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

TagContent
EnhancerAtlas ID
HS091-19062 
Organism
Homo sapiens 
Tissue/cell
HepG2 
Coordinate
chr17:16930420-16934750 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs11867934chr1716933404hg19
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Klf1MA0493.1chr17:16931496-16931507TGGGTGTGGCC-6.62
TBPMA0108.2chr17:16932545-16932560TCGGCCCTTTTATAG-6.24
ZNF263MA0528.1chr17:16932977-16932998AGAGGAGGAAGGAGGTAGAGG+6.41
ZNF263MA0528.1chr17:16932980-16933001GGAGGAAGGAGGTAGAGGGGG+6.4
Number of super-enhancer constituents: 29             
IDCoordinateTissue/cell
SE_05858chr17:16933788-16936262Brain_Hippocampus_Middle
SE_23636chr17:16930483-16933437Colon_Crypt_1
SE_24609chr17:16930592-16932594Colon_Crypt_2
SE_24609chr17:16932600-16933161Colon_Crypt_2
SE_26997chr17:16930360-16933050Esophagus
SE_27670chr17:16930495-16933448Fetal_Intestine
SE_28856chr17:16930404-16933447Fetal_Intestine_Large
SE_30353chr17:16930832-16932794Fetal_Muscle
SE_31426chr17:16930288-16933209Gastric
SE_34197chr17:16930666-16931595HCC1954
SE_34197chr17:16931634-16932103HCC1954
SE_34341chr17:16930398-16932866HCT-116
SE_34341chr17:16934057-16934838HCT-116
SE_34638chr17:16930171-16936299HeLa
SE_35971chr17:16930221-16933329HMEC
SE_35971chr17:16933788-16936282HMEC
SE_37027chr17:16930096-16938231HSMMtube
SE_42192chr17:16930502-16933069Lung
SE_47491chr17:16931621-16932114Pancreas
SE_52055chr17:16930615-16931613Skeletal_Muscle_Myoblast
SE_52055chr17:16931627-16932957Skeletal_Muscle_Myoblast
SE_52055chr17:16934171-16936222Skeletal_Muscle_Myoblast
SE_55953chr17:16934010-16941475u87
SE_57371chr17:16930601-16931654VACO_503
SE_57371chr17:16931698-16932552VACO_503
SE_58168chr17:16931647-16932117VACO_9m
SE_63843chr17:16930601-16933114HSMM
SE_63843chr17:16933946-16936222HSMM
SE_67627chr17:16934010-16941475u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr171693050816933600
Number: 1             
IDChromosomeStartEnd
GH17I017027chr171693037516936254
Enhancer Sequence
TTTTGAGATG GGGTCTCACT CTGTTGCCAA GGCTGGAGTG CAGTGGTGCC ATCACTGCTC 60
ACTGCAGCCT CAACCTCCCC AGCTCAAGTG ATCCTCCCAC CTCAGCCTCC CAAGTAGCTA 120
GGACTACAAG GGGCTCACAA TCACACCCAG CTAATCTTTG TATTTTTTTA GAGGCAGGGT 180
TTTTCCATGT TGCCCAGGCT GGTCTCCTGG GCTCAGGAGA TCCTTTCACC CCAGCCTCTC 240
AAAGTGCTGG GATTACCAGC GTGAGCTGCC ACACCTGCCT TTGCCTGTTC TTGAAATTCA 300
ACCAGAGCCT GGCCTTTTTG CCATCATGGT ATGTGGTGTC GTCTGTTCAA TAAAGATCTT 360
GAGCAAATTC TGGACCAGGC GTGTGGACGG GTAGGTGGAA CTCAACCCTC ATGCCCAGTT 420
TTCTCAGCCC TACCCTATGG TTCCAGAGTG ATGGCTGTGT GCACGATTCT GAAAGCTGTG 480
TGCGGTGCTG CTCAGGAGCC AGGAGGACAC TGGGCCACAC TGGGTGTGAA TCCTGGCCCC 540
CCACTTCCTG GCTGTGTGAA CGTGGGCCAG TTACCCAGAT CTCAGTTTCC CCAACTACAA 600
AGTGTGAGTA AGGATAATAC TTCCTCCTCA GACAGTTGTT GTGAGGATCA AGATATGAGC 660
TTAAACCGGG TGTGGTGGCT CAGACCTGTA ATCCCAGAAC TTTAGGAGGC TGAGGCAGGA 720
GGATCCCTTG AGTCTGGACG TTCCAAGATA CTGTGAGCTA TGATCACACC ACTGCCCTCC 780
AGCTTGGGTG ACAGAACACG ATCTCATCTC AAACATTTTT TTAAAATTAA TGAAAAAAAG 840
AGTCCATGCT TAGAATAATC CTGGCATTGG GCAAGTCATA CAGAAGTTGT TTTTATAACA 900
TGTTTTTTTT TTTCTCTCAT TATAAAAGTC ACACGTGTGT GTGGTTGCAA GGTCAGGTGG 960
CAATGGGTAC TCTGGTCCTT TTTCCTGGAG CTGCTGGACC ATCACAGGGC AGAGGGGGTC 1020
AGACTTCCTA GGGCGCCTCA CTCAGCTGCC CTTGTCCGCC TGGACAGACT TGCCTCTGGG 1080
TGTGGCCATT GCGAAGGAAT CCTGCCCCAT CGCTGACAAT GAGCTGCATT CTTCAGAGAG 1140
GCTGCCCCAG TCCCCCCAGC TGACGTAAGC CCTGGGCGTG GCAGGTGCAC TCAGGAGGCA 1200
GGGCTGCCTG CTCAGTGTTG GGTGGAGCCA CATGCCTGTC CAGGGCTGGG TCCACCCTGT 1260
GTGGACTGAG GCCACCATGT GCACGGTTTT CAGCTATGCC TCATTCGCTT GCTGTGTGAA 1320
TCTGGGCTGC AGGGCCTGCT GCTGTGTGCC ACAGGCCAGT GCCCTGCAGT GCAATTGTAC 1380
CTGAGGACCC AAGGTGGCCA GGGAAGCCCC AGGTGCGACT TGGCAGGGGA AGCAGGGGCT 1440
GTGGACGGAT GGAGAGCTGT CATGTGGAAA GGCAGTGTGT CCCCAGGCCG TGGCCCAGCC 1500
TCCAACACCC CCAAGTCCCC TCCAGGCCTC TCCAGACCAG GCCCACCACA TACTGCCTGT 1560
GCAACCTCGG GTGAGTGACC TCACCTCTCC AAGCCTCAAA GTCCTGATCC CCATTGGGAG 1620
GGTGCAGTCA GAGGGTGAGT CTGAGCCCCC TGGGGCCTGG CAGGCTCTGT ATGCATGGCA 1680
GCCACCTGCC CACACTCACC CCAGACATCT GCTCATTCCA GAAACCTCCT GGGAACATCC 1740
ACCATATGCC AGGCATAGTG TCAGACAGGA GGGGACAGAG AAAAACAAGA TCAACAACCG 1800
CCCTGCCCTT GTGGAGCTGG CGTTCTAGTA CCGGAGACAA AACAAGGTGC TTCCAAGGAG 1860
GAAGCCGTGC TCATCAGGTA ATCCGCATAA TCGCTCAGGA GGAGACTTGG CAGCCAGATG 1920
GAGACGCCAC CTGGGGTCTT AGGGGAACAG CATTCCAGGC AGAGGGAACT GCAGCTGCAA 1980
AGATCCTGAG GAGGAATGAG TGCCCAGCGT TTGAGAAGCA GAGCCGGCCT CTGGACGCCT 2040
GCCCTAGGGA GAAGGCTTTC CACCTCATTT TTAGGGTCCT AGGGGATCCC CTCCACTGTG 2100
AATGCACGAA TGCACAAGGA TGACATCGGC CCTTTTATAG AGGGGAAGTT CTTCCCGTAA 2160
ACAAACCAAA GTCCCTCTGG GGGACTTTGC AACTGAAGCT GAGCCTTCTC TTTTAGTCAC 2220
TCCCACCCCC CAGACCCAGA GCCAGCTGAT TCCTCCTGCA TCCTGCTCAC AGCTCCAGGA 2280
AAGCGTCCTG GTGGGGAAAG TCAGTGAAAC ACCAGGTGGC CTAAGGTATT TTCCCAGGAC 2340
CTCAATGTGA CTAGACAGGG CTAGCTTATC AACCCTGGGA TGCGATGAGA GGGGCAAAGC 2400
CCGGCAAAAG AAACTGGACC CAGGGCACTG AGGGAAGCCT AGGTCCCGTC TGAGTGCTCC 2460
GCACAGGGAT AGGAGGAGAG ACAGTCGGGG GTTTTGTGAG GGAGGGGATA GGTGGGTGGT 2520
AGTAATGAGG GGTGTTCAAG TCAGTGCCCA GCAACCAAGA GGAGGAAGGA GGTAGAGGGG 2580
GTGTCAAGCA AGCCGTAGCT TCAGGCACAG CTGGATCCAT AACCCTGAGG CTTGGGCTAT 2640
GATGGCTGTT GCCCAACCCC CACTCCCATA TCACCCAGGT CTCAGTCACC TTCCTCTCTG 2700
TGACACAACA GCCTCCTCCC TAGGGCTCCT TCCTTCCACT CTTGCCCCCA CAAATCCATT 2760
CTCCATATAT TGTTAAAACC ATGCCACTCT CCTGCTTAAC CCCTCCCCCC ATGGCTTCCT 2820
GACGCCCTCC ACATAAAGCA GAAACTCCTT ACCCAGGCCC CAGAGACCCC CGCTGACCTC 2880
CCCAACCCCA CCTCTCTCTC CTCTCCCCTC ACTGCCTCTG TCCTTTCTGT CCCTTGAACA 2940
CACCAAGCAC ATCCCCACCT GGCCAGCATT GCACCTGCTG TCCTGTCCCC CGGGTGCATC 3000
ACCATGTGGC CGCCCCTTCT CAGCAGGACA GCCTAGATGT CGCTGTCCTC GGCCATCTGG 3060
CCCCCAGCCT TCTGTCCACT CCCCACACCA GCCCTGTCCG GCAGCTCCTT CTGTGATGGA 3120
AGTGCTCTTT GTCCACTGTC ACCAGCCTCT GTCAGAAGCT ACCGGCCCCG TGTGGCTAAC 3180
AAGCCCCTGA AATGCGGCTA CTGCAATGGA AGAACTGGAC TCTTAATTTT CAATTACTCC 3240
AATTACTTGA AACTCATATA GCCACATGGG GCTAGTGGCC ACCATTTGGA CAGAGCGACT 3300
CCAATGTTCT ACATGGTGTA ATTTTATTTA CTAGCCCTTA GCACAAAGTG ACGTGATCTT 3360
AACTTCACTT GTTTTCTGTC TCTCTGACGA GAGTATCAGC TTTGTGAGGT GAGGATTGCC 3420
TCCGTCTTTT CCACTGCTGT ATGCCGGGGC TTAGTAGTGG GCCTGGCGTA TAGTAGATGC 3480
TTAATATGTA ATTGCTGAAT GAATGAATGA ATGAATGAAT GAATGAATGA ATGCATGCAT 3540
GAGTGAATGA ATGACTCCTG GGGCCATGAA CTCTGAATTT CTCCAAAAGG AATGCTAGTT 3600
CTGCCGGGGA TTGTTGCTGT GTGACCTAAG TCAGGATCTT GCCCTCTCTG GGCTCAGCAT 3660
CCTGACCAAG GGGTACCAGG GCCCCTCTGC TCCTAAGGCT CTGAGACTTC CTGCTGCTTA 3720
CTCTGTCCAA GCTGCCCCGT CTATCCTTCA TCCCCGATGC CCACCCCCAG TCTCCCCAGC 3780
CACTTCATAG GAAAGGGGCC AGACAGGCTT CCTGTCCCTG GAGCCTGTGT CTAGAGAGCC 3840
ATCAAAGCAG GCTGCCTGTA CCCGTCTCCT AGCAACAAAT GGCCTTAGGA AGTATTTGAG 3900
GGTGGGATAA AGTGGTGGCC ACTGTGGGGC TGTGTCCCAA ATCGACAGCT CTCCAGTTGG 3960
CCAAGGGCAA GTGTTTCCCA GGAGCCAGGC CAAGGCAGGC TGGCAGTCGT GGTACATGCA 4020
CCAGGAGTCG GCTCCAGGGT CCTCCAAGCC TGGGCCCTGC AGTCGGCCAC CCTTACCTTC 4080
TCGTGCCTGT GCTTGGGGTT CAGAGGTGGC AGGGGGTGCT TGGGCCCTAC ATGCTTCTTG 4140
TGGGGACCTG TAGGAACCAG GCATGAGGAA GTGAGGAGTG GGTGCTGACT GTCAGTGACT 4200
CGAACCCTGA CTGCCCCAGC ATCCAACACT CACACGCATG CACATGTGCC TACTCAGCCG 4260
GACACAACAC ACAACTATGC ATGCTGACAC GCACTTGTGC AGAGGCATAG GCACAGACTG 4320
CACTTACCTT 4330