| Tag | Content |
|---|
EnhancerAtlas ID | HS184-31466 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr9:123148480-123149710 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myod1 | MA0499.1 | chr9:123148660-123148673 | TGCAGCTGTTTCT | + | 6.29 | | Myog | MA0500.1 | chr9:123148659-123148670 | CTGCAGCTGTT | - | 6.02 | | Tcf12 | MA0521.1 | chr9:123148659-123148670 | CTGCAGCTGTT | - | 6.62 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_46508 | chr9:123145781-123150508 | Osteoblasts | | SE_56084 | chr9:123148691-123149587 | u87 | | SE_67660 | chr9:123148691-123149587 | u87 |
|
| | 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 |
| GH09I120385 | chr9 | 123147732 | 123150170 |
|
Enhancer Sequence | TGTGGCTACT GCCATCCCAG GTGAGCGCCG GCCTGAGGCG CGAGGATTTT ACTCTCCAGG 60
ACCCCGATAG GGACGTTGGG ATGTGGGCCT CGGAAGTGAG ATAAAAGCAC CATTTCCAAG 120
GTAGGGCAAG CAGGGGGCCC TGGGCCTGTC TCCCAATCCT CTCACTATAT ATTTAGTCCC 180
TGCAGCTGTT TCTCTCAGGT GCAGCTCCTC CAGCACACGT GGTGATTAAT TTCACTGAAG 240
GGAAATTGAC GCATTTTCTG ATTACTGCTT CAAAGCCTCC CGAATTCAGC TGCTGGTAAA 300
ATTAACTCAC CAGGGACAAT GGAGCTTTTT CCAAGGTCCA AATTGTCTTA TTTGCAGTTT 360
GTTCTTGGCA TTAATCCAGC CCAAACAAAC CAGGCTGCTC CTCCACCTCC CAGAAGAGGG 420
AGGGCCTTCA CTAGCCCAAG GTTGAAAGTA TTTTACGTGA CTCTAAACTG GCGGATAAAA 480
ATGCACTTCG TTTTAGATTA TTGTGTTCCT GAAAAGCTGT GGGTGACCTG AAGCAAATGG 540
CCAGCTGGGC TCCTGGAGCC CCTCCTCTGC AGCTCCTGCT CCAGGCGTGC CTGGGTTCAC 600
CAACCAGACG GGCCTGGGAT GTACCAGAAT CCAATGTGGA TCTCTCCTCC AATCCCTGCA 660
CCTCAAGCCC TTGCCAATGA CCAAGTTCAG CTCCCATGGG CTGTGCACTG ACCATGTGCC 720
AGGCAAGGTA GGACTCTTCC CCTGTGGGGA CATCTGAGCC CAGGTCTGAC TTCCAGGCCT 780
TGCCTGAGCT GCATCTACTA CACTGTACAA CCTCCTCCCC TCCTCCCCAC TGCCCCCGCA 840
ACCACACATG CTTACATTTG CGCACACCTG CCTGGAGGGT AAACACCCTG ACAGCAATAG 900
CTTAAGCACA ACCTTAGAAC GACCCTGTAT GGCAGACGCG TCTTAATGTT GTTCTGAGCT 960
AGAGAATCTA GGAGTGGCCA ACCCGGAGAT TTGTTCCTTG TTTGTGAGGA GTATCTGAGC 1020
CCCCAAGCCC GTCTCATGGG ACATGGGCTG TACAGGGAAC TGAGGCCCTG AGTTTTGGGT 1080
TAAAAAAAGG TTCCCAGGTA GAGGTCCTTG GGGGAAGGTT AAGTGAAAAT GCTATATAAA 1140
CTGCATGCTG TTTATAAGTG GTGATGGTTT TCCTGCCCCA CCTGGGCCGT GGGCTGTGTT 1200
GTTCAGCCGC TGCCACTGAA CCATCTGTTT 1230
|
