| Tag | Content |
|---|
EnhancerAtlas ID | HS098-36756 | Organism | Homo sapiens | Tissue/cell | HSMM | Coordinate | chr22:31259000-31259840 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Rhox11 | MA0629.1 | chr22:31259279-31259296 | AAGCTGCTGTAATTGAA | + | 6.09 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr22 | 31259093 | 31259264 | | chr22 | 31259285 | 31259814 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH22I030863 | chr22 | 31259261 | 31260025 |
| Enhancer Sequence | GGGCAGGCTC CTAACTCTTC ATGCCACACC CTTTCCTCTT CTGGGGGTGA CACTTGCAGA 60
ATACCATGTA ACATGTGGAA ACCACCCAAC AGCTGGAAGT GCAGAGGAGG CAGTCACCCA 120
GCAACTGGGC TGTTCGTTCT CAAACACGGT GACGTTGCTT GATATCCCCC AGACTCCCAC 180
CCCAAGCCTT TCTCTCTGTT ATCAGCATCT GGCCGATTGG ATTTTGTGAT CAGGCTCAGG 240
CAGCTTAACA GCCCTCCCAA ATCTAAATCA AAGTCACCAA AGCTGCTGTA ATTGAATGTT 300
GGAGGCGCCA ACCACACGGG CTGGGAATGG CTGTTTTCTG GCGAGGGTGC AGTTTTCTGG 360
CGAGGGTGCA GCGCCCCCGC AGTCCTCACT GGAAACCAAT GACACCACTG CGCTGTTTCT 420
CCTCAGAGCC CCCACGTGGG GGTGGAATGT CTTTTTGCAT AGCCAGACTG TGACAAAATA 480
GGATGCATGC CCTGCTTAAA GTCGGTAGTG CTCAAGATGC AATGAATGCC CTGCTCTGGG 540
GGTCTGGAGC CTTGTGATGG GAGTCCCAGA GAGCAGTGAC CGCTTGAGGA CAAGGTCATG 600
GGCTGGAAAG TTGCCAGGGC TCGGGGACTA GGCCTTGCCC ATTCCCAGTC CTGCATACTT 660
GAACTTCGCT CTGCAGAGAG GGGAGGGACA GCAGTGCCTG TCTCCATTAA TCACACTGTG 720
GGCCCGAGGG AGGTCCACTG GTCAGAGCGA ATCCTGCTGG TGACTGACAG TTGGATATCA 780
GCCTCCGACA CAGCAGCCCC TATACTGCAC TGATGCAGGC ATGCCTGCTG TGGGGAGTGG 840
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