EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS076-53306 
Organism
Homo sapiens 
Tissue/cell
H1 
Coordinate
chr8:24798940-24800990 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs6557786chr824799742hg19
TF binding sites/motifs
Number: 24             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
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
ZfxMA0146.2chr8:24800617-24800631CCCGCCTCGGCCTC+6.01
Znf423MA0116.1chr8:24800843-24800858GGAACCCAAGGGGGC+7.15
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr82480082424800925
chr82479946224799718
Number: 2             
IDChromosomeStartEnd
GH08I024941chr82479894324800313
GH08I024943chr82480068124800830
Enhancer Sequence
GCTAGAGTAC AATGGCTCTG TTATAACTCT CTGCAGCCTC AACCTCCTGG GTTCTATGAA 60
TCCTTCTGCC TCGGCCTCCC AAGTAGCAGG GACTACAGGC GCCACTACAC CCGGCTAATT 120
TTTATTTTTT TTGTAGAGAC CGGGTCTGCT ATGTTGCTCA GGGTGCTCTG GAGCTCCTGG 180
GCTTAAGCGA CCTTCCCTCC TTCGCCTCCC AACGCTCTGG GATTACACGT GTTAACCACC 240
GCGCCAGCCC TGCCCTTAGC TTATAAGGGA AAGGGAGAAG CTGCTCCTCT TCTCGCCTCT 300
CTTCTGTTAC AAAAAGCAAC CTGCTGCCTC CTCTGCCTCC CTTCTCCACT CCCCAGTGTA 360
AGAGTGAGCT GCAGATAAGC GTTATGTTTA CCAGGTCGTC TCACACTTAA TGTGCACAGG 420
AATCGCCTGG GTGTCCGGTT AAAATGCAGA TTCCGGTTGG GTGGGAGCCC TGGCGGGGGA 480
GGAGGGGGTC CAAAACTGCA TTTCCAACCA GCGGCGAAGG ATGCAAAGGC CGCTTGTCCA 540
CACTCCACCC AGGAATCCGT AGGAGGCCCC GCCCCGCCTC CCGGTGGCCT GGTGCTGGGC 600
CGCCCTCCCC CTCTTCCTTC CTCCCCAGCC TCCTAGCCCC TCCTCCTTCC TCCCCAACCT 660
CCTACCCCCT CCTTCTTCCT CCTTACCCCT CCTCCCTCCT CCTCCTCCCT CCTTTCTGCC 720
CACCTCCCTC CCCTTCTCCT TCCCCTGTCT TCCCCATCCC CACCGCAGCC TCGCCGCACC 780
CTCGGAGTCC AGCTTCTTCA CGTTAAACTC AGACTCCAGA GCGGCTGGGG CGTGGCTCTC 840
GGGGCCAGGC CTCGATGAGG AGGGGCACCG TCCAGAATGA CTGCGGATGC CCCCTTCCCA 900
GCCCCATGTT GGAGTCTGGG GTCCCAGAAC GGGCCGGCTC TGGAGGAGAC ACCTCTAGGC 960
TCCCCGAGTA GGGCAGGCGG CAGAAGTTCC CTAAGAGGAC ACCCCCACAC CACGATGCCC 1020
ACCTCCCGAC CCCCGCGCTG CCCACTCAGT CCTCTGGCCA CTGGGTTTCT GGCCGCAGAT 1080
CTCGCTGCCG CCTCCTCCTC CGGGCGCGGC CACCTGGAGA AAGATCCAGC AAAACCCTGA 1140
TTCCCGGCGC CTCCTCCCTC CCCCGCCCCT GTCCATCTCC AATGGCGGAG CTTTCTGCAA 1200
AGCCGCGTGG CTCTACCAGC TCTAAAGTAT TTCAAAAGTC TTGGAACTTG TTCGTTTGCG 1260
GGATGGGGGT CTCAATAGTT AAGGAATTGG AAGCTGCAGC ATTTTGCACC TTAGGGGGAG 1320
GGGCGGGATC TCTTACTGCA GGGGCTGTGG AGGCTGCACC CCGCACAGGT TTTGCCCCCG 1380
GGGGGCATCC TGGGGTCGTG CCCACCCACT AAGGAGACTG GAGCGGCTTT TTTTTTTTTT 1440
TTTTTTTTTT TAAAGACAGA GTCTCGCTCT GTCGCCCAGG CTGGAGTGCA GTAACGCAAT 1500
CTCGGCTCAC TGCAAGCTCC GCCTCCCAGG TTCACGCCAT TCTCCCGCCT CAGCCTCCCT 1560
AGTAGCTGGG ACTACAGGCG CCCGCCACCA TGCCCGGCTA ATTTTTTGTA TTTTTAGTAG 1620
AGACGGGGTT TCACTGTGTT AGCCAGGATG GTCTCGATCT CCTGACCTCA TGATCCGCCC 1680
GCCTCGGCCT CCCAAAGTGC TGGGATTACA GGCGTGAGGC ACCGCACCCG GCGGAGAAGC 1740
TTCTTAAGCT CCTGTCTCAG CCCTGGTCGT CCCTCCCCAG CCCAGAGCTC CTCCTCCCCC 1800
GACCACATGT GCATCCAGTC TGCCGGCGGA AAGAAACAAA GAGAGCAGGT GTGACCAGCG 1860
GCGATGCGAG CGTGGGTGGC GCCCGGGCAG AGCTGCAGGT GCAGGAACCC AAGGGGGCGG 1920
CTCCGGGCAA CAGCGGTGAT CGCGACAGTG AAACCAGAAA AAGTGGTATC TGGCCATTTT 1980
GATTTTTCAA AGCCTTTTAT CTCAGCTCAT TAGATTCTCA CGGGTTTAGG GAGGCGTGTT 2040
TAGGTTACTT 2050