Tag | Content |
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EnhancerAtlas ID | HS161-01299 |
Organism | Homo sapiens |
Tissue/cell | PC3 |
Coordinate | chr1:178653360-178654780 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2C | MA0497.1 | chr1:178654285-178654300 | TTCTATTTTGAGATT | - | 6.23 | Nr2f6(var.2) | MA0728.1 | chr1:178654656-178654671 | TGAACTCCTGACCTC | - | 6.22 |
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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 |
GH01I178683 | chr1 | 178652525 | 178655460 |
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Enhancer Sequence | CCTGAGGCTG GGAGCTTGAA ACTAGCCTGG CCAACATGGC GAAACCCTAT CTCTACTAAA 60 AATACAAAAA ATTAGCTGAA TGTGGTTGCA CATGCCTGTA ATTCCAGCTA CTCAGGAGGC 120 CGAGGCTGGA GAACTGCTTG AACCTGGGAG ACAGAGGTTG CAGGAAGCCA AGATCACACC 180 ACTGCACACC AGCCTGGGCA ACAGAGCGAG ACTCTGCATC AAAAAAAAAA AAAAAAAAAA 240 AAAAAAAGCA AAATTTATGT GGGGACAACA GTTAATAAAC AAGTAGATAA ATGAAACAAT 300 TACAGATTGT GAGAAGAAAT GAAGAGATGA AAAGCGTACC TTATTCAGAG AATGATGAGG 360 GTGGGCATGG GGGAGGGTGT CTGCTTGGGT GGTGAAGGCC AGGCTCTCTG AAGAGCTGAT 420 ACTGGAAAAC TTAACCAACC CATGTGTCCT CCTTTTGAAG CCCTCACAGG CCTTGGCATA 480 GAGGCTGAGC ACATGAAGAT CTGCTAAAGT GAATGGGAAA CTAGGGAAAT GAAAATAAAT 540 ATCTAGCTTA GTGTAAAAGT AAGGAAATAT TTTTTGAAAA TTGAAACCTG TTGGGTAAAG 600 GTCATGCTCT CTTAGAGCTT TTGAAAAAAA ACACATCATT TAACAGTCAT TAAGAAAAAA 660 TGTGTGACCA CAGGAACTGC AGAGTTCATA GGTTTCAATA CATATTTCAA AACAAGCCTC 720 AGAAATAACA ATCCAATGTG TCATTGCTAT ACAACTCCTT GAAAAATAAA TCCACAACAA 780 AAGGAAAAAA ATAAGACTAT TTTGCAGTCC AGATATCTAA GTATTAAAGA ACTTATAGGA 840 GCCTCTGAAA ATCCAGTAGG CATGTTTATG TCTTTATGAT GATCTTCTCC CCTGGATAAA 900 TTTGTTTTTA GAAAGAACTA AAAACTTCTA TTTTGAGATT GCTCTGTACA CATGCATGAT 960 ATTTGACCAT GTAGAGTCAT GAACATGCTC TGTCTATACA TTCACATACA TAAAGACAGG 1020 GGGATGTGGA AAGGATATGG ATTTAGTCAG ATAGAATTGG GTCCCAATTC TGGTTCCAGT 1080 ACTTTTTTTT TTTTTTGAAA CGCAGCTTCA CTCTGTCATC CAGGCTGTAT TGCAATGGTG 1140 TGATCTCAGC TCACTGCAAC ACCCGCCTCC CAGGTTCAAG CGATTCTCCT GCCTCAGCCT 1200 CCTGAGTAGC TGGAATTGCA GGCACCCACT GCCACACCTG GCTAATTTTT GTATTTTTAG 1260 CAGAGACGGG GTTCACCATG TTGGCCAGGC TGGTCTTGAA CTCCTGACCT CAGGTGATCC 1320 ACCAGCCCCA GCCTCCCAAA CTGCTGGGAT TACAGGCATG AGCCACCGCG CCCGGCCTGG 1380 TTCCACCACT TATTAGCTGT GTGATTTTGA ACAAGTTATT 1420
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