| Tag | Content |
|---|
EnhancerAtlas ID | HS098-49394 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr6:108169130-108170470 |
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 | AGACCCTCTT TCTGCCAGAA CGCACGGGCT GTGTGAGGGG CGTCCTACTG AGGGTCGGGC 60
TTGATGGCCC GGGTCGGTTA TATCTGTCCC CCGGCTAGGA GAGGCTCTGA GGCAATAACT 120
GCAGCTGTTC CCCTCCCCCA GGACGGGGGT CGGGGGTCGG GCCTTGGGGA GCCCCCTTAG 180
GAGGCAAGGC GCTAGAAACT AGAGAAGCGA CAGGGACCCT TTTTTTGCGT CTGAGTCCAA 240
GGAGAAACAG CTGGGTCTAA GGGAGACGGT CGGGACTCTG GGTCTGACTC AACGAATGCC 300
GGAGGCCACC CTGAGCTCCA GAGTGGTGGA GTCCGGGACG TGGCTGCGAG GGGTCTGTGG 360
GAGCCGGGGG CACGGCAGCG TCGCTCCAGC CCCACTGGCC GGCCCGGGAC TCCAAGAAGA 420
GGCAGCGGAT CTCCCAGTCC CTGACCAGCC TGGCCGGGCC CCGGTCGGCC ACCTCGCGCC 480
CCCTGGTGGC CACAGAGGGA GAAGCCGCCC GCTCATTTCT CCTGCTGCCG CTGGAATCCG 540
GACTCCGGGG GCTGAGCGCC TGGACCGGAA GGAGGAAGGG AACACGGCAG AGTCCTCGGG 600
GGAGCTAGGG CTTCGTGGGG CAGGAAGAAG ACAGTGGCCG TTTCCACCGA AGACACCACG 660
TGCAGTGTCT TCACAGGCAA AGCAATCCCA GCTGTGAATC CCACGGAGCA CCTACCTGCT 720
CACCAAATTC TGGTGGCAGA ACGAAGCCTC CGGTTGACGT CCCCAGGGGA GATCCCCCGT 780
CGCTCCTGAG AACACCTTTG CCGACTCCCC TCTGCAGGCA TTAGGCCATT GGGGAACTGA 840
ATGCTTTCCT GGCCCCACCA GTTAGCCACC TTGTGTGATA CGGAAATCTC ATCTTTTCAA 900
ATATAAGACT TGTCAAGCTG TAGGAAAAAT ACATGTGAAC ATCCTCCTCA CTCAGCAGTA 960
ACATCCTCAG GCTCTTGCAG CTAACCCAAA ATGAAAAGAT CGAGGTCTGA AGACTTGGTT 1020
TACATTATTC ACACAATGAT TTCATCCTCT TTCCCCTTCC CTCAAGGCTG TGGGAATGTT 1080
CTCTAAGAGG TGGAAGAATC CAGACTCAGG TGTTCTGAGT GAAAATCAAG GGCAAGGGTT 1140
GTGCTTACGC CCCACGCGGC TCTTCCCCCA CCCCGCCCGT CCCCCAGCAA GTTAAGGGCA 1200
GAGTGGTCAG AGCCAACGCT GTATTCAAGA TGGCTAATTT TATTGGTCAG TTTGGCCAGA 1260
CCAAGGTACC CAGATACTTG GTCAAACATT GATCTGGATG TTGCTGTGAA TGTATTTTTC 1320
AGATAAGAAT AACATTTAAG 1340
|
