Tag | Content |
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EnhancerAtlas ID | HS134-50471 |
Organism | Homo sapiens |
Tissue/cell | Mesendoderm |
Coordinate | chr6:7542320-7543630 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZIC4 | MA0751.1 | chr6:7543229-7543244 | GACCCCCCGGTGAGA | + | 6.07 |
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| Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
SE_02725 | chr6:7540501-7544887 | Astrocytes | SE_23573 | chr6:7541750-7543708 | Colon_Crypt_1 | SE_24139 | chr6:7541259-7543632 | Colon_Crypt_2 | SE_24814 | chr6:7541227-7543610 | Colon_Crypt_3 | SE_26973 | chr6:7540700-7543996 | Esophagus | SE_28040 | chr6:7540668-7551124 | Fetal_Intestine | SE_29087 | chr6:7540640-7551418 | Fetal_Intestine_Large | SE_36041 | chr6:7540816-7547851 | HMEC | SE_64620 | chr6:7540401-7548004 | NHEK |
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Enhancer Sequence | GGGTACCTGC CCGGAGAGCG CGGGCTGCGG GGCTCGCGGG ACAGGGAGGG ACCGTCCTCC 60 TCTGGACGAC TGGGAGACTC GGGTCCCGAA GGTGGAAAGG TTTTTTTGCC CCAGGTCCCG 120 AAAGAACTTC CCGGCCGCGC TGGGAGCAGG ACCGGGTGTC CTGACGCGTG CGGGGACAGG 180 TTGGCCCCTG TCCTGCGAAC AGGGACTCGG TCGTACCTTT CTCCCCTCCC GCGAGCCCGG 240 GCGGGTGGTC AGAGGGGGCG TCGGGCCCGC GCGGGGCTGT CCCCTGCCTG CTGGACACGG 300 CTGCAGCCGC CTTTGTCCCA GCCCGCGAAT GGGAGGTCAG GCGAGGTGGG GCTGCGACCA 360 CAAAACCCAA CCTCTCCAAC CGTAATCAAA GTAAAAGAGG AAAGGAGCGG GGCCCCGGTC 420 CTGTCTGGTG GCCGAGTGGT GCTCGGGGCT CCGCAGTCTC TACCGGCTCA CCCCCAATCC 480 CCAGTAACCC CGAGACCACG ACTGCAACGA CTCCTGGACT CCTCGGCCAC CCAAGGACGT 540 TTGTATCAAG GCTGCGCGTC CCGGCGGCGC GGGGTCCTGT CCCGAGGAGG CGCTTCGGCT 600 TCCCCTGTCC GGGAAACGAA ACTTCCCCGC CGGGGCGGCT GCCGGGCCCG GGTCTCGAAG 660 TTCGGCCGGG ACGTGCCTGT TACCTTCGGT CGTCCGCGCC GCAGCCCCCG CGGGCGAGCG 720 CACCTGGGGC CCTGCCTCTG AGCCTTTTGT TTCCTCCTTT TTAAAAACAC CGGATGAAAG 780 ACCCCAGTGT GCCTTGGATC GCAGAGCGCC GGCCGCATGT CTGCTTTGAT CCAGAATGTG 840 TGGGCAGGGG AGTGGGGGGG TGGGAGAGGA CGACGCTGGG GGCCCGCCCT GGCCTAGGCG 900 CCCCGGGAAG ACCCCCCGGT GAGAGGGTCA GCTTCTCCGG ATCCCAGCGG AAACAGACCG 960 AGGGCGTCAT TTGGGTGGGT GGGGAAGAGA TCCTGTCCCT GCTTTGACCG GGTCTCGGGA 1020 GCTGGACTCT AGATGCCCAC GTGAGCCGTG CGCGTTTTGC AGCCCGCCCC ACCTCCCCGC 1080 CCCCTGCTAG TTGTTCCCAC GTCGGGCTTT TGGGAAAGAG GCCCTGAGCG CCGGGACGTT 1140 ATTTACCAGG CGTTGTGGCC CTAGGCCTGG GAGGAGCAAC CTGAATGCGC TCCAGGGAGT 1200 TTTGTTTTGC AAGCAGTTTT GAAGGCAGGG ACTACTCGAG TTGCAACCTG TTTTCTGCTT 1260 AGATTCATTT ATTTATTTAT GGGGCATCCT GAAAATCTAT TTTCGCTTTT 1310
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