Tag | Content |
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EnhancerAtlas ID | HS092-00568 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr1:19888840-19891180 |
Target genes | Number: 14 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr1:19889003-19889014 | CATGAGTCACT | - | 6.14 | IRF1 | MA0050.2 | chr1:19890122-19890143 | CTTGAGTTTCTGTTTTGTTTT | + | 6.32 | IRF9 | MA0653.1 | chr1:19890126-19890141 | AGTTTCTGTTTTGTT | - | 6.02 | Lhx3 | MA0135.1 | chr1:19889066-19889079 | AAATTAATTATTG | + | 6.46 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I019562 | chr1 | 19889410 | 19891322 |
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Enhancer Sequence | TCAACCTCCC GAGTAGCTGG GATTACAGGC ATGCACCACC ACACCCAGCT AATTTTTGTG 60 TTTTTAGTAG AGACAGGGTT TCATCATGTT GGTCAGGCTA GTCTCGAACT CCTGACCTCA 120 AGTGATCTGC TGCCTCGGCC TCCCATAGTG CTGGGATTAC AGGCATGAGT CACTGTGCCC 180 GGCCTGGTTC TTGTCCATAG AAATGCAACT TGTGTCCGGT AGAATGAAAT TAATTATTGC 240 CTTGTGGATA TCAACCAACT TTGCCAGTTT CGTACCTAAT CTGTAAGTTC ACTTCCCTGT 300 TCCTTACGCG ACTATAACTG TGAGATATTT TGAACTAGTC GTAACATCTT ATCAATTCCC 360 TCATTACTTA ATGTGTTCCA CAAAATCTTT GATATGGGTT CATTTAATAT CTGTATGAAA 420 GTCATAATTT TATTGTTTTT GAAAATTACC CCTGGACTTA ATATATATAA GGTGCTTAGA 480 ATAGGGTCTG GCACCAAGTA TGGACTCAGT AAATGTTAGC TTTTGTAAGT AACGGATTAA 540 TAACATCCCT TGTTTTATAG ATGAACAGAA TGAAGTGCAG AGGAGACAAG CACATTTGCT 600 TAAATGGCAC TGCTTGCTGG AGATGGAGCA GGAGCTAGAA GCCAAGTCTC TGCTATCAAG 660 CCCCTGCTTT CTTGCTGCCA CCCCCGCCCC ACCCCTCTCC TACCCACAGT CCTCTCTGGC 720 TGTGCTTTGC TGACCCTACA CATTCTTTGG GTTTCATTCT GGATCCTTCT AGGCTAGGTT 780 AGCAGCCCCA ACCCCAACCT TTGTGTCTTC CCCTGTGAAG CTGGTATTGT AAATATATTG 840 CAACTATCAA TTTCTTCATC TAGGCCAGGT GAACTACTGG CTCATGCCTG TAATCCCAGC 900 ACTTTGGGAG GCCGAGGTAG GAGGATGGTT TGAGGCCAGG AGTTTGAGAC CAGTCTGGGC 960 AGGATAGTGA GACCCCACCT CTAAAAAATA AAAAAAGAAA ATCATCTTCA TCTAAGCCAT 1020 GAGCCACACA CAACCAAGGA CCGAAACTGT CTTGATTGCC ACCCAGCCTG GCACACAGCA 1080 AGTAGAAACA CCAGAAGTGA GGCCTCATAT AGGTGTGGTG TTCTCTCCCC TGGGGATGGG 1140 GAGCAGGGCT GCTTTCCAGA ACTGACTGGA AACCCTCTGC TCCTCCATCC TCTGACGGCC 1200 CAAAACTCCC CCAGGCTCCT GGCAGCTCTA GGCAATATCA AGCCTCCTAG AGAGGATGCC 1260 TGGAGCCACT AGCCTCTCAA GACTTGAGTT TCTGTTTTGT TTTTTTCCAA ATAAAATTCC 1320 AGAAATCCAG GTTTAAAAAT AACCAAGCAA TGCAATCTTC TCCACCAAGC TGCTTGGCAA 1380 AAACAAACCC TCAACAAAGA CTAGTGTGCA GTCTCACTTC ACACTTACTC ATTTTCGGCC 1440 GCCAACTCAG CTCTGTTTTG GGTGGGGAGG AAAAGCGGGA GGCAGGACTC CCAGGGGCAG 1500 AAGCGCAAGG GCACAGGCGC TGGGCAGAAG CTGGGCTGGA CCGTAGGGCC GCCCCGGCTT 1560 TGCAGGCACA CACCCGTTTG GGAAGACAGC TGCTAGAGAC TGCTGCGAAG TCCGGTTTTC 1620 CTTGGAGTCC CAACTTGCTG GTCTCCAGCC CTGGATCTGG CAAGAGATCA AAGCAGCCCT 1680 GGAAAATGGT CTCCATTCGT AATCCAGAAT TCATTCTCCT TCCCCGGGGA GACATCAGCT 1740 TCTGCCTGAG CCTGCCTTTC CCCATTATTA CTTAGGGAAC TGGCCGGTCA TAATGGGGAG 1800 CAGCATTTAT GCTCTTGCGG AACAACAACC TCAAGACTCC CCACTTTTTT TGACATGGTC 1860 TATTTTCTAA CCTGTCATCC TTTTTTTAAG GCCCATTTTG TGGGTGAGAA AAACGTGTGA 1920 TGGAAGAGAG GAAATTCAGG ACCAGAGGCC TGGAAAACTG TCAGATTTCA TATTTCCTCC 1980 TCCTTTGAAT CAGCATTAAT GCCCCTCAAT GGGGTTTTCC TGCAAATGCT TGTATAACTC 2040 CCTTTTAAAA CAATTTTTGC TGTTTTTTCC TTTCCCTGCC CCTGGGTAAG TTATTCCAAC 2100 TGACTACTTT CCACCTCAAA AGAAAGTAGT GGACAGGAAA AAAGTGGTCG TGTGGTCTGT 2160 TGGCTACAGC TCCAAGTGGA GCCAGGAGAT TTGGGTTCTA TTCTGAGCCT TTCTGAGAAC 2220 ATGACGAGGG GGAGGGACAC AAACTTGGCT CTTTTACTGG AGTCCAGGGA CTCCATGCCA 2280 ACAGGAGGAA GTTACTTATT CCGGATCAGA AGGGGACCAG GAACTGGCAT TTATTAAACA 2340
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