Tag | Content |
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EnhancerAtlas ID | HS190-01299 |
Organism | Homo sapiens |
Tissue/cell | Treg_cell |
Coordinate | chr1:229264960-229266380 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2A | MA0052.3 | chr1:229265011-229265023 | GCTAAAAATAAA | + | 6.04 | MEF2C | MA0497.1 | chr1:229265009-229265024 | TAGCTAAAAATAAAA | + | 6.32 | 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 | TTCTGCAAAA TCAATGCAGA GAAAGCAGAA AGGCTTTCAT TGAACCGTGT AGCTAAAAAT 60 AAAAGACCCA ACGAGCAAAG ATTCCCTAGT GCTGGGCAGG AGAGGGGATC AGGGAAGTAG 120 AAGAGAGAGG CAGCCTCTGA AGGGGCTCCC ACACAAGTGC AGGGCGGCAG CACCTTAGCC 180 GCAGAGCCCC GGGTGCTCTT CTTCCTGCCG GGACACCTGA GCCCACGTTC TCCTCTGCTG 240 CTTGCCTCTT AGCACTCAAG CTGAGGTGTC GAGACCACAT CCCAGAGGGC AAATGGCAGA 300 CAGTTAAGGA GCTGAGCAGC CAGCTGGGGT TGCTTCTTCG TCCCCAGAAG CCCCGCCAGC 360 AACTTCTGTA GACCTGCCCA TGGCCAGGAC CTCGTCACAA AGCCTCCTCT GGATGGGGGG 420 CCAGCCTCTT GCAGCTGCCC ACCCAACCAG GGTGCTCGTA GGTGTCAGGC AGGACTCAGC 480 AGCAGAGAGA CAAGTCTTTC TGAAAGCAGA AAGGGAGTGC TCATGGGGAA TTACATGACT 540 CCCGGAATCA TTAGGAGGCA GGTTCGCTTC CCAAAGCCAC GCCACAGGGC TGGATGCGGA 600 AGGACCTGCC TTCTGCTACA ATTAGGGAGG CCCCAGTCAC ACCGGGAAGC CAGGGCTAAA 660 ACTGCAATGC TTTTTCTAGG AGCTCTGCCC CTACATGGGT GCGTCCCTCC CTGCCTCTGT 720 CTCTCAGCTT AACCCTGCCT CAAATTTAGT CTCGTGACAG AAAAAATGGG ACTAATCTGA 780 TTGGCAGAAC CCACATCACA TCCAGAATCC TAGCGCAAAG GTGCTGGGAA GCGCAGACTT 840 GCTTTCCAGC TGTTGCAGAA CTAATGGCAC AGAGGAGGAA GCTGGGGTGG ATGCCACACA 900 CGCCCATCAG CCACGAGTTA GCAAAGGAAG CAGAGACCTA TTTCCAGGGG ACTTTGGCTT 960 CTGAGCTGCT GGTGGTGGGG GAAGGGAAAG GGAAGGGCAC TGGGGTGAAA ACAACCCTTC 1020 TTGCTTTCCT GTGCAGAGGA CTCAGGATGT GGTTGGTGAG CCCATCATCT GGGGAGACGC 1080 ATGAAGGGGA AAGGGGGAAA GAAAGCTTCA AAAGAAACAT GGCTGAAGGG TTCCCGTCCT 1140 GGAGAAGAAG GGGTGGTGCT GGCCGTGACA CTTACCCTAT TGCCTCACAG ACCTGGAGCG 1200 ATTGACCTCT CTTGTGCACA CCAGGGAGTG GGAGGGACAG GGGGATGAGG ACATAGGCCT 1260 GCCTTGAAGA GCTTGCACCC TAATGAGAAA GCTAGAGCTG AGAAGCGCAA AGACAGGATG 1320 GAACAGGCAG GGTCCTTACA GTGCTACAGA TGGGTAAGCT GAGGCCTGGG GGGTGACCAC 1380 CTGCCTGGCA TCCCCTGTGC CAACCTCCAC CCCCCAGCAG 1420
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