Tag | Content |
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EnhancerAtlas ID | HS060-06965 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr11:117948020-117949460 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr11:117948194-117948212 | CCTGCCTTCCTCTCTTCC | - | 7.53 | Klf1 | MA0493.1 | chr11:117948143-117948154 | GGCCACACCCA | + | 6.62 | ZNF263 | MA0528.1 | chr11:117948848-117948869 | CACCCTCTCTCCTCCTCCTCT | - | 6.53 | ZNF263 | MA0528.1 | chr11:117948845-117948866 | CCTCACCCTCTCTCCTCCTCC | - | 6.88 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_23705 | chr11:117945333-117948611 | Colon_Crypt_1 | SE_23705 | chr11:117948738-117951458 | Colon_Crypt_1 | SE_29489 | chr11:117946646-117951064 | Fetal_Intestine_Large |
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Enhancer Sequence | GTGAGTGTGG GGCCCTCTGC TCCCAAGACA CAGGAAGGGT GGGTCTCCCC ATGTAAGGCC 60 CTTCAAGCAG CCTGAGCATC CATCAGCTGA GAATTCTGTG ACACCTTCTA GGTTAAAAAA 120 AGAGGCCACA CCCAAATCCC CTCACACCCC AGCCCGGTAC ACGTCTCATA CCCACCTGCC 180 TTCCTCTCTT CCTCCATTGC CATGGTCCTT GGACCAGCTC ACCTAAGAAG CTGAGCACAG 240 AGCCAGGGCT GTCCTTCCCG ACTATTCTTT CCTGAATCCT GCATGTTCTT TTGCCCAATG 300 TCTCCAGGTC TGTTGGTTAG AGGTTGGCAC TATTTTTCCA AGGCAGGGGG CTGTTCTGAT 360 GCCACGGTTG CCCTCTGCCA CTCCCTGGGG AAACTGATTC CTTTTCTTTT TAAAGAAAAG 420 TGTAGACTGG GTGCAGTGGC TCACGCCTGT AGTCCCAGCA CTTTGCGAGG CTGAGGCAGA 480 CAGATCTCTC GAGGTCAGGA GTTTGAGACC AGCCTGGCCA GTATGGTGAA ACCCCATCCG 540 TACTAAAAAT ACAAAAAATT AGCCAGGCGT GGTGGCAGGT GCCTGTAATC CCAGCTACTT 600 GGGAGGCTGA GGCAGGAGAA TCGCTTGAAC TTGGGAGGCG GAGGTTGTGG TGAGCCAAGA 660 TTGTGCCATT GCACTCCAAC CTGGGCAACA AGAGTGAAAC TCCGTCTCAA AAAAAAAAAA 720 AAAAAAAAAA AAAAAAAAAG AAAGAAGGAA AAGAAAACAG TGCAGAGATG CCTCCAAACA 780 ATCTAGGGTG TTTGTGGTCA TCTTTTACTT GGTCTCTTTT CATGCCCTCA CCCTCTCTCC 840 TCCTCCTCTG AATACCTGGA GCGTCTTCGC TGTCTTGGGG CAAAGAGAAT CAACCCTATC 900 TTTCAAGGAG GACAGCTGAG GGCCAGGGAG GGGAAGAGAT AATAACTGGG TCTGAGGAGG 960 AACCCAGGGG TCTTCCTTCT CCAGTCCTTG GCCAAGAGGC AGCAATTGCC CAGCCACCAA 1020 AGTGAAAGGG AAGGGAAGAG AGGAAAGGAG AAGCCACTGT CCAAGGGGGA AGGGTGTGAC 1080 CTGCAGGGGC CCCTCGAGTG ATTGTCTCCT ATTCCCAACC TGAGCACTTC CCACGACACT 1140 CTTCTGAAAA TTCTGGCAAG AACAATTCTT AGTGCGGTTG TAGCTGATGA TCAGAAAGGG 1200 GAAGGGGCTT CCCTTTGAGC CAGGATCAAA GCACAAGCTT CCTGCTTTCC CATCCAAGGA 1260 GGCGCCCCAA AGTTTGGCCT GTGTGCAGAG ACGCTGTATC CCCTGGGGCT CCCAGGAGAG 1320 GAGAGCAGCT GTGGAGTCTA CCTAGCTGTG AGCTGCTTCT GGGTGGCAGG CACTGAGGAG 1380 ACCTGGGGTG TCTCTTGGGG GAGCAACAGA GAAGGGAATC ATTTCTAGGG CAGGTCACTA 1440
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