Tag | Content |
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EnhancerAtlas ID | HS184-29231 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr8:40248150-40249130 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
LMX1B | MA0703.2 | chr8:40248724-40248735 | TTAATTAAATT | - | 6.32 | PHOX2A | MA0713.1 | chr8:40248725-40248736 | TAATTAAATTA | - | 6.62 | PROP1 | MA0715.1 | chr8:40248725-40248736 | TAATTAAATTA | + | 6.32 | PROP1 | MA0715.1 | chr8:40248725-40248736 | TAATTAAATTA | - | 6.62 | Phox2b | MA0681.1 | chr8:40248725-40248736 | TAATTAAATTA | - | 6.62 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AATAAAAAGA AGAATTGTCC TTAAATAAAA CCTCTTCTAA ACTTTAAGGG GTACTGTCTG 60 CCTATAATGG ATTATAAATA ATGCCCTGCC TGTACCCTAT ATTACATTTT TCCTGCTAAA 120 ATGCAACCCT TTGCTCACAC AAAAAGTTAT CTGACACCTT TTATAACCTT CTAGCAAAAG 180 ATTATGTTGC GGGCCTGGGG TTGGGAGAGT AGGGGTGAGA TTTCCCCTAA TAAGTTGGAA 240 ATAAAAGAAA GAAGATTTGG TTCCAAGGAT TTAGCTAGTA AAATCCACAT GCAATGTTTA 300 GAAATCTAGA TGAGTAAATA AGAGACTGTC TGTAAATATG TGGCCAAAGG ATTTGAATAG 360 TCCTCTTATT CCTCCCAAGG TGACCTGGGT CTCAGAGAGG CAGGACAGGA ATGTGGTTAC 420 TATTTAGCAA GCAAAAGCCC CATCGATTGC ATTGCAATGT ATGAGCATAA AGGGACAGTC 480 TGGATCATAA AAAATACAGC TCAACAGAAC AAAAATTGGC TGTGTTTTTC CAGCATTGTC 540 CAATCTAAGA AGACACTGAA TCTGTAAGAC AACCTTAATT AAATTACTAG AGAGGTGTTC 600 TGTATCAAGG GGTAGGAATG ATTCATCACA CCTGACATGG CCTGGATAAA AATCTCCCAG 660 ACTCTCCACC TCCCTTTGCT CTGATTCCAC GCTTACTATG CAACTTTAGA GTTATTATTT 720 TGACCTCCCC TGGAAGAAGC TGTCTCCCAG CAGGAGAAAT GAGAATTCCT TTCATTGGAT 780 CAAAATATCT TCCATTATGT ACCAATAAGT TTTGCATCTT CTGATGTGCT TTGATTTTAA 840 TTTGGTTACT GTGAGTCAGT GCCCTTGATG CAGTTTGACT CCAGGACAAT GACAAAGTTT 900 AGGACTCATA GGCACAGTAA ATTCACCAAG GTGAATGCCT CCCTGTGAGA TCACTTGGTA 960 AAGAACCATC CAGCCTTCAT 980
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