Tag | Content |
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EnhancerAtlas ID | HS098-06654 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr10:33293790-33295740 |
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) |
Gfi1b | MA0483.1 | chr10:33295272-33295283 | TGCTGAGATTT | - | 6.32 | MEF2A | MA0052.3 | chr10:33295545-33295557 | ACTAAAAATAGA | + | 6.27 | MEF2B | MA0660.1 | chr10:33295545-33295557 | ACTAAAAATAGA | + | 6.32 | MEF2C | MA0497.1 | chr10:33295543-33295558 | CTACTAAAAATAGAA | + | 6.57 |
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| Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
SE_28190 | chr10:33293774-33295435 | Fetal_Intestine | SE_29371 | chr10:33293692-33295588 | Fetal_Intestine_Large | SE_34909 | chr10:33291964-33296307 | HeLa | SE_36090 | chr10:33292167-33295894 | HMEC | SE_41035 | chr10:33293661-33295531 | Left_Ventricle | SE_47141 | chr10:33291813-33297039 | Panc1 | SE_59892 | chr10:33232038-33295346 | Ly4 | SE_64578 | chr10:33292449-33296137 | NHEK | SE_67550 | chr10:33292033-33296654 | u87 |
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Enhancer Sequence | CCACTGTGCC GGCTACTTTT ATTTTTTTAG AGATGGGGGT CTCACTCTGT CGCTCAGGCT 60 GGAGTGCAGT GGCTGGATCA TAGCTCACCG CAGCCTTCAA CTCCTGGGCT CAAGGGATCT 120 TCCTGCTTCA GCCTCCTGAG TAGCTTGGAT TACAGAGGCA TGCCACCAAG CCCGGCTAAT 180 TTTTAAAAAG TTTTACTTTT TGTAGACGGG GACTCACTTT GTTGCCCAGG CTGGTCTCAA 240 AACTACTGTT TCACGTGATG CATTATTTTT TAACCTACAG CAGTGCTTCA AAGTCACAGA 300 GATTTTTGTC CTAGATCATT AGCTAAACTG CTTCTATTTA GAATTTTTTG TTGTTGTTTT 360 CTTAAAAAAA AAAATCTAGA AATAAAGGTA GGAACGTTTC TTTCCCCCCA AGGTTGAGAA 420 CAGTCTCTTT CATCTGTTTT CCAGAATTTT AATAACTGCT TCACAGCCTC TCCTGCGGGT 480 TAGATGTCCT GAGTGTGCTG ATGTTTGCAA CACTTCCCTT TTCTGCTGTT TGAATCATCT 540 GCAACTTCAC AGGGTTAGTA ATAAAGTCGG CTGACGGGCA GATCTCATCC TGACCCTGGC 600 AATAGTCACT CTTACCTAAG GCAACTGACT CAGGCTTCTC CTGGGCTCTT TTTTTCACCC 660 CACTAGGCAG ATTTCTCTCT ATATATGGTA ATAATGCTCC CAAGCAGAGG CCGCTGGCTT 720 CCCCAGGAAA ACTGGAAAGT GAAATCACAT ACCAGAGACT TTGTGGTACT GTGGCCACGG 780 TCGTTTTTCT GCTACTAAGG GTGAAAGTCG ATTATTAAAG CAATTGCATC TTCCAAGAGC 840 GATTTTCCCG CATCCCTCCG GGCTTGGGGG CTGCAGGGAC CCAGCCGGCA CACTCCGCAC 900 GCCCTGCGGA TGACTCACTG CGTTTGCACT GCCGCAGGCG GGCTCGGTGG TGGTGGTGAC 960 GCGGCCCGGC AGCCCGGGAA CGCAGGCGGG CTGCACCCTC TGGAAGCCAG CCCGGGTCTC 1020 CGCGCTGTCT TTCCCAACAT CAAAAATGCT GCTCCTATTT GCATAGTGCT TGACCTTAAT 1080 TGGAGTGCTG TTAGCGCCCG CGATTCTCAC CAAAACTTAG TGAAGTGTGG GTCAGTGATC 1140 TAGGCCCTTT ACTCGTCGGG GAAACTGAGG CTCAGATGAA TGTCTTGCCC AAAGTCACAC 1200 CTAAATTGCA CAGCTTAGAT GTAAATACAT AATTGCAGGG GGAGGCACTG TGCTTATGTC 1260 GCTCCATGCT GCGTTTTAGG TTTTCTTTAC AAGGGCCAAA CACCATCTGC TTTCATGTAA 1320 TAAACTTCCA TTCCACTTTA AATATATAGA AAGCAGCAGA GGAAGTTCAA GGGAGGGCAT 1380 GAGCAAGCAT GTATGGGAGT CCTATTTGTG GAAACATCAC TCCAAATCAG TTAGTTTTTT 1440 TCCTAGTGAA GTTGATCAAA AGAAAGCCCA AGTTATTCAG AATGCTGAGA TTTAAGGAAA 1500 TGTGTAAAAA TATTTATTTC TATCTTTTTA ATGTGATCTC ATTAGCTTTA AATAGCTGGT 1560 CTTCCTTGCT TTTTTGGGAG AGGAAAACAA CGTATCTTCA AAACAGTTAC CTAAAAATAG 1620 TAGAAGCTTT ACCAAGGGAG CCAGGCGTGA TGGCTCATGG CTGTAATCCC AGCACTTTGG 1680 GAGGCAGACG TGGGCACATC ACTTGAAGCC AAGAGTTCGA GATCAGCCTG GCCAACTTGG 1740 TGAAACCTCA TCTCTACTAA AAATAGAAAA ATAGGCCGGG CATGGTGGTG TGCACTTGTA 1800 ATCCCAGCTA CTCAGGAGGC TGAGGCGGGA GAATCGCTTG AACTCAGGAG GCTGAGGTTG 1860 CAGTGAGCTG AGATGGCGCC GCTGCACTCC AGCCTGGGCC ACAGGGCGAG ACTCTGTCTC 1920 AACAAACAAA CAAAAAGAAA CTTTACCAAG 1950
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