Tag | Content |
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EnhancerAtlas ID | HS028-00194 |
Organism | Homo sapiens |
Tissue/cell | Colo829 |
Coordinate | chr1:159199120-159200140 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr1:159199587-159199608 | ACTTGCTTTCACCTTCACTTC | + | 6.01 | Myod1 | MA0499.1 | chr1:159199551-159199564 | AGCAGCTGCCCCT | + | 6.18 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I159229 | chr1 | 159199105 | 159200234 |
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Enhancer Sequence | AAGATACCAG TCATCGAGAA GGATATGTTC AAAAGAAGGC CAGTCCCTTC TCTGGATGAG 60 ACGCTATCCT GGCTCAGTCC TGGATATGCC TGAGAGCAGG GAGGTATTGG TTTTTGCCTA 120 TGAGTGCCTG GGCTGTGGGC CCATCTCCAC ACACAGAGAG AATCAAAGGC GTAGAGAAAT 180 GTGTTTAGTT CGATGACAGG GCTAAGGCCC ACAGCTACAA TTTAGTCAGG ACATTGCCCT 240 TTGGCTGCCG CTCAGTGCCC ACAAATTCAG GATGTTGGCA CAGAAACAGG TGGTGTCCAT 300 CTGGGCTGGT GAAAGCACAT GATCTTCTCT TAACATGTGA TGAAGCAGGC ACCCAGAGCA 360 GCTCCCAAAC AGCAGGCTCT GTGGCCGCCT TCACTGCTGA TTCCATTACC ACTCCACCAC 420 AAGAGGTGAG GAGCAGCTGC CCCTCCGAAG GCCGTGCCCC AGGACCCACT TGCTTTCACC 480 TTCACTTCTC AGCTCCAGCC CTCCCCCACA GCTGTTTCAG AGGACAAAGA CACTTTATTG 540 CAATATGCAA AGCTCTCAGG ATGCAAACTA TATCTGGATT AACAACTATA AGTACAGTTT 600 TATTACTTCA GCTTGGCATT TGCTGACACA GAAAGCAAGT ATTTATTGTC ATCTCCATCC 660 TGCTTCCCAG TTTTAACTTT TGTTCTCCTG CCATCCAACT CCAATTCCAG AGTTATTTTC 720 TTTGCTTCCT CAGATTACTG AGGAGATAAT GTCCTTTCTA TTTGCCCTCA GGTCCACACC 780 TCGTTTTAAA GCCAAAGCTA TCACCCTGAC TACTGGATTC CAATCTGATG AGTGCTTAGT 840 TACTACCCCA AGATTTCCAT GAAGAAGCTG ATAAATGACA CATGTTTGAG AAAGCTTTAG 900 GGGTCTTGCA AGCACAAAGG AGTCAACTCC TGATTAGATG AGAAAGCTAA CTATGCAAAA 960 GGAAGGTGGC CAGTCTTTGT GATATTTCAT TGGTCATATT CCCCCTGAAA TGTTGTTTAA 1020
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