EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS197-20472 
Organism
Homo sapiens 
Tissue/cell
ZR75-30 
Coordinate
chr8:24797300-24800540 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs6557786chr824799742hg19
TF binding sites/motifs
Number: 24             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Atoh1MA0461.2chr8:24797911-24797921AACATATGTT+6.02
Atoh1MA0461.2chr8:24797911-24797921AACATATGTT-6.02
KLF5MA0599.1chr8:24799505-24799515GCCCCGCCCC+6.02
ZNF263MA0528.1chr8:24799646-24799667CCCTCCTTTCTGCCCACCTCC-6.16
ZNF263MA0528.1chr8:24799581-24799602CCTCCTTCCTCCCCAACCTCC-6.34
ZNF263MA0528.1chr8:24799601-24799622CTACCCCCTCCTTCTTCCTCC-6.36
ZNF263MA0528.1chr8:24799664-24799685TCCCTCCCCTTCTCCTTCCCC-6.42
ZNF263MA0528.1chr8:24799617-24799638CCTCCTTACCCCTCCTCCCTC-6.43
ZNF263MA0528.1chr8:24799665-24799686CCCTCCCCTTCTCCTTCCCCT-6.47
ZNF263MA0528.1chr8:24799546-24799567CCCCCTCTTCCTTCCTCCCCA-6.4
ZNF263MA0528.1chr8:24799597-24799618CCTCCTACCCCCTCCTTCTTC-6.52
ZNF263MA0528.1chr8:24799539-24799560CCGCCCTCCCCCTCTTCCTTC-6.53
ZNF263MA0528.1chr8:24799634-24799655CCTCCTCCTCCTCCCTCCTTT-6.83
ZNF263MA0528.1chr8:24799614-24799635CTTCCTCCTTACCCCTCCTCC-6.85
ZNF263MA0528.1chr8:24799658-24799679CCCACCTCCCTCCCCTTCTCC-6.89
ZNF263MA0528.1chr8:24799661-24799682ACCTCCCTCCCCTTCTCCTTC-6.92
ZNF263MA0528.1chr8:24799568-24799589CCTCCTAGCCCCTCCTCCTTC-6.93
ZNF263MA0528.1chr8:24799543-24799564CCTCCCCCTCTTCCTTCCTCC-6.96
ZNF263MA0528.1chr8:24799604-24799625CCCCCTCCTTCTTCCTCCTTA-7.08
ZNF263MA0528.1chr8:24799542-24799563CCCTCCCCCTCTTCCTTCCTC-7.17
ZNF263MA0528.1chr8:24799621-24799642CTTACCCCTCCTCCCTCCTCC-7.23
ZNF263MA0528.1chr8:24799624-24799645ACCCCTCCTCCCTCCTCCTCC-7.86
ZNF263MA0528.1chr8:24799630-24799651CCTCCCTCCTCCTCCTCCCTC-8.75
ZNF263MA0528.1chr8:24799627-24799648CCTCCTCCCTCCTCCTCCTCC-9.36
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr82479946224799718
Number: 1             
IDChromosomeStartEnd
GH08I024941chr82479894324800313
Enhancer Sequence
ACTGTGAAAA CAGAAAATTA GTATTGTAAA TGCTGCATCC CAAGGGCCTA AAGATGGTAT 60
CTGGCCCATA ATAGGTACTC AGAAAGTATG TCATGAATGA ATGAATGAAT GAATGAATGA 120
ATTGTAAAAT AAAAATAAAA TCCAACTCCC CCCACCTTCA GCAGATTAAA AGGAACCCTC 180
TTGGCCAAGG AGATCCCAGA AAACCTTTAA GTTTCCCAGC CATGAAGAGA CGGGAGGTTG 240
GTCATGCCTC ATTATGCCGT CTTTCTTATT AATCTTTACC AGATTATTTC TTAACAATTA 300
AACAGAAACT GGTCCTGGAG AAACAAAGAA TGGAAGCTTT GCTCCATCCT TGATGTCAGC 360
CAATTGCCAG ATAGATACCA CAGCCCAACT CCCCTCCCTT CTTGTGGTTT TGACACAGCA 420
GGTAACTGGT TTCACCATGC ATTCCTTTCA GATAAAATTC TCCTTTCCAT GGACTGGTTT 480
ACAGATGCTG TGCACAAGAC ACTCTGTGTC CTTTGCTTTA CCTTTTCACT TATAGAGCCT 540
AATTTTAATG CATTTAAATG TCTCCACTTC ACAGTGAACA TGGGACATGC ATAACATGCA 600
TGTTTGCTTA CAACATATGT TCGCGATCCT CTATTCATGA ATATTCATAG CTCCTCCTGT 660
AACCTGATGA ATATTATATT ACATTCAACC CATTTAGCAT AACACTCCTG TCCCACCCTT 720
GCTCTGGCAG AGTGCCTGCT TTTAGTCTGC ACAGGAGGCT CCACTTCCCA GCCTGCAAGT 780
TGCAACTTTT TTTAAGAAAT AAAACTCTAC TTTGCAAATT TATGGACGTT GTAATTTTTA 840
AGTCTACAGC AAGGATGTTA TACGTTTACT GGCATTACTG GCAGATATAG CCTACAGTAA 900
GCCTCCAAAC CTGGCATTCA GCTCCAGAGA AAGCGTTCAT GTTAAAGCTG ACAAAAACTG 960
ACCACCTCGT GAGCTCTCAG GCCCTGAGCT CTCCTTCGCA TCTTGTCTTC TCCTTCCTAG 1020
GCTTGTGCCT TCAAAGCACC AGGTCTGCTT GGTCCTGGGG CCAGGCTAAC GCTCTCCCTG 1080
GGATAGATAC AGGGTCCAGA GAAATATCTG GTGCTTGTTT TCCAACCATC GCCACCCCAA 1140
CCTGGGGGGA AGGCAGAGCT AATATTATAC AGGTGAAAGT TGCTTGAGGA GATGAGTGAG 1200
GCCTGTCTTA CGAAAGTAAC TGGCAAGGAG CTTTACAGAC GGCAACATGA AGCCAGATAG 1260
GATTTGCACC CGGCGGGTGA GGAAAACATT GCCCTGCCCG TGAATGTACA TTTTCACTTG 1320
GGTTCTGTCC TACCCCACCC CTCGCCCCCA TGAGTTTACA CTTCTCCCAC ACGGGGCTTG 1380
GACAGCCTCA GCAGGTCAAG CGGCTGAGGG TCCTGGAACA TCTTGTGCCC AATGGCCTGA 1440
CCTCAGCAGG CCTCCAAATG GAAGCCAAGT GCTGACCCTC AAGGGTCTAC AAAAGTTCCT 1500
TTATCAAACT CTACCCAGGA TAGTGAGGGG ATGTTTAGAA GACGGACAGG AATGAGCTTT 1560
TCCCTTGGCC AGGCCTTCCC CTTGCTTATT ACTTATTACT TATTATTATT AATAATATAG 1620
GATCTTGCTC TGTTATCCAG GCTAGAGTAC AATGGCTCTG TTATAACTCT CTGCAGCCTC 1680
AACCTCCTGG GTTCTATGAA TCCTTCTGCC TCGGCCTCCC AAGTAGCAGG GACTACAGGC 1740
GCCACTACAC CCGGCTAATT TTTATTTTTT TTGTAGAGAC CGGGTCTGCT ATGTTGCTCA 1800
GGGTGCTCTG GAGCTCCTGG GCTTAAGCGA CCTTCCCTCC TTCGCCTCCC AACGCTCTGG 1860
GATTACACGT GTTAACCACC GCGCCAGCCC TGCCCTTAGC TTATAAGGGA AAGGGAGAAG 1920
CTGCTCCTCT TCTCGCCTCT CTTCTGTTAC AAAAAGCAAC CTGCTGCCTC CTCTGCCTCC 1980
CTTCTCCACT CCCCAGTGTA AGAGTGAGCT GCAGATAAGC GTTATGTTTA CCAGGTCGTC 2040
TCACACTTAA TGTGCACAGG AATCGCCTGG GTGTCCGGTT AAAATGCAGA TTCCGGTTGG 2100
GTGGGAGCCC TGGCGGGGGA GGAGGGGGTC CAAAACTGCA TTTCCAACCA GCGGCGAAGG 2160
ATGCAAAGGC CGCTTGTCCA CACTCCACCC AGGAATCCGT AGGAGGCCCC GCCCCGCCTC 2220
CCGGTGGCCT GGTGCTGGGC CGCCCTCCCC CTCTTCCTTC CTCCCCAGCC TCCTAGCCCC 2280
TCCTCCTTCC TCCCCAACCT CCTACCCCCT CCTTCTTCCT CCTTACCCCT CCTCCCTCCT 2340
CCTCCTCCCT CCTTTCTGCC CACCTCCCTC CCCTTCTCCT TCCCCTGTCT TCCCCATCCC 2400
CACCGCAGCC TCGCCGCACC CTCGGAGTCC AGCTTCTTCA CGTTAAACTC AGACTCCAGA 2460
GCGGCTGGGG CGTGGCTCTC GGGGCCAGGC CTCGATGAGG AGGGGCACCG TCCAGAATGA 2520
CTGCGGATGC CCCCTTCCCA GCCCCATGTT GGAGTCTGGG GTCCCAGAAC GGGCCGGCTC 2580
TGGAGGAGAC ACCTCTAGGC TCCCCGAGTA GGGCAGGCGG CAGAAGTTCC CTAAGAGGAC 2640
ACCCCCACAC CACGATGCCC ACCTCCCGAC CCCCGCGCTG CCCACTCAGT CCTCTGGCCA 2700
CTGGGTTTCT GGCCGCAGAT CTCGCTGCCG CCTCCTCCTC CGGGCGCGGC CACCTGGAGA 2760
AAGATCCAGC AAAACCCTGA TTCCCGGCGC CTCCTCCCTC CCCCGCCCCT GTCCATCTCC 2820
AATGGCGGAG CTTTCTGCAA AGCCGCGTGG CTCTACCAGC TCTAAAGTAT TTCAAAAGTC 2880
TTGGAACTTG TTCGTTTGCG GGATGGGGGT CTCAATAGTT AAGGAATTGG AAGCTGCAGC 2940
ATTTTGCACC TTAGGGGGAG GGGCGGGATC TCTTACTGCA GGGGCTGTGG AGGCTGCACC 3000
CCGCACAGGT TTTGCCCCCG GGGGGCATCC TGGGGTCGTG CCCACCCACT AAGGAGACTG 3060
GAGCGGCTTT TTTTTTTTTT TTTTTTTTTT TAAAGACAGA GTCTCGCTCT GTCGCCCAGG 3120
CTGGAGTGCA GTAACGCAAT CTCGGCTCAC TGCAAGCTCC GCCTCCCAGG TTCACGCCAT 3180
TCTCCCGCCT CAGCCTCCCT AGTAGCTGGG ACTACAGGCG CCCGCCACCA TGCCCGGCTA 3240