Tag | Content |
---|
EnhancerAtlas ID | HS183-02552 |
Organism | Homo sapiens |
Tissue/cell | T47D-MTVL |
Coordinate | chr17:79301070-79303940 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr17:79303447-79303458 | GGTGACTCATG | + | 6.62 | JUND | MA0491.1 | chr17:79303447-79303458 | GGTGACTCATG | + | 6.02 | KLF16 | MA0741.1 | chr17:79302493-79302504 | GGGGGCGGGGC | - | 6.02 | KLF5 | MA0599.1 | chr17:79302494-79302504 | GGGGCGGGGC | - | 6.02 | SP1 | MA0079.4 | chr17:79302492-79302507 | TGGGGGCGGGGCCTC | - | 6.44 | SP4 | MA0685.1 | chr17:79302490-79302507 | GGTGGGGGCGGGGCCTC | - | 6.64 | ZNF263 | MA0528.1 | chr17:79303272-79303293 | AGAGGAGGGAGGAGGGAGGAG | + | 6.91 |
|
| Number of super-enhancer constituents: 28 | ID | Coordinate | Tissue/cell |
SE_23211 | chr17:79302108-79305098 | Colon_Crypt_1 | SE_26559 | chr17:79300946-79301389 | Esophagus | SE_26559 | chr17:79302232-79304772 | Esophagus | SE_27741 | chr17:79301633-79305758 | Fetal_Intestine | SE_28689 | chr17:79300868-79306340 | Fetal_Intestine_Large | SE_29929 | chr17:79301804-79304977 | Fetal_Muscle | SE_31718 | chr17:79302282-79304471 | Gastric | SE_34591 | chr17:79301530-79306049 | HCT-116 | SE_35230 | chr17:79301694-79305379 | HeLa | SE_41800 | chr17:79301805-79304593 | LNCaP | SE_42641 | chr17:79300771-79301571 | Lung | SE_42641 | chr17:79301708-79305193 | Lung | SE_47367 | chr17:79301586-79304906 | Panc1 | SE_48267 | chr17:79300913-79304968 | Psoas_Muscle | SE_49267 | chr17:79300756-79301454 | Right_Atrium | SE_49267 | chr17:79302245-79304134 | Right_Atrium | SE_50704 | chr17:79300768-79301473 | Sigmoid_Colon | SE_50704 | chr17:79302148-79304837 | Sigmoid_Colon | SE_52831 | chr17:79300804-79301493 | Small_Intestine | SE_52831 | chr17:79302321-79305169 | Small_Intestine | SE_53485 | chr17:79300595-79301475 | Spleen | SE_53485 | chr17:79302655-79304056 | Spleen | SE_56913 | chr17:79302223-79303451 | VACO_400 | SE_56913 | chr17:79303471-79305245 | VACO_400 | SE_57608 | chr17:79301790-79305121 | VACO_503 | SE_58079 | chr17:79301741-79305485 | VACO_9m | SE_65666 | chr17:79301842-79305088 | Pancreatic_islets | SE_69098 | chr17:79301779-79304921 | H9 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr17 | 79301764 | 79301840 | chr17 | 79301974 | 79302367 |
|
Enhancer Sequence | ATTCCTCAGT TAGCATAACG TCCCTGAGGT CCATCCACGC AGTAGCGGGT GTCAGATTTC 60 CTTCCTTTTC CAGGCTGAAC CCTGTTCCAC ACGTGGCTAG ACCACAACTT GTGTGTCTGT 120 CCACTCATGG GTCGACGGCA CTTGGGTGCT TCCACCTCCT GCTGGCCGTG ACCAGGGCTG 180 CTGTGGACTC TGGCGCTCTC GTCTGCACCA GCTGCTGCCT TCAGTTCTCT GGGGTCTGTA 240 GCCGGAGTGG CATCGTTGAG TCACGTGGGA ATCCTGTGCT CTGCTTTTTT TCTTTTCTTT 300 TCTTTTCTTT TTTCTTTTCT TCTTTTCTTG AGACAGAGTC TTGCTCTCTC ACCCAGGCTG 360 GAGTGCAGTG GTGCGATCTT GGCTCCCTGC AACCTCCACC TCCCGGGTTC AAGCGATTCT 420 CCTGCCTCAG CCTCCCAAGT AGCTGGGATT ACAGGTGTTC ACCACCACGC CTGGCTAACT 480 TTTGTCTTTT TAGTGGAGAT GGGGTTTCAC CATGTTGGCC AGGCTGGTCT CAAACTTCTG 540 ACCTCAGGTG ATCCGCCCAC CTTGACCTCC CAAAGTGCTG GCGTTACAGG CGTGAGCCAC 600 CGCACCCGGC CTATGCTCCA CTTTTTGAGA GGCCAACAAA CCCCACTTGC TTTTTCAATC 660 CAGATTTTAA CCTTTGAGGG AAAAGAAAGA TTTTTGTATC TATTCCTGGG CCGGGGTAGG 720 GGGGCTGTTG GGTGAGGAAC ACCCAAGAAC GGCTCAGGTG AGAGGGGTGG CCTCTAAGAC 780 CACATGGCCT GGACACAGCC TGGCAGGCAG ACCGAAGCAG CCGGGGCTGC CTGGAGGGCC 840 TCAGTTCTGC TCCTCCCCAG CTGCAGGATC TGAGCAGGAG GCCTCCTCAC TCTGCGCCTC 900 AGTTTCCTCA TCTTTATCTG GGGACGGAGC AGCCTCTACC TCTCAGAGCT AGTTGCGATC 960 ATGGTGGCAG CTGAGGCCCA GCCCTGGTAT GCAGTGAGGG TTCAACTGAG CCAGCCCCCA 1020 CTCGCCACAG GCTTGCCTGG GGAAGACAGG TGCATCAGCC CCGGGGTCCA TTTCGCAGTG 1080 GGGCTGATCC CAGCCCACCC TCACCCGCCC GGGAGCCTCG CCCTTCACCC CATGCATCTT 1140 CTCCCCTGAA TCACCCCCAG GGTCTCCAGG GCAGGAGCAG GGCTGGCAAG GGCAGGGCTC 1200 ACAGCCCCAT AGGGAGGACA CAGTGCCCGC AAGAGGGACT GGGCAAGAGG TGGACAGGCA 1260 GGGGGTGGGG GCATTCTGTG TGCCCCAGAG CCTGAGTTCG CAGGCTCTCA GCAGCCCGTG 1320 CTGGGCAGCA GTGTGGGCGT CTCTCCCGCA GGGCACCCTC TGCACTTTCC TGCAGACCTG 1380 CAGCAGCCCT TTCCTGAGGG ACACCTGGCT CCGGGCCCAG GGTGGGGGCG GGGCCTCGCG 1440 TGTCTCCCCC TTGATTTGTA AGAGTCCAGG GCTGTCGGCC ATGGCCACAC TGAGCACCCC 1500 TGGGAGCCAA GGCAGCTTAA GGACAAGGTG TGTATGAGGA CGGCGGGGCC CAGGGAGGAG 1560 AGGCTAGCCC AGGGCTACCC GGGTCCCCGG AGTAGGGGCA GGGGACTTGA AAATGAGCCC 1620 CCAAGGGGCT CTGATGGGGG CAATTCCAGG AGAGGCGTGG GCAGGTGTGG GGCTGGAGAG 1680 AGGCCTGTCC TTTTTCCCTT GCCCTGCACA CTGTCTGCAG GGTGGCAGAC CCAGGCTGCC 1740 TGGCGAGGCT GCTTCTGGAG GCCTGAGGAA GGCTGGGCTG AGGACTCCGC CTCTCCTCAA 1800 AGCCACAGCC TCCCTGCTCT GGGGCTACAT GTCGGGAAAA TCCCTGCCTG GGTTACCCCA 1860 GCTGGGGACT CAAGCTCTCT TTGGACCCTA CAGAAAGAGC TGGCCAGCCC CCAGGCCAGA 1920 AGGGCCGTCC GTGACCCACA GATGGCCCCA ACACACTGTA AAACACGCAT GATTTATTTT 1980 AGTGTGTGTT AGAAAAATAA AGCCAACACA TCAAGCCTGC AATTTCGCAG ATACTAACAC 2040 TTCGGACCAG GAAAAAAGAA GCCCATGACA TGGCACAGCG CTGTGGAGCG AGCGAGATCT 2100 GGGATGCGTA GGCCTGGACG GCTGAGGCTT GGAAACCCCT CCCCTCCCCA AACTTTCCCA 2160 CCATGCAGGG GCCCAGCAGG CCCTCAGCCC ACTCACCCCG CCAGAGGAGG GAGGAGGGAG 2220 GAGGGTCCGG GCCAGGTGGG AGCTTCTCCC CGGAGGCCTG AGGCAGCTTC CCTCCTCTCC 2280 CAGGAAGGGG CTGGCCCAGG CCCAGCTAGG ATGCTCCCAG CCCAGCTCCT ACCCGCCGGG 2340 TCTTTCCCGT TTGTCAGGCA GGCCGGCAGG CTGGGCTGGT GACTCATGAC TGGCTGGGCC 2400 ATCTGCCCTG CACCCCTGCC CCGGGCGAAG TGAGAAACCT GACCGGGCTC CAGCACAGAC 2460 AGGAAACCCC ACCCCAGGGC CTGCAGTGGG ACAGGTGTGG CCGCCCTCCA CCCCCACACA 2520 GGCCTCGGGG AGGGTGTCTG AGGCCGGCCT GGCCCTCTCT GCAGCACTGA AACACCAGCT 2580 GCCTCTCCCC AGCCCGGAAC TGGGGATCCA GTGTCCTCCG CACTGACCCC AGGCTCTGCT 2640 CTCCCTGGGA AGCACCCGCT TTGACAGTGG GGCCAAGGAC TGGGGTTCCC ACCCTCCTCT 2700 GCCCAGTGGA CTTTGTGGCC CCAGGCAGGT GGCATCAGCT CTCTGGGCCT AAGCTTCTCA 2760 TCTCTGCAGG GTTCATCAGC TCAACAAGCA TTTGTGGGTT CCTGAGACCT GAAGGCTCCA 2820 CTCCCCCACC TAAGCACACA ACAGTCCAGG CACCACCCAC ATCTCCCTCT 2870
|