Tag | Content |
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EnhancerAtlas ID | HS187-12966 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr2:25598730-25600060 |
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) |
CTCF | MA0139.1 | chr2:25599753-25599772 | GCGCGCCCCCTGGCGGCCA | - | 6.64 | MEF2B | MA0660.1 | chr2:25599914-25599926 | ACTATTTTTAGC | - | 6.11 | MEF2C | MA0497.1 | chr2:25599913-25599928 | GACTATTTTTAGCAC | - | 6.05 | TBX21 | MA0690.1 | chr2:25599392-25599402 | AAGGTGTGAA | + | 6.02 | ZNF143 | MA0088.2 | chr2:25598786-25598802 | GACCCACGATGCATTT | + | 6.24 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_59929 | chr2:25599094-25648690 | Ly4 | SE_60720 | chr2:25584365-25647609 | DHL6 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I025376 | chr2 | 25599172 | 25601348 |
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Enhancer Sequence | GCTCAGGGTG GCTGGGACTT ATGGACAAGA ACTCGGTGGA GCTGTTGCTT CCTCAAGACC 60 CACGATGCAT TTGGTAGCCC TCCCGGGGTC CTCCAGCACT GCAAAACAGC GCCAGCCCAG 120 GCTGTGGTGC TGCACGGCAG CCTGGCTCAC CCAGGAGTCA GTGATGCTGC AGTTTCTCAA 180 AAAACCGTCT ACCTAGGTTA AATTAGCCTG CTCAGTGGTC ACAGAGCAAT TAAGATGGAA 240 GTGCCCATCT TCCTTCCGTG ATGACCACCT GTGTTCCTCG CCAGGATTGA GGAAAGGGAC 300 CCAGTTCCAA AGGTCTGACA GGCATGTGGG TCCTAAAGCA GACGCCAACA GTCATGAGGG 360 AGCTCGGGGC TTAGGTAATG GCGGGTTTTC TAGCTCTACG AGAAATCAAC CTCAGCAAGA 420 ACGGGTATCA CCAGAGTGCA CCCGGTACCT GAGTGCTGGC CTCAGAGCTG AAAACACAGA 480 GAGTCAGCAG GGGCTTGGGC AGAGAAGAGG GCCCCACGCC CTTGGAAACA GGGAGCTCTG 540 CTTGCCTGAA GAGCCAGAGA GGGGCCACGG TGAGCGCAAC TCCGTGGAAA GCTCGTGGGG 600 ACACAGTGCC AACCAATGGG AAGATGAGCT ATGGGGGAGA AGAGACAGAG AGGAAAGGAC 660 GGAAGGTGTG AACACCCACC CCTTCTATTT TACCCTGACT GGGCCTTGGC AGGCTTGCCT 720 GGGACTCCAT CCGTGTGCGG CCAGGAGTTG ATCCCACCGT CTCTGCACAG ACCTCCTCAA 780 AGCCAAGGGC AGGGGTCTGC AGAGGTGGGT GAGGGATGCT GGGGAGCCAG CTGTGGGGCT 840 TCTCGCTTCA TTACAGTCAC TGCCCTTTAT AAATATTTAT AGCAGTTCTT CTGCTAAAAA 900 TAACATCCTG GAGCCCAGGG AGGAGGAAAA AATAAATGAA AATCACCGGG AACGGGACTT 960 GATCACGTGT GCCCGAGCCC AATCGACCCC TAAGGCGAGA GGCTGCGAGC AGCGCCCCCG 1020 GCGGCGCGCC CCCTGGCGGC CACGGAGTCC GCGGCGCAGA GACCCTCCCG CCCTCTCCGA 1080 GGAGGCTCAG CCCGGCTGCG GCGCGCGGCT GGGTCTCCGC CCCTCCCTCC CGGGCTGCAG 1140 GCGGCGGCAT CACACGGGGC GGGCGGAAGC CTAACCAGTG TGAGACTATT TTTAGCACCG 1200 TGGCCAGGGT GTGAATGTCT ACAGAGCCGA GCAAGGCCTG ACGCTTTCTT TGCACGCTGG 1260 AAGAAACCTG TTGGTTTTTA AAGGTCAAAG ATAAGGAAAC TTGTGCCCCC ACGTTCAGGA 1320 GCACCCCACG 1330
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