Tag | Content |
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EnhancerAtlas ID | HS141-01822 |
Organism | Homo sapiens |
Tissue/cell | NB4 |
Coordinate | chr1:229265200-229266640 |
Target genes | Number: 12 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr1:229265936-229265957 | GGGGGAAGGGAAAGGGAAGGG | + | 6.2 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_28465 | chr1:229264302-229269774 | Fetal_Intestine | SE_39448 | chr1:229264555-229268325 | Jurkat | SE_49840 | chr1:229264440-229269846 | RPMI-8402 | SE_66415 | chr1:229264555-229268325 | Jurkat |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I229128 | chr1 | 229264525 | 229269563 |
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Enhancer Sequence | CTTGCCTCTT AGCACTCAAG CTGAGGTGTC GAGACCACAT CCCAGAGGGC AAATGGCAGA 60 CAGTTAAGGA GCTGAGCAGC CAGCTGGGGT TGCTTCTTCG TCCCCAGAAG CCCCGCCAGC 120 AACTTCTGTA GACCTGCCCA TGGCCAGGAC CTCGTCACAA AGCCTCCTCT GGATGGGGGG 180 CCAGCCTCTT GCAGCTGCCC ACCCAACCAG GGTGCTCGTA GGTGTCAGGC AGGACTCAGC 240 AGCAGAGAGA CAAGTCTTTC TGAAAGCAGA AAGGGAGTGC TCATGGGGAA TTACATGACT 300 CCCGGAATCA TTAGGAGGCA GGTTCGCTTC CCAAAGCCAC GCCACAGGGC TGGATGCGGA 360 AGGACCTGCC TTCTGCTACA ATTAGGGAGG CCCCAGTCAC ACCGGGAAGC CAGGGCTAAA 420 ACTGCAATGC TTTTTCTAGG AGCTCTGCCC CTACATGGGT GCGTCCCTCC CTGCCTCTGT 480 CTCTCAGCTT AACCCTGCCT CAAATTTAGT CTCGTGACAG AAAAAATGGG ACTAATCTGA 540 TTGGCAGAAC CCACATCACA TCCAGAATCC TAGCGCAAAG GTGCTGGGAA GCGCAGACTT 600 GCTTTCCAGC TGTTGCAGAA CTAATGGCAC AGAGGAGGAA GCTGGGGTGG ATGCCACACA 660 CGCCCATCAG CCACGAGTTA GCAAAGGAAG CAGAGACCTA TTTCCAGGGG ACTTTGGCTT 720 CTGAGCTGCT GGTGGTGGGG GAAGGGAAAG GGAAGGGCAC TGGGGTGAAA ACAACCCTTC 780 TTGCTTTCCT GTGCAGAGGA CTCAGGATGT GGTTGGTGAG CCCATCATCT GGGGAGACGC 840 ATGAAGGGGA AAGGGGGAAA GAAAGCTTCA AAAGAAACAT GGCTGAAGGG TTCCCGTCCT 900 GGAGAAGAAG GGGTGGTGCT GGCCGTGACA CTTACCCTAT TGCCTCACAG ACCTGGAGCG 960 ATTGACCTCT CTTGTGCACA CCAGGGAGTG GGAGGGACAG GGGGATGAGG ACATAGGCCT 1020 GCCTTGAAGA GCTTGCACCC TAATGAGAAA GCTAGAGCTG AGAAGCGCAA AGACAGGATG 1080 GAACAGGCAG GGTCCTTACA GTGCTACAGA TGGGTAAGCT GAGGCCTGGG GGGTGACCAC 1140 CTGCCTGGCA TCCCCTGTGC CAACCTCCAC CCCCCAGCAG GCTACTTCCA TAGCGATCCA 1200 GGCTTCAGAG CATCTCAGGT TCCAGAGAGG CTCCAAAACG CACCAACTCA AAGTCTGTTT 1260 TACTGGAAAT GTTCATGAAA ATCTATTCCA TTACTATTTA GATTATCAAG GCACACCACA 1320 GGGTGAAGTT TAACATGCAG CAAAACTTTT CTCAAGCCTC TTTTTCCAGC TCTCTCACTG 1380 ATTCTCCAAA ACTTCTCTCT TACTCTCTGC TCCCAGCAAA GCCTTGCCTC CTGGCAGCCC 1440
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