| Tag | Content |
|---|
EnhancerAtlas ID | HS184-12918 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr16:89219420-89220490 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myod1 | MA0499.1 | chr16:89220331-89220344 | AGAGACAGCTGCG | - | 6 | | Myog | MA0500.1 | chr16:89220334-89220345 | GACAGCTGCGG | + | 6.32 | | TFAP2A | MA0003.3 | chr16:89220470-89220481 | CGCCTCAGGCT | + | 6.14 | | ZEB1 | MA0103.3 | chr16:89220060-89220071 | CCCACCTGCCC | + | 6.14 | | ZEB1 | MA0103.3 | chr16:89219434-89219445 | GGGCAGGTGGG | - | 6.14 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AGGCCTACGG GCAGGGGCAG GTGGGCAGGG GGACTGTGCT GGGTCTCTGG CCGCGTCTGG 60
ACGGCAGGCG ACACTTTCTC CACAAAAAGC GTCAAGAAAC CACGACACTT GGTTTCTGGA 120
CTTTTCCGCG GAACAGTAAC CAGAACAATC GCCATGAAGG TTCGTTTCTG TCATGGCTCA 180
GTGCAGCCTG GACGCCCTGG ACCAGCCCCT CCTGCGCCTG GGCCACGGCC GCTGCCTTCA 240
GGGCATCACT GGTGGGCGGC ACAACCATCC TCCCTTTGGG GGGTTAATTT CATTTCTTTC 300
CTCCCTTCTT TAATGGTGAA TGGAGGAGCA CCGAGCACCA CTGCAGTCTC AGTTTCAGAT 360
CCCAGCGCCT CGTCCCTGCC CACTGCCCTC GGCCCCGCCC GCCTGCATTG GCAGTGCCCT 420
GGCCCCACCC ACCCGTGTCA GCACCGCCCA CCGCCCTGGC ACCACCCACC GAGTTCTCGC 480
CCATGAGGAA GGGGGACCCT GAGTGGAGGT TTCAAACCTT AGGGGCCGTC CCTGCCGTGC 540
AGGGCTCTGT GAGGCCTCTT GCCACATAGG CTTGTGTCTG CAGGACTGTG CGGCATTTAC 600
TCCCATCTCA AATACCCCAT ACAGGGCAGA CTGCCCCTGC CCCACCTGCC CACCCACTCC 660
CCAGCCTCTT CCGCACGCCT CCTCTGGAAG GGGAACGGGC CACAGAGTGA AATGGGGCCT 720
TCCAGCTCCA GTGCGGGGAC TTGGAAGGCC TGGCCCGGTG TGGGGGCCCC TCTGCCCTGC 780
AGGCCACTCT GTGCAGGCCT ATCCTCAGGT GTGCCCTCGC CCAAGGCCTG CACGCACCAT 840
GGCTTCTGTG GTACCAGTGA TAACACCATG CCGGGCACCT CCTGCAGTCA CCACCCCTGG 900
GCTGCTAGGG CAGAGACAGC TGCGGTGGCC CGGTGCACCT GCCTGGCCTC AGGATGGCCG 960
AGGCGCCTGG CAAGGCTGCA GGGTCCCAGG GGCACCTGTC CGTACTGCTG GGCGCCTGAG 1020
TTCCTCCTGC TGGGCACTGT CAGGGCAGTG CGCCTCAGGC TGTGCTTGTC 1070
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