Tag | Content |
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EnhancerAtlas ID | HS187-01949 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr1:182112380-182113750 |
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 | chr1:182112476-182112495 | TGGCCACCAGAGGGCGCTA | + | 10.32 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_09815 | chr1:182112138-182120273 | CD14 | SE_31808 | chr1:182110721-182115150 | Gastric |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I182142 | chr1 | 182111858 | 182119706 |
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Enhancer Sequence | AGCACAAGTG AACCTTCACA AAGCTGGGCT AAGTGATATT AACGTAGCTG CTATTAACCA 60 GAAATTCCCA GTCAAGTCAA CCAGGCTTGG CAGTGGTGGC CACCAGAGGG CGCTAGAGTA 120 GAGTCCGTGG GAGAACTTCA GCGGTGGCCC TGCAGGTTTG AGAGGCACCT TCCCGGAGGA 180 TGGATTTGAA GGGCTGAGGG TCCAGCAGTT CTGTGGGTTG GCGGCTCACA GGAGAAAGCA 240 TGAAGACATA CTTCCATCCT CACACCCCCG AAGGTCCTTG CCTGGACTGG AAGCTAAAGA 300 AGCGCATGCT ACATTGTTTT CCTAGTGACA AAAATCCCAG CTGGCCTCTG GTTAACTTTT 360 CAAACAAATG GCACTGATGT GATATTGGGC GAACTCTAGG TGTCACTGAC CTAATAAAAA 420 GAAAAAAGCT ATTTGCTTCC CATTTTCCGA TGCAGTGAGG ATTTCACAGT GATCTCAAAC 480 ACAGTGAAAT ACATAAAAAG AGCCTAGCTT AATGGGGGCA CCCAGCAAAT GCCCAATAAA 540 CATCTGTTCC CTTTCCTCAA TAAACCCCAT TTGCCTCTCA GCCTGCAGCC TCCCACACTG 600 GTGGACCCAC GTGCCCCTCA GAAGTGAAGC TTTTGGCCCC TGTAAAGCAG CAGCCCCTCT 660 GGCCAGAGAG TCTTTTGTCC CAGAGCCTTT GTTGTTCCAG ATTTCTCACT GTGAGGCCTC 720 AGCAGCTGCC AGGGGGCCAC CCCAGGAGCT GGAATCAGAG CTCAGAAAGA CAGCAGTCCT 780 TCTTCTGCTC CTTTCTGGGC CCGCATGCCC CAGCCCCACA CCCAGCCTCA ACCACACTGC 840 CCTGCACACC CTCACCGTGC CCCCACTTCT CCACAATGTG TTTCTAATCT GCCCAGGAAC 900 AGTCACCAGC TCACTTTTCC TGCCTGGTCT CATTAGCGTG GCCTCTGGGC CTGGGCCTGG 960 GTGTGTAGCC CAGAGGCTTG CACGGAGGTG ATCAGATTGC AGGGAACAGT ATGTTTCCCT 1020 CCCTGCCTCT GCTTGTTTTC TTCAGGGGCC AGGGCCAGCC AGCTGAGCTG TCTTCCTCTT 1080 CCCCGGCTTC TCATCCTCCC TCACACATGG TCTGACTTCA GTGGGTGGGG GGATGAGCAG 1140 AGGGTGTGAC ACACACGAGT GTGCATGACT GGCATGTAGG GAGTGTGAGT TGTGGGCAGG 1200 TTTCTTAAGG GGAGGCAAGG CTGCTACTAC TCCGGGAAAC AGGCCTGGGA GCCAGGGGGA 1260 GTGGAGGAGG AAGGCCAAGC TGGGGATTTG TACAGACCAG TTCTGGCCAG ATCTCTTAAA 1320 ATGTTTTGTT CTTGCATTGC TGCTGCTGCT GCTGTTGGTT TTTTTCCCCC 1370
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