Tag | Content |
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EnhancerAtlas ID | HS096-00110 |
Organism | Homo sapiens |
Tissue/cell | hNCC |
Coordinate | chr1:234905030-234907180 |
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) |
ALX3 | MA0634.1 | chr1:234906047-234906057 | TTTAATTAGA | - | 6.02 | EWSR1-FLI1 | MA0149.1 | chr1:234905838-234905856 | GGAAGGAAGGAACTTAGG | + | 6.66 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_09448 | chr1:234906101-234915704 | CD14 | SE_47205 | chr1:234902504-234911573 | Panc1 | SE_61976 | chr1:234893860-234914718 | Toledo |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I234766 | chr1 | 234902616 | 234912525 |
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Enhancer Sequence | TACAGGATCA AATCCAGTCC CAGTCAGTTT CAGCTGAGAA ACTCAGGTGT GGGCCCAGAG 60 AGTTTAAGAT CACTTGTCCA AATGTTGTGA ATGCCAGAGG CAACACTGGA CTCAGGTGTT 120 CTGGGCAGTA ACCTTTGCTC CTCTCTCCCT ACCACATGCC CCCCAGGCCA GCTGGCCCTT 180 CTGACCAGCA CCATCTGTCT GATGTCTCTT TGCCATTACT CGGAGGCCTA ACCTCAGCAC 240 TGACAGGCTG CTTGACCTGG AACCTCGCCA CTATGTCCTA GCCATGCTCC CTGACACCCC 300 CGCTCTCTAG CAAAACTACT CCCTTCTTCC TCTGCATGCG ATTAATTATC TCATACAGCA 360 TCTCTTTTCT TTTCCCACTG TATTCCTGTT GGTTCAAGAT GTGTCTGCAT TCCTTACCAT 420 TTTACCGGGA ACAGTGTCTT TTTCATCTTT GTCTCTCCAG TGCCTCAATT GCGCCTACCA 480 CGCATGTATT ATACAAATGC GCAGCTTGCT GTGTGACCAT GGCCCAATTG TTCACCGTCT 540 CTGGGCCTTC TCTTGGATTT ATAAAATTAA CGGGGCACTA CTGACTTATC TCACAGAGCG 600 GCTGTGTCCT AATGTATATA TTGTTGCATA AATATCTTGG AAATGCAGTG GCCAACGACA 660 GCGCTCAACA ATAAATGCTG TGTGCTGAGA GCAAGTGTTA GAGAACTTGA AAGGAGGCTC 720 TTCTCTCTGT GATGAAAGAA ACGGAAGGTG GCTCTGCAGA TCCCCTCAGA TGATGCACGC 780 TGTGGACCCG AGCACCGAGC CTGGGTGGGG AAGGAAGGAA CTTAGGAGAG GTGTGAGGGC 840 AAGGGCGTCT TGTGGAGAGA GCTTGACCAA ACCCTGACCC TCCTCTTTGT AGAGCCCCCG 900 GGCTCGTCTG CAGGGTCTGT GCAGGCCGCC TGCCCCCTGC GCCAGCAGGC GAGGAGGACA 960 GCCTCCCCTT CTCAGCAGGA CCCCTAGCCC TGCAGAGGGA GCTGGGAGCT GGCTGCTTTT 1020 AATTAGAGCC GCTTCTTTCC TGTTTTCCTT CGCGGCTGGT TTCCGAGCTT CCCTCACCCT 1080 CTGCTGATTC CCCCAAGCAA TTTTTTTAAG CATCCAAACC GTCTGGGATA AGAAAGGAGA 1140 AAGCTATCAT TATGTGTGTG AGCTGTGCGG TGGCTTCCGC TGGCTTCCCA GACGTTTGGA 1200 GGTCGTCAAA AGGCTGGCTC TGCTGTCTGG ACATGGCCTG AGGAAGCCTG GTGCCAGCTT 1260 TCTGCTTCCT ATGCCACCAG CTCTGCTTAT GTATATATTG AGCACCTGCT GTGTGCCAGG 1320 CCCCCAGATG AGCAAATATA GCGTCAGCCC AAAAAGCTGA GAACTATTGT CATGGCTCTC 1380 TTAGGTCTAG AGCTGTGGCA GTGATCACCA GCACGCTGAC AGAGGTGTGA ACGGAGCACC 1440 CCAGACATGG AGCAGGAATG AGAACGACTG GCACGATGGG TTGCACCAAC GAGAACCTTA 1500 CAAGGAGAAC ACAGCCTCAA TCTGGCTCCC GTTCCCTTTA GAACTCACTC TCGTTCATGG 1560 CTCGTGGAAC CCACATTCAT TCGGAACGCA AGAGGCTCCA GAAGGGCTGT CAGATTTAGC 1620 AAAGAAAAAT GCAGCATGCA CAGTGAGATG TGAACTTCAG ATAAACAACA TATAATTGTT 1680 TAGTGTAAGT ATGCTCTAAA TATTGCATGG GACATGCTTT TTATTATAAC ATTGAAGGTA 1740 TATTTGCACT AAAAAAGGGA TGTGTTGTTT ATCCGAAATT CTCATTTCAC TAGGCATCCG 1800 GTATTTTATC TGGCAACTCT TTTCCAAGGT CAACAGAGAG TCCTAGACCA TAGACCAGAA 1860 AGTCCATTCT ACCCGACACT GGGCTACAAG AAATGTATAT TTGTGGGGAT CAGCCACACT 1920 GGGAGAAAGA TAGCTGTCTC ATGTCACCAG GGTAGATGAA GAAAGGGTTC TAAAGCCTAG 1980 CAGCATTCAT ATGATAGGTA CCTGGGCTTG TTTTCAAAGA TCAGCAATCA AGGGGAAATG 2040 ACAGAGACGC TGGAGGAGGC TGGTCCTCCC AGAAGCTAGT GGCTTGACCC AAGAAGGAAG 2100 AAAATGGCGG CTGCCTTCCC GGACCCAGGC TGTAGGCCGG GAATTCCCAG 2150
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