| Tag | Content |
|---|
EnhancerAtlas ID | HS051-05417 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr11:123138100-123139530 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BHLHE40 | MA0464.2 | chr11:123139055-123139065 | GTCACGTGAT | - | 6.02 | | MITF | MA0620.2 | chr11:123139051-123139069 | AGATGTCACGTGATCATC | + | 6.09 | | MITF | MA0620.2 | chr11:123139051-123139069 | AGATGTCACGTGATCATC | - | 6.09 | | TFEB | MA0692.1 | chr11:123139055-123139065 | GTCACGTGAT | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TATGTTATAG ATAGATTACC TTGTTGCTTT AAAAAATGCA TACGTGAAGA CCGGGCACAG 60
ACGCTCACAC CTGTAATCCC AGCACTTTGG GAGGCTGAGG TAAGTGGATG GTTTGAACCT 120
AGGAGTTCAA GACCAGCCTT GGCAATATAG CAAAACCCTG TCTCCACTAA AAATACAAAA 180
ATTAGCTGGG TGTGGTGGTG TGTGCCTATA GTCCCAGCTA CTTGGGAGGC TGAGGCGGGA 240
GGATTGCTTG AGCCCAGGAG GTTGAGACTG CAGTGAGCCC TGAGTACACC ACTGAACTCT 300
AGCCTGGGCA ACAGAGTGAG ACTCTGTCTC AAAAAAAAAA AAAAAAAAAA AAAAAAGGAC 360
AAGTAATGTA TAATTATCTT TAATGGAGTT AAGTAGATCC AACAGGAAGT TTACAAAACA 420
TTAAGAAAGT GTTAGGTGCT GGGTTCTGTG TTTTGTCTTT GTGGTTTTGT TTCTGTTTTG 480
TCCTTGTATT TTAACCCAAC TTGGCATGTG GACCACTCAG AAAGTGAAAT AAATGTAATG 540
CTAAAATTTT TTTTTTTTAC TTCATGCCTT CCTCAGCCAG GACTTTGAGC TTCTTTCCCA 600
CCCTCCTATT TGAAGCAGAG ATTTTAATAA TATAACTTCA TCTACTTTCC TTTCCAAACG 660
GTAGGTGCAT CAGGGATCAG CAGACAGCTG CCAGGCGAAC AGGGGAGTGC ACGGGCCAGG 720
CAGGGGTTGC CCGTAAGCCC GCCACGGGAG GACTGGATTT CTGGGCAGAC AAGGAGGCGA 780
GACTGACAGT CACTTCTGAG TGGTCCCCTC GGTGCTGTCA CCGAACTTGA GACATGTAAT 840
CGTGATTTCA TCAAAGCCTT GATAGTTGCT ACTGTCTCTG TTCTCTTCTA TTTATTCGGT 900
GTGTAAGAGG GATGTTCACT GGTGCCTGTG AAGATGGTCA CAGCAAACAT TAGATGTCAC 960
GTGATCATCC TATTTGTTTC TAACTTCAGA GGAAAGGAAA GCACAGCTGG TTCCTCCTCA 1020
GTGCCATTGT TTCCCTCATC ACAAAGGATT TTAAACTCCT GCCATGTGGA CCCATCTCAT 1080
CTTCAGCTGT ACATCACTGA CTGCTTTGAG CAGAATCTTG GGATCAATAC TCTGCTCTAA 1140
ACATGACCCA AGAGCTCCAT CTGCATCATG AATGAAGAGG CGGCTGCTTC CCAGCATCTG 1200
GTTTCTGGGA GAGCAGGGGG CCAGGTCTGC CCAGGCAGAA TCTGACAGAG CTCAGGTACC 1260
TGCTGCTCAT GCACATTTCA GAGAGCAGTG AAACTTAAAA TGCATCCAGC AATTTCACTT 1320
CTAAAATCTG CTGTCCAGAA ATGCCCATGA ATGTTCACAG AAATGTTCAC TGGACGGTGT 1380
TTCTTTTGTC ATTCCTTTAA CAACAAAAAG GGTTGAAAAT AATCCAAATG 1430
|
