Tag | Content |
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EnhancerAtlas ID | HS098-56614 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr9:2411420-2412950 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MYCN | MA0104.4 | chr9:2411542-2411554 | GGCCACGTGGCT | + | 6.37 | MYCN | MA0104.4 | chr9:2411542-2411554 | GGCCACGTGGCT | - | 6.37 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr9 | 2411475 | 2412000 | chr9 | 2412000 | 2412200 |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I002411 | chr9 | 2411061 | 2414680 |
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Enhancer Sequence | CCTTTGCAAA ATATAATCTC ATATTGATTA TCACAGTCAT TAAGTTTGTG CGGAATTATT 60 TCATCTTCCT CTTCTGTGAA GCATATGGTA GGACTGTCAT TCTCCTTTTT AAATTTAGGT 120 GTGGCCACGT GGCTTGCTTT GGCCAATAAA ATGTGAGTAG ATGATATGCC TTTGCGGTGG 180 AAGCTTTAAG AGCTAATGTG TGCTTCATCA CATTCTTTCC ATTCTCCCAC AGAGACTGAC 240 AGCATTCCTG GTGGTGTTGC TTTTTTAAGC TTAGATCCCA GAAAGAGATT ATGCAGAGTA 300 GAGTTTCTAG TTGATTTATG GTTGAAATGG AGTCTGAGAA ACAAATCTTT GTCATGTAAG 360 ATTGTTTTTT GGGGCTGCTC GTTATTGTAA CATAATGTAG TCTTTTTTGA TTGATACAAG 420 GATCAGCGGC ACAGCTTATT TCTTACTGTA TTCCCACATG TTAGCACAAG GCCTGGTACA 480 GAAAGTATTT GTGATTTGTT GAATCAAATT TTAGAATCAG AGTTCTTCAA CGCCTGTGGT 540 GACAATGCAA AGATGGGGGC TGATATTCTG TGCCATTTGG TCTTGAGTTC TCAATACATT 600 CCATTCATTT TTCCAGCTGG AGGGACGAAG AATGACATTT GACTTAGTCG CAAATGGAAA 660 TCATTTTGTT TGGTACAAAG CCCATTGGAA AAAGGAAGAC AAAGGGCATT TCTTTCAGTG 720 GTAACCTGCT ACTGCATTTC CTGTAAACAC TAAATATTCT CCTCTGTTAG CCTATGAGAA 780 ATGGTGCTAG GTGGGAGAAG AGGCAAGGGT TTTCTTGTTT GTTTGTCTCT TAGCTCAAAA 840 GAATCAGGGG AGAAATCTCT TCTAATTACA GAGTTATGTG CTTTGGAAGG ACTTTTTTAT 900 TCATTAAGTC TGCCCACTGC CTATAAGTAA TCTATCTTGG AAAAGATGTT TTATTCTTAG 960 AAGTATGAAA CCATTTTTGG TCTCTGAAGC AAGATGATTG GATCCACCAA TAGAAAGTCA 1020 TATTCTCTTG GTCAGATAAA TATTTTATGC ATTTTATTTT TCAAATAAGT AGAGCAGTCA 1080 TGTTATTTAC TATCTAAGCA TAGAGACATT TGATCATGAA AGAGGGCACT GTTACCATTT 1140 ATACTAGGAC AACTAGCATA AAATGGTATT TTCCTGGGCA AACTATATGA ACACCTTACA 1200 AATAAGGCCA CTTATGAATG TAACTTTCAT AACATGTAAT CAAGTCATTA AGTCCCTTAT 1260 TCTGAGAAGA GCCAGCTGAC CAGGAGACCA AAAGGCCAAG AGAAAGAATG TCATCCTCAA 1320 TTAAGCATTT CAGTGAGTAA ATCATGATTC CATTAGTTGA TTGTTACTAA ACTTTCTTAA 1380 GACATGCCCT TAGTGAAACC TTTTACACCA GCGTACAAAT GCATGGACTA TTTGCCTGAA 1440 CTAGAAGGTC CTTCCCCGTC AGCAACCCCT GACTATAAGA CCCAGACTAA ATGTTATTTC 1500 CTCTGAAATG GCTTCTTCAC CATTCCTGGA 1530
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