EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS157-07063 
Organism
Homo sapiens 
Tissue/cell
PANC-1 
Coordinate
chr19:18130490-18133640 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs12984174chr1918132540hg19
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
MITFMA0620.2chr19:18133079-18133097TGTGGTCATGTGACCACA+6.44
MITFMA0620.2chr19:18133079-18133097TGTGGTCATGTGACCACA-6.44
Nr2f6(var.2)MA0728.1chr19:18130678-18130693TGAACTTCTGACCTC-6.38
RARAMA0729.1chr19:18130675-18130693TCTTGAACTTCTGACCTC-6.88
RREB1MA0073.1chr19:18132340-18132360CACCCCCCCACCCCCCACCT+6.22
RREB1MA0073.1chr19:18131314-18131334GGGGTGGGGGTGGGGGTGGG-6.27
RREB1MA0073.1chr19:18131320-18131340GGGGTGGGGGTGGGAGGGGG-7.19
Number of super-enhancer constituents: 21             
IDCoordinateTissue/cell
SE_03528chr19:18130671-18131169Brain_Angular_Gyrus
SE_03528chr19:18131311-18133631Brain_Angular_Gyrus
SE_04156chr19:18130327-18135495Brain_Anterior_Caudate
SE_05027chr19:18129368-18135719Brain_Cingulate_Gyrus
SE_05917chr19:18129420-18135750Brain_Hippocampus_Middle
SE_07191chr19:18123490-18135726Brain_Hippocampus_Middle_150
SE_08048chr19:18129556-18135507Brain_Inferior_Temporal_Lobe
SE_11531chr19:18130225-18136150CD20
SE_17546chr19:18130687-18135928CD4p_CD25-_CD45RAp_Naive
SE_32095chr19:18130664-18133651Gastric
SE_33722chr19:18132360-18135625H2171
SE_41200chr19:18130424-18135677Left_Ventricle
SE_42935chr19:18130491-18135643Lung
SE_48098chr19:18117499-18135641Psoas_Muscle
SE_48877chr19:18130441-18133652Right_Atrium
SE_50498chr19:18130482-18133715Sigmoid_Colon
SE_51440chr19:18125584-18135837Skeletal_Muscle
SE_55387chr19:18131327-18132959Thymus
SE_55387chr19:18132966-18133608Thymus
SE_61722chr19:18124231-18170119Toledo
SE_65475chr19:18130282-18133763Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 5             
ChromosomeStartEnd
chr191813178718132922
chr191813304518133309
chr191813199118132570
chr191813107018131394
chr191813094918131445
Number: 1             
IDChromosomeStartEnd
GH19I018019chr191813058418136229
Enhancer Sequence
ACAGCATTGT CCAAGCTGGA GTGGAAAGCC TCGATCTCGG CTCACTGCAA ACTCTGCCAC 60
CCGAGTTCAA GCAATTCTCA TGCCTTGGCC TCCTGACTAG CTGGGATTAC AGGCACCCAT 120
CACCACGCCC AGCTAATTTT TGTATTTTTA GTAGAGACAG GGTTTCACCA TGTTGCCCAG 180
GCTGGTCTTG AACTTCTGAC CTCAGGTGAT CTGCCCATCT TGGCCTCCCA AAGTGCTGGG 240
ATTACAGGCG TGAGCCACCA TGCCCAGCTC AGATGAAGAT TCTGATGGGG GTGGAGGTGT 300
CATCCCTTGC ACTTGCTCCC AAGACCTCCT AGAGTCAGAC GTGTCCCCCA TGCAGAGTCA 360
AATGCTAGGT CTCTATCTCT CAGTGTCTCT GTCTGTTTCA TTCTGACTCT CACCATCTTT 420
TCTTTCCCAT CTCTGTCTCT CTCTCAATAT CTGTCTTGCT TACTGTCTCT GTCTCTGTCT 480
CTCAGTCTTA TTGCCTCTGT ACTTCTGTCT CTTTCTCCCT GTCTCTGTCT CCCTCTGCCT 540
CTGATTCTCT CACTATCTCT CTTGGCTACC ATCTCTCTGT CTCTTTGGGT CCCTGACTCT 600
CTCACCATCT CTGCCTCCTG CCCTGGCCCG GCCAGCTGGG GGACAAGGGG TGACAAGCAG 660
TCAGGGCGCC CGCTGCTTGT TTTCCCACCC ACGCTGGCAG GGAGCCCAGC CCAGCCGGGC 720
CACTGTTCAG GAATCCTCCA GCCTCCCCGC TCCAGCCACC AGGCGCGGCC ACCGCCAGCC 780
TCTCCTCCCA GCACATTCTG TCCCAAGCAA AGAGCGCCAG AGATGGGGTG GGGGTGGGGG 840
TGGGAGGGGG ACGCATTCCT GCTGAGCTCC AGTTACAGGA CAGCTTGTCC TGGTGGCCCC 900
ACCAGCACAA CCTCCTGATG GCTCCCCATC CTGCTGTGGG GTTAGACCTT CCTGAATGAA 960
GCCAAAGCCC CTCTGCCAGT TCGTGCCCAC CTCAGGGCCT TTGCACCAGC CATACCTTCC 1020
ACCTGGCACT CTGTCTCCCT AGATCTCCCC AAGACCTCCT CCGCCTGCAC ATCTGAGACC 1080
TCACATCACC TTCTCAGCAA GTCCCCTCTG TCCCTAGGCC CGGGCACCCC AAATTCCCCT 1140
CCTGCTGCCC CAGTGCATTT AATTTCCTGG TCCTCCCCAT GTCCCTGGGG TTACATATTC 1200
ACTTGTTTGT TGATGTGGTG TCTATTACAC CAGGTCCCCA CTGTGTCCCA GCACCCTGAA 1260
CACACAGTAG GTGGCTTAGT GAAGGTTTTT ACAATTGACA TCTATTCCTC CCAAAGCTCA 1320
GCCCGCCCAG GCTCATCCAT GTGGATCCAC AGTTCTGACC ACCCCACCTC TGCCTCACCC 1380
TGCCTCCGCC ACCCCTGCAC CCTAATGCAG CAGGATTTCC CAAGCCCCCC TGCCTTGGCC 1440
CAGGGAGTTA TCTCCACCAG ATCCACCTTT CTGAGCGAGG AGCTGGGTGC ATTGAGGGGC 1500
AGGGGCGGCT GGAGTTCAGA TGCACCTTTT GAGCGAGGGG CTGGGCCTCT CTGTCGCTGG 1560
GCTCCAGGCA CAGGGCAGTC ATGATGTACA CACACACGTG CAAACACACA CGCACACACA 1620
TAAGCCTGTC AGCAACATAG AAACACCAGC CAGTGAACTC GGGCACAAGC AGCCGGGCAC 1680
AGAGTGTTCA CCAGGTGCTC ACATGTGGAG TACCCCAACT CCTAGGAGGA TGCGGTTATG 1740
GCCTGGATCC TACAGGTGGG GCCCAGACAT GGGCTTTGAA CCCACGCCAG GGTATGCACA 1800
AACCTATCCA AACACACGCG TGTCTGCCCT AGCTTCCCTC ACCCGGGAGT CACCCCCCCA 1860
CCCCCCACCT TGTTTTTGAT GTTCAGGAAA GTCCCCAGAA AGCACTGGGC CCGGGCAAGG 1920
GGCCAGGAGG AAATGGTGAC TCAGCCGGTG GCCATCAGTG CCTGCCACGC TGGGCTGGGT 1980
GGACTGCGCG GCCCGATCTG GGAGGATCCA CAGAAAACAA CAATAAAAGA TGAGGGCGTG 2040
GGTGCGGGGT AAAAAGGACT CAGCCCAAGA ATGATCAGAG AGGGGATGGA TCCCCCTGTG 2100
CTCCAACACT TCAACCCTGC TGGGCCTGAT TGACAAGTGG GGAAACTGAG ACACAGGGAA 2160
CAAGTGACTT CGCCAAGGCC CACCAGCCAA GATGGTACAG GCAAGGGGAT CCCTAAGTCC 2220
TTAACACAGG GGTCTGGAGG AATGTCTACC TGCCCTGCCC TTTTTTTTTT TTTTTTTTTT 2280
GGAGACAGGG TCTCACTCTG TCCGTCAGGC TGGAATGCAG TGGCATGATC TCAGCTGACT 2340
GCAATCTCCG CCTCCTGCCT CAGCCTCCCA AGTAGCTGGG ATTACCGGCG CCTGTCCCTA 2400
TGCCCAGGTA ATTTTTGTAT TTTTAGTAGA GATGGGGTTT CACCATGTTG GCCAGGCTGG 2460
TCTCAAACTC CTGACCTCAG GTGATCTGCC CACCTCGGCC TGCCAAAGTG CTGGGATTAC 2520
AGGCGTGAGC CACAGTGCCC GGCTCCCTGC CCCACTTTCT GAGACCCAGA TCCACTTCCT 2580
GGTTTCCTGT GTGGTCATGT GACCACACTT GGCCAATTGG AGCCTTTTGT TATCACAGGC 2640
ACAGGGATTG GGTCAGGGCT GGGCACGTGA TCCTGCCTGA GCCAATCATG CTACGAGTTT 2700
GGAGACTCCC TGGAAGAAGG CCTAGAAGTA AGGAAAACCA TCTTGGACGC ATGATGATGG 2760
CAGTGGATCA GAGTCCCAAG GACACTGGTG AAGATCAGAG CAGGACTCAC ACAACCTCAG 2820
ATCCCTGTGG AGTCAGGGTG GAACCAGAGG GAAGGCTGAA GGCTGGAGGG TCCTGAGAGG 2880
CCTTGCAGAA AGAGAGGACA TTGGAGCTGG GGCTTTGATG GATGAAGAGG AACTAGGGAA 2940
AGGCATTTCA AGCAGAGGGA ACAGCCTGTG CAACCACAGC AGGCAGGTGG GAGCTAGGCG 3000
TGTCCTCAGC CACCCCAGTG GCCCCATGGG GCTGGAGCAT AGAGAGGCAT CTGCAAATGT 3060
GTTTATTTGT TTATTGAGAC GGAGTTTTGC TCTTGTTGCC CAGGCTGGAG TGCAGTGGCG 3120
CAATCTTGGC TCACTGCAAC CTCCGCCTCC 3150