| Tag | Content |
|---|
EnhancerAtlas ID | HS108-35308 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr6:108169110-108170460 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr6:108169603-108169622 | TCGCGCCCCCTGGTGGCCA | - | 8.78 | | Myod1 | MA0499.1 | chr6:108169249-108169262 | TGCAGCTGTTCCC | + | 6.98 | | Myog | MA0500.1 | chr6:108169248-108169259 | CTGCAGCTGTT | - | 6.02 | | Tcf12 | MA0521.1 | chr6:108169248-108169259 | CTGCAGCTGTT | - | 6.62 |
|
| | 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 |
| GH06I107847 | chr6 | 108169005 | 108170204 |
|
Enhancer Sequence | TTGGGGTGTG CTGGATCTGG AGACCCTCTT TCTGCCAGAA CGCACGGGCT GTGTGAGGGG 60
CGTCCTACTG AGGGTCGGGC TTGATGGCCC GGGTCGGTTA TATCTGTCCC CCGGCTAGGA 120
GAGGCTCTGA GGCAATAACT GCAGCTGTTC CCCTCCCCCA GGACGGGGGT CGGGGGTCGG 180
GCCTTGGGGA GCCCCCTTAG GAGGCAAGGC GCTAGAAACT AGAGAAGCGA CAGGGACCCT 240
TTTTTTGCGT CTGAGTCCAA GGAGAAACAG CTGGGTCTAA GGGAGACGGT CGGGACTCTG 300
GGTCTGACTC AACGAATGCC GGAGGCCACC CTGAGCTCCA GAGTGGTGGA GTCCGGGACG 360
TGGCTGCGAG GGGTCTGTGG GAGCCGGGGG CACGGCAGCG TCGCTCCAGC CCCACTGGCC 420
GGCCCGGGAC TCCAAGAAGA GGCAGCGGAT CTCCCAGTCC CTGACCAGCC TGGCCGGGCC 480
CCGGTCGGCC ACCTCGCGCC CCCTGGTGGC CACAGAGGGA GAAGCCGCCC GCTCATTTCT 540
CCTGCTGCCG CTGGAATCCG GACTCCGGGG GCTGAGCGCC TGGACCGGAA GGAGGAAGGG 600
AACACGGCAG AGTCCTCGGG GGAGCTAGGG CTTCGTGGGG CAGGAAGAAG ACAGTGGCCG 660
TTTCCACCGA AGACACCACG TGCAGTGTCT TCACAGGCAA AGCAATCCCA GCTGTGAATC 720
CCACGGAGCA CCTACCTGCT CACCAAATTC TGGTGGCAGA ACGAAGCCTC CGGTTGACGT 780
CCCCAGGGGA GATCCCCCGT CGCTCCTGAG AACACCTTTG CCGACTCCCC TCTGCAGGCA 840
TTAGGCCATT GGGGAACTGA ATGCTTTCCT GGCCCCACCA GTTAGCCACC TTGTGTGATA 900
CGGAAATCTC ATCTTTTCAA ATATAAGACT TGTCAAGCTG TAGGAAAAAT ACATGTGAAC 960
ATCCTCCTCA CTCAGCAGTA ACATCCTCAG GCTCTTGCAG CTAACCCAAA ATGAAAAGAT 1020
CGAGGTCTGA AGACTTGGTT TACATTATTC ACACAATGAT TTCATCCTCT TTCCCCTTCC 1080
CTCAAGGCTG TGGGAATGTT CTCTAAGAGG TGGAAGAATC CAGACTCAGG TGTTCTGAGT 1140
GAAAATCAAG GGCAAGGGTT GTGCTTACGC CCCACGCGGC TCTTCCCCCA CCCCGCCCGT 1200
CCCCCAGCAA GTTAAGGGCA GAGTGGTCAG AGCCAACGCT GTATTCAAGA TGGCTAATTT 1260
TATTGGTCAG TTTGGCCAGA CCAAGGTACC CAGATACTTG GTCAAACATT GATCTGGATG 1320
TTGCTGTGAA TGTATTTTTC AGATAAGAAT 1350
|
