Tag | Content |
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EnhancerAtlas ID | HS051-01934 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr1:182112280-182114660 |
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 | HNF1A | MA0046.2 | chr1:182114120-182114135 | AGTTAATAATTAAAG | + | 6.15 | HNF1B | MA0153.2 | chr1:182114121-182114134 | GTTAATAATTAAA | + | 6.24 | IRF1 | MA0050.2 | chr1:182113888-182113909 | AAAAAAAAAAAGAAAGTAGAA | - | 6.99 |
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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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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I182142 | chr1 | 182111858 | 182119706 |
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Enhancer Sequence | GTCCCCATGA AAATAACGTA GATGAAGCAG CAGAGAACTG ACAAAGGCTG TGGAAACATG 60 GAAAGAGTAA TGATAACGCA GAAATCAGAG GTGAAGTAAA AGCACAAGTG AACCTTCACA 120 AAGCTGGGCT AAGTGATATT AACGTAGCTG CTATTAACCA GAAATTCCCA GTCAAGTCAA 180 CCAGGCTTGG CAGTGGTGGC CACCAGAGGG CGCTAGAGTA GAGTCCGTGG GAGAACTTCA 240 GCGGTGGCCC TGCAGGTTTG AGAGGCACCT TCCCGGAGGA TGGATTTGAA GGGCTGAGGG 300 TCCAGCAGTT CTGTGGGTTG GCGGCTCACA GGAGAAAGCA TGAAGACATA CTTCCATCCT 360 CACACCCCCG AAGGTCCTTG CCTGGACTGG AAGCTAAAGA AGCGCATGCT ACATTGTTTT 420 CCTAGTGACA AAAATCCCAG CTGGCCTCTG GTTAACTTTT CAAACAAATG GCACTGATGT 480 GATATTGGGC GAACTCTAGG TGTCACTGAC CTAATAAAAA GAAAAAAGCT ATTTGCTTCC 540 CATTTTCCGA TGCAGTGAGG ATTTCACAGT GATCTCAAAC ACAGTGAAAT ACATAAAAAG 600 AGCCTAGCTT AATGGGGGCA CCCAGCAAAT GCCCAATAAA CATCTGTTCC CTTTCCTCAA 660 TAAACCCCAT TTGCCTCTCA GCCTGCAGCC TCCCACACTG GTGGACCCAC GTGCCCCTCA 720 GAAGTGAAGC TTTTGGCCCC TGTAAAGCAG CAGCCCCTCT GGCCAGAGAG TCTTTTGTCC 780 CAGAGCCTTT GTTGTTCCAG ATTTCTCACT GTGAGGCCTC AGCAGCTGCC AGGGGGCCAC 840 CCCAGGAGCT GGAATCAGAG CTCAGAAAGA CAGCAGTCCT TCTTCTGCTC CTTTCTGGGC 900 CCGCATGCCC CAGCCCCACA CCCAGCCTCA ACCACACTGC CCTGCACACC CTCACCGTGC 960 CCCCACTTCT CCACAATGTG TTTCTAATCT GCCCAGGAAC AGTCACCAGC TCACTTTTCC 1020 TGCCTGGTCT CATTAGCGTG GCCTCTGGGC CTGGGCCTGG GTGTGTAGCC CAGAGGCTTG 1080 CACGGAGGTG ATCAGATTGC AGGGAACAGT ATGTTTCCCT CCCTGCCTCT GCTTGTTTTC 1140 TTCAGGGGCC AGGGCCAGCC AGCTGAGCTG TCTTCCTCTT CCCCGGCTTC TCATCCTCCC 1200 TCACACATGG TCTGACTTCA GTGGGTGGGG GGATGAGCAG AGGGTGTGAC ACACACGAGT 1260 GTGCATGACT GGCATGTAGG GAGTGTGAGT TGTGGGCAGG TTTCTTAAGG GGAGGCAAGG 1320 CTGCTACTAC TCCGGGAAAC AGGCCTGGGA GCCAGGGGGA GTGGAGGAGG AAGGCCAAGC 1380 TGGGGATTTG TACAGACCAG TTCTGGCCAG ATCTCTTAAA ATGTTTTGTT CTTGCATTGC 1440 TGCTGCTGCT GCTGTTGGTT TTTTTCCCCC CTTCCCTGTG CTGAGCTGTC ATTTCTTAGT 1500 CCAGCCAGGC CCTTATGAAC TTCTGGTTCC TCTAAACGGT AAACACCCTG GTTTTCCAGA 1560 CTACACCATA GCTCTCTTTT CTTATTTGCC TTCAAAATAC ACTTTAAAAA AAAAAAAAAG 1620 AAAGTAGAAA ATGGCAATAT CAGTGATAAG GGCAGGGCAT GCACTGAAAA AGAACAGTTC 1680 AATCTAACAT TTATCGAGCC TGCCACCTTC CTCAGCTTTA TTCTCTCCTT TCTTGTTCTT 1740 GGTAACAGCA GATAAGAAAT CAGCTGTGGG TCAATACGTG AAAAATGTTC ACTCTTTTAG 1800 AGTAGTATTA AAATAAATAT TTTCAATGAC AACATTAAGC AGTTAATAAT TAAAGCATGT 1860 GCATATGTAT ACTTAAAAGG GGCTGGAGTC CCTTCTGTCC AAATCAAATT TTCCACAAGC 1920 GTTGGTAACA AGGTGGCTGG GAATGTTGAG ATGTGAGACT GGCCTTCCAA GGATCAGGAG 1980 GGCAGCTGGT GGTGGGTCTG CTCTCTCTCA TCACTCTCAG TGGCGACATC ACCGTCCATC 2040 CTCCCCAGTA CTAAGATCTG CTTCAGGAAA GAGCCTGAAA CCAGCCACAT GTATCTCATG 2100 TTGGTGAAGG AAAATCACAG TAGTGGTCCT CAGTGGGACT CTAAAATGAC TTCACATCAG 2160 CCTCATTTGG TAAATGAGGA AACTGAGGCT CCAAGAGGTG ATGTGTGTCA CCCAAGTTTC 2220 CATAGCAGAG CTAGAAAAAG ACCTTGTTCC TGGGGTCCTG GGAGAGGGTC CTACTGCCCA 2280 GCTCTGACGG ATGAAAGGAA GGCTTTTTTC CATGGTACCA GCTGTTGCTA TGGGCAACCC 2340 TAGAGATCAC TCTGTGGGGT GTGGGATCCT TCGGGAGAGC 2380
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