EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS043-00481 
Organism
Homo sapiens 
Tissue/cell
Fetal_heart 
Coordinate
chr1:16492580-16495290 
TF binding sites/motifs
Number: 21             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr1:16492748-16492766CCTTCCTTCCTTCTTCCT-6.71
EWSR1-FLI1MA0149.1chr1:16492759-16492777TCTTCCTTCCTTCCCACC-6.98
EWSR1-FLI1MA0149.1chr1:16492755-16492773TCCTTCTTCCTTCCTTCC-7.2
EWSR1-FLI1MA0149.1chr1:16492736-16492754CCATCCATCCTTCCTTCC-7.88
EWSR1-FLI1MA0149.1chr1:16492744-16492762CCTTCCTTCCTTCCTTCT-9.09
EWSR1-FLI1MA0149.1chr1:16492740-16492758CCATCCTTCCTTCCTTCC-9.55
PLAG1MA0163.1chr1:16494542-16494556TCCCCTTGGGCCCC-7.12
RFX1MA0509.2chr1:16494467-16494483CGTCGCCATGGAAACC+6.38
RFX1MA0509.2chr1:16494467-16494483CGTCGCCATGGAAACC-6.4
RFX2MA0600.2chr1:16494467-16494483CGTCGCCATGGAAACC+6.6
RFX2MA0600.2chr1:16494467-16494483CGTCGCCATGGAAACC-6.73
RFX5MA0510.2chr1:16494467-16494483CGTCGCCATGGAAACC-6.26
RFX5MA0510.2chr1:16494467-16494483CGTCGCCATGGAAACC+6.27
RREB1MA0073.1chr1:16494145-16494165GGTGGGGGAGTGGGTGGGGG-7.01
ZNF263MA0528.1chr1:16492751-16492772TCCTTCCTTCTTCCTTCCTTC-6.01
ZNF263MA0528.1chr1:16492740-16492761CCATCCTTCCTTCCTTCCTTC-6.04
ZNF263MA0528.1chr1:16494579-16494600TCTCTCCGCCCCTCCTCCCCA-6.12
ZNF263MA0528.1chr1:16494004-16494025GGAGGAGAGGCAGGTGGGAGG+6.37
ZNF263MA0528.1chr1:16492743-16492764TCCTTCCTTCCTTCCTTCTTC-6.48
ZNF263MA0528.1chr1:16492747-16492768TCCTTCCTTCCTTCTTCCTTC-6.76
ZNF263MA0528.1chr1:16494576-16494597CTCTCTCTCCGCCCCTCCTCC-7.1
Number of super-enhancer constituents: 17             
IDCoordinateTissue/cell
SE_23091chr1:16493730-16494938Colon_Crypt_1
SE_23091chr1:16495015-16496277Colon_Crypt_1
SE_23751chr1:16493699-16494633Colon_Crypt_2
SE_24743chr1:16493660-16494922Colon_Crypt_3
SE_26540chr1:16492616-16493248Esophagus
SE_26540chr1:16493665-16496410Esophagus
SE_31527chr1:16493631-16494622Gastric
SE_34268chr1:16493420-16495012HCT-116
SE_34628chr1:16493224-16496455HeLa
SE_47150chr1:16493248-16496088Panc1
SE_56795chr1:16492706-16493355VACO_400
SE_56795chr1:16493661-16494984VACO_400
SE_56795chr1:16495015-16496331VACO_400
SE_57357chr1:16493697-16494611VACO_503
SE_57939chr1:16493722-16494629VACO_9m
SE_65472chr1:16490206-16493455Pancreatic_islets
SE_65472chr1:16493525-16494995Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr11649380016494448
Number: 3             
IDChromosomeStartEnd
GH01I016161chr11648808916492643
GH01I016166chr11649270716493355
GH01I016167chr11649363016496219
Enhancer Sequence
TTCTCTAGAA CCCACCCATC TATCCCCCCA CCCCTTCAGC TGTGTCCTTC ATCTGTCAAT 60
CTGTCCATCC ATCCAGCCAT CCATCCATCC ATCCATCCAT CCATCCATCC ATCCAGCCAT 120
CCATCCATCC ATCCAGCCAT CCATCCATCC ATCCAGCCAT CCATCCTTCC TTCCTTCCTT 180
CTTCCTTCCT TCCCACCTTG GCCCAGCCCC TCTCAGCCCC CTCTGCATCC CATCCATCAC 240
TTCTCAGACA GGCCTCCCCA GCCAGGTAGT CACCTCCTAG CGGCTCCATC TGTCTGTCTG 300
TCTACCAACC CATCCATCCA TCTGTCTGCC AGCCCATCCA TCATGCCACA GGCCACTTGT 360
CCATTCTTGC CACCTTTCAC ATGTTCCCTA GTTAGGCCCC TGTGGTATCC CCCAGCCAGC 420
GCAGTGTAGG TGGGGGGCGT GTGTTCATGT CAGTAGATAT GTCTGTGGCC GCCAGCATGC 480
CTTGTGCTGA GCAGAGGGCA AGGGACCTGG ATGAGGAGCT GGGGAGGGGT TGGGGACAGG 540
AAGACTGGGA ACCTCTTGGT GGGGGGCACA GCAGCTTCCC TGTGTATTCT CCCTGTGGTC 600
TGTTGCACCA TAGGCATCAA TGGCCTGCTC AAAAATAAAT ACACGACTGG AAAACTCTCC 660
CACCTCCATT CTTTTTCCTT TTTGGGGGGG TGGTGGGGAC AGAGTCTTGC TTTGTCCTCC 720
AGGCTGGAGT GCAGTGGCAC GATCTCAGCC CACTGCAACC TCCACCTCCT GAGTTCAAGC 780
AGTTCTCCTG TCTCAGCCTC CCAAGTTGCT GGGATTACAG GCCTGCGCCA CCACGCCTGG 840
CTAATTTTTG TTTTTTGGTT TTGTTTTTTC TTTTCCGGGA TGGAGTCTTG CTCTGTCACC 900
CAGGCTGGAG TGCAATGGCC GGATCTTGGC TCACTACAAC CTCCGCCTCC CGGATTCAAG 960
TGATTCTCCT GCCTCAGCCT CCCAAGTAGC TGGTATTACA GGCACGCGCC ACCACGCCTG 1020
GTTAATTTTT GTATTTTTAG CAGAGATGGG GTTTCACCAT TTTGGCCAGG CTGGTCTCGA 1080
ACTCCTGACC TCAGGTGATC CACCTGCCTC TGCCTCCCAA AATGCTGGGA TTACCGGCAT 1140
GAGCCACTGT GCCCGGCTTC CGTTCTTCCT GATTACTTAA GAGGGGCCTG ACTAATGCCC 1200
AGCATGGTTG GGGACCCAGG CCCCTCAAGC CCTGGAAGTC CCTTGCCTGG GGTCATCCAG 1260
TCTCCTCCCT CAAAGGGCTC TCACTCCCCA CCGCCGCTCC CTCTCCTCTT CCTGCTGCTG 1320
AGAGACGAGA GACCAGCAGA AAGAGACTTG GAGAGACGGA GACACAGAGG CAGATGGAGA 1380
ATGCTGGGCG CCCGGGAAAG CCCAGGAAGG AGCCCGGGCC ACGTGGAGGA GAGGCAGGTG 1440
GGAGGAGGCA GGAGAGAGCA AGGCTGCCCA GGACAATGGA GCGGGACCGG AGGAGACGCG 1500
GGGAGGGACG CGGGCCAGGG GTGCGGTGGG GGGCACGGGG TGGAACTCCG GGTCCCGTAG 1560
GGCGGGGTGG GGGAGTGGGT GGGGGGATGG CCCACCTGCC GTGGGAGCGG GTCCGGAGGA 1620
AGCTAGGGTC TCGGGGTGGG AAGTGCTGTG TAGAAGCGAG CGCAAGAGGC GAGAGGAAGC 1680
GCGGCGGGGC GGCCCCTGTC CCAGCCTCAC CCCCATCCCC CCAAGTCTCG CACCCCGGTC 1740
CGCCCCAGCT TCCGGCTCCG CAGGTGCCGC CTTTGAGGGC CGCCGCTCGC AGTTTACCGC 1800
GGAGCCGGAG CCAGAGCCCC TTCCCCGCGG CGAGGAACTG CCTCTGCGTC TCGTAAAAGG 1860
GGTCTGGGCC TGGGGGGCGG CGGCCTCCGT CGCCATGGAA ACCGGGGCGG GGAGGCGGCG 1920
GCCCGGAGAG CCCCATGCAC TTTGCATACC ATTGCAGGTT CCTCCCCTTG GGCCCCGCCA 1980
GCCTCGCTGG GCCCGCCTCT CTCTCCGCCC CTCCTCCCCA AACCCATCAC CCTTGCCTTT 2040
ATTTGTCTTA AATTTATTTT AAAATGTATT TATTTATTTT TTTCAAACAG GATCTCGCTC 2100
TGTCACCCAG GCCAGAGTGC AGTGGTGCGA TCATGACTCT CTACAGCCTT CCATCTCCCC 2160
AGGCTCAGGT GATCCTCCCA CCCCAGTTTC CCAATAGCTG GGACCACCAC GCCTGGCTAA 2220
TTTTGTGTGT GTGTGTGGTG ATGTCGCCCT CTGTCACCCA GGCTGGAGTG CCGTGGCCAG 2280
ATCTTGGCCC ACTGCAACCT CCGCCTCCCA GGTTCAAGCA ATTCTCCTGC CTTAGCCTCC 2340
TGAGTAGCTG GGATTACAGG CGCGTGCCAT CACACCCGGC TAATTTTTTT GGTATTTTTA 2400
GTAGAGACGG GGTTTCACCA CGTTGACCAG GCTGATCTCA AACTCCTGAC CTCGTGATCT 2460
GCCTGCCTCA GCCTCCCAAA GTGCTGAGAT TACAGGCGTG AGCCACCGTG CCTGGCAATG 2520
CCCGGCAATT TTTGTATTAT AGAGACAGGG TCTTGCCATG TTGCCCAGGC TGGTGTTAAA 2580
CTCCTGGACT CAAACAACCT GCCCACCTCC GCCTCCCAAA GTGTTAGGAT TACAGGCATG 2640
AGCCACTGCA CTCGGCCACC CCTGCCTTTA AAAGTCACCT CCTCCAGGAA GCTTTCAGCC 2700
ACCACCACCA 2710