Tag | Content |
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EnhancerAtlas ID | HS012-15766 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr19:56178570-56179870 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Gata4 | MA0482.1 | chr19:56179366-56179377 | TCTTATCTCTT | + | 6.02 | MYC | MA0147.3 | chr19:56179734-56179746 | GGGCACGTGGCG | - | 6.74 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_23398 | chr19:56178044-56179214 | Colon_Crypt_1 | SE_23398 | chr19:56179431-56180404 | Colon_Crypt_1 | SE_23969 | chr19:56179550-56179870 | Colon_Crypt_2 | SE_27904 | chr19:56178304-56180119 | Fetal_Intestine | SE_29198 | chr19:56178255-56180189 | Fetal_Intestine_Large |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I055666 | chr19 | 56178334 | 56181342 |
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Enhancer Sequence | TGTGGGGGCA TCTCCCCTCC TTCCATGGGC ACAGCGGCTC ATGCTTCTGA GGCTCTTTCC 60 CATTTCCTGT CTTACCTATT CCTTCCCAGC ATCAGGATGG AGGTGGGATG GGGCCACTCA 120 CACTTGGTGT GGAGGCTGCA GAGGAAGGGG AGGCCATATG GCCTAGGTTT TGAACTTGGG 180 AGTCAGGCTG GTTGGTTACC GGGGCCTGGC ATAGCTGATA TCTGACAGGA CGGCGTCAAG 240 TTACATTGGC AGAGCCTGTG GGGTCTCAGG TTGAATCATC CCACCAGCAG GCACTTGTCT 300 GTGAGTCCAG AGTTCAGTGG ATAGGGCAGG ATCGAGGGCC AGTAAATTCA GCTGATAAGC 360 CCCCACTCTG GTATGTCAGC CCTCGAAGAC ACTGGATCCT GCATCCCACA GTCAGCCCAC 420 AGTTCCCAGT GAGATCAGAG CAGCTAATGC TGCGGATGCT GTTCTGAGAC TTCCCGGGCA 480 GCCGCGGCTG CTCATCGTGT CGTGCCACCC CTGTGAGGGC AGTTGCACCC CTGCAGTGGC 540 ACCTGCAGTT CTGACAGGGC GTGAAGGGAA GGGACTGAGC TTTTTTTTTT TTTTCCTTTG 600 AGATGGAGTC TCACTCTGTT GCTCAGGCTG GAGTGCAGTG GAGTGATCTC GGCTCACTGC 660 AACCTCCGCC TCCTGGGTTC ACGCCATTCT TCTGCCTCAG CCTCCTGAGT AGCTGGGACT 720 ACAGGTGCAC GCTACCACAG CCCGCTAATT TTTGTGTTTT TAGAGAGACG GGGTTTCACC 780 ATGTTGGACA GGATGGTCTT ATCTCTTGAC CTTGTGATCT GCCCGCCTTG GCCTCCCAAA 840 GTGCTGAGAT TACAGGCGTG AGCCCCCGCG CCCGGCCGGG ACTGAGCTTT AATGGGAGCC 900 TTGCCTGGGT GGCTGTCAGA GAAGGGGTGG GGTGTGTTGT GACTCACCAG TAGGTCCCGA 960 GCCCAGGTGA CCTGCCAGCA TTCCACAGCA GCAGGTAGCA GATGTGGGTG TGAACTTTGT 1020 GCCTTTGGAG CGTTCTGGAG GATGTTCTAG TTTGAGGTTC CCCTGAGGCT GGGCAGATTT 1080 GGGAGACATG GTGCGTTCTC CCCGAGGAGC CTCTGTGTGC CACTGCCCAG GACCCTCACT 1140 GGTCAGATAA GGCTGGGGTG GGGTGGGCAC GTGGCGACCC CTCCCTCGTC AGATCAGGCA 1200 GGAAGTGTTC TCTTTGGCAA TTGAGGAGCT CGCCGTAGAC TGTCCAGGTT TTGGGAGATA 1260 ACCTGGTACT GGAATTGAAG TCCTCCTCTT CTCTACCCAT 1300
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