Tag | Content |
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EnhancerAtlas ID | HS026-16913 | Organism | Homo sapiens | Tissue/cell | CNCC | Coordinate | chr2:16360900-16362130 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
LMX1B | MA0703.2 | chr2:16361319-16361330 | TTAATTAAAAT | - | 6.62 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GTCTTTGGGG AAGACCAAGA AGCATGTGGC CTGCTCCTTG TCCTCACTCA TGACCTGCTT 60 GGTGAGAGCA GATAGTGACA AGCAAGGTTG TTTTATGGCA CGTGGGTGGG TAGCTGGGGC 120 TATGAGAAAA CTTCAGATGG GTGAAGGCTG ATCAGGGAAG GTTCCTGGAG GAGGGCAGAG 180 AGGCTCTCTG AGCATTCCAG GTGGGGAGAA ACCCCTGGAG AAAAAGTCTG GAAGCAGGAG 240 GACCCAGGCA GGCACCTGCA GGGAGGCTGA GGCTGTGGAG TGGAGAAGCT CCAGTGCTGC 300 CAGCCTGGCT CAGGAGCCTG TTTGTCTGTT TTCAATGTTT ATGGGATAGA ACAGCTTCTT 360 TACAGTGATC TCTTTTTAAT GGAGTTATTA TAGAGCAAAA GACGTGTTTA CCGGAAAGTT 420 TAATTAAAAT GTACTTCCTT GGGAATTATG TCCCAGGAGC AAATGAGTTT AAGCAGGTCA 480 CTTGGCACAC ACCCGTCCGG AGGTGCTGAT CTCATTCCGG ACTCCAGGGA GAGGTGTGGG 540 AGGGGGTCTG AGCAAGGCAG GAGAGGAAGT GAGGTGGGGG CAGGGGAGGC AGCGAAGGGC 600 AAGTGTGTTT GCTGTTCCTG TAGGAGCTTG TCTCGGGCAG ACTTTCCAGG CTGTGGGGAA 660 GCAATTGCTC CTCCTGCCTG GGAGCCAGCC TTCTGCAAGG GGCTTGAGAC ACAGTAGACA 720 GCTGCTTCTG TGATCTCCAA GTGAATTTTC CAGACAAATG ATTCCTGCCT GCCTGATGAT 780 AAGTCAGGCT CTTCCACCTT GTTACCTAGG GTACCTTCTT CAGCCCTGCA GGGGCCTTTG 840 AAATTTGAAA ATTGCTACTA AAGCTGTCAA AGAGTTCACT CTGGTGGAGG ATGAGATGAG 900 AAAGACAAGA CAGCCCCAGC AAATGAATCC ATCAGCAGGG CCTTGCTGGG TGTGAAGAGG 960 TCCTTGGTCC TAACCAAGGT ACAAGGAGAT ATAAGGCACA GCTTTTGCCC TTGATTCTCT 1020 CTCTTGTTGG AAAAGCAAGA AGGTCTAGAA ACATTTATTA AGTCCTCAAC ATGGTCTGGC 1080 CCTCTTCAGC ATGATAGTGG TCTAAACCCC AAAATAACTG CCAAACGATT GGTTTAGCAT 1140 CCGTGGTGCC ATTTTGGAGA ATTCTGAACA AGGCACGATG GGTGCAAAGT GATGGGGTTG 1200 GCGAGTGGTG GGTCTGAGCC TGGATCTCGG 1230
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