| Tag | Content |
|---|
EnhancerAtlas ID | HS051-14126 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr19:30321660-30323080 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr19:30322524-30322536 | AAACAAACAAAC | - | 6.32 | | IRF1 | MA0050.2 | chr19:30322545-30322566 | AAAAAGAAAATGAAAATGAGT | - | 6.61 | | Klf12 | MA0742.1 | chr19:30322236-30322251 | AAGATGGGTGTGGTC | - | 6.18 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr19 | 30322926 | 30323060 | | chr19 | 30322162 | 30322300 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I029830 | chr19 | 30321661 | 30323070 |
|
Enhancer Sequence | TAATTTGCTG CAGATACTTC AGTTCCTGCA CCGACAGACA ATTGCAGTCT GTATCCAATG 60
AGCACAGATT TTTTCCTACC TCGTCCCAAT TCCAAATTTA ACTTCAGAAG ACTCTAATGT 120
ACTCAGTTGC ATAGGCTTAC CAGGTACTCT TTCCTGGGAG CCTCACATGG GAGGGCAACA 180
CTATCCTTTA TTCAATAAAC AGCATCCCCC ACCTTTTAAA TCATTTTCCT GATCAATGCC 240
AATTCCAAAA GTTGTGTGGT ATCTGATTAT GCAGTGCGGT TCAAGTCAAA TGCTGGCTTC 300
CTTGGGGTTG GTGAGTGAGG TGCCCTCGAT GGAGTCCCTG CTAAGTGTAC ACTGCCAGTC 360
CTGGAGACAT GAACTCAAGG GAGCCTGGGA GACCGGGGAA GCCCTGGAGT CCCCGGAGGG 420
CACTGGTATG AAATGAAAAG GTGGCACTCT AGGAGCAGAG CAGCAGCAGG ACTCAAGCTC 480
GGGAGGTGGG GCTGTGGAAT GCTCTCCAGC AGTCACAAAA GCCCTCACAA ATAGGGTAGA 540
GGAAGGCCAC ATCACAAGGG GCTTTTGCCG TCAACTAAGA TGGGTGTGGT CTCCCCCGCA 600
GCAGGAAGCC GGTGTTTGTA AGACAGGAGT GACTTGCTCA GAGCCGGTTT GGAGGAAGAG 660
GTTGATGAAC AAGTACAGAG TTATGTGTCT TTGTGCCGTA AGAAAATGAC TGTGCAAGTC 720
GGGCGTGGTG GTGTGCACCT GTAATCCCAG CTATTGGGAG GCTGAGATGG GAAGTATCGC 780
TTGAGCCCAG GGGTTTGAGG CTGCAGTGAG GCATGATCAC ACCACTGTAC TCCAGCCTGT 840
GCAACAGAAC GAGACCCTAT CTCAAAACAA ACAAACAAAA AATCAAAAAA GAAAATGAAA 900
ATGAGTGTGT AGTGTGTGGA GGACAAGCAG GCAGGCAATG AGGACATTCG TAAAATCAGC 960
TGCATCACCA TCATTTCTAA ATGGCGCTGC CTGCATATCT CCCCAGGCCC CCGTGATTCT 1020
GCTCCTGTGC CCCTGCCCAG GCCTCTGCCT ACAGTGGCTG GACCCCACCT CCTGCAGGAG 1080
TGCACCCCTG ACGTTGGCCC ACACTGATGT CATTTCTTCA CTGGGTTCTG GAGGCAGTTG 1140
ACTCATGTGG GAAGCCGGCT CTGCCACTTC CCAGAGTGGT CTTGGGCTCT GTGCTTCATT 1200
TCTCCAAGCT TCGTGTTTCC CAGCTGTGAC CTGAGGATGA CAACATAGTG CTTCCCCCAT 1260
GGAACCGAGG GGAGATGAAA TGAGGTCACG CATAGATATG TTGAGCACAG CGCTTGGCAC 1320
ATTAAAGAGA AACAGCAAAT GACAGCTGAT CCCTCTTATT GCCACCACTG GGTTCACTGT 1380
CACTGAGCTA GGCTGTTCTG TGAAGGATTG AGCATTCTCT 1420
|
