EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS012-02613 
Organism
Homo sapiens 
Tissue/cell
Caco-2 
Coordinate
chr11:17006600-17010050 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs11024102chr1117008605hg19
TF binding sites/motifs
Number: 19             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr11:17009946-17009964CCTTCCTGCCTTCCTTCC-10.35
EWSR1-FLI1MA0149.1chr11:17009989-17010007TCTTCCTTTCTTCCTTTC-7.18
EWSR1-FLI1MA0149.1chr11:17009942-17009960ACTGCCTTCCTGCCTTCC-7.21
EWSR1-FLI1MA0149.1chr11:17009974-17009992CTTTCCTTCCTTCTTTCT-7.22
EWSR1-FLI1MA0149.1chr11:17009985-17010003TCTTTCTTCCTTTCTTCC-7.2
EWSR1-FLI1MA0149.1chr11:17008409-17008427GGAAGGGAGGCAGGAAAG+7.67
EWSR1-FLI1MA0149.1chr11:17009970-17009988CCTTCTTTCCTTCCTTCT-7.68
EWSR1-FLI1MA0149.1chr11:17009958-17009976CCTTCCTTCTTTCCTTCT-7.69
EWSR1-FLI1MA0149.1chr11:17009962-17009980CCTTCTTTCCTTCTTTCC-7.85
EWSR1-FLI1MA0149.1chr11:17009950-17009968CCTGCCTTCCTTCCTTCT-8.16
EWSR1-FLI1MA0149.1chr11:17009966-17009984CTTTCCTTCTTTCCTTCC-8.48
EWSR1-FLI1MA0149.1chr11:17009954-17009972CCTTCCTTCCTTCTTTCC-9.47
IRF1MA0050.2chr11:17008138-17008159TATTTATTTCACTTTCACTTT+6.96
PRDM1MA0508.2chr11:17008146-17008156TCACTTTCAC+6.02
SNAI2MA0745.2chr11:17009563-17009573TGCACCTGTT-6.02
ZNF263MA0528.1chr11:17008941-17008962GCTCCCTCCTTTTCCTCCTTA-6.37
ZNF263MA0528.1chr11:17009946-17009967CCTTCCTGCCTTCCTTCCTTC-6.46
ZNF263MA0528.1chr11:17009966-17009987CTTTCCTTCTTTCCTTCCTTC-6.47
ZNF740MA0753.2chr11:17008805-17008818CCACACCCCCCAC+6.03
Number of super-enhancer constituents: 11             
IDCoordinateTissue/cell
SE_23209chr11:17006345-17010079Colon_Crypt_1
SE_24588chr11:17006954-17010047Colon_Crypt_2
SE_27642chr11:17005603-17011510Fetal_Intestine
SE_28618chr11:17005858-17011943Fetal_Intestine_Large
SE_31464chr11:17005871-17010093Gastric
SE_42048chr11:17006935-17008802LNCaP
SE_42048chr11:17008809-17010048LNCaP
SE_48027chr11:17006917-17007272Pancreas
SE_48027chr11:17007452-17009993Pancreas
SE_50712chr11:17006304-17010109Sigmoid_Colon
SE_52571chr11:17006346-17010116Small_Intestine
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 4             
ChromosomeStartEnd
chr111700720317009519
chr111700970817009844
chr111700692617007190
chr111700812117009806
Number: 1             
IDChromosomeStartEnd
GH11I016978chr111700039417011590
Enhancer Sequence
GGGTGCCAGC GGGCTGGGCA CCTCCTCACC CTGTCTGCAT GTTCTTCTTC CTCAAGGAAG 60
GAAGCCTTCA GAAGCCCTTG AGGCAGATGC CTCTGCCTCA TTCATCTAAG AATGCCCAGC 120
ACCTGGCCCA GGGTTGGCAT GCAGGTGCCC ACTACACGTT TATGAATAAA CCAACCCACT 180
CCTAGGCACC TAGTTGTGTC CTTACATTTT GATTTCTTTA CACATTGCTT TGTGAATTGC 240
TGTTCATTTT ACTGAATGTG AGGACAGGCA GAAATTCCAA GTACACTTGC TTCTCAACCT 300
TTTGGCTAAT ATCAAGTATA GAAATTCCAG ATACACAAAA CTGAACTAGA ATGGACCCTG 360
CCTTGAAGAA ATTTACAACA ATGTGAGAGA GATGTAGACA CAAAAAGGTG TAACATGAAG 420
CAGGACAGTC ACGTGAGCAG CAAATGCAGT GCCAAGAGTG CAAGGGGCAA GAGAGCTCTT 480
GGGGTGGGGG TGGGGACAGC CACACACAAC AGCTAGACAG CCTAAGAGGG GCAGGGAAGG 540
CGGAACCACT TATCCATCCG TTCATTCCGC ATTAACATTT TAAGTTTTCT TGCTTGAAGA 600
AACACTGTGC TTGTTACTTA ATACTGTGCT GAGTGCTGGG GACAGATATG TGAATCAATC 660
AAACATAAAG ATAATTCACA GGCTAATGAG GGAGAGACAG AGAGACATTA CACAGACTAA 720
GGTGATATGT GGCAAGAGAG GATGCTAGCA TGCAAGCTCC ATGCCCACAG GCACCCTCCT 780
TTTGTTCACT ACTGTACTCC TCAGTACAAC ACTGTCAGGC TCAGAAAAGC TTCTCAGTAC 840
ATAACAAATG AATGAAAGCA CTGCTAACTA AATGAATGAA AGCACAAATG GAGGGATATC 900
ACAAACCCTT GATGGCGGGT GGCCACAGAT GGCTTCCCAG GTAATGCCTG AGTCTTAAAG 960
GATGCATAGG AATTACCTGG ATGGAAGGGG GCATTCCTAC AAAAGCAAAG ACAAAGAAGC 1020
AAGAGAGTGC TACAGCTTAT GATGTTGTGG AGTGTGTTCA GGCCAGAGGG GAATGGTGTG 1080
CTTTAACAGG ACACAGACAC AGGAAGAGAA GCCCAAGTCA GGACACCTCT GAAGGCCCTC 1140
ATCAGGAAGC ATATCAGGAT GAGGTATTTG GGCCCCTGTA GGGAGAACAG GATGGAGGCA 1200
AGAAAACCAG TCGGAACCAT CTGCACCGCT GCAGATATGA GTTGGTGACA GTGGGGTCTT 1260
TAGGAGGCAC CAGAGAAAGG ACTAATCACA AGAATCTGTT ACAAATCACA GGTGCAAGAC 1320
CCCATGGAGA AGGGAGGCAT CGAATGAGCC CAGACACATT TTGAGTACAT AAGAAAAGTG 1380
CAGCCCCACC AGAGCCCTCC TGGGAATGCT GCAAAGCTGC TGGGGAGATG CCAGCAGAAC 1440
CATGTCACAC CTTGCCCACA GTCACCAAAG TGGGGACCCT ACTGACTGGC TGGAGGCAAG 1500
GAGGAAGTCA GGGGAGAGAA ACCATAAAAA TTGCTCACTA TTTATTTCAC TTTCACTTTG 1560
AGCACACAAG TGGGGAGAAG ACGCCCTGGC CCAGGAGTAG AGAAACCTGG CTGGAGTCCC 1620
AGCTGTCACC AACAACCTGA GTAACCTTGG GCAGGTGACT TCACCGCTGG GGCTCAGCTT 1680
CCCCATCTAT AAACCAGAGC TTCCACCATG AGCCCCACCT CTACCAACAT CCTGGAAAGG 1740
CCCCAATCAG ATAAGTATCA GCTCTGCATA GCTTTATGTA GCACCTACTA TATGATCTTC 1800
CTTGTACCAG GAAGGGAGGC AGGAAAGGGG CAGGCCGAGC CCCTGCCCAG AGAAGGTTTT 1860
AACAAGGTGG TCCAAGCAGG TACTGCAGAA CACCGGCAAG GGCATTTCCA GCCACATTCT 1920
CCAGCCAGTC TTACTGCCCA GCCCAACCCA GCCCAGGGAA GGCGGAGAGG AAGCAGTGAG 1980
CTGTTTTACA ATCCATCAAA TTAATTGCCC CAAATGGGAA ATTTGCAGGC CTCCTACAGC 2040
CTCCTGTGTA TTCCATAATC TCCCATGGCC CTAATCTGCT GAGAAAGAAT GTGTGGGCTG 2100
TAATCTTTTC AGCCCACTGT TCACAGGGGC AATGCCTTGG AAAAACCTCA GTCCCCACCA 2160
GTGATCACTC CCTCCCAACC AAAAGCCTCC CCGACCTCCC ATCCCCCACA CCCCCCACTG 2220
ACCTGGTGGC CAGCCAAGGC CTGGCTCCGC CCCCCAGAAG CCAGCTAGGC CAACCTTGGC 2280
CTTGACTTTG ACCTCGGAAA GGAGACCTGC CCAACCAGCT CCTTTGGTAA ATACAACTTT 2340
TGCTCCCTCC TTTTCCTCCT TAAGACAGAA CAGCCTGGCA GGAGGCAGAA CCAGGAGAAA 2400
TGGCTTCCGA GTAGAGACGC ACCCTTGAGG CGTGGTGAAA ACAGCCCCAG GTGAGGTGCT 2460
GGGCATTGGT TCTAACCTTT GCTTACCCTA TCCCTGCTAG GAAACCCACT TCCCATCTCT 2520
GGACCTCATC TTCATTTGAG AAATGAAGGG AATGTAAAAC AGCCTCCCAG GAACTCCTTA 2580
CCCCACCCCT TTAAACAAGT TGCTTCTTTG CTTCTGCTGT AACCTTTGCC TGCTCCTTTT 2640
CCTGCATAAT GAAGCCTCTG TCTAGGCCCA ACTCAAATGT CACTTTCCCC ACGAAGGCTT 2700
CCTGGATCCC TCCCTTCTCA ACACCTGTCC CAAACTCTTT CTGCCTCCTA CACTCAACTA 2760
GCCTTGAGGG CAGAGGATTC TTTTACTCAT TGCTACTGTC AGGAAACTCA TTTGATAACA 2820
TATTTCAGAG AGCTCTGGAC AAACCTAGGG CCAAAACCTA TTTCATTCTC TAAAATACCT 2880
GGCATGGCAC AGATCCTGGG TCACCACCAC TGGGTGAAGT TTTCTCAGAC AGTGTGTGGA 2940
AGGCCAGGCT CCCTGAAGTT GACTGCACCT GTTAATAACC AGTGTCTGTA CCCTCTCTCC 3000
TTAACAAAGT GCTTTCCTAC TCACTACCTC ACCTACAGGG GAAGGACTGA TGTGATCCCC 3060
TTTCACAGAG AAGGCAAATG TCTTGCCCCA GGTCAGGCAG CTGTAAGGGG CTAAGCCAGG 3120
ATCCAAACCC AGGTCTCCTA ATTCTGGTTC TAACTTTGTG TTCCTCCCAC CGTACCTGAG 3180
GGAACATGCA AAGCTGAGCC TATTGAGAAG ATCTGGGCTT GGAGAGAGAT GCAATCTAAA 3240
CCTCTCCTTA GGGCTGCCCT GGGAGCCACA TCCAGAGCAG CCAAGGGACA GTCAGGAACT 3300
CTGGGCAGAG GAATGGCAGA AGGCATTTAC TCCATACTCT CCACTGCCTT CCTGCCTTCC 3360
TTCCTTCTTT CCTTCTTTCC TTCCTTCTTT CTTCCTTTCT TCCTTTCTTT GAGACAGAGT 3420
TTCACTCTTG TTGCCCAGGC TGGAGTGCAA 3450