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

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EnhancerAtlas ID
HS092-04856 
Organism
Homo sapiens 
Tissue/cell
HFF 
Coordinate
chr1:223673310-223674520 
Target genes
Number: 9             
NameEnsembl ID
TF binding sites/motifs
Number: 8             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Stat6MA0520.1chr1:223674140-223674155GGTTTCCAGAGAAAC+6.15
ZNF263MA0528.1chr1:223674484-223674505TCCTCCTCCTCTCCCTCCTCC-11.18
ZNF263MA0528.1chr1:223674475-223674496GACTCTCCCTCCTCCTCCTCT-6.16
ZNF263MA0528.1chr1:223674481-223674502CCCTCCTCCTCCTCTCCCTCC-6.27
ZNF263MA0528.1chr1:223674478-223674499TCTCCCTCCTCCTCCTCTCCC-7.21
ZNF263MA0528.1chr1:223674493-223674514TCTCCCTCCTCCGCTTCCTCC-7.61
ZNF263MA0528.1chr1:223674499-223674520TCCTCCGCTTCCTCCTCCCCC-8.07
ZNF263MA0528.1chr1:223674496-223674517CCCTCCTCCGCTTCCTCCTCC-9.06
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1223673532223673875
Number: 1             
IDChromosomeStartEnd
GH01I223499chr1223673147223674962
Enhancer Sequence
GTAGCATCTG AAGCAGCCAC TGGGACCAGG CTTGCCACCC TTTCAGAGGG GTGTGAGGTG 60
CAGGGCAAAG GGTCTGTAAA GGCTGGCAGG GAAGTGGGAA GCAGTGGAGA GCCAGGACCA 120
GCCCTGGGCA CCCAGAGGGG TTAGGGACCC TGCCACCCCT CCCAGGTTTC CAAACAAGGC 180
CTGTGCCTGC CTGGGCTCTG ACAGTCAGCC AACAAACAGG CATTTCCAGG TCTGCACCAG 240
GCCCCGGGGA TACAAAGAGG AGTGAGAGTT CCTGCCCTCC CTGGATCCTG CGGGGAAGGC 300
TGACAGATAC ACCAATCCTG TGTCACGGGA ACTGGGGATT GGGGGGAATG ATGGGCAGGG 360
GGCATCAGGG TTATCTGAGA AAGCTTCCCA GAGGAGGCGG TCCCTGGCTG AATTGAAGAA 420
ATTGCTGGGA GCTTCTCAAC AAGAGCATTA GAAGGGAGTT GGGGGCACGA AGTGGGTGCT 480
CATGTCAGGA GAAAAATCCA CAAAGGCCTC TCATATGCAC TCTGCGCCCT CCTCTCATTT 540
TTCCAGGGTC CTGCTCCCAG CTGTGCAAGC TGCAAGGAAG AACGAGCCCC CTCCTCCAAG 600
GCCTCGACGG TCCACTCAGT CACCCACTTA AGAATTCACC AAATAAGTAA TGACTAAGTC 660
TGACTGGGAG AAAATGAAAG CTCTCTTGGA GGGGAAAACA AGTTACTCAT GCAACCAAGA 720
GCATATCCTT GGCACCCTCC ATGAGTGGAG CCACGGCAGG AGGGGCAGAC AGGAACAAAC 780
GGTGGCCATG AATCATGCTG TGTGCGAGCT CCTTTGTTTC TAAGGCATGT GGTTTCCAGA 840
GAAACCAGGG AACACTGCCT TCAGGTAAAC ACGCCCACCA CCCATGCTTC TTGGAACAGG 900
CTCTGTCCTC CAGGAGCCCC ATTAAAGAGG CCTAGCTGCT TACATTTGTC AGTTGTACTT 960
CCACAGGGGG GATTTCAAGT GCTAGCTGGC CAAGTCATCC AACGGGTGGC AATGGACCTT 1020
CTGTTGGCCG GGAGCATCCT ACCCCGTGCC AGGTCCCTGG TCCCACTCTG CCCACCACCC 1080
TCTCACCCCC AGAAGAAGAC TCCTCTGGTT GATGAGTTTG GCAGAAGAGT CTTGGTTTGG 1140
TCAGTTCAGC CCTTCTGCTC ATGCTGACTC TCCCTCCTCC TCCTCTCCCT CCTCCGCTTC 1200
CTCCTCCCCC 1210