| Tag | Content |
|---|
EnhancerAtlas ID | HS034-11822 | Organism | Homo sapiens | Tissue/cell | ECC-1 | Coordinate | chr16:89219350-89220490 | 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 | CCGAGGTCGA AGCCAGTTGC CCCTGGAGAG CGAGAGACTG GGCTGGGCCG ACTCCCACCT 60
CTGTCGCGAG AGGCCTACGG GCAGGGGCAG GTGGGCAGGG GGACTGTGCT GGGTCTCTGG 120
CCGCGTCTGG ACGGCAGGCG ACACTTTCTC CACAAAAAGC GTCAAGAAAC CACGACACTT 180
GGTTTCTGGA CTTTTCCGCG GAACAGTAAC CAGAACAATC GCCATGAAGG TTCGTTTCTG 240
TCATGGCTCA GTGCAGCCTG GACGCCCTGG ACCAGCCCCT CCTGCGCCTG GGCCACGGCC 300
GCTGCCTTCA GGGCATCACT GGTGGGCGGC ACAACCATCC TCCCTTTGGG GGGTTAATTT 360
CATTTCTTTC CTCCCTTCTT TAATGGTGAA TGGAGGAGCA CCGAGCACCA CTGCAGTCTC 420
AGTTTCAGAT CCCAGCGCCT CGTCCCTGCC CACTGCCCTC GGCCCCGCCC GCCTGCATTG 480
GCAGTGCCCT GGCCCCACCC ACCCGTGTCA GCACCGCCCA CCGCCCTGGC ACCACCCACC 540
GAGTTCTCGC CCATGAGGAA GGGGGACCCT GAGTGGAGGT TTCAAACCTT AGGGGCCGTC 600
CCTGCCGTGC AGGGCTCTGT GAGGCCTCTT GCCACATAGG CTTGTGTCTG CAGGACTGTG 660
CGGCATTTAC TCCCATCTCA AATACCCCAT ACAGGGCAGA CTGCCCCTGC CCCACCTGCC 720
CACCCACTCC CCAGCCTCTT CCGCACGCCT CCTCTGGAAG GGGAACGGGC CACAGAGTGA 780
AATGGGGCCT TCCAGCTCCA GTGCGGGGAC TTGGAAGGCC TGGCCCGGTG TGGGGGCCCC 840
TCTGCCCTGC AGGCCACTCT GTGCAGGCCT ATCCTCAGGT GTGCCCTCGC CCAAGGCCTG 900
CACGCACCAT GGCTTCTGTG GTACCAGTGA TAACACCATG CCGGGCACCT CCTGCAGTCA 960
CCACCCCTGG GCTGCTAGGG CAGAGACAGC TGCGGTGGCC CGGTGCACCT GCCTGGCCTC 1020
AGGATGGCCG AGGCGCCTGG CAAGGCTGCA GGGTCCCAGG GGCACCTGTC CGTACTGCTG 1080
GGCGCCTGAG TTCCTCCTGC TGGGCACTGT CAGGGCAGTG CGCCTCAGGC TGTGCTTGTC 1140
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