Tag | Content |
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EnhancerAtlas ID | HS184-24094 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr5:63443560-63444670 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MAFG | MA0659.1 | chr5:63443892-63443913 | ATCATGCTGGGTCAGCAATTC | + | 6.37 | MAFG | MA0659.1 | chr5:63443892-63443913 | ATCATGCTGGGTCAGCAATTC | - | 6.6 | MAFK | MA0496.2 | chr5:63443893-63443912 | TCATGCTGGGTCAGCAATT | - | 6.28 | MAFK | MA0496.2 | chr5:63443893-63443912 | TCATGCTGGGTCAGCAATT | + | 6.52 | NFAT5 | MA0606.1 | chr5:63443925-63443935 | AATGGAAAAT | - | 6.02 | NFATC1 | MA0624.1 | chr5:63443925-63443935 | AATGGAAAAT | - | 6.02 | NFATC3 | MA0625.1 | chr5:63443925-63443935 | AATGGAAAAT | - | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CCCCCACTCC ATATCTCCAT TCCAAGCTAT ATTGCTTGTG TAATCTTGGA TTTACCTTTT 60 CCTGTTATGT ATGTCTTGTA TGTCTCCTCC CGACTGTTCA ATGAGGGCAC AGATTTCTGT 120 CTGTTTCACT CACCGCTGTA TCTGCAGTGC CTCGTATTTC TTCCACAAAG GATCTTCTCA 180 ATAAATGGTA CTTAATTTTT TAAATGCAGC TTTTCATTAC ACACTAGCAA CTGGAAAGGC 240 ATGCAATTCT ATTTCCAAAA TTCATTAAAC AAACGTGGTA AACATTCAGG CCAGAAGGCG 300 GCAGCAAAGC TTCATCAGCC CAGCAACCGG CCATCATGCT GGGTCAGCAA TTCAGAGGCG 360 CAACTAATGG AAAATTAGGC AGAACAGCTT TTCACCAGGG AGTCTGAGCT GAAGGAGGTG 420 AGGCCAGAGA ACTGAGCTGG TTAGGACTGC ACCCTGGCCA AAGAGCAGGG AGACAGATAG 480 GAAGAGAGAG AAAGGCAAGG CTTGTCCAGG AGAATGAGAC CCACATTAGG GGCTCACAGA 540 ATGAACATTC AGGTTGTCAG GGAACTTAAT CAGGTGCCAG AAAATTTGGC ATATTATCTC 600 AGCAAACTCA GGTAAACCTT TTGGCGATGT CCACAGGGAG GTTCCCTTTC AGATAACAAG 660 TCTATTTATC ACTGTAGCTA GAATCTGGGA GCCAAAATAT ACCTACCCCT ATTAAGACAG 720 GAGAATTATG CCAGTCCCAA CAAGTGTGTC ACCAAGCCGA CAAAAATAAG TAAAGTACAA 780 TCCCTAGCCT CTTGAGGATT ACAATCCACG GCAGAAAAGA TATGAAAGCT AATAATTAGC 840 TTTCCCTGAG GGCCATGTTT CTTTTCACAA TTGCAGTGCC ACATCTCATA CTTTGTTAAA 900 GAAAAATAAA GATGGCAAGT GCTTAGGTCT AGGCTGCTGC AGAAGAAAAC CAGATGTAGG 960 AGGAACTGTG ACTCTGCCTC TCATGCAGGC CTGAATCTGG AGTGTGGTCC TCCTGTGGGG 1020 TTGCACTTAC TCTGGATTTT TCCAGAAAGA CTGTCTATAG GTGCCTGCAT GCTGTGTTCC 1080 TGTGAGGGAA GCCCCAGCTG TGTCTGTGGT 1110
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