Tag | Content |
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EnhancerAtlas ID | HS051-05366 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr11:121243300-121244430 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr11:121244408-121244420 | AAACAAACAAAC | - | 6.32 | IRF1 | MA0050.2 | chr11:121243964-121243985 | ATTTACTTTCTTTTTCAGATT | + | 6.92 | ZNF263 | MA0528.1 | chr11:121243527-121243548 | GGTAGAGGGGGAGGTGGGGGA | + | 6.06 |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I121371 | chr11 | 121242341 | 121245978 |
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Enhancer Sequence | AGCACAAAAA CTGCAGGAAC CCTACAGTGT CCTCCTTCTC CACATCTTCC AGATGAGAGG 60 CTGCCACCAG GGTTACTAGG GAACCCATAG TAAGTAGGGT CTTGGGAGTT AGACCCCCTA 120 CTACCTTCTG TTGAGTGAGT GGCAGACAAG GAAGTGGGGG GATGGTGGAC TGGAACATGC 180 AGGAGAAGGA GGGAACAGAT CTGGTTCAGG AAGTTCAGAG AGGTCAGGGT AGAGGGGGAG 240 GTGGGGGATC TCCAAGAGGA AAGGAAGGGA TTTAGAGGAT TCCTTTAAAA GAGATAAAAC 300 ATTAGAGAGT CTTTGGTTAG CACTTCTGAG TTGTTTGTTG GCCTCCTGTG AGGAGGTGAG 360 GTGATCTTCC CCGCCTTTGC TACTCTCCAG GTACCACTGA AAGTAGCTCT CCCATCCTGG 420 TTGTTTTTGT GCCTGTGTTT TCCATCCTAG TTCACAGGTA TGCTAATTTG TGCATCTCAA 480 AAGATCCCCA TCTAGGCCAT GGTAACTTGG AGTCTGCTTT GGTTATAAGG GTCCACTTGG 540 TTAAACATTT GCATGACAAC TCGCCATAAG TATTTTGCAG GTACCCGGCT GGAGTTTCTA 600 AAGGTGGAGC TTTATGTTGC ACAGCTGCTG GGTTTTAGCC AACCTAGAGG TCTTGTTCCC 660 CATAATTTAC TTTCTTTTTC AGATTTACCA AGTCAGGAAG TGTCAGACCC AGGGTGTTCT 720 GCTTGCAGAC CTAGCTTTTC AGGGCTGTTA CTCCCTGAAC CAATTCGATC CACCTGTGTC 780 ATGGCTGTGT GGCACAGTGT GTCGGGGCTC AAGGTGCGGG AGGGGTCAGC TCCGTATATG 840 CACCTGCCAG CTGAGATTAG GCTCGAAGTG TGTTCTTCTG AGGGGGTAAC CTACTCAGAG 900 CCGCTGCACG TCTTAGGGAG CGTTCCCCCG AGACCCTCTC ATATGATTCT CAGTTGCCTG 960 AAAATGCCCT GAAAGGCTGA GGGGAGCATG GTGCTCTTAT TTCTTTGGAG TGGAAAATTC 1020 CACACTCATA AGCGAGAGGG GCTTCGAGTT GGTCAAATCT AATAAGAGAA GGATGAAAAC 1080 ATACAGAAAA ACCCCCGAAT AAGACAGAAA ACAAACAAAC AAAACAGCTA 1130
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