Tag | Content |
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EnhancerAtlas ID | HS111-00630 |
Organism | Homo sapiens |
Tissue/cell | KB |
Coordinate | chr10:33293580-33295710 |
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 | CTGCAACCTC CACCTCCCAG GTTCAAGCGA TTCTCCCACC TCAGCCCACC GAGTAGCTGG 60 GATTACAGGC GCCCACCACC AGGCCCAGCT AATTTTCATA TTTTTGGTAG AGACGGGATT 120 TCACCATGTT GGCCAGGCTG GTCTCGAAGT CCTGACCTCA GGTGATCTGC CCGCCTCAGC 180 CTCCCAAAGT GCTGGGATTA CAGGTGTAAG CCACTGTGCC GGCTACTTTT ATTTTTTTAG 240 AGATGGGGGT CTCACTCTGT CGCTCAGGCT GGAGTGCAGT GGCTGGATCA TAGCTCACCG 300 CAGCCTTCAA CTCCTGGGCT CAAGGGATCT TCCTGCTTCA GCCTCCTGAG TAGCTTGGAT 360 TACAGAGGCA TGCCACCAAG CCCGGCTAAT TTTTAAAAAG TTTTACTTTT TGTAGACGGG 420 GACTCACTTT GTTGCCCAGG CTGGTCTCAA AACTACTGTT TCACGTGATG CATTATTTTT 480 TAACCTACAG CAGTGCTTCA AAGTCACAGA GATTTTTGTC CTAGATCATT AGCTAAACTG 540 CTTCTATTTA GAATTTTTTG TTGTTGTTTT CTTAAAAAAA AAAATCTAGA AATAAAGGTA 600 GGAACGTTTC TTTCCCCCCA AGGTTGAGAA CAGTCTCTTT CATCTGTTTT CCAGAATTTT 660 AATAACTGCT TCACAGCCTC TCCTGCGGGT TAGATGTCCT GAGTGTGCTG ATGTTTGCAA 720 CACTTCCCTT TTCTGCTGTT TGAATCATCT GCAACTTCAC AGGGTTAGTA ATAAAGTCGG 780 CTGACGGGCA GATCTCATCC TGACCCTGGC AATAGTCACT CTTACCTAAG GCAACTGACT 840 CAGGCTTCTC CTGGGCTCTT TTTTTCACCC CACTAGGCAG ATTTCTCTCT ATATATGGTA 900 ATAATGCTCC CAAGCAGAGG CCGCTGGCTT CCCCAGGAAA ACTGGAAAGT GAAATCACAT 960 ACCAGAGACT TTGTGGTACT GTGGCCACGG TCGTTTTTCT GCTACTAAGG GTGAAAGTCG 1020 ATTATTAAAG CAATTGCATC TTCCAAGAGC GATTTTCCCG CATCCCTCCG GGCTTGGGGG 1080 CTGCAGGGAC CCAGCCGGCA CACTCCGCAC GCCCTGCGGA TGACTCACTG CGTTTGCACT 1140 GCCGCAGGCG GGCTCGGTGG TGGTGGTGAC GCGGCCCGGC AGCCCGGGAA CGCAGGCGGG 1200 CTGCACCCTC TGGAAGCCAG CCCGGGTCTC CGCGCTGTCT TTCCCAACAT CAAAAATGCT 1260 GCTCCTATTT GCATAGTGCT TGACCTTAAT TGGAGTGCTG TTAGCGCCCG CGATTCTCAC 1320 CAAAACTTAG TGAAGTGTGG GTCAGTGATC TAGGCCCTTT ACTCGTCGGG GAAACTGAGG 1380 CTCAGATGAA TGTCTTGCCC AAAGTCACAC CTAAATTGCA CAGCTTAGAT GTAAATACAT 1440 AATTGCAGGG GGAGGCACTG TGCTTATGTC GCTCCATGCT GCGTTTTAGG TTTTCTTTAC 1500 AAGGGCCAAA CACCATCTGC TTTCATGTAA TAAACTTCCA TTCCACTTTA AATATATAGA 1560 AAGCAGCAGA GGAAGTTCAA GGGAGGGCAT GAGCAAGCAT GTATGGGAGT CCTATTTGTG 1620 GAAACATCAC TCCAAATCAG TTAGTTTTTT TCCTAGTGAA GTTGATCAAA AGAAAGCCCA 1680 AGTTATTCAG AATGCTGAGA TTTAAGGAAA TGTGTAAAAA TATTTATTTC TATCTTTTTA 1740 ATGTGATCTC ATTAGCTTTA AATAGCTGGT CTTCCTTGCT TTTTTGGGAG AGGAAAACAA 1800 CGTATCTTCA AAACAGTTAC CTAAAAATAG TAGAAGCTTT ACCAAGGGAG CCAGGCGTGA 1860 TGGCTCATGG CTGTAATCCC AGCACTTTGG GAGGCAGACG TGGGCACATC ACTTGAAGCC 1920 AAGAGTTCGA GATCAGCCTG GCCAACTTGG TGAAACCTCA TCTCTACTAA AAATAGAAAA 1980 ATAGGCCGGG CATGGTGGTG TGCACTTGTA ATCCCAGCTA CTCAGGAGGC TGAGGCGGGA 2040 GAATCGCTTG AACTCAGGAG GCTGAGGTTG CAGTGAGCTG AGATGGCGCC GCTGCACTCC 2100 AGCCTGGGCC ACAGGGCGAG ACTCTGTCTC 2130
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