| Tag | Content |
|---|
EnhancerAtlas ID | HS139-13500 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr12:104764740-104766180 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GLI2 | MA0734.2 | chr12:104765722-104765737 | CGTCTTGTGTGGTCT | - | 6.17 | | LHX2 | MA0700.1 | chr12:104765557-104765567 | GTTAATTAGT | - | 6.02 | | SOX10 | MA0442.2 | chr12:104765323-104765334 | TTCTTTGTTTT | - | 6.62 | | mix-a | MA0621.1 | chr12:104765556-104765567 | AGTTAATTAGT | + | 6.14 |
|
| | 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 |
| GH12I104370 | chr12 | 104764596 | 104766378 |
|
Enhancer Sequence | GGGATTACAG GCATGAGCCA CCACACATTT TGCTTTTTAA AGCATTTACT TTAAAAATCT 60
CACCTCTTTC AATCCTCGTT CTGTTCATTG TTTGCTCCAA GTTCGAGGGG CCTGTCAGTT 120
CTTCCTGCAA ATAAAATCAG TGAACAACCC TGTAGGTACA CTTCAAGGTA TACAGGGGAG 180
CAGAGAATGC CGCCTGGGTA GGGGCGAGTG TTACTTCAGC GGCAGGGAAA GCCTCTGTCA 240
ATATTTGCGA GGAAGAGACG TCTCCAGAAG TAAGAAAGGC CACATTATGG AAATGGCATG 300
TTTTATGCAG GGAGACACTT GAGAATCAGG GAGAGTCAAT AAAGGGGCTA AGAAGGGTCA 360
AGAACTTGGG TTTGAGAATA AGGCGAGTCT ACTAGTTGAG AAGGAGAATA AGGCTTCGGT 420
AAGCCAGCCC CACCTGCCAC CTTGCCACCC CTTTTTAGGA AATAAGGGAC AGTTGCCAGG 480
GGCTGTTTTG TGACATAATC TAGAGGTATT TATGCCAAAA GGACTGACGG AAATACCACC 540
ACTGCCAACC ACGACAGCAT CCTGGTTCCC TAAACGGATG GGCTTCTTTG TTTTCCTTTG 600
TCACAAGGAA TTAGAGGAAT GTGGCTACAC CCGCAGCTTC TAACACCAGC TAGCCTGGGT 660
TCACATCCTG GATGAATCAC TTACTGTGTA ACCTCAGGCA TATTGTTTAA CCTCTCTGTG 720
CCTCAGCATC CTCAGCTGGA AAATGGGGGT GGCAATAGCA GCACCTCCCT TGTGTGGTTG 780
TCAGGACAAA ATAAGTTAAC TCAGGGAAGT AAGGAAAGTT AATTAGTAAA TAAGTTAACT 840
CTGGGTAAGT AAGGTATCGA GGACGGGGGC TGGCCTCTAG AACGTGCTGT GTTAGTGTTG 900
GTGATTCTTA CGTGTGAACC AGCAGCAGAT GGAAGGTCTG GCCGTTGAGG GATGCTACTT 960
TTTTCCTGAC GATGACTATG AACGTCTTGT GTGGTCTAAG ACAGCAGTCC TTTTTGGCAT 1020
CAGGGACCGG TTTCATGGAG GACGATTTTT TCCACGGTCG GGGGGTGAGG GGGGTCAGGA 1080
TGGTTTTGGG ATGAAACTGT TCCACCTCAG ATCATCAGAC ATTAGTTGGA TTCTCATAAG 1140
CAGTACACAA CTTAGATCCC TCGCATGCCC AGTTCACGAT AAGGTTCATG GTCCCATGAG 1200
AATCTAATGC CACCACTGAT CTGACAGGAG GCGGGGCTCA GACGATGATG CCAGGGATAA 1260
GGGGCGGCTG TAAATACAGA TGAAGCTTCG CTCACTTGCC CGCAGTGACT CGCCCCACTT 1320
CCTGCTGTGG GGCCCAGTTC CTAACAGGCC ACAGAGCGGA TGAGTACCGG TCCACAGCCC 1380
AGAGGCTGGG GACCCCTTGT CTCAGAGACA TCTTGAGAAC CTCTTTATTT CCTCTTTGTT 1440
|
