Tag | Content |
---|
EnhancerAtlas ID | HS147-18908 | Organism | Homo sapiens | Tissue/cell | NHEK | Coordinate | chr18:4831140-4832820 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TP63 | MA0525.2 | chr18:4831320-4831338 | GACAAGTTACAACTTGTA | + | 6.71 | TP63 | MA0525.2 | chr18:4831320-4831338 | GACAAGTTACAACTTGTA | - | 6.82 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TAGATGATTG ATTGATCAAT CAATAGATAG GGAAATGAAA AATGAAGCAC CTATGTTATG 60 TCAGGGAAAC TAGTTCTTTG TGATATTCAC AATTAGAAAA TTAGCCTGAG TAATGCTGTT 120 TCCCCACACC CATACTCAAA GGTGATGTGA TAAGAGCTGA TGAAAATGCT CCATACAAGT 180 GACAAGTTAC AACTTGTAGA TGGGGGGTGG AAAATAATGT CTTCTCTTCA CTTAGACACA 240 AGAGAAGATA TAAAAGGAGG AAAGAAAAGC TCTGATCCTT GCAGACAGGA TGGAAGGGAT 300 CCTAGGTTCT GATGGTAACA TATTGCAACG TCAATCAGAT CTTTCCAAGA GCCAGATAGC 360 CCCACGTGTT TCAGCTTTTA TAACCTAGGA ATTCAAAAGT AAAGACTTTG AAAGATTAAT 420 AGAAATGTGT CTTGAAGAAA GTTATGTAAT GCTTTTCAAT GACAAAGAGA ATTCTTATAC 480 ACTTTCACAC ATGCACACAC ATAATCACTC AAACCTGTTA TTTGAGATGA TTTTCACAAA 540 TCTCTGTTGT TACCTATGTC CTGTTTATTG CTAATAGGAA GCCTGAGCAG AGGGGACCGA 600 CAATACTCTT GGGAAGGGCC AATCTTCTTA TGCTTCTGAA TCATAGTGTC CTCATCTATT 660 AATATGATGG AGTGGTTACT TTAATATACT TTAAGCTCTA TCATATTATG GTTTTACGTT 720 TGGTATGTAA GTGATCTGTG AAAAGAATAA AAGATTATGG GAATTCCCTT GTCCCATTGC 780 ACACCCTTTA ATCTGCCTGG AGGCACAATT CTGTACATTG TGTCTTTGGA GTTCTCTTGG 840 CAGCCAGCTT TCAGTTGGGA TGGGTCAGTG AGAGGCAGCA GCAAGAGACA GTTGTCTTGG 900 AGAGAGAAAA TGGATTGTTT TCCAAGTTCT TACCCTGCTT GGTGCCACTT ATTTGCCAGG 960 AACTACATTC CGCCAGCTCC CACCAGGCAG CCCTAAGACC CAATTCCAGC TCTGCCTGGA 1020 GGAAGGTAAC AGCTTCCTGC TCTGATAGTT GCTAAGCGTT TCATCATCCC TTCATCCTGC 1080 CTACACCTCT GAAAGCAGTC CTTTCATTGA AGTTTCTTTA TTGAAACATC TGGCGTAAAT 1140 TCTGTTTCCT GCTGCAACTC CGATTGACTA GAAAGGTCAA AAATCCAAGT CATTTGTATT 1200 TGATTTTGGA ATATATTTTC AGTTGTATTT TTTAAAAAAT ACATTGGTCT AATGTTTTAG 1260 AAATCCATAC CACTTTAAAG ACAAAATGTA TCCAGTGAAC CTCTAATTCA GGAAAAACTA 1320 TAAAAAGTTC CATTTAATCA CCTGTTCAGT ATTCCTTCCT GCTTCTCAGT CCAAACTCCC 1380 AGTAATCCAT CTTGCAGACA AATGCAAAGC ACTGGCAGAG ATTTACCTGT GAGGCTGATG 1440 CACTTCTCAG TTGGAAGTAA TAATTAAATG TTTTGATTTA AAATGTTTCT CACTAGAGAG 1500 TTGACTGTAT TAATGGTGGG AACACAGACA TAAAACACTG AATTTTAGCT GCTTTAGGTA 1560 TTATGCTCTG CTGAACTGTA TTAATAGGAA CTCAAAAGCA ATATTTGTTT CATATTACTC 1620 ACAGTGGTCT GTGAATTACA TTGCAAGACG GAAAGTCTGA ATTCAGTTCT TGCTTTTGAG 1680
|
| |
|
|
|