| Tag | Content |
|---|
EnhancerAtlas ID | HS095-02166 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr1:159199000-159200070 |
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 |
|
| | 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 |
| GH01I159229 | chr1 | 159199105 | 159200234 |
|
Enhancer Sequence | GGCTAAACAT AGGCCTAAAT CTTTCTTACA GGAGCCAAAC ATTAAGTTTA GAAGCAACCT 60
TTTAATTCAT TAACTAGTCA ATGATTTGAC TCTGTAACCA GATCTTCATT ATACATTTTC 120
AAGATACCAG TCATCGAGAA GGATATGTTC AAAAGAAGGC CAGTCCCTTC TCTGGATGAG 180
ACGCTATCCT GGCTCAGTCC TGGATATGCC TGAGAGCAGG GAGGTATTGG TTTTTGCCTA 240
TGAGTGCCTG GGCTGTGGGC CCATCTCCAC ACACAGAGAG AATCAAAGGC GTAGAGAAAT 300
GTGTTTAGTT CGATGACAGG GCTAAGGCCC ACAGCTACAA TTTAGTCAGG ACATTGCCCT 360
TTGGCTGCCG CTCAGTGCCC ACAAATTCAG GATGTTGGCA CAGAAACAGG TGGTGTCCAT 420
CTGGGCTGGT GAAAGCACAT GATCTTCTCT TAACATGTGA TGAAGCAGGC ACCCAGAGCA 480
GCTCCCAAAC AGCAGGCTCT GTGGCCGCCT TCACTGCTGA TTCCATTACC ACTCCACCAC 540
AAGAGGTGAG GAGCAGCTGC CCCTCCGAAG GCCGTGCCCC AGGACCCACT TGCTTTCACC 600
TTCACTTCTC AGCTCCAGCC CTCCCCCACA GCTGTTTCAG AGGACAAAGA CACTTTATTG 660
CAATATGCAA AGCTCTCAGG ATGCAAACTA TATCTGGATT AACAACTATA AGTACAGTTT 720
TATTACTTCA GCTTGGCATT TGCTGACACA GAAAGCAAGT ATTTATTGTC ATCTCCATCC 780
TGCTTCCCAG TTTTAACTTT TGTTCTCCTG CCATCCAACT CCAATTCCAG AGTTATTTTC 840
TTTGCTTCCT CAGATTACTG AGGAGATAAT GTCCTTTCTA TTTGCCCTCA GGTCCACACC 900
TCGTTTTAAA GCCAAAGCTA TCACCCTGAC TACTGGATTC CAATCTGATG AGTGCTTAGT 960
TACTACCCCA AGATTTCCAT GAAGAAGCTG ATAAATGACA CATGTTTGAG AAAGCTTTAG 1020
GGGTCTTGCA AGCACAAAGG AGTCAACTCC TGATTAGATG AGAAAGCTAA 1070
|
