Tag | Content |
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EnhancerAtlas ID | HS133-02361 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:151537530-151538630 |
Target genes | Number: 25 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:151538456-151538474 | CCTTTCTTCATTCCTTCC | - | 7.88 | RREB1 | MA0073.1 | chr1:151537593-151537613 | CCCCACCCCACCCCACCTCG | + | 6.42 | ZNF263 | MA0528.1 | chr1:151538509-151538530 | CCCTCCCTTTCACCTTCCTCT | - | 6.16 | ZNF263 | MA0528.1 | chr1:151538440-151538461 | TCCTTCTTCCTCTTCTCCTTT | - | 6.21 | ZNF263 | MA0528.1 | chr1:151538444-151538465 | TCTTCCTCTTCTCCTTTCTTC | - | 6.32 | ZNF263 | MA0528.1 | chr1:151538491-151538512 | CTTTTTCTCTCTCCCTCCCCC | - | 6.38 | ZNF263 | MA0528.1 | chr1:151538497-151538518 | CTCTCTCCCTCCCCCTCCCTT | - | 6.66 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 151537867 | 151538409 | chr1 | 151537982 | 151538216 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I151565 | chr1 | 151537512 | 151538763 |
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Enhancer Sequence | TATTAATCTT GTATATAGTT ATGTCTAACC TGGGATGGGA AGTTCCTCAA GGTTAGGAGT 60 TCACCCCACC CCACCCCACC TCGTGTCTGT ATCCTCACCC TCCCATTCCC CCCAGGTCTG 120 GGATGTAGAA GGCATCAGTA AATGTTTGTT AGACTGAACA GATTGGGTAA GTCTTTCCTG 180 GGAGGGATAA TCCTGGGATC CTGCTTTTCA GTTTTTCCAA AACTCGAGGA CAGAAATGTC 240 CTCAGGAGAG CAGAGCTGTC TCTTTGTGAC TTCGCCCTCA TCCTTTAGAT TCTGAGTTGT 300 ATCCTTGATT TGCATTTTGG TTCAGGCAGA GTCTTGCTCC AGCAGCAGCC CCTGCCTTCA 360 TTCCCTTGAG GGGAACAGTG GCCCAGCAGC TGGTGCAAGG AAAGTTCTTT GTCTTGGGCA 420 TGCACTTGTG TGGTGGAAAT TACCTAATTT TTGCTTTGGC TGAAGGTAGG TCTTTCAGTG 480 CTTGAGCTCA CATCTGGCTG GTGGGAGCTA CTTTGTCAGG TATCAGAAGA ACCTAATGTG 540 TGCAGAGACT GGCCCAAAGT CCAGCCCCCT TGTTTGCACA AACCGGCTGT CATATGATGA 600 ATAATCAGGC TTTGGGTCAG AAATAATTGA AAAAGATCTT CCCTTTGTAA TTTTTGCTTT 660 GTCAAACTTT ATCAGGATCC CTGGGGGCAA GGGAAGCTCT TTGTTTGTGG CAGGCAGCTG 720 CATGTATTCC CTGGCTAAGA AGAATGGGCT ACACATACTT TTCCATCTGC TGAAAGATTT 780 TAGCCTGAGG TTTTTTTCAT CCTCCCTACA AGACTTTCAA GGCCCTTTCA AGGCCGCATA 840 ACATCTCTCC ACCCCCTCTT GTTTCTATTT TCTCATGGAA CGCTAGAAAT CTTTTCTTCT 900 TTCGCTTCGT TCCTTCTTCC TCTTCTCCTT TCTTCATTCC TTCCTTTTTC TCCCTCCCTT 960 TCTTTTTCTC TCTCCCTCCC CCTCCCTTTC ACCTTCCTCT CCCTCTCCCT GTCCTTCTCT 1020 TTCTAAGATT TGAGTGTTAG GAGAATAATG TTTCAAAGTT GGTTGCTTTC ATCTGTTTTA 1080 ACTACCAATT TTATTTTTCT 1100
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