| Tag | Content |
|---|
EnhancerAtlas ID | HS184-16589 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr2:100252670-100253900 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SOX10 | MA0442.2 | chr2:100253724-100253735 | AAAACAAAGCA | + | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH02I099636 | chr2 | 100252644 | 100255510 |
| Enhancer Sequence | GATGAGGAAC TGTGGCCTAA TGTGGCTCCC TGACTCACTG GCTGGGAACA GGGTGAACAG 60
GGCCACAGGG AGGCCATGTG GGGAGCTGCC AGGGCTTCAG ACTCTTGGCC TGGGCTGGGC 120
TTCATCGAGG CCCTGTCCAG TCGGCTGGAT TGGGGCCAGT GAGCAGGCTT ACTTTGTCTG 180
TGAAATAGAA AAAGGGGCCA TGGACTCACC CTTCACAAGC AGTTGGTTCA CTTCAACATT 240
TTAATGGAAC CGACCTGAAA TTAATGAGCA CTGTCACACT GAGTAAATAC TGCCTCTCGG 300
GATGAGAGCG GCAATGGGTA GAAGGCAGTG TGACAATTCA AACCCAAGGC CACGGACAAT 360
TACATAGAGG AAGTCTGTTC AGAATTTGGC GGATCGAATG GCTGTCCCCA AATAACAGGC 420
ATGCAGATGG CTGGAGTCTG ATGCTGCCTG GCGAGGGCAG AGGCAGATGC TGCATTCTGA 480
GGGCCAGCAA GAGGACACGA CGTGGCAGTG GGCCAGCCAG CCACAGCCGG GAGCCAGCAC 540
AGGAAAGGGA GTTGGACGGA GTCAGAAGGT CAGGCCGCCC CAGTGAACAG GGAGCACATT 600
AACCTTTCCA AAGCCACGGG GGAGCTTATC AGGCTCCAAA ATGCAGTCAT CAAAGGCCAG 660
CCAGCCCAGT GCAGCCAAGG CTGGCCCGGG GCTACCTCTG GGAGCAGGTC ACGGGGCGGC 720
AGCCTGTGAG CGGAGGTGAG GGCAGGCCCT GTGCCCAGAG TGAGCAGCTG CAGGGTGGTG 780
TGCTCCAGCT GGCTCTGGGA GTCCCAGGCT GGAGAGTGGA ATGGTCAGGG TGGGACTGTT 840
CCAGGGGTGG GAAAAGGGGG GAAATGGAGA GGACGGGAGT GGGTAGAGGG TGCTGGCCTG 900
AAGGGCTCTT AAAGCCAGAG AGAACAGACT CCATGGGCTT TGGCCAGTTT TCTTTACTAA 960
AAGGAGATGA AAAACAGAAC AAAACAAAAC AGATTTGATA TCATGACTTT AACTCCCATG 1020
AAAAGTAGTT AAGTAGTTTG GTTTTAAACA AAGCAAAACA AAGCAAAACA CCTCAGTCTA 1080
TCTATTGGCT TTAAAACCAC CCACTCATCA CAGATGCTTT TGCGGCACGG CCTCCGCCCA 1140
CTGCAGGCAC AGGCATGAGT GATGAAGACA GTGGCACCTG TGTTCAGAAA CACATACGGG 1200
CACTGAAATG CATCTTTTTT GAATCTTTTT 1230
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