| Tag | Content |
|---|
EnhancerAtlas ID | HS101-01383 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:44021970-44026820 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr1:44024432-44024450 | GGAGGGGAGGGAGGCAGG | + | 6.34 | | Mafb | MA0117.2 | chr1:44023524-44023536 | AAAATGCTGACT | + | 7.22 | | RREB1 | MA0073.1 | chr1:44022452-44022472 | TGGTGGTGGTTGCTGTGGGG | - | 6.93 |
|
| | Number of super-enhancer constituents: 27 | ID | Coordinate | Tissue/cell |
| SE_00616 | chr1:44009256-44025211 | Adipose_Nuclei | | SE_04240 | chr1:44023611-44026224 | Brain_Anterior_Caudate | | SE_05040 | chr1:44023306-44027093 | Brain_Cingulate_Gyrus | | SE_05962 | chr1:44023210-44026924 | Brain_Hippocampus_Middle | | SE_07193 | chr1:44023786-44025089 | Brain_Hippocampus_Middle_150 | | SE_08033 | chr1:44023627-44026877 | Brain_Inferior_Temporal_Lobe | | SE_23218 | chr1:44022089-44026653 | Colon_Crypt_1 | | SE_23829 | chr1:44022157-44023119 | Colon_Crypt_2 | | SE_23829 | chr1:44023263-44026674 | Colon_Crypt_2 | | SE_24870 | chr1:44022071-44023154 | Colon_Crypt_3 | | SE_24870 | chr1:44023259-44025244 | Colon_Crypt_3 | | SE_24870 | chr1:44025899-44026852 | Colon_Crypt_3 | | SE_26649 | chr1:44022053-44025193 | Esophagus | | SE_27645 | chr1:44022136-44025907 | Fetal_Intestine | | SE_28595 | chr1:44022065-44026100 | Fetal_Intestine_Large | | SE_31538 | chr1:44022050-44025040 | Gastric | | SE_33537 | chr1:44023245-44025799 | H2171 | | SE_41575 | chr1:44022120-44023117 | LNCaP | | SE_41575 | chr1:44024391-44026778 | LNCaP | | SE_50363 | chr1:44021974-44023142 | Sigmoid_Colon | | SE_50363 | chr1:44023204-44026309 | Sigmoid_Colon | | SE_52524 | chr1:44022166-44025322 | Small_Intestine | | SE_56987 | chr1:44022407-44023150 | VACO_400 | | SE_56987 | chr1:44023728-44024680 | VACO_400 | | SE_65452 | chr1:44022315-44025132 | Pancreatic_islets | | SE_65452 | chr1:44026172-44027003 | Pancreatic_islets | | SE_69138 | chr1:44023472-44026821 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH01I043560 | chr1 | 44025900 | 44027003 | | GH01I043556 | chr1 | 44022192 | 44025767 |
|
Enhancer Sequence | TTGCCAGGCT GGAGTGCAGT GGTGAGATCT CGGCTCACTG CAACCTCCAC CTCCCGAGTT 60
CAAGTGATTG TCCTGCCTCA GCCTCCCAAG TAGCTGGGAC TACTGGCAGG TGCCACCACG 120
CCCAGCTAAT GTTTGTATTT TTAGTAGAGA CGGGGTTTCA CCATGTTGGC CAGGCTGGTC 180
TCGAACTCCT GACCTCGCCC GCCTTGGCCT CCCAAAGTGC TGGGATTACA GGCCTGAGGC 240
ACTGCGTCCA GTGTCGGTTA CTGTTTTGCA TCTGTGTCTT GTATGAGTCC GTGGGCTCTA 300
CAAGCTTAGA GGAGCCATAG AGGACAGTGG TTAAGACTCT GGACCACTCA CTTCTCGTGT 360
GTCTTTGGGT TAGTAACTAT GCCTCTGACC CTCATTTGCT CCATCTGTAA ATGGATATAA 420
TGCCTACCAC CCAAGCTGGT TTGGAAGATT GAATGCTGTG TATGAAGCGC TTCCCAGGAG 480
TGTGGTGGTG GTTGCTGTGG GGCTGGAAGC TGTACATCTT GAGGCCTCAC CACGTGAGCT 540
GAAGGTGGTT GGCCTCCGTG CTGCGTGGCA TCATCCGGGT GATGCAGCTC CACTGCCTGC 600
TCCCACGGGG GGACATACCT GTGCAATAGG AACTCAGAGA ACAGGCCCTG GGCCAGCATC 660
ACTGATTGCT GAGTGTTCTC AGGCTCCTCC CTGCCACTTC TGACCTGTTT CCCCACTCGT 720
GACCTGGGGG CAAGTATTTC AATGCTGCCC AGTCCTCCTA TTGGCAGCTG TCCTAGCAGG 780
GAGCCATCTG CCCTGCCCTG GCATTTGGGA GGTGGCTGAA GGACCAGAGG CCCCAGAGGG 840
CTTCTTTTCA GGCTCTCAGA TTGGGGAACA GGGCCTCCTT GTTAGTATTG AAAGAGGAGT 900
CCTTCAAAAG CGCCTAAGCC CCAGGTCCTG GGTCAGGAGC CCTCTTACCT CTGCCACTGC 960
CCTGGGCAGC CTTACCTTTC AAAGGGTTGA GGAGGATGGA GGTGGTCTTT CAGGCCTGGG 1020
GTGAGGAGGA CGGACTTCAG ACTGACAGGA GGGGCTGGGT GTGGTGGCTC ACGCCTGTAA 1080
TCCCAGCACT TTGGGAGGCA GAGGCCTGCA CATCACTTGA GGTCAGGAGT TCGAGACCAG 1140
CCTGGCCAAC ATGGCAAAAC CCCATCTCTA CCAAAAAATA CAAAATTAAC TGGGCGTGGT 1200
GGCGCACGCC TGTAGTCCCA GCTACTTGGG AGGCTGAGGC AGGAGAATTG CTTGAACCCA 1260
GGAGGAGGAG GTTGCAGTGA GCTGAGATTG CGCCACTGCA CTCCAGCCTG GGCGACAGGA 1320
GACTCCATCT CAAAAAAAAA AAAAAAAAAG AGGACCTGCA GGAGGTGCCT CCGTTTGGTT 1380
TCTCTACCAG GGGCCAGCAG TATATGTTTG CGCTTCTGGG GTGTGAGAAG TGTCTGATGA 1440
GGCTGGGGAG AGTGTGGCGC AAGTACCCAG ACCCTGTCCA TGCTCCGGGG AAGGGTGTGG 1500
AGCTGTGGGC CTGAGTGAGC CCCTCCTGCT TCTGAAACAT AGCACCAGGA AGACAAAATG 1560
CTGACTTATC CTGCTGGTCT GTATAACCTT GGCCAGCATT GGGCTTGACA GAAAGGCGTG 1620
CCGCAGGAGG GCCAGAGGGA AGCAGCCCAG AGGGTGAACA CCCGCCCCCT GCCCCGCCTC 1680
ACCCCACCCC TCCCCTCCCT CCTAGGAGGA TCAAGAAAGC TGGGTGCCTG CAGGAACTGG 1740
GTGAAAGGAT GGTTGGACTT GGACTGGAGC TCTGGGGTGG GGCCGGCAGG AGCCAGGGCC 1800
ATTCTTGGGA GGCCACCACA GGGTACGAGG AGGGCTGGGG AGGGGATGGA GCTAGTTGGG 1860
GTCGGGGAAG TAAGAGTCCT TCCTGAGTTG CACACAGCTC TCCCTGTGAG CTGGTCTCCT 1920
TGGAGAATGG CTGAGGGCTG TCTGGGGTGA ACTGGCTCAG GTGAAGATCA GTGTGCCCCC 1980
AAAAAGGAGT CCAGGCCTGC AGTCTGTTCT GTGCCCTCTG CCTTTGCCTC ATGTCACACC 2040
AGGCCCAACT GCTGTGGCTC CAGGGCCACT CCCACCACAG CCCGTGGGAG TGCCCCCCCA 2100
AATCCCCCAC AGCCGTGCCC TTTGCACCTC GCATCTGAGC AGGATTGTTA TTCCCAGTGT 2160
GGCCTCCCCT TGACACCCCC GCCAGGACTG CATACGAGGT GGGGGTGCCC AGCACAAGCT 2220
GGCCGGGGTG AGCCTGTCCT GGCTGTGATG AGCGTGGGGC CCGCCGCCCA GCGTTCCTGT 2280
CTGAGTGGTA ATTGAAGCCA TTAGCGCGCC AGCCTCTCCC TCGCCGGGTA ATGGCAGGAA 2340
AAGCTCTTCT CGCTCCGCAC TCTTGAGGCG GCGGCTGAAT CACTCCCCCT CCAACCCGCC 2400
CGCTGCCGCC ACTGAGACAG GGAATCTGAC ATTTTCCCTC ACCAGGGAGG GGGAGCCCTG 2460
GGGGAGGGGA GGGAGGCAGG CCTGGATTCC TGGCCTTTCC CTCCAGGAGG TTGAGGGGCA 2520
GTGAAGGTCT TGGAGCTCAG TCTGTAAGTC ATGGATTCAC CTGGGGCCGC AGATTTCAGG 2580
CCTGGAAGGA CTGGCCGGGA AAGCCCAGGA GGCCGCCAGA CATTCAGTGG TGTGGGGAGG 2640
GCACTGATGA CTTTGGGTAG GTTCTGGGAG GGACAAGGAG GCGGGGAGAA GAAAGAAGCT 2700
GTGGAGCAGA GATGAGCTGT TTTGGACTTC TCCTGGGGGG CTTAGCTCCA AGGGTTCTGA 2760
GTACAGGTAG CATTACTTGT CTTGGGGTCA TTGATAGGGC AGATAACGTG CACTGTTCGT 2820
GTGGTGTGGG TGCCCTGTGT GCCATGTTTA AGGCAGTGTT TGTGTGAAGT GTGTGGTGCA 2880
GTGTGTGCAG CAGGGGTGCT GCCTTGCAAG CTGTGCGCAC AGAACGGGGT GTGCAGCGGT 2940
CAGCGCACAC GTTACCATCA GGCAGTGGGG AAGGGGCAGT GTGTGCAGGA GGCACTGCAT 3000
GCTGTATGGG CTGTGTATGC AGCGCGCAGT GTTTGTGTGC ACGTGTGTGC GTCAGGCAGT 3060
GCGTGGTGTG GTGGTAAGCA GGTAGTGAGT ACCTTATGGG CTATGTATAC AGCAAGGCAT 3120
ATGCATCAGG CAGTGTGTGG GCAGTAGGCA GTGTGTGTGT GTGTTATCAG GCAGTATATG 3180
TGTGCGGTGT GCCGTGCGGC AGGCTACCTG TGTTTATATC GGGTAGTGTG TGTGTGTTTA 3240
TGTGCAGCAA GGGTGTGCAG TAGGTGTGCA GTAGACTGTG TGCAGCAGGC GTGTGTGTGT 3300
GTACAGCAGG TGGTGTGCAG CAGGCAGTGT GTGTATGTAT CAGGCGGGGT GTGGTGTGTG 3360
TTTATGTGCA GCATGCGGCG AGTACTTTGT GTGGTGTACA GCAGGTGGTG TGCGGCAGGC 3420
TGTGTGTATG TATCAGGCTC TGTGTGTGTG TGTGTGTGTT TGTACAGCAG GTGGTGTGCA 3480
GCAGGCAGTG TGTTTATCAG GCAGTGTGTG GTGTGTGTGT GCATCTTTAT GTGCAGCGAG 3540
TAGTTTGTGG GGTGTGCAGC AGGTGGTGTG TAGCAGGCTA TGTATGTATC AGGCTGTGTG 3600
TGTGTGTGCG CGCGTGTGTA CAGCAGGTGG TGTGTAGCAA GCTGTGTGTA TGTGTCAGGC 3660
AGTGTGTTTA TGTGTGTGTG TCCAGCAGGT GGTGTGTAGC AGGCTGTGTA TGTATCAGGC 3720
AGTGTGTGTG TGCGCAGCGG GTAGTTTGCA GGGGTGTACA GCAAGCAGTG TGCATGGTAT 3780
GTACAGCAGA TGGTGTGCAG CAGGCAGTGT GTGTGTGTGT GTGTGTACAA TAGGTGGCAT 3840
GCAGTGGGCA GTGCATTTGT GTGCATGCAG CAGGCTGTGG TGTGTACAGC AGGTGGTGTG 3900
CAGCAGACTG TGTGTTTGTA TGCATCAGGC CGTGTGTGTG TGCAGCAGGC AGTGTGTGTG 3960
TGTGTACATG CGCACACGCA ACAGGCACTA TATTTGTGCA GCAGGCCATG TGTGTGGTGC 4020
ATACAGCAGG TGGTGTGCAG CAGGCTGTGT GCTTGTACAT GCAGCACATA GTGTATGTGT 4080
GTTGATGTCA GACAATGCAT GTGCATGTGT GTGGAGTGCA CAGCAGGTGA TGTGCAGCAG 4140
GCTGTGTGTG TAGGTGTGCC TCGGGAGTGT GTGGGGGTGG GAGTGGACAG CAGGTGGTGT 4200
GTGCCTTACA ACCTGTGTGG GCAGCAGCAG GAGTGGGCAG CAAGCAGCCC GAGCTGAAGT 4260
GTGGTGGGGT CAGTCTGGCA CTGGCAGGAG GTCGGAGATG CTGTGTCTGG GCTCATTGTC 4320
TCTGGGACCC CGCAGGATCC CTGTTTGGAG CTGTTGGTCC GCCAGGAAGT TCGACAGAGT 4380
TGGATGTGGC CAGAATGGTC TGGCTGAGCT GTTCTCAGCA CCTGTTGTGG TCGACCTCAG 4440
CAGCTCCTCT GTAGCCAGGC CAGGAGGTGG GGTGCACCAG ATAGGGATCC TGCCCAGACC 4500
TGCCTGCAGG AGGTCTTGGG ACCCTTTCCT CTCCCTCCCC TACCCCACCA AGCCCACAGT 4560
CCCTTCTGTC TGTTCCCACC TGGCCTCAGT GTCCAGCCAG CACCATACCA CCTATGCCAT 4620
GCGGGCCAGG GAATCCAGGT GTCTCGATGG AGTGCCTGGT GTTGCCAGCC TTGGAGCAGG 4680
CTCTGGGGAA GGGCTGTCCG GCACATGAAG TAGTGACCAG GGTGGGGGCT AATCAGTGCT 4740
GTACTGGGCT TGGACCTCTG GGTTCTGCAG GAGCTCTGAC CCTGGCTGGC TTTGGGGCTC 4800
GTGGGATGAC GAAGGACCTC TTGATATACC CCCTGACCAC TCCACAACAC 4850
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