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

TagContent
EnhancerAtlas ID
HS157-06828 
Organism
Homo sapiens 
Tissue/cell
PANC-1 
Coordinate
chr19:2492330-2496730 
TF binding sites/motifs
Number: 19             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
IRF1MA0050.2chr19:2493320-2493341CTTTATTTTTATTTTCATTTT+6.21
KLF5MA0599.1chr19:2494845-2494855GCCCCGCCCC+6.02
MEF2AMA0052.3chr19:2495843-2495855GCTATTTTTAGC-6.44
MEF2BMA0660.1chr19:2495843-2495855GCTATTTTTAGC-6.92
MEF2CMA0497.1chr19:2495842-2495857GGCTATTTTTAGCCG-6.18
NR2C2MA0504.1chr19:2496163-2496178TGACCTTTCACCTCC-6.86
Nr2f6MA0677.1chr19:2496163-2496177TGACCTTTCACCTC-6.6
PLAG1MA0163.1chr19:2493058-2493072GAGGCCCTGGGGGG+6.18
RREB1MA0073.1chr19:2493293-2493313TGTGTGTTTGTGTGTTGGGT-6.19
RxraMA0512.2chr19:2496163-2496177TGACCTTTCACCTC-6.8
Sox3MA0514.1chr19:2496367-2496377CCTTTGTTTT+6.02
ZNF263MA0528.1chr19:2495893-2495914CTCTCCTCCTCCTCCTCCTCC-10.75
ZNF263MA0528.1chr19:2495896-2495917TCCTCCTCCTCCTCCTCCTCC-12.34
ZNF263MA0528.1chr19:2495887-2495908CCCTGCCTCTCCTCCTCCTCC-6.26
ZNF263MA0528.1chr19:2495703-2495724GAGGGAGGGCAGGGTGGGGGG+6.31
ZNF263MA0528.1chr19:2493040-2493061GGAGGAGGAGATGGGAGTGAG+6.35
ZNF263MA0528.1chr19:2495884-2495905CCGCCCTGCCTCTCCTCCTCC-6.52
ZNF263MA0528.1chr19:2495890-2495911TGCCTCTCCTCCTCCTCCTCC-8.02
ZfxMA0146.2chr19:2495638-2495652CCCGCCTGGGCCTG+6.37
Number of super-enhancer constituents: 12             
IDCoordinateTissue/cell
SE_24383chr19:2494354-2496521Colon_Crypt_2
SE_25170chr19:2493927-2496709Colon_Crypt_3
SE_27369chr19:2493818-2496400Esophagus
SE_31940chr19:2493882-2496463Gastric
SE_37152chr19:2490278-2499382HSMMtube
SE_41828chr19:2494229-2496540LNCaP
SE_43297chr19:2493861-2496458Lung
SE_44558chr19:2493529-2496658NHDF-Ad
SE_48020chr19:2494513-2496167Pancreas
SE_50943chr19:2493885-2496560Sigmoid_Colon
SE_54295chr19:2494465-2496352Spleen
SE_65706chr19:2493855-2496674Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr1924947052495117
chr1924957802495940
Number: 1             
IDChromosomeStartEnd
GH19I002490chr1924906592497696
Enhancer Sequence
TGCAATGGTG TGATCTCGGC TCACCGCAAA CTCCGCCTCC GGCTTCAAGT GATTCTCCCA 60
CCTCAGCCTC CCGAGTAGCT GGGATTACAG GTGCATGCCA CCACATCTGG CTAATTTTTG 120
TATTTTTAGT AGAGACAGGG TTTCACCTTG TTGGTCAGGC TGGTCTTGAA CCCCTGACCT 180
CAAGTGATCT GCCCACCTTG GCCTCCTAAA GTGCTGGGAT AACAGACGTC AGCCACCGTG 240
CCCGGCCAGG ATTTTGGACA CACAAATATC CCCTCTCTTC CCCTGCAAGC CTACCTGTGC 300
TACCCACCCC AGCCATCCCC TCCTGAGGTG TCTGTCCTTC CATGCCTGAA GGGGTTCATG 360
GGAGTGTGGG GAGTCCTACA CCCCACCTGT GATTTTCCAT CATTTGAGTT CTCCTATGGC 420
TCAGACCATT GCCTGCAGGA AGCTCCAGAA ACAGCCAGGG TTGGTGGGAT TAGAACTGCA 480
CAGGTGGGGA GGTGATGCCC ATATACCCTA AGAAACTATC CTTCCATTTC ACAGCCGGAG 540
AAACCGAGGC CCAGAGACAG GAAGGTCTTC TTGTTGAGCT AAGAAGAGAA ATAGAGGGAT 600
GATAAACGGA TGCCCTGACT GGGCCCCCTC AACCATCTCC TCTTGCAGCC AGAAACAGTA 660
GGTTCCTACC GCCAACAAGG GTGGGGACAG GAAGGTGGGG GACCAGGGTG GGAGGAGGAG 720
ATGGGAGTGA GGCCCTGGGG GGAGGTGGAG CCTATGTCCT GGAGACAGAC ACAGAGGTGG 780
GCGGTCCGGA GACACCCACC TCCTCAGACA GGCACGGGCT CTGGCAGCTG GTGACAGAGA 840
CACAATCTGG GGCACATAGG CACTGTCTGT CCCTCCTGCC GCCGATCTTC CTCCCCAGCC 900
TCTGATGGGG ATTCTAGGGG CTGCTGGGGC CCCTGCAATT GTTTTGGCAT GAGTGTGCAT 960
ACCTGTGTGT TTGTGTGTTG GGTGCACATG CTTTATTTTT ATTTTCATTT TATTTATTCC 1020
ATTTCATTTC ATTTATTTCA TTTCATTTCA TTTTTTGAGA CTGAGTCGTG TTCTGTCACC 1080
CAGGCTGGAG TGCAGTGGCA CTATCTCAAC TCATTGCAAC CTCCGCCTCC CAGGTTCAAG 1140
CGATTCTCCT GCTTCAGCCT CCGGAGTAGC TGGGACTACA GGTGCCCACC ACCATGGCCG 1200
GCTAATTTTT TGTATTTTTA GTAGAGATGA GGTTTCACCA CGCTGATCAG GCTGGTCTCA 1260
AACACCTGAC CTCAAGTGAT CCGCCCACCT GGGCCTCCCA AAGTGCTGGG ATTACAGGCA 1320
TAAACCACCG CGCCCGGCCT CACTGAGCAT GTTTTGAAGG CGAGTGCGTT CCTCTTGACT 1380
GCTGAACTTT CATTCTATGA ACCGACCTCC GTTGACCTGT TCCCCTCTGA ATGGAGGGGT 1440
ATTTGAGCTC TTCCCAGGTT TTGGTGATGA GGAACAAAGC TGCTACGTGC ATTTACCTCC 1500
TGGTCTCTGT GTGCTCCTAA GTTGTGTATT TCTTTCAGAT AGTACCAAGA GAAGTGAGGT 1560
TGCTGGGTCC CCGTAACCTT ATAGGGTAAA TACTATTATT ACATCCACTT TGTTGATCGG 1620
GAGAATAGAC GCCGCCAGGC CTCCTGTCTC TCGCTTTCAC ACAAAGGCAC ATACGGCAGA 1680
CACGGACCCC CATCACTCAT CCATCACTTT CCCATCACTC ACCGCAGACC CTCCAGGACC 1740
CACGCAGAAA CCCAGGGCTC CCCCACGGTG CACGCAGCAC CCAGGCTGCC CGCCCTCCAC 1800
CCAGGGCCGC GTCACGCCCG ACACCCCCGG AACAGACGCC TATGAGGCCT GCAGCTCCAG 1860
ACGGGCTGCA GACACACAGC GATTTGTTCA TCTTTCCAGC CACCCCGTCT GGTCCTGACA 1920
GTAATTAGCT CCCAGACTGG TGGGGAGACG GTGAACAGCC TGAGAGTCAT CGCCCACGGC 1980
TCCACGCCCA CAGGCCACGG GCACCGGGAG AGAGGGTGAA TGAGTGTGTG TGTGTGTGTG 2040
AGTGTGTGTG TCCGGAATCT GTACTCTCCA GCCAGGGCTC CCCATCCTCC TGCAAAGGGC 2100
CAGCACCGTG CACGGGTACC CACGGCGCCT TCCAAGGGGA ACGTGCACAG GCATACCCAC 2160
TGTTCATTCC ACGAAGGATC GTGCACACGC ATGCCTACCT TTGCATTTCA CGCGGGATTG 2220
TGCACACGCA TGTCCACCGT GCCTTCCACG CGGGATCGTG CACACGCATG TCCACGAACT 2280
CCTGCACACC TACACCCACC AGGCCTGCCC ATGCGATGCG TCCCTGCAGA CCCACTGTGG 2340
ACGCCTGCTT GTCGGCGTCC TGCGCATCCC GCGTGAGTGG AGTGTGCACT CGTGGAGGGG 2400
GCGACTGAGT GCGGGGCAAG CGCAAGCGCA AGCACACTGG GCTCGCGGAG GGTGGAGAGA 2460
GGCCGTGCGC GTTCCCGGGG CTGGCGCGGA GGTGGGGTCA GCGGCGCGGG AGAACGCCCC 2520
GCCCCGCTAC CGCCAGCCCG GAAGACCCAC GGCGGCGGGC GCTGGCGTCA CGGGTTTCCA 2580
CTGGGGCCCC GGCGCCGGGG CCGGGATTCC CTGGCGCAGG AACGCCCGTG ACGGCGGCGC 2640
CTGCCTGCGT CGGCCACGCT GGGAGGTTTG AGCCTGGGGA TGACATCAGC CCCTGCGTTT 2700
CTGGAGCTGG CCCGGGCGGG ACGGGGACTT GGAGAAAGCA GTGACACCCA CTTTCGTTGA 2760
CTGCCAACCC GTGCAGAGCG CTTAGTGCGT GTCCGACCGT GAGCTGAGCG CTGTGATGCG 2820
GGTGCTGTTA ATGTCCCATT GCACAGATGG GGAAACTGAG GCCGGCGCAC TGCCCGCCCC 2880
GCCGGGCCCC CAGAGTGAGG GCCCGGGGCT GGGAGCAGCC TTTTCCCAGC GCCCTCTGCA 2940
GTGTAGAGTC CCACCAGCTT GTCTCCCGCT CTCTCCTGCA CAAGCCGGCT CAGAGAGGGT 3000
CTGCGGGTGT CCTGGCACCA CCCAGCAAGT TGGGTGCTGC AGCCAGCTCT GTCCATACAG 3060
TTGGTCTCTG CCCAGCTGCG GTGGCCAGGG GCGGTGCCTG AGCCAGGGCG CCCGGGCGGC 3120
CCGGTGGGGT GTGCCCAGCC GCTGCCTTCC TGCTGACGCC GGTGCCAAGG GATCTAAATA 3180
TAGCCTGGGA GGAGGCAAGG GCTATTTTTA ACGCGAGTGG CTTGGCCCCT CCCAGTTCCC 3240
GGGTCAGGAG CCCTTTGGTC CAGGATTTTG GGGAGGGGCA GGGGCGAGGG GGAGCCAGGG 3300
GCCCCACACC CGCCTGGGCC TGCCCCTCTG CCCACACCTG GCCCTGGAAG ACTCTAGGGG 3360
ACGAAGGGCC GTAGAGGGAG GGCAGGGTGG GGGGGCTGTC GCAGGTCACC TTTCTTAAAC 3420
GCCACCTCCT CTCTAGCTGC CGACCAGCCC TGGCCTTTTG TTGGGCCCAG AGACTGCTTT 3480
CTATTTTGGG AAGGTGTTGG AATAATTTCC TTGGCTATTT TTAGCCGGTT CGGGGATTCC 3540
TCCACTCAGG CTGGCCGCCC TGCCTCTCCT CCTCCTCCTC CTCCTCCTAG TCGTCTTCCT 3600
CCTCCCGGCA GACCCAAGGG CGGCCTCCTT CATGGAGGGC AGTCAGGGAC ACACAGTCCC 3660
TGAGCCAGAC CCAGAATGGG GAGACCCCTA TATTTCCTGG GTCGGGGAGG GAAGGGAGCT 3720
CTGAAGGGCG TTCCCACGTT CCAGGTGAGC AGGACTTTCA GACCTCTGGG AATCCATGAC 3780
GCCAGGTATC TGAATTCTGT CTCCAGGGCA GGGTGGGGCG ACCCAGCAGC CTCTGACCTT 3840
TCACCTCCTT TCAGGGTTGT CACAGGAAAG TGGCCTGCTG AGAACAGACC TTGACTCCCA 3900
CATCCCTAGG CTAGGGGCTC CCATGTTCCC AAGAGGAAGA TCAGTGTGAT GAGGGTAAAC 3960
TGAGGCACAG AGGGGACACT GGGATGGGAC ACATCTTGGG CTCATTCCCT GATGGTTTCA 4020
TTTCCTTCCA CATTCTACCT TTGTTTTTAA TTTTTTTTTT TGATTGTTTT GAGACAAGAC 4080
GGAGTCTCAC TCTGTCACCC AGGCTGGAAG AGTATGCAGT GGCACAATCT CGGCTCTCTG 4140
CAACCTCTGT CCTCTGGGTT CAAGCGATTC TCCAGCTTCA GCCCCCTGAG TAGCTGGGAT 4200
TACAGGTGCA CGCCACCATG CCCAGCTAAG TTTTGTATTT TTAGTAGAGA CGGGGTTTCA 4260
CCATGTTGGC CAGGCTGGTC TCGAACTCCT GACCGCAGGT GATCCACCTG CCTCTCCTCC 4320
CAGAGTGATA GGATTACATG CGTGAGCCAC TGTGCCTGGC AGCAGCGCCG TCATAGCTTA 4380
TGGCAGCCTT GACTTCCTGG 4400