Tag | Content |
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EnhancerAtlas ID | HS197-09615 |
Organism | Homo sapiens |
Tissue/cell | ZR75-30 |
Coordinate | chr17:79300960-79303940 |
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 |
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| 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 |
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| 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 |
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Enhancer Sequence | CCCCCCCGCC AGTCCCTGGT GACCCCAAAT CTTCTGTCTG TCTTTGTGAA TGGCCTGTTC 60 TAGAAGTTGC ACAGAAGTGG AAGCACACAC CACGTCCCTT TCTGTCTGGA ATTCCTCAGT 120 TAGCATAACG TCCCTGAGGT CCATCCACGC AGTAGCGGGT GTCAGATTTC CTTCCTTTTC 180 CAGGCTGAAC CCTGTTCCAC ACGTGGCTAG ACCACAACTT GTGTGTCTGT CCACTCATGG 240 GTCGACGGCA CTTGGGTGCT TCCACCTCCT GCTGGCCGTG ACCAGGGCTG CTGTGGACTC 300 TGGCGCTCTC GTCTGCACCA GCTGCTGCCT TCAGTTCTCT GGGGTCTGTA GCCGGAGTGG 360 CATCGTTGAG TCACGTGGGA ATCCTGTGCT CTGCTTTTTT TCTTTTCTTT TCTTTTCTTT 420 TTTCTTTTCT TCTTTTCTTG AGACAGAGTC TTGCTCTCTC ACCCAGGCTG GAGTGCAGTG 480 GTGCGATCTT GGCTCCCTGC AACCTCCACC TCCCGGGTTC AAGCGATTCT CCTGCCTCAG 540 CCTCCCAAGT AGCTGGGATT ACAGGTGTTC ACCACCACGC CTGGCTAACT TTTGTCTTTT 600 TAGTGGAGAT GGGGTTTCAC CATGTTGGCC AGGCTGGTCT CAAACTTCTG ACCTCAGGTG 660 ATCCGCCCAC CTTGACCTCC CAAAGTGCTG GCGTTACAGG CGTGAGCCAC CGCACCCGGC 720 CTATGCTCCA CTTTTTGAGA GGCCAACAAA CCCCACTTGC TTTTTCAATC CAGATTTTAA 780 CCTTTGAGGG AAAAGAAAGA TTTTTGTATC TATTCCTGGG CCGGGGTAGG GGGGCTGTTG 840 GGTGAGGAAC ACCCAAGAAC GGCTCAGGTG AGAGGGGTGG CCTCTAAGAC CACATGGCCT 900 GGACACAGCC TGGCAGGCAG ACCGAAGCAG CCGGGGCTGC CTGGAGGGCC TCAGTTCTGC 960 TCCTCCCCAG CTGCAGGATC TGAGCAGGAG GCCTCCTCAC TCTGCGCCTC AGTTTCCTCA 1020 TCTTTATCTG GGGACGGAGC AGCCTCTACC TCTCAGAGCT AGTTGCGATC ATGGTGGCAG 1080 CTGAGGCCCA GCCCTGGTAT GCAGTGAGGG TTCAACTGAG CCAGCCCCCA CTCGCCACAG 1140 GCTTGCCTGG GGAAGACAGG TGCATCAGCC CCGGGGTCCA TTTCGCAGTG GGGCTGATCC 1200 CAGCCCACCC TCACCCGCCC GGGAGCCTCG CCCTTCACCC CATGCATCTT CTCCCCTGAA 1260 TCACCCCCAG GGTCTCCAGG GCAGGAGCAG GGCTGGCAAG GGCAGGGCTC ACAGCCCCAT 1320 AGGGAGGACA CAGTGCCCGC AAGAGGGACT GGGCAAGAGG TGGACAGGCA GGGGGTGGGG 1380 GCATTCTGTG TGCCCCAGAG CCTGAGTTCG CAGGCTCTCA GCAGCCCGTG CTGGGCAGCA 1440 GTGTGGGCGT CTCTCCCGCA GGGCACCCTC TGCACTTTCC TGCAGACCTG CAGCAGCCCT 1500 TTCCTGAGGG ACACCTGGCT CCGGGCCCAG GGTGGGGGCG GGGCCTCGCG TGTCTCCCCC 1560 TTGATTTGTA AGAGTCCAGG GCTGTCGGCC ATGGCCACAC TGAGCACCCC TGGGAGCCAA 1620 GGCAGCTTAA GGACAAGGTG TGTATGAGGA CGGCGGGGCC CAGGGAGGAG AGGCTAGCCC 1680 AGGGCTACCC GGGTCCCCGG AGTAGGGGCA GGGGACTTGA AAATGAGCCC CCAAGGGGCT 1740 CTGATGGGGG CAATTCCAGG AGAGGCGTGG GCAGGTGTGG GGCTGGAGAG AGGCCTGTCC 1800 TTTTTCCCTT GCCCTGCACA CTGTCTGCAG GGTGGCAGAC CCAGGCTGCC TGGCGAGGCT 1860 GCTTCTGGAG GCCTGAGGAA GGCTGGGCTG AGGACTCCGC CTCTCCTCAA AGCCACAGCC 1920 TCCCTGCTCT GGGGCTACAT GTCGGGAAAA TCCCTGCCTG GGTTACCCCA GCTGGGGACT 1980 CAAGCTCTCT TTGGACCCTA CAGAAAGAGC TGGCCAGCCC CCAGGCCAGA AGGGCCGTCC 2040 GTGACCCACA GATGGCCCCA ACACACTGTA AAACACGCAT GATTTATTTT AGTGTGTGTT 2100 AGAAAAATAA AGCCAACACA TCAAGCCTGC AATTTCGCAG ATACTAACAC TTCGGACCAG 2160 GAAAAAAGAA GCCCATGACA TGGCACAGCG CTGTGGAGCG AGCGAGATCT GGGATGCGTA 2220 GGCCTGGACG GCTGAGGCTT GGAAACCCCT CCCCTCCCCA AACTTTCCCA CCATGCAGGG 2280 GCCCAGCAGG CCCTCAGCCC ACTCACCCCG CCAGAGGAGG GAGGAGGGAG GAGGGTCCGG 2340 GCCAGGTGGG AGCTTCTCCC CGGAGGCCTG AGGCAGCTTC CCTCCTCTCC CAGGAAGGGG 2400 CTGGCCCAGG CCCAGCTAGG ATGCTCCCAG CCCAGCTCCT ACCCGCCGGG TCTTTCCCGT 2460 TTGTCAGGCA GGCCGGCAGG CTGGGCTGGT GACTCATGAC TGGCTGGGCC ATCTGCCCTG 2520 CACCCCTGCC CCGGGCGAAG TGAGAAACCT GACCGGGCTC CAGCACAGAC AGGAAACCCC 2580 ACCCCAGGGC CTGCAGTGGG ACAGGTGTGG CCGCCCTCCA CCCCCACACA GGCCTCGGGG 2640 AGGGTGTCTG AGGCCGGCCT GGCCCTCTCT GCAGCACTGA AACACCAGCT GCCTCTCCCC 2700 AGCCCGGAAC TGGGGATCCA GTGTCCTCCG CACTGACCCC AGGCTCTGCT CTCCCTGGGA 2760 AGCACCCGCT TTGACAGTGG GGCCAAGGAC TGGGGTTCCC ACCCTCCTCT GCCCAGTGGA 2820 CTTTGTGGCC CCAGGCAGGT GGCATCAGCT CTCTGGGCCT AAGCTTCTCA TCTCTGCAGG 2880 GTTCATCAGC TCAACAAGCA TTTGTGGGTT CCTGAGACCT GAAGGCTCCA CTCCCCCACC 2940 TAAGCACACA ACAGTCCAGG CACCACCCAC ATCTCCCTCT 2980
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