Tag | Content |
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EnhancerAtlas ID | HS012-10811 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr12:89766110-89767330 |
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 | chr12:89766479-89766491 | AAACAAACAAAC | - | 6.32 | Foxd3 | MA0041.1 | chr12:89766483-89766495 | AAACAAACAAAC | - | 6.32 | HNF4G | MA0484.1 | chr12:89766805-89766820 | TGGCCTTTGTTCTTT | - | 6.14 | MAX | MA0058.3 | chr12:89767024-89767034 | ACCACGTGCT | + | 6.02 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_27644 | chr12:89763300-89771362 | Fetal_Intestine | SE_28566 | chr12:89761572-89775819 | Fetal_Intestine_Large | SE_35929 | chr12:89761762-89771214 | HMEC | SE_38298 | chr12:89761862-89771214 | HUVEC | SE_41177 | chr12:89766532-89767330 | Left_Ventricle | SE_48925 | chr12:89766309-89767299 | Right_Atrium | SE_50215 | chr12:89766250-89767304 | Sigmoid_Colon |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I089368 | chr12 | 89761900 | 89775589 |
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Enhancer Sequence | TTCAATAAAT GATTTTCACT TAAGCATTTG TTCACGCAGT CACTTCATTC ATTTATTTAT 60 CATAAAACAT TTATCAAGGT CCTATTCTAT ACTGACACTA TGCTGGGCTC AAGAGATGCT 120 GAGGCTTTTT GGGCAAGAAG GTTGAAGACT AGGCAGGGAG AGAGACCTGA ACTAAAGCAG 180 GAGAAGGCAA GGTGTAGTAT ACACATCATG GAGACATGTA TAAAGCATTC CTGGAACCCA 240 GAGGAACCAG GAAGTGCTGC TCATAAAAGA TGCTTTTTGA ACTAGATCTT GAAGAGTGAG 300 TAGCCCGAGG AGTTTGGGCT TGCGAATTCT AGATAACAAG AACAGCTTGC CAAAAGGGAT 360 AAAGTTGTGA AACAAACAAA CAAACAAAAA ACAGGGTTTG GAGCCAGGAG GACTTTGGTG 420 TGAGTGGTGT TTGGCCATTC TGCCTGGTGC CTTCCTTTGA ATTTAGGTTC GACCCCCTGT 480 GGGGGCCACA GAGAGTCACC TGCAGCTCAG TCTTACCCCA GGTGCTGGGC CCAAGTCTGC 540 TCTTAGAGGA AATGTAAGTA GCTTATATCA CTCAGTATCG GGTCAGCTAG GCTCTGGGTT 600 CTGTTCTGAG CTCCTGCTCT ATTTCTAGCT GTGAAGTTTC CACTTGATTC CTGTCACAGG 660 CTCTACCTTG TATTCCAGTT CAAATAACTG GGCTTTGGCC TTTGTTCTTT CTTCTACATT 720 CTGCCTCTAA GTTTCTCTAA GACTGGAATT TTGCCTTTCC TTATCAGTCC TTCCTAGAAC 780 TTCAGTCCCT CCCAGAACTT CAGTCCCCTC CTTGGCCCTG GGGCCTCACT CCAGGCTGCT 840 TGATCCACTT ATGGTTATTG CTTGCTGGGT TCACCTTCTT CTCCTTTCTG CAGGTGGAAC 900 ACAGACTGAT GACAACCACG TGCTGAGATC CCCTGTTACT GCCTAGACAC AAATTGCTAT 960 CTAGGTCCTG TTTCACTGCC TGGCAGAACT GCCTTGCTAC TTCTGGTTTG GCTCGCCATT 1020 GCCTGAATTC CTAAACTCCA TTCTGAATAT TACTAGTGAA AAATGCACGG CAGGGCGCAG 1080 TGGCTCATGC CTGTAACCCC AGCCCTTTGG GAGGCTGAGG CAGGTGACTC ACCTGAGGTC 1140 AGGAGTTCGA GACCAGCCTG GCGAACATGG TGAAACCTCG TCTTTACTAA AAATACAAAA 1200 ATTAGCCAGG CATGGTAGTG 1220
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