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

TagContent
EnhancerAtlas ID
HS184-13532 
Organism
Homo sapiens 
Tissue/cell
T47D 
Coordinate
chr17:39940270-39942830 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs7213095chr1739940768hg19
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr17:39941248-39941266GGGAGCAGGGAAGGCAGG+6.16
ZNF263MA0528.1chr17:39941249-39941270GGAGCAGGGAAGGCAGGGGGC+6.05
ZNF263MA0528.1chr17:39940642-39940663TTCTCCTCCTCCCCCGCATCC-6.42
ZNF263MA0528.1chr17:39942365-39942386GGGGGAGTAGGGAGGGAGGGA+6.54
ZNF263MA0528.1chr17:39941655-39941676GAGGCAGGAAGAGAAGGAAGA+7.1
ZNF263MA0528.1chr17:39940645-39940666TCCTCCTCCCCCGCATCCCCC-7.33
ZNF263MA0528.1chr17:39940636-39940657CCTACCTTCTCCTCCTCCCCC-7.62
Number of super-enhancer constituents: 24             
IDCoordinateTissue/cell
SE_23177chr17:39940171-39943078Colon_Crypt_1
SE_23845chr17:39940284-39943074Colon_Crypt_2
SE_24826chr17:39940186-39940762Colon_Crypt_3
SE_24826chr17:39941043-39943220Colon_Crypt_3
SE_26576chr17:39937446-39946643Esophagus
SE_27684chr17:39940016-39944181Fetal_Intestine
SE_28604chr17:39939290-39944303Fetal_Intestine_Large
SE_31640chr17:39940077-39943753Gastric
SE_35990chr17:39939244-39944308HMEC
SE_40900chr17:39937341-39943942Left_Ventricle
SE_41716chr17:39940081-39943081LNCaP
SE_42558chr17:39937451-39943776Lung
SE_47748chr17:39940258-39940577Pancreas
SE_47748chr17:39940822-39943075Pancreas
SE_48895chr17:39940059-39943716Right_Atrium
SE_49575chr17:39940710-39941117Right_Ventricle
SE_49575chr17:39941148-39943079Right_Ventricle
SE_50269chr17:39940113-39944232Sigmoid_Colon
SE_52578chr17:39940064-39943923Small_Intestine
SE_56909chr17:39940155-39943059VACO_400
SE_57643chr17:39940618-39943012VACO_503
SE_58007chr17:39940842-39943111VACO_9m
SE_64699chr17:39939300-39943189NHEK
SE_68966chr17:39939590-39943107H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr173994140039942611
chr173994053939940600
chr173994063739940800
Enhancer Sequence
GGTCACTGAG GCTCAGGTAA TGAGAGACAG AGCTGGGTCT CAAACCCAGC TCAGTTCAAG 60
CCCAAAGCCC TGTGCTCAGA ACTGCCCCAC TGTCCCATCT CTCCAAATAA ACAGTCCTTC 120
TGTAGACTAG TCAATTGACC CATCTCACTC TAAGGTGGCT CCAGGATGGG AAAAAGGTTG 180
GCAGCCCTAG CCCGACCTTT TTCGTTCCTA TGCACTGCAT TCTCAAAGCC TCGGCCCTGG 240
CAGCCCAAAC AGAGGCTCCA GAGGGAATGG GGTGGAGCCA GGGTGCAAGG GAGGGGTGGA 300
GTGGGGGTGG GAGGGCTCAA GTCACCCAAG CTGGGGCTTG ATCTAGCAAG AAATGACTAA 360
CTGGGTCCTA CCTTCTCCTC CTCCCCCGCA TCCCCCAGTC CAGTCAGTGG CCAGTTTTCA 420
CCAAGCACCT CCTAGCAGTA CTTCCTCAGT ATTATCTTTT CATCACAGCC ACAAACCAGA 480
TTAGCTAAAC TAATCATGTA GCCAACATAA TTACAATGCC CTCCCCTCCT CCACCTTGGC 540
ACAGAGAAGA GGGAAAGCAG GTTATTTTTG CCCAAACTCC CTGCTCCTGT TGCTCCCCAG 600
AGGTGCAGAA TCCCATCCCC CGGCAGAAAA GGATCTGAGT TCCCACACTG ACTTCCCCCT 660
AGCACAGGGC TGAGCGTGAT CCCCACCCAG GATAAAGGGG CTGAGTCTGG GCCCCCAGCC 720
TCACTCCCCC ATCTACAACA AAGAAAGAGG TGGTAGACTC TTCCCCTCCA AGCACTCTCG 780
ATCCCCGCCC CCCACAATCT TTCTCCCACC CCCAGGACTG AGAGAGAACC CAACTGTTGT 840
ATTCTCTCTC TGTTCCCCAA CGAGGCTGGG CTCCAAATCC TGCAAAAAGA CCACATTTCA 900
GATTTTTTTT TTAAACCGGG GTACAAACCC TGATCAAGAT CCCCAATTCT GGGTGGGGGG 960
GGGCGGTCTC AGGAAATTGG GAGCAGGGAA GGCAGGGGGC CCGATGCAGC TCTGCCTGAG 1020
AGAGTCTAGC ATTGAAGAAA CCTTCCCCCA AAAAGCCTTC CTGCGGTCTC ACTTTCCCTG 1080
TCAAATTCTT TCAGGAAAGC GGGTGGGAAA GGTCTGTGCA GGCCTCCAGA AAGCATGCAC 1140
CTTCACAATT CAGAAATCAA ATGGAAGGCA AGTCCCACAG CCTCATGCGC TTCTGCCTCA 1200
ATAACCAGCC AGCTAAGTAA TGTGGGGGAT GGGGTAGAGG CAAAAAAAAA AAGACAAGAA 1260
CAACCACTCC CCCCACCTTC CTCAGTTTGG CCCAGCCCTG CCCCACCCCC ATTCCTGGGG 1320
AGGGGGCAGA GCTTGAGAGA CAACCACTTA CGCAGGCCTT GTCTGAGGGG GTGTGGTGGT 1380
CCCAGGAGGC AGGAAGAGAA GGAAGAAGCT GCTTCCCCTC TCAGCACTTT CCACCCCCCA 1440
CCCCGGCCCC TACCTCAGGC CCCTGGGGCC CAGCGAACAG GATGAATGTG GGGGCAGGGA 1500
AGACAGGGTC GGAGCCCAGG CACCGGCCCA GGTTCAGCCA GGGGCCGGCT GGGGGAAGGG 1560
GTTTTGCACC AGGAAGGACC CCCTAAGCCT AAAGGAAGTT TTGGGCAAGG AGACGGGAAA 1620
ACCCCCAGAT AAAGCTGCTG TGAATACTTC CTCCTGCAAA GTTTGTTTTG GGTGATTTTT 1680
TCCAACAATA AGAGGTTAGA GAAGACGGGT CCTGTTCCCC TACCAACACT CTGGCAGCCA 1740
CAGCTACTGG AAACTGGGCC AGGTGACCCT GAATTCTTCA TCCGTGCACA GACCCCACCC 1800
CCCAGACCCC AGGGCGAGCC ACGGGTGCCA GACACCAGCT GGACACTGAG CCGAGCCCTG 1860
CACCCCCCAG TCACTCCATC CCACCTCCGC TGAAGAAGCC AGAGCCGGGC TCCCACCGGC 1920
GTGGAGGGAG GCGCCGCAGG TAGTATCGAC GAGGCTCTGG GAGCTGGAGG GCAGGGCCTC 1980
TGGACTCCGT GCGCTCACCT GCTCGGCAGG TGGGGCCAGA GTCGCTGGGA AAATGTGCGC 2040
TCGGCCCCCA CAGTTGGGCA AGCTGGGCGC AAACAATAGG GCCCCACCCA GGCCTGGGGG 2100
AGTAGGGAGG GAGGGAAAGC GAGGATGACG CGTGGGGTGG GGTGAGGGTG GCCCCAAAGA 2160
GACCAGCGGC AGCAAGTTCC CCAAACGGTA AATTCCTGAC TGCAGCGTGA GCCCTGGGAC 2220
GCAGTCGAAG CAGAGCAAAG TCTCCCCCGC CAGCCCAGGG CGAGAGTCAG GGACGCGGCG 2280
TCGGGCGAGC TGCGCGGGCC CCGGGGGAGG CGCGACCCCG GAGGCACCTG TCCGGATCCC 2340
TCCCCGCCTT GCTCAGATCT CTGGTTCGCG GAGCTCCGAG GCGCGCTCGG CCCGAACCGC 2400
GCGACCCCCA AGTCGCCGCG CCCAGGACCC CAGCGCGCCC CCTGCCGCCG GTGCAGGGTG 2460
GCGCTCGATG GCACCGGCCC TCACCTGCCC AGGGACGGCT GGGACCGGCC CCGCGGCCGC 2520
TCGCCACCCC TCTGTCCCCA ACGATACCTG CGCCCCCGAT 2560