Tag | Content |
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EnhancerAtlas ID | HS148-04727 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr12:116194960-116197500 |
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) |
HOXA13 | MA0650.2 | chr12:116196657-116196668 | GCCAATAAAAC | + | 6.14 | IRF1 | MA0050.2 | chr12:116196886-116196907 | AAAAGGAAAGAGAAAGTGCCT | - | 7.11 | SPIC | MA0687.1 | chr12:116196462-116196476 | AGAAAGGGGAAGAA | + | 6.03 | Stat6 | MA0520.1 | chr12:116195159-116195174 | ATTTCTCAGGAAATG | - | 9.03 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I115753 | chr12 | 116191517 | 116197215 |
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Enhancer Sequence | ATTGGAAGCA ATTGACTCTC AGCAAATGTT GGTCTTTTAT AAAGTTCATA ATTTCCCAGT 60 AAATTATTTT TAGTTACTAA ACATCTTAAA CATGAAGGAT CTTAAAAGAA TTCCTCATCT 120 GCCACCACAC ATACATGCAC AGAAAAAAAT TATAAAGTTT TCTAAAAGTG CGTTTTTAAA 180 AGACCTCAGA AACGGAAATA TTTCTCAGGA AATGTCGAAC ACAAATGTCT ATATAATATC 240 TACATGAAAT AATAAATCAA AATCAGTTTT TTTCATCTGA CAAAACACAA TAAACGGGTT 300 TAGAATATTG TTTGAAGCAT TTTTTTTAGC TTTCCAAAAG ACCAATAATA GATGATGCCC 360 TATTGGGAAA GATAACATGT GTTTTCTTGT AGCTTGGTGG GAAAAATATT TTTTGCTCTT 420 TGTAAAGGAA ATCAGATATA TATTTGGGGG AAAAGAATAT AATGTTTCAC TGTGATACGG 480 TCCAACAAAA ACCCAGGAAA TTCAAGGTTC AACTGATGCT TGGCTAAAAA TTCACACCAT 540 TGTGCCCCTT TACTGATGGC AGATTTCGAA GCCCAGAATG TATGGGTGAA CCTCAAGTTT 600 CCTAACTTCA GCCTCTTATG TCTAAACATC AAATTGTTAT TTAACTATTA GCCGGTGTTA 660 GACTGCCTGC CATTTTTTTT CTTTTGTTTT CCCTTGGATA TTTTATATCT TTGCTGATCT 720 TTCCAGCACA TCACCTGAAA CGTATATACT GCATTTTAAT CCCAATGGCT GATGCTATCT 780 CTGGATAAGC TGAATTTCTT TTTCAATGGG AAGGGTATTG GACGAGAGAG AAGAATCACA 840 GAATAGCAGG GTGTTTGAGC TGAGAGAAAC TGGGGATACA GAGAAAGTAA GAGAAAACAC 900 AGATGGAATG AAAAGCTGGA GAACTGGGAT AGAAGGGGAC CCAGAATTGT CAATGGATTT 960 CTTTTGGTCT ATGCCTAGAA ATACATTAAC TGTTAGGGAG TCTTCCCTTC AGGAAAGTCT 1020 CAGTTCCAGA ATCAAATTAT AGGACCCAAC ACATTGTCAA ATATTTAAAC CTCTAGTGCC 1080 ATACCATTTG TAGATTTCGA GATCATTACT TTACTACTAG ATTGTTAATT ACAATGAAGT 1140 AATGGCAGAC TGGGCTTGTA GATTTTATGG ATGCCGCTTC TGTGTGAGTG ATTGTTAATA 1200 CTAAAAGCTT AAACTTTAAC TGCATTTTAA GCATCTGGGA CTGGAGCGAA AGCGGGAGCT 1260 GTGAGTAAAT GCTTTCAGCA GGTATGTAGT TAGTTATTAA AATGGGCTTT GAAGCTCTCT 1320 TTTGGTGTAT TTCTGCATAT TTTAAGGGTC CAGGCCAAAA AGAAAAAAAA CACTTTTTTT 1380 TTAATGCACT TAATTTGGAT TTCATTGAAT TTTCTTCACG CACTGATGTT AGGATATTTT 1440 GACAAATGTA ATTCCCCAAC CCCTCTGTAT GAAAGAAAAG AAACTCTTTT TTGAAGAGAT 1500 TTAGAAAGGG GAAGAAAAAT CCTTTTTAAA AGGCTTAAGG GTAAGGAGGG GTAAAGCGAA 1560 TAAGTGGTAG GGGAGGCTTT TATTTTCTAA AGCTCAAATT CCAAAGAAGA AGGACAGTCC 1620 ACGTAAGAAC TGAAACTAAT TTACCTGAAC CCTTTGTCAC TGCCTGGCTC TTGACTATTA 1680 AATGATTCTT TTCAGTAGCC AATAAAACCA AATCAAAAGC ATGTTTTGGA TGGAGGGGTG 1740 GTGCCAGGCA ATTCCCCCCA CATGAAAAGC CAAACTATGC TGTGTTTGTT TTGGTTTTCC 1800 CCTAAGAGGA TTTTCAGAGA AGGGGCTGGG GTTTGGGCCA CCCTCCTTGG CCCCACTCCT 1860 ATGAGGGAAT ATAGGGGACT GTTTCGTTCT CGTCCACGAA GCTAAACTGC CCATCGGTAT 1920 TACCCAAAAA GGAAAGAGAA AGTGCCTGCC CTGCAGTCAG GTCTACAAAC CCTGATGTTT 1980 TGTCTTTGTT TCCCTCTCAA AGGCTGTTTT AAGATCCCTG CCAATGCAAA GACTTGGGGA 2040 ACTGTTTGTC ACTTTTCAGA AAACAGCTCA GACTTTCTGG GCCTTAATAT CCCTACCTTT 2100 AAACAGCACC GATATTCACT GCCTTCTGTC TTCGAAGATG CTAGAGATGT TGTTTTCAAA 2160 GATTTGGGAA TCCTTAAAAG CAAAGAGCTA CATAAAAATA CAGAGATTAA AAAAAATGGC 2220 AGCCCACTTC TTTCCATTCC TGATGCCCAG TTTGGTTTGA ATACGTAAGA ATTCTGTAAC 2280 AGTGCCTAAT AACGATTACT AATAACAAAA GTATCTAACA CAGAGTGGGC CTTCAATATT 2340 GAATATTTAA CCTTAGTAGA GGTATTAGCC TTTCAAACTC TTCCCATCTT TAAACTGGAA 2400 GGGAATTTTT GCCCTATTTT ATCAAGTAGT GGAAGACATG AAGATAAGAC AGTTCGATAA 2460 TTACAGTCCC CGGAATTTCC ATGCTTGAAC AAGGATTTGA GGTACCTTAT TTCAAGTCTC 2520 TTTTCCAGAC AATGAAATGC 2540
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