EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS023-24076 
Organism
Homo sapiens 
Tissue/cell
CD8+ 
Coordinate
chr8:24798240-24801000 
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
GTTAAAGCTG ACAAAAACTG ACCACCTCGT GAGCTCTCAG GCCCTGAGCT CTCCTTCGCA 60
TCTTGTCTTC TCCTTCCTAG GCTTGTGCCT TCAAAGCACC AGGTCTGCTT GGTCCTGGGG 120
CCAGGCTAAC GCTCTCCCTG GGATAGATAC AGGGTCCAGA GAAATATCTG GTGCTTGTTT 180
TCCAACCATC GCCACCCCAA CCTGGGGGGA AGGCAGAGCT AATATTATAC AGGTGAAAGT 240
TGCTTGAGGA GATGAGTGAG GCCTGTCTTA CGAAAGTAAC TGGCAAGGAG CTTTACAGAC 300
GGCAACATGA AGCCAGATAG GATTTGCACC CGGCGGGTGA GGAAAACATT GCCCTGCCCG 360
TGAATGTACA TTTTCACTTG GGTTCTGTCC TACCCCACCC CTCGCCCCCA TGAGTTTACA 420
CTTCTCCCAC ACGGGGCTTG GACAGCCTCA GCAGGTCAAG CGGCTGAGGG TCCTGGAACA 480
TCTTGTGCCC AATGGCCTGA CCTCAGCAGG CCTCCAAATG GAAGCCAAGT GCTGACCCTC 540
AAGGGTCTAC AAAAGTTCCT TTATCAAACT CTACCCAGGA TAGTGAGGGG ATGTTTAGAA 600
GACGGACAGG AATGAGCTTT TCCCTTGGCC AGGCCTTCCC CTTGCTTATT ACTTATTACT 660
TATTATTATT AATAATATAG GATCTTGCTC TGTTATCCAG GCTAGAGTAC AATGGCTCTG 720
TTATAACTCT CTGCAGCCTC AACCTCCTGG GTTCTATGAA TCCTTCTGCC TCGGCCTCCC 780
AAGTAGCAGG GACTACAGGC GCCACTACAC CCGGCTAATT TTTATTTTTT TTGTAGAGAC 840
CGGGTCTGCT ATGTTGCTCA GGGTGCTCTG GAGCTCCTGG GCTTAAGCGA CCTTCCCTCC 900
TTCGCCTCCC AACGCTCTGG GATTACACGT GTTAACCACC GCGCCAGCCC TGCCCTTAGC 960
TTATAAGGGA AAGGGAGAAG CTGCTCCTCT TCTCGCCTCT CTTCTGTTAC AAAAAGCAAC 1020
CTGCTGCCTC CTCTGCCTCC CTTCTCCACT CCCCAGTGTA AGAGTGAGCT GCAGATAAGC 1080
GTTATGTTTA CCAGGTCGTC TCACACTTAA TGTGCACAGG AATCGCCTGG GTGTCCGGTT 1140
AAAATGCAGA TTCCGGTTGG GTGGGAGCCC TGGCGGGGGA GGAGGGGGTC CAAAACTGCA 1200
TTTCCAACCA GCGGCGAAGG ATGCAAAGGC CGCTTGTCCA CACTCCACCC AGGAATCCGT 1260
AGGAGGCCCC GCCCCGCCTC CCGGTGGCCT GGTGCTGGGC CGCCCTCCCC CTCTTCCTTC 1320
CTCCCCAGCC TCCTAGCCCC TCCTCCTTCC TCCCCAACCT CCTACCCCCT CCTTCTTCCT 1380
CCTTACCCCT CCTCCCTCCT CCTCCTCCCT CCTTTCTGCC CACCTCCCTC CCCTTCTCCT 1440
TCCCCTGTCT TCCCCATCCC CACCGCAGCC TCGCCGCACC CTCGGAGTCC AGCTTCTTCA 1500
CGTTAAACTC AGACTCCAGA GCGGCTGGGG CGTGGCTCTC GGGGCCAGGC CTCGATGAGG 1560
AGGGGCACCG TCCAGAATGA CTGCGGATGC CCCCTTCCCA GCCCCATGTT GGAGTCTGGG 1620
GTCCCAGAAC GGGCCGGCTC TGGAGGAGAC ACCTCTAGGC TCCCCGAGTA GGGCAGGCGG 1680
CAGAAGTTCC CTAAGAGGAC ACCCCCACAC CACGATGCCC ACCTCCCGAC CCCCGCGCTG 1740
CCCACTCAGT CCTCTGGCCA CTGGGTTTCT GGCCGCAGAT CTCGCTGCCG CCTCCTCCTC 1800
CGGGCGCGGC CACCTGGAGA AAGATCCAGC AAAACCCTGA TTCCCGGCGC CTCCTCCCTC 1860
CCCCGCCCCT GTCCATCTCC AATGGCGGAG CTTTCTGCAA AGCCGCGTGG CTCTACCAGC 1920
TCTAAAGTAT TTCAAAAGTC TTGGAACTTG TTCGTTTGCG GGATGGGGGT CTCAATAGTT 1980
AAGGAATTGG AAGCTGCAGC ATTTTGCACC TTAGGGGGAG GGGCGGGATC TCTTACTGCA 2040
GGGGCTGTGG AGGCTGCACC CCGCACAGGT TTTGCCCCCG GGGGGCATCC TGGGGTCGTG 2100
CCCACCCACT AAGGAGACTG GAGCGGCTTT TTTTTTTTTT TTTTTTTTTT TAAAGACAGA 2160
GTCTCGCTCT GTCGCCCAGG CTGGAGTGCA GTAACGCAAT CTCGGCTCAC TGCAAGCTCC 2220
GCCTCCCAGG TTCACGCCAT TCTCCCGCCT CAGCCTCCCT AGTAGCTGGG ACTACAGGCG 2280
CCCGCCACCA TGCCCGGCTA ATTTTTTGTA TTTTTAGTAG AGACGGGGTT TCACTGTGTT 2340
AGCCAGGATG GTCTCGATCT CCTGACCTCA TGATCCGCCC GCCTCGGCCT CCCAAAGTGC 2400
TGGGATTACA GGCGTGAGGC ACCGCACCCG GCGGAGAAGC TTCTTAAGCT CCTGTCTCAG 2460
CCCTGGTCGT CCCTCCCCAG CCCAGAGCTC CTCCTCCCCC GACCACATGT GCATCCAGTC 2520
TGCCGGCGGA AAGAAACAAA GAGAGCAGGT GTGACCAGCG GCGATGCGAG CGTGGGTGGC 2580
GCCCGGGCAG AGCTGCAGGT GCAGGAACCC AAGGGGGCGG CTCCGGGCAA CAGCGGTGAT 2640
CGCGACAGTG AAACCAGAAA AAGTGGTATC TGGCCATTTT GATTTTTCAA AGCCTTTTAT 2700
CTCAGCTCAT TAGATTCTCA CGGGTTTAGG GAGGCGTGTT TAGGTTACTT TAAAAAATAT 2760