| Tag | Content |
|---|
EnhancerAtlas ID | HS051-20410 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr3:185278870-185280200 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Arntl | MA0603.1 | chr3:185279311-185279321 | GGTCACGTGC | + | 6.02 | | EWSR1-FLI1 | MA0149.1 | chr3:185279945-185279963 | TCTTCCTTCCTTCCTCTT | - | 6.04 | | Foxd3 | MA0041.1 | chr3:185279648-185279660 | GAATGTTTGTTT | + | 7.22 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_29288 | chr3:185278960-185280302 | Fetal_Intestine_Large | | SE_32145 | chr3:185278687-185279995 | Gastric |
|
| | 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 |
| GH03I185561 | chr3 | 185278989 | 185280188 |
|
Enhancer Sequence | GCCCAAGGGA CAGTTCTTAG ATAAGACCCC CTGGTCAGCG AACATCGGTA TGATCGGGTG 60
ACCACGTCTC TCAACCAACT TCCCTGCTGG AGGGGTGCCT CCAGGAGGGA AGGAAAGTGG 120
CTGATTATGA TTGTCCTCCT AATATGCAAG TTCCCATTTC CTATTTCCAG CATCAGCCTT 180
TCTGGCCTTG TCTTTTTTCT GTTTTTCTGG AGTACGAGGG GAGTTTGCAT GCTGCCTCCT 240
GGGTTTTATT CCAGCTAGCT GTAGCTTTCT TGCTGCCTAC AGAGGCCTGG GGCAGGAGAG 300
TTGCTAAGAT GCCAGGGAGT GCCCATTTGG TCACTGGCAG TCTGGGCAGG TTACCCCTTT 360
CTGGGTTTAT GGTGACGGAG GGGAGGCCAA AAGGCACAGA GCAGGCAGCT CCAGCCAGGT 420
CCTGAGGATC CGCCTCACCA CGGTCACGTG CCTTAGTAAC TGTGCCCAGG AAGTGGCCTG 480
CTGCTGCTTT TCCTACTTCT GCCCTTCCCT GCCACCCCTC GCATGTCTCA GTTGACAAGC 540
AATTTGTTGT CTTCCCTGGC CCCCTAGGGA AAGCGGTAAA AAACAGTCCA TGTGCACCCC 600
AACCTTACTA GCCTAAGGTG GGCAAAGGAG TGTGAAGCAG CCTAGAGTAC AGAGCCCTGG 660
GGGAGGAGCC CGCTAATAAG GGGCGCTCTC CTGTAGCCAT ATATTAAATG CTAACTAGGC 720
TAAGGTGGAG GAGCTCTGCC AGCTGCTGTC ATCTTCAGAA GACAGACACA GCAGTAAGGA 780
ATGTTTGTTT TGCTTTTTTA TAAAATGTTT AAAAACACTG TGGCTAAGAA ACTTCAAAGC 840
AGACCCTGTG CTGCATGTGT GCTCCTCCCC TAAGCCCCTC TGCTTGGGGG TGGTAAAAAT 900
AATAAAAAGA ACATTTTCAG TACCTTACCT AACAGGGTTG GCTCCAGGCG TAGGTGGCCT 960
AGAAGATAAG GGGAGTGGTT TTCTCCCAGC CTGTTACTCT CTTGCCTCCA GCCTCCGCGC 1020
TTACACACAC ACTTTACCAC CCTGTCATTC TCTAGCCTCT TACTGCCACT TGTAGTCTTC 1080
CTTCCTTCCT CTTAGGGTAA GGACAGCAAC AAGTGGCAGG CTATTAAAAA TAGAAGCTGC 1140
CTAAGGAGCC CAGAACGAAT AAAAAGAAAC CAGCCACAAC CCTACTTTCC CGAGCTCACT 1200
TCTAAGACAT TCCAGCTAAA GGCTGATGCA GGAAAATGGC CAACACCAAA GGACATTTTT 1260
TAAAGTTTTT TTTTTTTTTT TCTGTTTTCT ACACACTTAA GCTAACTCAA TGCAGGTTTA 1320
TTATCCTGGC 1330
|
