Tag | Content |
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EnhancerAtlas ID | HS055-00491 |
Organism | Homo sapiens |
Tissue/cell | FT33 |
Coordinate | chr1:151525050-151527430 |
Target genes | Number: 16 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:151526019-151526037 | GGAGGGGAGGAATGAAAG | + | 6.23 | FOXC1 | MA0032.2 | chr1:151526515-151526526 | TAAGTAAACAT | + | 6.02 | Nr2f6(var.2) | MA0728.1 | chr1:151527398-151527413 | TGAACTCCTGACCTC | - | 6.22 | POU2F2 | MA0507.1 | chr1:151526119-151526132 | TACATTTGCATTT | + | 6.03 |
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| Number: 2 | ID | Chromosome | Start | End |
GH01I151552 | chr1 | 151525095 | 151525575 | GH01I151553 | chr1 | 151526301 | 151526343 |
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Enhancer Sequence | ACGCCGGTAA TCCCAGCTAC TTGGGAGGCT GAGGCAGGAG AATTGCTTGA GCCCGGGAGG 60 TGGAGGTTGC AGTGAGCCGA GATCGTGCCA CTGCACTCCA GCCTGGCCGA CAGAGCGAGA 120 GGGACTCTGT CTCAAAAAAA AAAAAAAAAA AAAAAAAAAG GCATACAGAT TTATTTGATC 180 ATAGTTTTAG GTGACATAGG AACCTTCTGA ATGAAGACCC AAATATACAG AGGAAAACGT 240 CCATTATTTT TAAATTTTCA ATTTTTATTA TTTTTTAAAA GCTAGCCTTA CTGAATCAGA 300 AGCAGTCCAT TCTTAGATTT GAAAAAGTAT AGGCAGCTGT GTAGAAATAT GATTGGACAA 360 AAAGGGTATG ATCTAATGCT GAGAGACTAA ATGGGGAAAC CCAGCAAGGC CTGTCTGTCT 420 AGATTCTTCT TGACCTCTCT AAGCATTCCT TCCAGGTGTG AGACAGGGCC CTCTCTGGAA 480 TGGGGGTCTT ATGACTTCAG ATCAAGCAAG GTGGGTCAGA TAATTTTTTT TTTTTTAGAT 540 GGAGTCTTGC TCTTGTCCCC AGGCTGGAGT GCAGTGGCAC GATCTTGGCT CACAGCAACC 600 TCCACCTCCC AGGTTCAAGC AATTCTCCTG CCTCAGCCTC CTGAGTAGCT GGGACTACAG 660 GCACCTGACA CCACGCCTGG CTAATTTTTC TATTTGTAGT AGAGATGGGG TTTCGCCATG 720 TTGGCCAGGC TGGTCTCGAA CTCCTGACCT CGTGATCTGC CCACGCCTCC CAAAGTGCTG 780 AGATTACAGG CATGAGCCAC TGCACCCGGC CAGATAATTT CTTTATAGCT AGCTTTTAAT 840 AGAAAGAGAG GTGGAAAGTC AGAGTAATAT TTTTAGGTTT TATGGCTGGC TTTGGGGAAA 900 AGGGGTTCTG GTTTCTATGA CCCACCTTGA GAAGAGGGAT TCTAGTTTCT ATGGCTAGCC 960 CCGGGATGGG GAGGGGAGGA ATGAAAGGCC AGAAAAGAGG TCAGGAGAAA GTCAGAGAAA 1020 ACTTTTTTCT TCCGAGGTCT TCATTTTGGG GTATCATATT CTGAGATCCT ACATTTGCAT 1080 TTCTGTTGGG TAGAGTAACT AGTGGTGGAA TTGCTGTGCC TTAGAGTACT TTTGTGTTTA 1140 TCTTTGGTCC ATGCTTCTGA ATTTTCCAGC GATTGTGTTG CTGCGCAATC CCAGCATCAG 1200 TGTCTCAGAG TGTCGGTTGT TCCACATCTG CTGAACACTT CGTATTTTTT TTTTATCCAT 1260 TTCATGTTAG TCATTCTGAT AGGTATTTTG TGGCATTGTT TTGTGGTTTT ACTTTCCAGC 1320 TCTTTGATAA TGCCTAATGA AGTTGAACCC CTTGTCATAT GTTTAATGAC TGTTTGGGTA 1380 TCCTCACAAT GATGTGTCTG TTGGCATCTT CTGCCTGTTT TTCTATTGGG CTGCATGTCT 1440 GGCTGGCTGT CTCCCTTTCT TTCTTTAAGT AAACATTTTA TTTTGAAATA ATTTTAAATT 1500 TACAGAAAAG TTGCAAAGTA GTACAGAGAA CTCTTATATA CCCTTCATCC AGTTTTCCCA 1560 CAATGTTAAC ATCTTATGTC ACCATGGCAC GTTTGTCATA TAAAGAAATT AATGTTGGTA 1620 CAATGCTGTT AACAAAGTTG TAGACTATCT GGGTTTCACC ACTTTTTCCA CTAATATCTT 1680 TTTTCTGATC CAGGATTCAG TCCAGGATCC CATGTTAATC ATTTTGTTTA GTAGGAATTC 1740 TTTATATATT CTGGACATCT TTTGTCAGAT ATACATATAG TGAATTTCTT TTGCTCTGTG 1800 GGTTGCCATG CAGTGTTTTT TTAAATTTTA TTTTATTGTT ATTGAGACAG AGTCTTGCTC 1860 TGTTGCCCAG GTCGGAGTGC AGTGGCACGA TCTTGGCTCA CTGCAACCTC TGCCTCCCGG 1920 GTTCAGGCAA TTCTCCCGTC TCAGCCTCCT GAGTAGCTGG GACTACAGGC ACGTGCTACC 1980 ACACCCGGCT AATTTTTGTA TTTTTAGTAG AGATGGGGTT TCAACATGTT GGCCAGGCTG 2040 GTCTCGAACT CCTGACCTCG TGATCTACCT ACCTTGGCCT CCCCAAAGTG CTGGGACTGT 2100 GAACCACTGT GCCCGGCCCC CTTTTTTTTT TTTTTTTTTT TTTTTTTGAG ACAGAGTCTC 2160 ACTCCGTTGC CCAGACTGGA GTGCAATAGC ACAGTCTTGG CTCACTGCAA CCTCTGCCTC 2220 CAGAGTTCAA GCGATCCTCC TGCCTCAGCC TCCTGAGTAG CTGGGACTAC AGGCATGTGC 2280 CACCACTCCT GGGTAATTTT TGTATTTTCA GTAGAGACAG GGTTTCAGCA TGTTGGCCAG 2340 GCTGGTCTTG AACTCCTGAC CTCAGGTGAT CCACCCACCT 2380
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