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

TagContent
EnhancerAtlas ID
HS159-02942 
Organism
Homo sapiens 
Tissue/cell
Pancreatic_islet 
Coordinate
chr19:2506580-2508710 
Target genes
Number: 4             
NameEnsembl ID
TF binding sites/motifs
Number: 19             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
MEF2AMA0052.3chr19:2508201-2508213TCTATTTTTAGT-6.27
MEF2BMA0660.1chr19:2508201-2508213TCTATTTTTAGT-6.32
Nr2f6(var.2)MA0728.1chr19:2506835-2506850TGAACTCCTGACCTC-6.22
Nr5a2MA0505.1chr19:2506827-2506842GCTGGCCTTGAACTC-8.25
RARAMA0729.1chr19:2506832-2506850CCTTGAACTCCTGACCTC-6.73
RREB1MA0073.1chr19:2508016-2508036GTGGTGTGTGTGTTTTGTGT-6.04
RREB1MA0073.1chr19:2508007-2508027TGTGTGTGTGTGGTGTGTGT-6.16
ZNF263MA0528.1chr19:2507593-2507614CCCTCCCTCCCTCCCTCTCTC-6.11
ZNF263MA0528.1chr19:2507513-2507534TTCCCTCCCCTCCCCTCCCCA-6.23
ZNF263MA0528.1chr19:2507545-2507566CTCTTTCTCTCTCCCTCCCTC-6.23
ZNF263MA0528.1chr19:2507581-2507602TTTCTCTCTCTCCCCTCCCTC-6.23
ZNF263MA0528.1chr19:2507523-2507544TCCCCTCCCCACCCCTCCCCT-6.56
ZNF263MA0528.1chr19:2507626-2507647TTTCTCTCTCTCCCCTCCCCC-6.65
ZNF263MA0528.1chr19:2507634-2507655TCTCCCCTCCCCCCCTTCTCT-6.69
ZNF263MA0528.1chr19:2507549-2507570TTCTCTCTCCCTCCCTCCCTC-6.99
ZNF263MA0528.1chr19:2507589-2507610TCTCCCCTCCCTCCCTCCCTC-7.53
ZNF263MA0528.1chr19:2507585-2507606TCTCTCTCCCCTCCCTCCCTC-7.54
ZfxMA0146.2chr19:2506860-2506874CCCGCCTCGGCCTC+6.01
ZfxMA0146.2chr19:2507899-2507913CCCGCCTCGGCCTC+6.01
Number of super-enhancer constituents: 8             
IDCoordinateTissue/cell
SE_24383chr19:2507083-2507568Colon_Crypt_2
SE_25170chr19:2506877-2507592Colon_Crypt_3
SE_27369chr19:2506975-2507651Esophagus
SE_31940chr19:2506925-2507690Gastric
SE_41828chr19:2506999-2507555LNCaP
SE_48020chr19:2506970-2507608Pancreas
SE_54295chr19:2506798-2507812Spleen
SE_65706chr19:2506996-2508346Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1925072062507458
Number: 1             
IDChromosomeStartEnd
GH19I002506chr1925065112507797
Enhancer Sequence
AGAAATAATC TAAATGTCCA TCAATAGTAT ATAATTTTTT TTTTTTTGAG ATGGAGTCTC 60
GCTCTGTTGC CCAGGCTGGA GTGCAGTGGC ACAATCTTGG CTCACTGCAA CCTCTGCCCC 120
CCAGGTTCAT TGCCTGCCTC ATCTTCCTGA GTAGCTGGGA TCACAGGTGC CTGCCACCAT 180
GCCTGGCTAA TTTTTATTTT TTATTTTGGT ATTTTTAGTA GAGACGGGGT TTCACCATGT 240
TGACCAGGCT GGCCTTGAAC TCCTGACCTC AGGTGATCCT CCCGCCTCGG CCTCTCAAAG 300
TGCTGGGATT TCAGGTGTGA GCCACCGCGT CCGGCTAAGC ATGTAAATTA AATTACTCTG 360
GAGTTGTTAA AATGCACTGA TTTTTAAAAA ATTATTATTT TTATATCTTT TTTGTTTTCC 420
TTCATAAAAA TGCAATGACT TAGCAAGCTG TCGGTCATAG GAAGTTAAGC GAAAAAAAAA 480
AAAAGCTAAG CCAGCCTCAG AGCAGTCTGT GTTGAGTGAG TCCAGTTTTA AAAACAAATG 540
GCAAGTGTTG GTATGAAATA GTGCCGATCT CCATTACAGA AGACGGTCTT GGGCACATGT 600
GCGGGAGCCC TACGGTCTGG CTGAAAATGC TGCCCAGTTC TGGCCGTACC ACTTTCTAGC 660
TGTGGACTCA AGGGAGTTGT TTACCTTCTG TCAGTCCATG TTTATTCATC TGCACAATCA 720
ATGCGTAGAA CCATAGCCCT TACCTCACAG CGTTTCCGGG AGGATCAGAT GACACAATCC 780
GAGGAAATGA ACCATTATTG CTACTTACTG TCACTGCTTT CTTCTGAGGC CAACGTTTGG 840
GCACGCCTAG AAGTTTGAAG GATTTGCCTC AGCTGTGAAC AAATGGTGGC TACAGGTGCT 900
GAGAATGGGT CTGAAGAAGG GCGTGGAGGG ATCTTCCCTC CCCTCCCCTC CCCACCCCTC 960
CCCTTCTCTT TCTCTCTCCC TCCCTCCCTC TCTTCTTTTT CTTTCTCTCT CTCCCCTCCC 1020
TCCCTCCCTC TCTCTCTCTT TCTTTTTTTC TCTCTCTCCC CTCCCCCCCT TCTCTCTTTT 1080
CTTTCTTTCT CTTTTTTGAC AGAGTCTCAC TTTGTCGCCC AGTCTGGAGT GCAGTGGTGT 1140
GATCTCAGCT CACTGCAACC TCTGCCTCCC AGATTCACGC CATTCTCCTG CCTCAGCCTC 1200
CTGAGTAGCT GGGATTACAG GCGTGCGCCA CCACGCCCGG CTAATTTTTG TATATTTAGT 1260
GGAGACGGCG TTTCACCGTG TTAGCCAGGA TGGTCTCCAT CTCCTGACCT CGTGATCCGC 1320
CCGCCTCGGC CTCCCAAAGT GCTGGGATTA CAGGCATGAG CCACCGTGCC CGGCCGCATG 1380
TGGGTTTTTC AATGGCTATT ATTTAAGCAT CTTCCATGTC CTTTGTGTGT GTGTGTGTGG 1440
TGTGTGTGTT TTGTGTTTTT TTTGTTTTTG ACAAGAGTCT CGCTCTGTTG CCCAGGCTGG 1500
AGTGCAGTGG CGTGATCTCA GCTCACTACA ACCTCCACCT CCCAGGTTCA AACGATTCTC 1560
CTGCCTCAGC CTCCTGGGTA GGTGGGACTA CAGGTGCATG CCACCACACC CAGCTAATGT 1620
TTCTATTTTT AGTGGAAACG GGGTTTCACC ATGTTGGCCA GGCTGGTCTC GAACTTCTGA 1680
CCTCAGGTGA TCCGCCCACC TCAGTCTTCC AAAGTGCTGG GATTACAGGC ATGAGCCACA 1740
GTGCCCAGCC AAGGATGACT TTTGAATGCT GTATGATTTT ATGTAACTTC TTCTTCTTCT 1800
TCTTTTTTTT TGAGACGGAG TTTCACTCTT GTTGCCCAGG CTGGAGTGTA ATGGCACGAC 1860
CTCAGCTCAC TGCAACCTCC GCCTCCCAGG TTCAAGTGAT TCTCCTGCCT CAGCCTCCCG 1920
AGTAGCTGGG ATTACAAGCA TGGGCCACCA CACCCGGCTA ATTTTTTTGT ATTTTTAGTA 1980
GAAACGGGGT TTCTCCATGT TGGTCAGGCT ACTCTTGAAC TCCCGACCTG AGGTGATCTG 2040
CCAGCCTCGG CCTCCCAAAG CATTGGGATT ACAGGCGTGA GCCACTGTGC CCGGCCTATT 2100
TTATGTAACT TCTATAGTTA TTATATTTTG 2130