Tag | Content |
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EnhancerAtlas ID | HS051-07517 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr13:73633950-73634990 |
Target genes | |
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) |
GATA2 | MA0036.3 | chr13:73634907-73634918 | TTCTTATCTTT | + | 6.62 | TCFL5 | MA0632.2 | chr13:73634000-73634010 | TCACGCGCAC | + | 6.02 |
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| Number of super-enhancer constituents: 11 | ID | Coordinate | Tissue/cell |
SE_23235 | chr13:73633053-73637700 | Colon_Crypt_1 | SE_24316 | chr13:73633076-73635399 | Colon_Crypt_2 | SE_24929 | chr13:73631683-73639879 | Colon_Crypt_3 | SE_26421 | chr13:73633805-73642018 | Duodenum_Smooth_Muscle | SE_27687 | chr13:73628614-73651570 | Fetal_Intestine | SE_28601 | chr13:73628476-73654730 | Fetal_Intestine_Large | SE_34966 | chr13:73627061-73637367 | HeLa | SE_36569 | chr13:73629841-73637236 | HMEC | SE_57068 | chr13:73633119-73635477 | VACO_400 | SE_57507 | chr13:73633139-73634965 | VACO_503 | SE_64296 | chr13:73628716-73641168 | NHEK |
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Enhancer Sequence | CTGCCCCGGC GGGTCGGCCT GGGAGAGGTA AGAGGGAGGG AACTGGGTGC TCACGCGCAC 60 CTTAGTTGTT TTTCTTACAC TTGAGGGACG AAACCTTGTA CCTTACGCTC AGTTTTACTT 120 AAATTACGCC TTCGCCTGTA CCGCTCTCCA ATGCCAAGGC ATTGGAGCCC TCCCCCCCAT 180 CCCCATCGTC TCGGGTTAAG TAGAAACGCA AATTGGGGTG CTGGGGAGAG GTTCCCCAAG 240 GTTTCATACC CGGTGGCTCA ACCTGCTTTA GAAGCGATTG CGGGCCGCGT TTGGAAAATG 300 AGAGTTAGGA AAGCTAAGGT TGTGTCGGAG CGCTTATTTT TCCTTAAAAA AAAAAAAAAA 360 AAAAAAAGAC CGGGGGTGTT GTTTTCTTCG TGTGCACGTA AATTTCCTCC CGGAGCCGCG 420 TTGAAAGCTG GCAGTTGGCT TTTACACTTG CCCAGCAGCC GAATTAGAGC AACCGCCTGT 480 TTCTTTCGCC CACGCAGGGA GTCATATAGC CCAGAAAAAA CTTCCCGGGA CTTTTAGCCT 540 GTCCCAAGGA AAAAAAAATT GGAAACATAC CCACATGCAA ACAGCTGGAA GAGCTAAAAT 600 CAGAAACCAC TAACCGCCGC GGGAGCGCAG TGCACGAAAG GGTTTAGTTC AGTTTATTTC 660 AAGACACTTC ATTTAGTAGC TCTTTGGCGT GTCGTATATT TGCTACCCAG CGCCTACTCC 720 GTGGGGTCTG CCAGGGTCTT GCTGTGAGAG GGCAGTGGCG TTTGTCAGAG ATGTGACTCA 780 CATGATGAGA GCGTTAATTT TTATTTTTAA ATCATGTCTA TCCGGGAAAC CCCGTCCGCA 840 TCCACACCAA GGTCCGAGAT GAAACGCATT TGAAATGAAG TAGTAGCAGA AAATGACTGT 900 CTTATTTACC TGTTAAGGTG CCACAGCTAA TATATGCGCC ATTCCATCTA GTTGGTTTTC 960 TTATCTTTCG AAATTTCCTT TTCAGTGTTA AAAAATGTAG GCTTAAGTTA TACTAGGAGA 1020 GAAGATAGCT GGAAAAGGCT 1040
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