| Tag | Content |
|---|
EnhancerAtlas ID | HS139-50115 | Organism | Homo sapiens | Tissue/cell | Myotube | Coordinate | chr7:32731490-32732980 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr7:32731669-32731688 | TAGCCAGCAGATGGCACTA | + | 7.97 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr7 | 32731794 | 32732055 | | chr7 | 32732282 | 32732456 | | chr7 | 32732366 | 32732625 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH07I032691 | chr7 | 32731540 | 32732212 |
| Enhancer Sequence | AGAGGTGGGT GGGTGAGGGA GAGAAGAGCC ACTGAGATCA TCACAACTCA AACAAAACTA 60
AAACAAGTGT AATACATGTC CCTTGAGTTC TCTTGCTTTC TCCCATTTTC TATTAAAACA 120
TGTGCAAACT AGCACCTTAA CACTTTTTGT AATTTCATGA CAAATGCTAT CATATTTCAT 180
AGCCAGCAGA TGGCACTAAG TATACATAAA ATGAACATTT TGCACACTGT CACTTTTTTT 240
TTTTTTCTCT TGAGACAGTC TCACTCTGTT GCCCACGCTG CAGTGCAGTG GCGCAATCGT 300
GTCTCTCTGC ATCATGGGCT CCAGCGATCC TCCTGCCTCA GCTTCCCGAG TAGCTGGGAC 360
CACAAGCGCC TACCTCCTAC TTATTTTAAA AGAGTTCAAT CCAGGCTCTA CTGTTCTCAA 420
GGGACTTTTC TCCATACTAG GAACTCTAAA ATCTGACAAT GGTCTGGATC TCTGAGATAG 480
GCAAGGCATC TTGTAGGTAC AGGGTCCTCT CTTCTGCCAG GGGCTACTGT GCTGTAGTCT 540
CAGAGGGATT TCATCAGGGG ATCCCAGTAA GGTTGTAAAA TGAATAATGA TCTTGGTGGC 600
ACCACACCAT CTCTGTGTAG TGAGGAAAAC TTATGTAAAA CTGGAACGGG TGAAGGGGTG 660
AAACTAGGAA GGTTTCATAG CTGTTAGAAG AGGGGGAACA GGATTGGGTG GGTAAAGCCT 720
TCAGCTGTGA GGCCTGTTGA CATCTATGAA AGAGGAAGAA AGCAGGAGAG CCTCCAGCTG 780
CAAAGGACAG CTGACCAGGG CTTGGCTTGC TCAGTGAGCA GCTTCAGAGC AAAGATTGCC 840
TGATGAAGCA GTTCAGCATT GGGCTGAAAC AGCCAGGCCC TACAGTACCC TTCTAATCTG 900
GTTTGGCTCT GTCCCCACCC AAAATCTCAT CTTCAATTGT AATCCCCATA ATCCCCACAA 960
GTCAAGGGAG AGACCAGGTG GATATAATTG AATCATGGGG GTGTTTTCTC CCATGCTGTT 1020
CTCCTGATAG TGAGTTCTCA CGAGAGCTGA TGATTTTGTA AGTGTTTGGT AGTTTCTCCT 1080
GCGTTCATTT CTCCTTCCTG CCACCTTGTG AAGAAGGTGG CTTGCTTCCC CTTAACCTTT 1140
TGCCATGATT GTAAGTTTCC TGAGGCCTCC CCAGTCATGC TGAACTGTGA GTCAATTAAG 1200
CCTCTTTCCT TTATAAATTA CCCAGTCTTG GGTATTTCCT TAGAGCAATG TGAGAACAGA 1260
CTAGTATATC TTCCTTGCTC AGTCATTGGC TGGGGGTTGC CTAGGAAGAA GAATGTGGTC 1320
CAGCGTGAAT GCCATGCAGA TGCTGATGGC TCTACAGTTG AAGGCTGTCA GTTAACTCTG 1380
TTCCCTGCAG CTGGGCAGCA GGTTCTCAGA GGAATACCCT AGAGGTTGTG TACTTTTGTG 1440
GCTGCCACAC CATCCTTATT AAAGAAATAA CTCTCATATG TATGATCCCC 1490
|
| |
|
|
|
