACACAA AGGCAAGGGC AGGAAGGAAG GAGGAAAAAA 780
AAAGGAAGGA AAGTTATTAC CTCTGGGTAG AAGGTTACTG TAGACTAGCT CTATTTTATT 840
TGTGCTTTTC TGTATCCCCG CCCTGACTTT TTTTTTTACT TCCAGCATAC TTTAGATTTT 900
TAATTTAAAA AGTTAAGGCA CATATTTTTT AAAGGAGAAT AAAGAAAGAA TAGTGAAAAA 960
GAGGAAGAAA GGAAGGTGAC CCATTCACTC ACTGATTCAT TCACAAAGCA GAGACCAGAA 1020
AGGAAGCAAG AATCCAATGT CATCTGACAT TGGATTTGAG AACATTTATT GGCAGTGTGC 1080
CTCTGGCATA CTTACCTAAC ACCTCTCTCT AAGCTTTATT ATCCTCGGCA GTAAAATGGA 1140
AAAATAATAC CTAAGTTACA AGACTGCCAT GGGGATAAAA AGAGGTGATA TATGCTAAGT 1200
GGCTAACAAG TGGTAGGTGC TCAATAATCA GTAGCTCATG GGAAGCCATG GAAGTTATGA 1260
CGATCTTTGG AGTCAGAGAT ACCCAGATCC AAAGTCTGAC TCCAGCACTT 1310