EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS139-39584 
Organism
Homo sapiens 
Tissue/cell
Myotube 
Coordinate
chr3:186130920-186133500 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs9853115chr3186131600hg19
TF binding sites/motifs
Number: 28             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr3:186133087-186133105TCTTCCTTCCTTCCTTCC-10.05
EWSR1-FLI1MA0149.1chr3:186133091-186133109CCTTCCTTCCTTCCTTCC-10.83
EWSR1-FLI1MA0149.1chr3:186133095-186133113CCTTCCTTCCTTCCTTCC-10.83
EWSR1-FLI1MA0149.1chr3:186133099-186133117CCTTCCTTCCTTCCTTCC-10.83
EWSR1-FLI1MA0149.1chr3:186133103-186133121CCTTCCTTCCTTCCTTCC-10.83
EWSR1-FLI1MA0149.1chr3:186133107-186133125CCTTCCTTCCTTCCTTCC-10.83
EWSR1-FLI1MA0149.1chr3:186133111-186133129CCTTCCTTCCTTCCTTCC-10.83
EWSR1-FLI1MA0149.1chr3:186133115-186133133CCTTCCTTCCTTCCTTCC-10.83
EWSR1-FLI1MA0149.1chr3:186133119-186133137CCTTCCTTCCTTCCTTCC-10.83
EWSR1-FLI1MA0149.1chr3:186133127-186133145CCTTCCTTCCCTTGTTTC-6.18
EWSR1-FLI1MA0149.1chr3:186133123-186133141CCTTCCTTCCTTCCCTTG-6.84
EWSR1-FLI1MA0149.1chr3:186133079-186133097CTTTTCTTTCTTCCTTCC-6.98
EWSR1-FLI1MA0149.1chr3:186133083-186133101TCTTTCTTCCTTCCTTCC-8.26
JUN(var.2)MA0489.1chr3:186132576-186132590AAAAGGTGAGTCAT+6.45
MAXMA0058.3chr3:186130978-186130988ACCACGTGCT+6.02
MEF2AMA0052.3chr3:186131764-186131776GCTATTTTTAGT-6.18
MEF2BMA0660.1chr3:186131764-186131776GCTATTTTTAGT-6.62
MEF2CMA0497.1chr3:186131763-186131778GGCTATTTTTAGTTC-6.41
NFYAMA0060.3chr3:186132412-186132423TCTGATTGGCT-6.32
ZNF263MA0528.1chr3:186133083-186133104TCTTTCTTCCTTCCTTCCTTC-6.36
ZNF263MA0528.1chr3:186133091-186133112CCTTCCTTCCTTCCTTCCTTC-6.94
ZNF263MA0528.1chr3:186133095-186133116CCTTCCTTCCTTCCTTCCTTC-6.94
ZNF263MA0528.1chr3:186133099-186133120CCTTCCTTCCTTCCTTCCTTC-6.94
ZNF263MA0528.1chr3:186133103-186133124CCTTCCTTCCTTCCTTCCTTC-6.94
ZNF263MA0528.1chr3:186133107-186133128CCTTCCTTCCTTCCTTCCTTC-6.94
ZNF263MA0528.1chr3:186133111-186133132CCTTCCTTCCTTCCTTCCTTC-6.94
ZNF263MA0528.1chr3:186133115-186133136CCTTCCTTCCTTCCTTCCTTC-6.94
ZNF263MA0528.1chr3:186133087-186133108TCTTCCTTCCTTCCTTCCTTC-7.03
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr3186131140186131200
chr3186131407186132227
Number: 1             
IDChromosomeStartEnd
GH03I186413chr3186131314186133044
Enhancer Sequence
GGGTCACCTG CAAGCGGCAT AAGGCAGGCT GTGAACCCAG GTCTGCCTGA TTCCAAAAAC 60
CACGTGCTCT TAACCACTGT ACTCCATTAC CATGTGTGGA GTGCCTACTG GGTGCCAAAA 120
TATAGCATAA GACAGAAGCA GCCAAGGCCA TTCCCGGGGA CCCCAGACCC CAAGGGAAAT 180
GCCTTCCTTC CCCCCAGCCC CTGGAGATGT CCTTGGCTGC CTCCTTCTCA CTGTGCTCTT 240
GACCTTGGCT ACTCTTGGGC AGTACCCAAA AGACCCAGGG AACACACTTC CCCTATTCCA 300
TGTCTCTCAG GACAAATGAG GAATTACAAA TAAACCGTAT TAATTCATCT GTGAACTCCA 360
AGCCTCTGGC ACAGTACCCG GCAATATTTT ACATGGTATA TAGCACCTAA CAGGCTATAT 420
TCAAAAAATA TCAGAAGATA GACGGGAGGA GACGGTCACC ATGCCAGGCA GGGAATGTTT 480
CCAGGGAGAA CTGTAGCTGC AGGGAGTGGG ACTTATCCTG ACTGCCCTGG GAGATCGCTA 540
ATTTAGAGCA CACCAGTGTG ACAGTACATT TCTTTTGAAA TGCAACTCAA AATCCGCTTC 600
CTCCAGGAGG AATGCCAAGT GGCGTCCCGG AACAGGACAA GTTGTACTTC ACAGGAGATG 660
GGAAGCTAGA GGGGGGAAAT GCCATCATTA ATCCACCAAG CAGCAGGGGG TGGGGGCGCT 720
TGCCTCCAAC AGGCATGGCT GGAAAAATAA GCAGCTCTGG CTTGTGCTCC TCCCTGTGTC 780
CCTGCCACGA CTGTGAAGGG CTAAGAACAC AGCAGAAAAG GTTCCAGTTC ATTTACAAGC 840
CTCGGCTATT TTTAGTTCAT CGATCCCTGG GCGCGGTGTG TGTGTGTTGA GGGGGGCCGG 900
GGGACGGGGC TTGCAGAGCT CACGGTTTGA GGTGGAAGCT GGGGAAAGCT TTAGAATTCT 960
TTTCATAGAA CAGGTACTCT GTTCACTACG CACCATCCAG CCTCTGGAGA CCTAACCGCT 1020
TTTCTTGGGG CAGGAAGAAG GAGCAGTGTC AGGGGAGGGA GGAGACTGAA ATGAGAAAGG 1080
GAACGAGGCA AGAGGCGGTG ACGCCCTTGT GCCAATGACC AAATTGGGTC AGAAAGAACA 1140
ACCTTTTGAA TGCAAGTCAG GAAATGTGAA TCGCTGCCTC AGCAGGGCCA GGTGCATGCC 1200
TAGTGGGTGC CGGCCCAGCC TGACCAGGGA ACTGTGACTG TACCTCCTGC CGCTCTAGAG 1260
AACCAGACCG ATGACCATCT AGAAGTGCAC TGATCTTTAT TCCTTGCCTG GTGCCCTGTG 1320
GCCAGTTCAA TTCCTATTAT CAACCCCTCC TTAAAGCTGT CAGGGAAAAG GAAGGAGAAG 1380
TTCACATTTA AAGATGGATC TAAATGGTGA AAGAGGTGAA AATCATTGCC TTAAAAGAGA 1440
TCACCTGTGG ATTTTGTGAG TTATTAATTC TATGATCCCT ACCGTGTCTG ATTCTGATTG 1500
GCTATATATA AATTAAAAAA CGGCTCTTTT TTCATATCAC CTCTACAGCC CCTGCAAGTT 1560
AAAAATATCA TTACCCGGCT TTTCTCCTTC TAAGTGTAGG CTGCTTGATT TAAGACATTT 1620
TGCAAACTTG TCTTTGTTCC AAGGATTTTT AAGCAAAAAA GGTGAGTCAT AGTAGCAACT 1680
CAATAGATGT TGAGCTGATT TGTGTTACTA AGAAGTTGTG GGTAAATTGC AGTTTTGAAT 1740
TTTTGGAAAC GGAATCATAT TGTAAATGTC CTGGACAGTT CAACAGTTGT GGGACTCCTC 1800
TGGCGAGTCC TATGCAGAAA CCTCCTCTTA CTTGAGTCAC TCAGCAGCAT TCGATGCAAT 1860
CACCCATGGC TTCCTTCTTG AAACGGGTGT GATTCCTTGA CCCTCACACT CACTTGGCTT 1920
GTCCCCAGGT TGCTGACTGT TCCTTCTCAG GCTCCTCTGC TGTCCTCCCT GCCTCTACCA 1980
CACCTCAGTG TACTGGAAGG ACCTGCATTC TACCTTTGTT CCTCCTGGCT TCATTTCCTC 2040
CTTCCTAGAG AAAACTGGAG GATGCCCATC CTGGCACTCT GATGACTCTC AAATTTCTGC 2100
CTGCCTTTTC TTTTCTTTTC TTTTCTTTTC TTTTCTTTTC TTTTCTTTTC TTTTCTTTTC 2160
TTTTCTTTCT TCCTTCCTTC CTTCCTTCCT TCCTTCCTTC CTTCCTTCCT TCCTTCCCTT 2220
GTTTCTTTCT TTCTCTCTCT CCTTTTTTTT TGTCTTGCTC TATCACTCAG GCTGGAGTGC 2280
AGTGTCATGA TCTCAACTCA CTGCAGCCTC TGCCTCCCGG GTTCAAGCAA TTCTAGTGCC 2340
TCAGCCTCCT GAGTAGCTGG GATTACAGGC GCCAGCCACC ACTCCTGGAT AATTGTTTTG 2400
TATTTTTAGT AGAGATGGGG TTTCACTATG TTGGCCAGCC TTGTCTTAAA CCTCTGACCT 2460
CAGGTGATCT GCCCACCTCG GCCTCCCAAA GTGCTGGGAT TAGAGGCTTG AGCCACCGCA 2520
CCTGGTCGAC TGCCAAATTT CTATCTCTAG CTGGATCTCT CGCTGAGTTC TAGATGTGCA 2580