| Tag | Content |
|---|
EnhancerAtlas ID | HS062-04059 | Organism | Homo sapiens | Tissue/cell | GM18486 | Coordinate | chr12:99092290-99093180 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NKX2-3 | MA0672.1 | chr12:99092588-99092598 | TTCAAGTGGT | - | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr12 | 99092368 | 99092958 | | chr12 | 99092996 | 99093059 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH12I098698 | chr12 | 99092466 | 99093370 |
| Enhancer Sequence | TGTTGCAAGT AGAAAAGTTT TGGTTTTGGC CATGTTTCTT AGTATATATA ATACTTCTTT 60
TTACTCGAGA GATTTGAAAA TGTACCTGGC CAGAAAAATT AGGTTTTACC TGGGAGTTGT 120
GCTTTGGAAG CTGACTTAAA GCCTGAGCAG CAGCTTTCTC CCCCAACCCC CATCCTTCTC 180
CGTGGCCAAC CTTTGGTTTG GGCATGGGCA GTCATTATCA CTCTGTGAGG CTGAGACACT 240
GCTCATGGCC CAGAGGAGTG AAGGTGGATC TTCTTGAAGG CCTTTGTCTT TTGTGCTATT 300
CAAGTGGTCC TACTAGTGAG CAAAGTTTAC AGTATTTTGT ATCTCATTCC TCAGGATCCA 360
GTTAGTTTTG TAGCCCTATC TGGCCCTGCC AAGCACACAA AGAGTCTTGC TTGTCCCTGT 420
TTTCAGAGAC TTCCTTATGT CTCTGGATGC TCTGCTAGGT CACGACCTAA CTTGGACTGG 480
GTCCTGTGTA GTCTTCCTGC TGTGCATGTG GTAGGTTCGT GAAACACACT TCATTCCTGG 540
CACAGCAGAG GGCAGCAGTG GCAAGTCGTG AGTCTCTTCA TCTTACCACC TTTCTTCCAC 600
TTGTGTCCTT ACTGTCAACA TGTAATTTTT AGCTTCCACA CCATGCAAGA CTCTTAACTT 660
TTTATTTAAT TTTATGTTCT GCATTTTGGG CAGTGCTTCT AATTTTTTCT TTTTAAGAAC 720
GTAATAATGA AACTGGAGAT CTTAATTTAA AAGCCTTACA AAAAGTCATG CATAGGTAAA 780
AATAATTCAT CAAGTGAAGT GAATAAGTTT ATGTGGCATT TAATTTAGGA AAAATTCTAG 840
AAGTGTGATT ATAGAGTAAA ACAAACTTTT TCTTTTTTAT TACTTTAATT 890
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