| Tag | Content |
|---|
EnhancerAtlas ID | HS098-07264 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr10:70825000-70826270 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOS | MA0476.1 | chr10:70825916-70825927 | TGTGACTCATT | + | 6.62 | | RREB1 | MA0073.1 | chr10:70826130-70826150 | ACACCAACCAACCCACCAAA | + | 6.11 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_09172 | chr10:70820083-70831788 | CD14 | | SE_53458 | chr10:70824406-70826563 | Spleen | | SE_56698 | chr10:70824100-70826766 | 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 |
| GH10I069064 | chr10 | 70823757 | 70826555 |
|
Enhancer Sequence | GGGTACTCTC CAAGCTGTCA TTGTGGGTTC TGTATCCTGC CCTCAGAGCT CAAGGCTTTA 60
TAGGGTCAAG CAAACTGCTC TTCGGAGTAC AGTGTGATTC TATGTGATAA ATGCTCTGCC 120
AAATCAACCA AGGTTTGCAA AGCACTGGAC GTACACTTTG GAGGGGAAAA TAATACAGGG 180
CTCTGCTGTG TGGAAGCTTC CAGAAGAGCG AACCTGACCA AGAACCATCC CTCCCTCCCC 240
ACACCATGGG TGTACAGCTG GCCCTCTGGG GCCTTGGAGT ATAGAGGAAG AGGGAGAACC 300
CACAGACATG CATAAGCTTG CTCTAGGCTG CCCGGGTTTC CAGCTGGGCA CCTTTGGTTT 360
TTCTTCCACT TCAGCTTCTG GCAGCTGGGG TTGGGGTAAG GGACCAGAGA GCTGCATTTA 420
TGTAGGAGAC AGTCTTGGTG GGGTGGAGTA AATGAATGTG TGCTCTTGTT TTTGTTTCTA 480
GGGAAACAGT GGAAAAGTTG CTAAATGTGG AAACCCAAGC TGTGGGTCTC TTTCTGGGGT 540
TTCTTTCTCA TCCTCTGTGT GGAGTGGCAA GTGGAGAGGA GAAAGTTTCA GAGGGAAGCC 600
AACCCACGCA GTAATTCCCC CAGGGACACA GGCTGAACTT GCAATCCCAG CGGGCAGGAG 660
GCGGGTTCGG GATTTCCTGG CTGGTCAGTA GGGTTAGAGG GTTCATTCTG AAATAAAGGG 720
GGTTTTCCCT CCATCACCAA TGAGATCAGA AGAGCTACCG TTTGGAAATA CAACCCTGTG 780
TGGAGGTAGT TTCAGCTCTG CTGGTGACTA AAGCTTGGGA GTGGGGACTT CCTCAAACAC 840
TTTTCTTCAG TCACTTTGAA AATGTCTGAC TCTTCTGGCT CCCTCAGACT GGAGTCTGTT 900
TTGCTGGGGC TTTTAGTGTG ACTCATTTTG TATGTCTTCC AAGGTGTCTT CACATTTAAC 960
AAAAATGGTT TGCTGGTTTC TTGTGTCTTT AAGGCCCAAG GACCTTAAGC TCTGTGAGGA 1020
CCATGGCTGC CTGGTGACTC GCTGGGCCTC CAGTGACCTC AGCACAGGAC CTGGACAGAC 1080
TGTGTTCTCC ACATACATGG CTTGTTCCAC AAACACTGCA GTTTTCCACA ACACCAACCA 1140
ACCCACCAAA CAAACAACCC AAATCACGCC AGTCCTGTCA TGGGGAATGG TTTTGTCATT 1200
TTAGCACATG AACCAGAATG GCAGGAGCCA GGAGAGAAAA GCATGTAGCT CTTCCAAAAA 1260
AGCTAATAAG 1270
|
