| Tag | Content |
|---|
EnhancerAtlas ID | HS121-37869 | Organism | Homo sapiens | Tissue/cell | LNCaP | Coordinate | chr9:136644010-136645030 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFE2L1 | MA0089.2 | chr9:136644035-136644050 | CAGTGACTCAGCAGC | + | 6.01 | | Nfe2l2 | MA0150.2 | chr9:136644033-136644048 | CTCAGTGACTCAGCA | + | 6.6 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr9 | 136644597 | 136644729 | | chr9 | 136644520 | 136644570 |
| Enhancer Sequence | CCTGCAAAGG ATAGGACAGC TCACTCAGTG ACTCAGCAGC TCACTCGGTG ACTGACTTGG 60
CCCCGGCCCG CAGCCCACCC CATCACCAAG CTCGGCCTCC CCCAGCACAC ACAGCCTTGC 120
GCCTGCATCT CCCTTCCCTA AATCCTTCCC ATAAGCCTCA TGTCTTTTTG ATAAATATCA 180
TAATTATTTA TGCAATAGAC AGATTCAGGG GTCATCATGG AACAGCAACT TATTTTCAGA 240
TGGCACTTTG TGTTTTCTTC CAAACACCCT TCAGATCTGT GGCCCACAGG CAGCTGTGCG 300
GGGCAGAAGA CGGGGGATCC CTCGTGTCAG AGACGGGCGA CGGGTCAGCA GGCCCAGCAG 360
CTTGCCCAAG GCCACAGAGC TCACAGAGGT GCTCTGGGCC TGAAATGGGG GTCCTGGCTG 420
TGCCTCCAGG GAATGTGGAG GCTGCTCTTA GACAAGCCTT GCTCTGACCC AGCCCTGCCT 480
GTAGCTCTCA AGGAGCCCAT GGCTCTCCCA GCCCAGCTCC CGCCTGGCCC AGCAGCAGCA 540
GCAGCATTTT TCATCTTTTG TCCTCTGCCG ATGAGGGTGA GGCTGTACTG AGCACTGCCT 600
GGACTGCACT CAAGTTTGCA GAGAACACGA TGCTTTTTAC GCTGTGTCTA GAAGCACGTT 660
TCCATTAAGC AACCCGCAGC AAGGCAGGAA GGGGATGGAG AACGTGGTGG GAGAACAGCA 720
GCGCCTTTTG ATCTCAGGTC TCTGGCTGCA GTTCGGTGGC CCTCCCTGGC TAGAAGGCCC 780
TTGCTCCTCT GCAGGCTGGG TCCTGTCCCT ACAGCCTGGT GCTGCCTTAT CAGAAACAGA 840
GCCACCTCCC AAGGAGGTGC CATAGAGGCC AGAGAGGCAA GAGGGAGGGG GCCCAGATGG 900
CAGCATCCAG GAGCCTGGAG CGTCTGGTGG CTGGGCAGAC CTGGCCATCA CCACACCTAG 960
GCCCTGGCTC AGCTCCCAGG TGATGGCTGA CATGGGTGAT AGCAGAGGGC CCAGGTCCAG 1020
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