Tag | Content |
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EnhancerAtlas ID | HS051-11975 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr17:47080970-47081900 |
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) |
ZNF263 | MA0528.1 | chr17:47081148-47081169 | GAGGGAGAGAGGGAGGGAGGG | + | 6.8 | ZNF263 | MA0528.1 | chr17:47081144-47081165 | GGGGGAGGGAGAGAGGGAGGG | + | 8.54 |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_28143 | chr17:47080506-47082110 | Fetal_Intestine | SE_29263 | chr17:47080553-47082196 | Fetal_Intestine_Large | SE_40473 | chr17:47080843-47082145 | K562 | SE_67981 | chr17:47049476-47113351 | TC32 | SE_68412 | chr17:47048796-47109684 | TC71 | SE_68710 | chr17:47081098-47081977 | H9 |
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Enhancer Sequence | TTCGTTCCCT ATCCTCTTAA AAGATTCTTG AAATGTGGCT AATGTTTTCC AGAAAGTGCA 60 GCTTAGAATT TGGGATGGGA GTGTTAGGGA GAGAAAAGGG GAGGAAAAAA GCAGCAGGGG 120 GAGACTGGAG AAATCAGACG AGTTAGTCCC GGCTTGGAAA TTCCAGACGG GGAGGGGGGA 180 GGGAGAGAGG GAGGGAGGGG AGATACGGGG TTGGGTGGAT TTCCCGCTTC CCTTTTAAAG 240 GGGAGCGGCT GGAGTCTCAC AGTGTTACCC ACGGGAGAGG GGTCGGAGAC GGGTGGTAGA 300 CTCAGCTCAG GGCAAGGCTA TATTTGCTTT TGGAGTTGCC GGCCTTCCCT TCCCCTTTCA 360 AAAAAGAGAG AGAGTAGAGA GAGAGAAAGT GGCGGCGGCG CTGCAGGCTC TTCCTGGAGC 420 GCTCGCCCCG GCCCGGCGGC CCTAACCTTC CCCGCCCGCC CCCGCGCCAG TCCCAGCCCG 480 GCAATCTCGT CTCGCTCTGA GGTGGGGCCG CCCGCCTGCC TTCTCTTAAC AAGCCCCTGA 540 CAGAGAACAT CCGCTGGCCT GGGTCTCCGA GGAGGACTTC CCCTCTCAGA TCCCTGAGAC 600 CCCAGGAGAT CCCAGGCCGC TTGTGGTGCG CCTTAGTCCT GGGAACCCCA GATCGCAAAC 660 CTCGCAGCAG ATACCCCACG AGAGGGTTCC CCCTCACCGG CTGCGGGCTG CGGGCTGCAG 720 ACCCTTTCCA GCACCTGGGC TGCCTCAGGA GCTCTCCATT CTAAGGCAAA AAGCCAGTGG 780 GTAAATGTGA AGTGAAAAGA GGCAAGAAGA GAGGAAGAGT AGGTAAAGGG AAAATAGGAT 840 GAGACAGTTG GAGAGAAAAT GGAAGTGCAA GTAGCTGTTC CTCTCTCCCA GTAGCTGGGG 900 TCTTGGCCTG AGAAATAGAA CCTTAAAGAG 930
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