| Tag | Content |
|---|
EnhancerAtlas ID | HS051-05738 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr12:8861910-8862810 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr12:8862275-8862296 | CCCTGGTTTCACTTTCTGTGG | + | 6.04 | | IRF2 | MA0051.1 | chr12:8862259-8862277 | GGACAGGTTTCACTTTCC | - | 7.16 | | Myod1 | MA0499.1 | chr12:8862161-8862174 | AGCAGCTGTTGCT | + | 6.59 | | POU2F2 | MA0507.1 | chr12:8862425-8862438 | ATATGCAAATTAT | - | 6.44 | | Pou2f3 | MA0627.1 | chr12:8862423-8862439 | TAATATGCAAATTATC | + | 6.53 | | RUNX1 | MA0002.2 | chr12:8862288-8862299 | TTCTGTGGTTT | + | 6.32 |
|
| | 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 |
| GH12I008709 | chr12 | 8861797 | 8862830 |
|
Enhancer Sequence | TTTTGACTTG TCAGCATTTC TGTTTTTTCC TGTTTTTCTT TTTTCTTTAT GTTAGCAGAT 60
GGGAAAAATA GAAAAGTAGA TGTTTTGAAA TTCTGTTAAG AGGAAACAGC TGTGCCCAAG 120
GCTAGGAGAG AACCATTGAG GGGCAGAAGC AGGCAGGCAC GCCTGGAGCC TCTACCTTTG 180
GGATTGAAGT CTTCACCCAA CACTTCTGGC ATCTCAGATG TGAATCCAGT TGGAGCACCC 240
CTAAGAAGGC AAGCAGCTGT TGCTGCAGCA GCCCTTGGGG AGGCCCCATC GCTTGGGCAC 300
CGAGGAAGGC TAGCCGCATG TCCTCCTGTG GGAATGGCAG TGTACCACTG GACAGGTTTC 360
ACTTTCCCTG GTTTCACTTT CTGTGGTTTC AGTTACGCCC TGACACAGTA CAACAGGATA 420
TTTTGAGAGT GGGAGAGACA CCGCATTCAT ATAACTTTTA TCATAGTATA TTGTTATAAT 480
TGTTCTATTT TATTGCTAAC ATCTTACTGT GCCTAATATG CAAATTATCA TAGATATGTA 540
TGTTTAGGAA AAAACATAGT ATATGTACTA TCTGCAGTTT CAGGCATCCA CTGGGGGTCT 600
TGGAATTATC CCTTGTGGAT ATGGAGGGAC TACTGTACCT GGTAATCAGA GATTTAATGT 660
AGAAAAATGT GGTTTTTGTT TTGTTTTGTT TTGAGATGGA GTCTTGCTGT TTTCCAGGCT 720
GGAGTCCAGT GGCATCATCT GGGGTCACTG CAGTTTCGAC TTCCCAGATT CAAGTGATTC 780
TCCTGCCTCC GCCACCTGAG TAGCTGGGTT TACAAGCATG CACCAACACA CCCGGCTATT 840
TTTTTTTTTT GTATTTTTAG TAGAGATGGA GTCTTAATCA TGTCAGCCAG GCTGGTCTTG 900
|
