Tag | Content |
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EnhancerAtlas ID | HS094-12038 |
Organism | Homo sapiens |
Tissue/cell | hMADS-3 |
Coordinate | chr14:20880290-20881560 |
Target genes | Number: 15 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
POU2F2 | MA0507.1 | chr14:20880695-20880708 | ATATGCAAATACA | - | 6.41 | ZNF263 | MA0528.1 | chr14:20881304-20881325 | TCTCCTTCAGCCTTCTCCTCC | - | 6.03 | ZNF263 | MA0528.1 | chr14:20881285-20881306 | CTCTCTTCCTGTCCCTCCCTC | - | 6.44 | ZNF263 | MA0528.1 | chr14:20881319-20881340 | TCCTCCTCCTTTCTCACCTCC | - | 6.6 | ZNF263 | MA0528.1 | chr14:20881307-20881328 | CCTTCAGCCTTCTCCTCCTCC | - | 7.22 | Znf423 | MA0116.1 | chr14:20881544-20881559 | GAAACCCTGGGTGCC | - | 6.9 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_28028 | chr14:20879130-20888428 | Fetal_Intestine | SE_29051 | chr14:20879173-20888453 | Fetal_Intestine_Large |
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Enhancer Sequence | ACAACAATAT CTCACTGGAC GTCAGTGTGA CAAACACGTA AAAAATGATG GCTTCTGTGC 60 CCAATACACT TTGCTCATGT CGTTGCCCTA TATAAGCCCC CAAGGAAAGG AGTGGGGAAA 120 CTCAGAATTG ACTCAGATTT TTTTTAAAAG AGATCTCAAG CCAAAAATAA ACAGAAAAAT 180 AAGGACAGTT TATTTGAGCA ACATAGTGAG ACTGTCCTAT CCTTAAAAGG ACAGTCTCAC 240 TATTTTGCTC ATTTTATTGT TTTGCACCCT GGAGTTTTTG AAAGGAGATT CGGCTGAACC 300 ACAAATGGAA AGTTAAAGTT CCGTCCCCAC TTCCATCTCT AGTTCCCTTC TCTGGAAGTA 360 AACATTGCTC ACAGTTTTAT ACTAACAGTT TCACAGTTTC TATGCATATG CAAATACATG 420 CCTTCACCAT CACCACTGCT TTTGCTTTTG CTTTACACAA ACAGGATCAT AAGTTAGATG 480 CTATTCTGCA CTTAGTATAT CTCAGAGACC TTGCCCTGTT AACACATTAA TACCCACCTC 540 ACTCTTTCCT TTTTTTTTTT TTTTTTTTTT TGAGGCGGAG TCTGGCTCTG TTGTTCAGCT 600 CACTGCAATC TCTGCCTGCC GAGTTCAAGC GATTCTCCTG CCTTAGCCTT CCGAGTAACT 660 GGGATTACAG GCGCCCACCA CCATGCCCGG CTAATTTTTT TGTATTTTCA GTAGAGAGGG 720 TTTTCACCAT GTTGGTCAGG CTGGTCTCAA ACTCCTGACC TCAGGTGATC CCCAACCTCC 780 GCCTCCCAAA GTGCTGGGAT TACAGGCGTG AACCACCGCG CCCGGCCTCC ACCTCACTCT 840 TCAAGTGGCT GTATGGTAGT CTAGCACATT TAAGCACAGT CTGGGTTTCT ATTATCACAA 900 ACGGTTCTCA TACTACCATT TGTTGGTGAC AGCCACTGTC CCCTTTCGAT GGGCACACAG 960 GGCAAGGAAG TAAGAGGGGA TGATTCTTAC GTGGTCTCTC TTCCTGTCCC TCCCTCTCCT 1020 TCAGCCTTCT CCTCCTCCTT TCTCACCTCC CCTTTCACGC AGTATACACT CCCTCCCCTT 1080 CCCGGAGCCG CCGGGAGGAG CAGGGTGGAT GCACCCCTAG CTGAGTCTCG GGTGGTTCCT 1140 AACCGGCCCC GCCAGGCACT TCCCACCCAG CTCTCAGCCT CAGAGCCCAG CGCCCTAGAC 1200 CCAGGGCCAG GGCAAGTTCT GCCTGCGCTC GGACCCTACC TTAGACTGGG GCTGGAAACC 1260 CTGGGTGCCT 1270
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