Tag | Content |
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EnhancerAtlas ID | HS055-02417 |
Organism | Homo sapiens |
Tissue/cell | FT33 |
Coordinate | chr13:110697770-110700560 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ALX3 | MA0634.1 | chr13:110700501-110700511 | TCTAATTAAA | + | 6.02 | BCL6B | MA0731.1 | chr13:110697938-110697955 | TACATTCTAGGAATCCA | + | 6.46 | IRF1 | MA0050.2 | chr13:110699152-110699173 | AAAGAAAAAGAAAAAGAAAAA | - | 6.17 |
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| Number: 1 | ID | Chromosome | Start | End |
GH13I110046 | chr13 | 110699279 | 110700391 |
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Enhancer Sequence | CCAGCTCACC TTCCGAGAAA GCTGGCTCAC GAAAACACAG AGCAACTGTG GCGATCTTTT 60 GACTGCTCTC TATACACTTT GAAAAAGTCC TCCTTTAATA TTCAAAGCGA CCCTGTTCGC 120 TGTACTTTTG CAGTGATCCG GTATCGTTCC AGGCACAGTT CTGCGGGCTA CATTCTAGGA 180 ATCCACCAAC AACCTTCAGA ATCCCCCTAT AAGAAATGGC AGTTGCATTT CATTTATGGC 240 ACCTTTTAAT GGATGAATAA ATTTGAGCAT AAGAAATTAT TTAAACAAAA TTGCAATTCT 300 GACAGCTGAG CCGATGGAGA AAGAAACCCA AAAGACCTGT CTCCCTTTCG CATTACCTCA 360 CCTCCTCAAG TCATTCCCTT GTTTTCTGTA GAACTCTATC AGCAGATAGA GGAGGGAAGG 420 AGAGGTTGAC CATGTTTCTG AAAAATAGTG GCTGAAACTT TAATGCAAAC TTCATAGAAA 480 CACATTAGAG GCCCACAGGT GGATGACGCA GGAAAGCATG GTGACCTGCT GATTCTGTCC 540 TGAGGCCTCC CACCTTCTCC TGCATCACAG AATCCTTCAC GGCTGTTCTT TCTCCCCAAA 600 ACATCAAACC GCCTCTGACC ACCCTGAATC TCTGTGACCT GAGAGTTCCA CTGAAGTCCA 660 CACACAGAGG GAAGGACTTT GACTTCTCAG TCCAAACTTC CTTTCACTTT AAAAAAAAAA 720 AAAAAAGTTG TGTAATATCC CCCACTCTCC AGCATTGATA ACCGGTAAGT ATATTTGCAA 780 TTTCACAGGA TTTGCCCAAC GCAAAAAAAA CACTTTTTAA TTATCTACTT CTTGCTTGGA 840 ACAGTCTTAT GATTCAAGAA CTGAATCTTA GAGTGGCATT TCAGGCACTG TCCTGTGGAG 900 AGGGGGAGTA GGAGGTGGGT CCAGTTGAAA CAGCGCTTGG GAAGGAGGTA GCCCTCCTCT 960 CCTGCTTGGT GGTTGCCCCC TGATAGGACA CTTTTGAGCA ATGTCTTATT TCATGGTCTC 1020 TACAAAATAA AAAAGGAAAA TATAGCTTCT TCTCCTTAAC CAAGAGAGCC CGTCCCAATC 1080 CCCTAATCCT CCTTAAAAAT ATCCAGACAG GCCAGGCGCG GTGGCTCATG CCTGTAATTC 1140 CAGCACTTTG GAAGGCCAAG GCCGGTAGAT CACAAAGTCA GGAGATCGAG ACTATCCTGG 1200 CTAACACGGC AAAACCCCAT CTCTACTAAA AATAGGAAAA TTAGCCAGGC GTGTAGTCCC 1260 AGCTACTCGG GAGGCTGAGG CAGGAGAATG GCATGAATCC GGGAGGCGGA GCTTGCAGCG 1320 AGCCGAGATG GCGCCACTGC ACTCCAGTCT GGGTGACAGA GACAGACTCC ATCTCAAAGA 1380 AAAAAGAAAA AGAAAAAGAA AAAAAATATA TATATATCCA AACAGCCCTT GTAGGTGCTC 1440 ATGGTCTAAT GCAGAAAGCT TGAAACATTG AGCTGGACTG AAAGTCTGGG AGGAGCCCTT 1500 TCATATTTCA ACACTGGGCC TGGAAAATGC TTTTTGTAAA TGGACAGCTT AGATTCTGCC 1560 CAACAGCCAG GATTGTAAAG TTTATTCGCG TGCACAGTGG TCTCGAAAGC ACTTCCGTAT 1620 AATTAGGAGT GATTGTACTC ACTTGTCAAA TCTGACCAAT AGATTTTAAT TCTCCAAAAC 1680 TCAGCCCATA CATTTCCCAA GGCACAATCA TACATATCAT AAACTATTAT GTTCAAATCA 1740 TAGTAATCTT CAAAATACAA GATAAATAAA ATGCAACATT TCAAGCCTAC TTTCAAAAAA 1800 AATTTAGGTC TAACGATTCT TACTCTCACT GCCTGCTCTA GAAGAGAAAG AGTGTACAAT 1860 AGTACAAAAA TTAATATAGA AACTGCTGCA CCCACTGTTT CTGAGATTGT TTCTCCAGGC 1920 CCTCCAAAGC AATCATGCAA ACTAGTTTAA TTTTTAAAAA TTGTTGGAGT GCTTTATGCT 1980 TGAGTTCTTG TAAGAGATTT AAGATAAAAC AAACACACAC AATCTGTAAA TACCAGCATT 2040 AAAAACACCC ATGTAGGCAG AAGTACACAA AACCACAGGA GATTTTAAAA AGGTGGTGGG 2100 GGTGGGGGGC TTCGAAAAGA TCTGCAGGAA ACAGACGGTG GTTGAAATGG CCTTATTTCC 2160 AGGCCACCCC AGGCTCCTCG TCCCCCGCTC CTGACTTGAA GTGAGCTGGT GGACTCCCTC 2220 CCCTTCTCCA TATCTGTGAT CCAGCTTCCT GCTCACCCGC CCACAGCCCT CAAGTGGACT 2280 GACTACTTTG GCCTCTCTCC CACTGCACTC CAGACAAATC CATTTGTATT CGCACCAGTA 2340 AACATACTCT TGCCAACTGA ACCATTGATA AAACTATGTT ACGACAACCT CCTTTCAAAT 2400 GAGAATGAGC AACTCCTGAG TGACCTCATG GGAGGGGCCA GCCATGCACT GCACAGCTCC 2460 AACTTCATTC CCCAATTTAG CAGACAGTTA CTGAATATCC TTTTACCGTA GGCTGAGCTT 2520 ACCAAGATGA ACACCCGCAG AGGGAGTAGA GTCTAGTCAA GGGGTGCGCT GGACACCAGA 2580 GCTCCTGTGG TTACCCAGCT TCACCAATAG CTGTTTTCAG GTTTTTAAAA AATTAGCCAT 2640 TTTCAATACC ATTCAGGACA TAGGCATGGG CAAAGACTTC ATGATTAACA CAAAAAGCAA 2700 TGGCAACAAA AGCCAAAATT GACAAATGGG ATCTAATTAA ACTAAAGAGC TTCTGCACAG 2760 TGAAAGAAAC TATCATCAGA GTGAACAGGC 2790
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