Tag | Content |
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EnhancerAtlas ID | HS121-38373 |
Organism | Homo sapiens |
Tissue/cell | LNCaP |
Coordinate | chrX:24750570-24751870 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HOXA13 | MA0650.2 | chrX:24750744-24750755 | GTTTTATTGGG | - | 6.62 | MSC | MA0665.1 | chrX:24751457-24751467 | AACAGCTGTT | + | 6.02 | MSC | MA0665.1 | chrX:24751457-24751467 | AACAGCTGTT | - | 6.02 | MYF6 | MA0667.1 | chrX:24751457-24751467 | AACAGCTGTT | + | 6.02 | MYF6 | MA0667.1 | chrX:24751457-24751467 | AACAGCTGTT | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH0XI024733 | chrX | 24751147 | 24751781 |
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Enhancer Sequence | GGTATGTATT TTTTTTTAAG CTGGCTTACT AACAGCTTGA TTTGAATTTC CTTATTTTTT 60 CTCCAGCTAT TGGATCAGTA ACTTGTTTTT CAAAAATTGT TTTCAAGAAT AGTGCATATT 120 GTTAAAGAGG GTTTTGTTTT TTTTTGTTTT TTTTTTTTTT GCCATGGAAA CTAAGTTTTA 180 TTGGGTTGGT TGCCTCCTAT TCAGCTGGTT CATTTTTTTT TTTCTAGGAG AAGTCTGGAG 240 TCTATTTGAC ATCTTTTTTT TGTTTCAATG GTTGCTCTAC TGAGGTTGAG TAGTTTTTTC 300 CTGGGTCAAA ATTAGACTTT ATTTTCTGAT GTCATTCTAA TAGCCTATCA TAGAAGCTTG 360 ATCAAAGTTT TCTGTGTGAT GAGGCAAGAT GCCAAGGAAT AAATATTTAC CTATTTGGGA 420 GGAGTTATAG TAATAAGAAT TGGAGTTGGG TTGTGCTATG CATAAAATTC AATGGATGAA 480 ACAATTCCAC CAAGTTCTGC ATATGTGTTT TATGAGTCAG TCTCCAAGGA GGATTCTGAT 540 ATATTCCATG TTGAGAGCTT GGCCAGTTAC CTAAGCATTT TGCTGTTTTT TAAAAAAGGG 600 AATAATACCA TTGACCTATT ATATTTCCTG GGATCTTTTT CAGCCCAGAA GCAGAGATTA 660 ACTTGGCGAG CCTCTCGTCT GGTTTTCTTG GGTGTTAGGA AAGTAGGACT AAAACATGCA 720 GAGAAGGGAG TATGAGATAT GATTGTTGTG AAGTTTTCCC CCTTAAGTGG GTGGAACACA 780 TGGAACAAAA TGGTGATGAG AATAGCCTGG AAAATATGTA GAAGAGAGCA ATCATGAGTT 840 CATTTCAACA CGCATTTATT CACTTCCTCT ATGTACGTCA CTATGTGAAC AGCTGTTGTG 900 TATGGTAAGG AACTTACAGT GTGTAATAGG GGAAGCTTTG GTCAATTTTA CCTTTTCAGA 960 AGGCTGAACT GAGTTTCTCC GCTGTATGTT GCTTGCGGCA TTGGTGGTGG TGGGATTTCC 1020 TTTGAGGAAG ACTGCTAAAA TCTTCCATTC TGGCTTCAGT GGATAGATAG CAAATGTTTC 1080 ATCAAAGCAG TTTTAACAAC TGCAGGGACT TAGGGTTCTG TGCTTGACCA TTCTTTTGAG 1140 GTCATCAACA TGACCAGTGG AAGTATTTGA TGACCCTCCT AATTCTTTAG GGTTGGGGGG 1200 AATATATTTA AGACAGTTTC GTTTGGAAAC ATGTACTATA TGATTACCTG AAATTAGACT 1260 AAGATGGGTG TTGGAATCTT TATTTTTTTT CCTTTTTACA 1300
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