Tag | Content |
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EnhancerAtlas ID | HS105-39529 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr19:18425340-18426830 |
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) |
TFAP2A | MA0003.3 | chr19:18426046-18426057 | CGCCTCAGGCT | + | 6.14 | Zfx | MA0146.2 | chr19:18425930-18425944 | CCCGCCTCGGCCTC | + | 6.01 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_01679 | chr19:18424972-18425806 | Aorta | SE_24690 | chr19:18426536-18427064 | Colon_Crypt_3 |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I018314 | chr19 | 18424973 | 18425806 |
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Enhancer Sequence | GGTAAGTATC CGCTCCACGG AGTATCGTCT GGCTATAAGG AATGAGGCAC TGACACAGGC 60 CACAGGGTGG ATGAACCTCA AAAACACGTT GCTGAGTGAC AACCACCAGG CTCGAAAGGC 120 CTCATGGTCT CCGTTCGCAT GCATGGGAAA TATCCGGAAT AGGCAACCCC ACAGAGACGG 180 CAGCTGCCTC ATGCTCATCA GGGACTGGGG CTGGGAAGTG ACTGCTGATG GAAATGGGCT 240 TTCCTTTTGT GGAGACGGAA ATGTTCCGGC CTAGATAAAG GTGGTGGTTA CACAACCTGT 300 GACTGCACCA AATGCCACTA AATTGTGCAC TTTAACTGAA GTGTTAGTAT GTAATATTAT 360 CCTTTTTTTT TTGAGATGGA GTCTCGCTCT GTCACCCAGG CTGGAGTGCA GTGGCGCGAT 420 CTCAGCTCAC TGCAAGCTCC GCCTCCCGGG TTCACGCCAT TCTCCTGCCT CTGCCTTCCA 480 AGTAGCTGGG ACTGCAGGTG CCCGCCATCA CGCCCGGCTA ATTTTTTTGT ATTTTTAGTA 540 GAGACGGGGT TTCACCGTGT TAGCCAGGAT GGTCTCGATC TCCTGATCTG CCCGCCTCGG 600 CCTCCCAAAG TGCTGGGATT ACAGGCATAG AGCCACCACG CCCGGCCAAT ATTATCATTT 660 TTTGGAGACA GGGTTTCACT GTCACCCAGC GACCTGCAAC CTCAAACGCC TCAGGCTCAG 720 GTGATCCTCC TGCCTTAGGC TCCCAACTAA CTGGAACTAC AGGTGCACGC CACTACACCC 780 AGCTAATTTT TATATTTTAT GGAGAGACGT GGTTTCTCCA TGTTGCCTAG ACTGGTCTCT 840 GAACTCCTGG GCTGAAGCCA TCCTCTAGCC TCAGCCTCCC AAAGTGCTGG AATTATAGGC 900 CTGAGCCACC ATGCCCAACC TGAAGTTCTT TTTATTTTTT TAAGTGACAG GGTCTTGCTA 960 TATTGCCCAG GTTGGATTTG AACTCCTGGG CTCAAGTGAT CCTTCCACCT CATTAATTTT 1020 CTTTTTCTAG AGACAAGGTT TCACTCTGTC GCTCAGACTG GAGCGCAGTG GTATGATCAT 1080 AGCTCACTGC AGCCTCAAAC TCCTGGGATC AGTCGATCCT CTTGCCTCAG TCTCCTGAGT 1140 AGCTGTGACT ATAGGCACAC ACCACCTCAT CTGGCTAATT TTAAGTTTTT CTTCTTGCCC 1200 AGGCTGATCT CGAACTCCTG AGCTCAAGCG ATCCTCCTGT CTTGGCCTCC CAAAGTGCTG 1260 GGATTACAGG CGCGAGCCAC TGCAACTGGC CCATTAAATT TTTAGTAAGT ATGTATGTAT 1320 TACTCTTACA AGCAGCAGAA ATGACAGGAG TGTGGACACT CCTGGGGAGG GAGAAGAGAG 1380 CAAACTGCCA TGCTGGTGGA CAGGCAGGCC AGGAAGCCGT CTGCTCAGCC ACCGCCCCTG 1440 TGCTGAGGCT GGCCCCCTCT CAAACAGGCT TTCCCAGACC ACTGAGTACT 1490
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