EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS088-47505 
Organism
Homo sapiens 
Tissue/cell
HeLa-S3 
Coordinate
chr7:2490550-2492470 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs11486794chr72491918hg19
TF binding sites/motifs
Number: 47             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CTCFMA0139.1chr7:2491204-2491223CTTCCACCAGGGGGCAGCC+6.98
EWSR1-FLI1MA0149.1chr7:2492308-2492326CCTTCCCTCCCTCCCTTC-6.02
EWSR1-FLI1MA0149.1chr7:2492264-2492282CTTTCCTTCTTTCTTTTC-6.24
EWSR1-FLI1MA0149.1chr7:2492309-2492327CTTCCCTCCCTCCCTTCC-6.36
EWSR1-FLI1MA0149.1chr7:2492300-2492318CCTCCCTCCCTTCCCTCC-6.92
EWSR1-FLI1MA0149.1chr7:2492304-2492322CCTCCCTTCCCTCCCTCC-6.96
EWSR1-FLI1MA0149.1chr7:2492336-2492354CCTTCCTTCCTTTCTCTC-7.26
EWSR1-FLI1MA0149.1chr7:2492328-2492346CCCTTCTTCCTTCCTTCC-8.03
EWSR1-FLI1MA0149.1chr7:2492284-2492302TCTTCTTTCCTTCCTTCC-8.2
EWSR1-FLI1MA0149.1chr7:2492292-2492310CCTTCCTTCCTCCCTCCC-8.32
EWSR1-FLI1MA0149.1chr7:2492296-2492314CCTTCCTCCCTCCCTTCC-8.62
EWSR1-FLI1MA0149.1chr7:2492332-2492350TCTTCCTTCCTTCCTTTC-8.73
EWSR1-FLI1MA0149.1chr7:2492288-2492306CTTTCCTTCCTTCCTCCC-8.84
ZNF263MA0528.1chr7:2492291-2492312TCCTTCCTTCCTCCCTCCCTT-6.09
ZNF263MA0528.1chr7:2492379-2492400CCCCCATCCCCTCCCTCTCCC-6.16
ZNF263MA0528.1chr7:2492386-2492407CCCCTCCCTCTCCCCTCCCCT-6.25
ZNF263MA0528.1chr7:2492317-2492338CCTCCCTTCCCCCCTTCTTCC-6.2
ZNF263MA0528.1chr7:2492343-2492364TCCTTTCTCTCCCCCTCCCCA-6.34
ZNF263MA0528.1chr7:2492268-2492289CCTTCTTTCTTTTCCTTCTTC-6.37
ZNF263MA0528.1chr7:2492350-2492371TCTCCCCCTCCCCACTCCCTC-6.3
ZNF263MA0528.1chr7:2492324-2492345TCCCCCCTTCTTCCTTCCTTC-6.47
ZNF263MA0528.1chr7:2492230-2492251TCCCCTCTCCTCCCCTCCCCT-6.49
ZNF263MA0528.1chr7:2492354-2492375CCCCTCCCCACTCCCTCCCTC-6.56
ZNF263MA0528.1chr7:2492358-2492379TCCCCACTCCCTCCCTCCCCT-6.5
ZNF263MA0528.1chr7:2492309-2492330CTTCCCTCCCTCCCTTCCCCC-6.61
ZNF263MA0528.1chr7:2492280-2492301TCCTTCTTCTTTCCTTCCTTC-6.62
ZNF263MA0528.1chr7:2492370-2492391CCCTCCCCTCCCCCATCCCCT-6.64
ZNF263MA0528.1chr7:2492391-2492412CCCTCTCCCCTCCCCTCCTCG-6.66
ZNF263MA0528.1chr7:2492237-2492258TCCTCCCCTCCCCTTTCCTTC-6.77
ZNF263MA0528.1chr7:2492287-2492308TCTTTCCTTCCTTCCTCCCTC-6.79
ZNF263MA0528.1chr7:2492308-2492329CCTTCCCTCCCTCCCTTCCCC-6.7
ZNF263MA0528.1chr7:2492304-2492325CCTCCCTTCCCTCCCTCCCTT-6.85
ZNF263MA0528.1chr7:2492296-2492317CCTTCCTCCCTCCCTTCCCTC-6.8
ZNF263MA0528.1chr7:2492190-2492211TCCCCTCCCCTCCCCTCCCCT-6.91
ZNF263MA0528.1chr7:2492195-2492216TCCCCTCCCCTCCCCTCCCCT-6.91
ZNF263MA0528.1chr7:2492200-2492221TCCCCTCCCCTCCCCTCCCCT-6.91
ZNF263MA0528.1chr7:2492205-2492226TCCCCTCCCCTCCCCTCCCCT-6.91
ZNF263MA0528.1chr7:2492210-2492231TCCCCTCCCCTCCCCTCCCCT-6.91
ZNF263MA0528.1chr7:2492215-2492236TCCCCTCCCCTCCCCTCCCCT-6.91
ZNF263MA0528.1chr7:2492284-2492305TCTTCTTTCCTTCCTTCCTCC-6.99
ZNF263MA0528.1chr7:2492375-2492396CCCTCCCCCATCCCCTCCCTC-7.01
ZNF263MA0528.1chr7:2492316-2492337CCCTCCCTTCCCCCCTTCTTC-7.04
ZNF263MA0528.1chr7:2492225-2492246TCCCCTCCCCTCTCCTCCCCT-7.13
ZNF263MA0528.1chr7:2492363-2492384ACTCCCTCCCTCCCCTCCCCC-7.13
ZNF263MA0528.1chr7:2492300-2492321CCTCCCTCCCTTCCCTCCCTC-7.54
ZNF263MA0528.1chr7:2492320-2492341CCCTTCCCCCCTTCTTCCTTC-7.54
ZNF263MA0528.1chr7:2492222-2492243CCCTCCCCTCCCCTCTCCTCC-8.37
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr724913232492175
Number: 1             
IDChromosomeStartEnd
GH07I002451chr724907862492610
Enhancer Sequence
CCAGCCTGGC CTGGCATCTC CTGGACCCCC GCAGGGGTGG CAGCTCAGCC CCTTGTGGGT 60
TTTTTCTTTG GGGGGACAGA CTCTCGCCCT GTCACCCAGG CTGAGGTGCA GTGGCACGAT 120
CTCGGCTCAC TGCAACATCC ACCTCCCGGG TTCAAGCGAT TCTCCTGCCT CAGTCTCTTG 180
AGTAGCTGGG ATTACAGGCG CCTGCCACCA TGCCCAGCTG TTTTGTATTT TTAGTAGAGA 240
TGGGGTTTCG CCATGTTGGC CAGGCTGGTA TCGAACTCCT GATCTCAGGT GATCTGCCTG 300
CCTCAGCCTC CCAAAGTGGT AGGATTGCAG GTGTGAGCCA CTGCGCCTGG CCCTGTTCCA 360
GGATCTTGGC TCTCTGTCCC GGGCAGGGTG CTTCCGGGCC TCTTTGATTC TGGCCACAAT 420
GCTGAGCCTG TCCCGCAGCC CTGGGAGTGG CCCCCAGACC TTCCACTGCC CCAGGAATGG 480
CTGACGCAAC TATTCCCCCC AACCAGTGAG ACCTGTGCCT GCCCGAGGAA GGTGTGAGCC 540
GGGCCATTTA GAGGAGCTCC CTCGGGTGGA TCCACCTCTG AGTCCTGGGC CTGCAGCCTG 600
GCACAGGGCT CCTGGAGGGG CTGCATGGAG CTGGGCAGGC CGGGCCCTGG GCATCTTCCA 660
CCAGGGGGCA GCCACGGCTC AGGAACGCGA CCTGCGGCGC ACCCTTGGCT AAACGCGGCT 720
GCACGCAGGG CATGGGGTGG CCGGCCAAAG CGCATGTGAA CCTGGTAATG CAATGTCCCC 780
CGTGGGTCCG AAAGCCCTGA GGCCACCCGA GTGAGCATCC CTCCAGCCCT GAGGCCACCC 840
TCCCGGGCCT CTGAGACACG GTCCCTGTGT GGGTGGCTGT ACAGTCCCGG TTCTGGACAG 900
GCCGTGGGGG GCACAGGAAG TGGCTGCTCA GCCCCCTGGG CGGCTGGACC AGGAGGGCAC 960
TGGGTGATCT GGGGGCACCG TGGCAGGGCT GGGCCTGGTC ACCCAGGCTC TGACGCCCTC 1020
GTGATTCCTG TCTGCTGGGC CCCACAGCGC CCTCAGCACC ATGCTGGCCA TGCTGGCCAG 1080
AGCTGTCTTC CTCCCACCAA ACACTGTCCG TGAGGGCGAC CTGTTTCCAG TTTGAACCAA 1140
GTTCACACTG ACTCCACCAC TCACTTGCTG TTGGGTCACT GCTCTGGGCC CCTCTGGGGG 1200
ACTCAAGGAG CTGAGTGGCT CCGACTCCCC AGGCCTGAAG CCCCAAGACG CGCTGCCAGG 1260
ACCACGCTGG CTGAGGCCAC TCTTTGAGCC CCTCCCCCAC AGGTGGCCGA GCACACACAG 1320
TCCAGTGGGC TGAGGTGGCC CCAAGGGCAG GAACGTGGCA TCTCTTCCCA CCAGTCAGTG 1380
GCTCTGGGGG CACAAGGACT TGTCGGGGGA AGGAGGCAGC AACCGCAGGT CAGAAGCTGG 1440
AAGCAGCGGC CACTCAGCAA ATGACACAGC TGAGCCGGAA AACCCAGTCC CAGGGCTGTG 1500
AAGAGCTGGG GCCGGCCTCA CGGGGGCTCC CCAGTTTCCC CTGCCCGGCC CTGGGCCGGC 1560
CTCACGGGGG CTCCCCAGTT TCCCCTGCCC GGCCCTGCCC TGCCCTGCCC TGCCCTGCCC 1620
TGCCCTGCCC TGCCCTGCCC TCCCCTCCCC TCCCCTCCCC TCCCCTCCCC TCCCCTCCCC 1680
TCCCCTCTCC TCCCCTCCCC TTTCCTTCCT TTTTCTTTCC TTCTTTCTTT TCCTTCTTCT 1740
TTCCTTCCTT CCTCCCTCCC TTCCCTCCCT CCCTTCCCCC CTTCTTCCTT CCTTCCTTTC 1800
TCTCCCCCTC CCCACTCCCT CCCTCCCCTC CCCCATCCCC TCCCTCTCCC CTCCCCTCCT 1860
CGTCCCTTTG TCAGGGTCTT GCTCTGTTGC CCAGGCTGGA GTGTAGTGAT GCAGTGAGCT 1920