Tag | Content |
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EnhancerAtlas ID | HS182-10285 | Organism | Homo sapiens | Tissue/cell | Spleen | Coordinate | chr18:9965570-9966870 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HSF1 | MA0486.2 | chr18:9966183-9966196 | GAAAATTCCAGAA | - | 6.17 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ACTTCCTTTC TGCACATTAG AACAGGTAAA AGGAACATGG TGTCAAAAGC AGCCTAATTT 60 CACTCTTCTC ATTTGCTCAG ACACAACTGA TCTAGATTTC TAACAATGCC AGTTGCCTTA 120 TTTTGGGAAA CAATTTGGAG TTAACAGGGA TTGTATTCCA TTGATTTGCT AGGGGGAGAC 180 CCCAGCAATG TGGAAACCAT TCTAAAATGT GAGGAATATG TATTAGCGGT ATGTAAGTGA 240 CTGTCCACAA GAGGTAGTAA GGAATTGCAG GAATGCTACC TGCTTATGAA TGTTTTCTCA 300 CCAGGCTACA AGGACAGCTG TTCCCCTGCC TGGCTTGACT CCCCTCTCTA GAGCAAGTCA 360 TGAATGGGTT AGGACAGTCA GGGTGGGCAG AATAAAAAGG AGAACAGCAA GCTGTGCTTA 420 AGTGGAGAAC CAAGCAAGAA AAGATGGATC TAGATGTTTG TTTTTGCAAC TGGACTTCAT 480 TTTTTTGTAT TATATTCTGA TTTCCTTCTG GGCAGTGGTA TTACAGCAGT CCCCCCCCCA 540 CCCCCTTATC TGTGGTTTCA CTTCCTGTGG TTTCTGTTAT CTGTGGTCAA CTGTTATCTG 600 AAAATATTAA GTGGAAAATT CCAGAAATTA TAAGCTTTAA ATTGCATGCC TTTCTGAGTA 660 ACATGATGAA ATCTCATGCC TTCCCACTGC GTCCCACTGG GGACCTGAAT CCTTCCTTTC 720 TCCAGTGGAA TCATGCTGGA TGCTCCCCAC CTGAGTCGTT GACATGGTCT GCTCCTGACA 780 CCCAACCATC AGCATCGTCA TGGCTCGATG ATCCAGGATT ACCTGGAGTG AGTGATCCTC 840 CGATCTGTCA TCAGAGGGTC AACAGCAGCC TCATGCTGCA TCACCTCACT TCCTGTCGTA 900 GGCCTGCTCC TCTCACATCT TCACCAGAAG AAGGCTGATG CAGATGACCG CGGCTTATGA 960 CACTTTAACT TGGGATTTGA CTGTAAGGTG ATGCAAAGGT GATCTGCACT CAGGAAAACC 1020 CATACTTCCA GTACCATTCA ACATTGTTTT CCACTACAGC ACAGCATTCA GTAAATTACA 1080 CGAGACATTT GACACTTCAT AATGAAGTGG GCTTTGTGTT AGAGGACTTT GCTCAACTGT 1140 AGGCTAATGT AAGTGTTCTG AGCACGTTTC GGGTAGGCCA GGCTAAGCCA TGATGTTTGG 1200 TAGATGAGGT GTATTAAGTG TATTTTTGAT ATGCAGTATT TTAATGTGTG ATGGGTTTAT 1260 TGGGACATAA GCCATTGTAG GTTGAGCAGC ATATGTACAG 1300
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