Tag | Content |
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EnhancerAtlas ID | HS024-04827 |
Organism | Homo sapiens |
Tissue/cell | Cerebellum |
Coordinate | chr14:101837700-101839310 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr14:101837740-101837758 | GAAAGGAAGGAGGGCTGG | + | 6.04 | MSC | MA0665.1 | chr14:101837908-101837918 | AACAGCTGTT | + | 6.02 | MSC | MA0665.1 | chr14:101837908-101837918 | AACAGCTGTT | - | 6.02 | MYF6 | MA0667.1 | chr14:101837908-101837918 | AACAGCTGTT | + | 6.02 | MYF6 | MA0667.1 | chr14:101837908-101837918 | AACAGCTGTT | - | 6.02 |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I101370 | chr14 | 101837287 | 101837933 |
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Enhancer Sequence | CTGCACATCC TCTTGCAGAG CTTGGGAAGG ACCCAGACAG GAAAGGAAGG AGGGCTGGAG 60 CTGGGGTCTT CCCAGTGGAA ACCTAGGCCA TGGGGCTCAC TATACAGTGG TACCGGAGGC 120 ACCTCTCAGA TCCCAGTGGA AATGGCTTTG TGGAAGGCAT AGATTTCGTA GGTGAACAAA 180 GCTGGTCTCA CTCCCAGTCT CATCGTTCAA CAGCTGTTTG ATGAACAGCA CTTGTGTCAC 240 CTGGTAAGTC TCCACTCCTC ACTGTCAACG GGGTCAAGAC CTCCTACCTC CACCGGACTG 300 TTGTCAAGAC TGAGATGAAT GCAAAGTGCC TCGCCCAGCG CCTGGCTCAG AGAACTGACT 360 TCATAAATGG CCGCTCTCAT TAGTAATAAT TTTATAATAA GAACAAAGAC AGAGTTGGTG 420 ACATGGGAGT ATTTCTGAAC TCAGACTAAC AGGGAAACAA CATCCAGGTT TCCTAGGGGC 480 CCAGCCATCT GTGTTCGAAT AAAAACGTGA ATTAGCCAAC AATGTTCGCC AGCCCCACCA 540 TGTACCTGGC AAATGTTTAC TGGCTTTCTC TGCTCTGTCG GACCTGGAGG AAAAGTAGAA 600 TCAGAAATTC CTCTGCAGGA GCTCTGTTCT GTTTCACTTC CAGAAACCAC TGGCTGTCAG 660 GCCACTGCAG TACTCGCACA CTCCAGTTCG GGAAAGAAGT CCCAGTTCCT GGCACGGCGA 720 AGGCTTTCCC TCAATCTGTA AGCAAGACCT GGTCACTGAA GACACAGTGA ATGCAACTCT 780 CCTTCTTGGG TGGCTCTCCT GGAAGAGACA CTCATCAAAG AAGTCGCCAT TCCTAGGCAT 840 CGAGTTGTGT CATACTGGTG ACTTAGCTTG ATAATGAAAA TCTCAAGAAT CAAACTACTC 900 CAAAAAATAA AATTCAGCCA AAGTTTTCCC CAAACCCCTC TACATCAAAA GTCAGCAAAC 960 TATGGCCCAA GGGCCAAATT TAACCCACCA CCTGGTTTTT GTAAATAAAG CTTTATTGGC 1020 ACACAGCCAC GTCCATTTCT TTATATATCA CCTATGGCTG TGTTCACACT ACAGTGGCAG 1080 AGTTGAATTG TCGGCTGTGA CAGAGACCCA CAGAGCCCAC GATGTTCACC ATCTGGCCCT 1140 TGCAGAGAAA GTGGGCTGGC CCCCGCTCCA CATAAACATG GGACAGGTGT CAGCCTCCCC 1200 AACCCCACGC TGCCATGGCC TCTGGCAGGG GTCTGATGCT CCTCTGATCC TGAGCAGAGA 1260 TGGCAAGTAG GTCCCCCTGA GCGGCAGGGT GGGGTGCAGA CTGCATTTCC AGGCTCGTCT 1320 GCAAGAGCTG AGTTGACTGG GGGGCAACGG ACATCTCCCT GAAAATCTTG GCTGGTGTCC 1380 AGTGGACAAT TTGCATGTGG AGCCTGGAAA TACTGGAGTG TGGTCTCACA CACCTAACCC 1440 ATATTAGCAG CTCCTTAGAT GACAGTGATA AAAGCTTCCA TTTGGCAACC GCTTTTATGT 1500 TTATAAAGTG GTTCGTATCC CTTGTTTCAC TTAGTTCTCA GGTCAATCTC ATGAGGCACC 1560 TTGTTTCTTA ATTTGCAGCT GAGGAGACTT ACTCAGAGGG TGATGTGTGG 1610
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