Tag | Content |
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EnhancerAtlas ID | HS139-19522 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr15:85186960-85188070 |
Target genes | |
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) |
SNAI2 | MA0745.2 | chr15:85187290-85187300 | TGCACCTGTT | - | 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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Enhancer Sequence | ATACAGAAAA GAGAGGCTTG ACAATGAGTC CCTAATTTTA TTTTAAAATA ATTTTCTTTC 60 TATTTTTAAT AGAGATGGGG TTTCACCATG TTGACCAGGA TGGTCTTGAA CTCCTAGCCT 120 CAAGCGATCC TCCCATCTCA GCCTCCCAAA ATGCTGGGAT TACAGGCACC CAGCCCCTAA 180 AATACTTTTT ATAATTTGTT CTATGGTACC AAAACAGGCT ATTGGATGAG GAATCAAGGC 240 ACTTAAAAGG CTAACCACGG GCAAGTAGCA TCTGCCCTCA GTGTTGGCAG CTGATGACTC 300 CGTGGGGCAT GTAACCATGA GCATCCGTTG TGCACCTGTT ATGCGTGAGG CTCGAAGGCT 360 AATTCTGGAC AAGTATTAGC TCTTTTAATC CTCAGAACTG TATGACACAG ATACTGTTAT 420 TTTACCCAGG AAACTGAGGC TTAAGAGACT TCTTCAAACC TTTTCAAGTT GCCCCAGAGT 480 CCAGTCCCCT ACCTCTGGGT CCCTTTCAGC AGATGGCCTT GTCTCCTACT CGATGGGGGA 540 AACAGAAGCC TTTGGAGAGA AATACCTTCA CGTCCCTGCA CGATCTAGCT GCACACACAC 600 TCATTCCATC CTGCCATCTT CCTGGTACTG AAGAGCCAGC CCCTCTACCT GAGCTTGGCT 660 CTTCTGTTCT TTCTGGATCC TGGCATTTCC AATCATCCTT TCTTGCTCTC TTAATGATTT 720 TTTTCAACCC CCACCTGCCT CGACGGATCC TTCCTGTTGG CTTTTAGATA CCCACATTAA 780 GTGCCGCAAG CAACTAGCTA CCACCAGACC AGAACCAGGG GCCTGCTGAC CTAGCTGGCT 840 TGCTACTTTT TTTTTTTTTT TTTTTTTTGA GACAGAGTCT TGCTCTGTCG CCAGTCTGGA 900 GTGCAGTGGC GTCATCTCAG CTCACTGCAA CCTCTGACTC CCGGGTTCAA GCGATTCCCC 960 TGCCTCAGCC TCCCAAGTAG GTGGGACTAC AGGCGTGCAC CAAAACACCC GGCTAATTTT 1020 TTTTATTTTC ATAGAGACGG GGTTTCACCA TGTTGGCCAC GATGGTCTCG ATCTCCTGAC 1080 CTTGTGATCC ACCCGCCTCG ACCTCCCAAA 1110
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