Tag | Content |
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EnhancerAtlas ID | HS197-05032 |
Organism | Homo sapiens |
Tissue/cell | ZR75-30 |
Coordinate | chr12:56273880-56275780 |
Target genes | Number: 29 | Name | Ensembl ID |
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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) |
HES2 | MA0616.2 | chr12:56273929-56273939 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr12:56273929-56273939 | GGCACGTGCC | - | 6.02 | IRF1 | MA0050.2 | chr12:56275279-56275300 | TTTTTCTTTTTCTTTTTTTTT | + | 6.09 | Nr2f6(var.2) | MA0728.1 | chr12:56274506-56274521 | AAGGTCAGGAGTTCA | + | 6.04 | Nr2f6(var.2) | MA0728.1 | chr12:56275507-56275522 | TGAACTCCTGACCTC | - | 6.22 | ONECUT1 | MA0679.1 | chr12:56275646-56275660 | AAAAAATCAATAAC | + | 7.1 | ONECUT2 | MA0756.1 | chr12:56275646-56275660 | AAAAAATCAATAAC | + | 7.28 | ONECUT3 | MA0757.1 | chr12:56275646-56275660 | AAAAAATCAATAAC | + | 7.95 | RARA | MA0729.1 | chr12:56274506-56274524 | AAGGTCAGGAGTTCAAGG | + | 6.5 |
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| Number: 2 | ID | Chromosome | Start | End |
GH12I055880 | chr12 | 56274781 | 56274930 | GH12I055881 | chr12 | 56274941 | 56275257 |
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Enhancer Sequence | TGACAAAACA CCGTCTCTAC TAAAAATACA AAAATTAGCT GAGCGTGGTG GCACGTGCCT 60 GTAATCCCAG CTATTCAGTT GGCTAAGGCA CGAGACTCGC TTGAATCGGG AGGCGGAGGT 120 TCCAGTGAGC CGAGATTGTG CCACTGCACT CTAGCTTGGG CAACAGAGTG AGAGTAGGTC 180 TCCAAAAAAA AAAAACAAAA AAAAAAATTA GCTGGCTGTG GTGGCGGGCG CCTATAATCC 240 CAGCCACTCA GGAGGCTGAG GGAGAAGAAT CACTTGAACC TGGGAGGTGG AGGCTGCAGT 300 GTGTGGAGAT TGTGCCACTG CACTCCAGCC TGGGTGACAG AGGGAGATTG GGTCTCCAAA 360 AAAAAAAAAA GTAAAAAAAA AAAAAAAGAT GTAATTCTGT GACATCAACA ACTGAAAGGG 420 GTGGGGATAG AGCTATAAAG GAGCAGAGTT GCCAGGCACA GTGGCTCACG CCTTTAATCC 480 CAGCACTTTG GGAGGCTGAG GCAAGAGGAT TGCTTGAGCT CAGGAGTTCA AGACCATCTT 540 GGGCAACATT GCATGACCTC ATTGCTGGGC GCAGTGGTTT ATGTCTGTAA TCCCAGCACT 600 TTGGGAGGCT GAGGCAGGCA GATCACAAGG TCAGGAGTTC AAGGACGGCC TGACCAATAT 660 GGTGAAACCC CGTCTGTACT AAAAATACAA AAATTAGCTG GGCGTGGTGG CCTATGCCTG 720 TAGTCCCTGC TACTCAGGAG GCTGAGATAG GAGAATCGCT ATAACCCGGG AGGCAGAGGT 780 TGCAGTGAGC CGAGATTGTA CCACTGCACT CCAGCCTGGG TGACAGAGTG AGACTCCGTC 840 AAAAAACAAA AAACTTTAGA ATGCTAAATG TCATCCCCAT GGAAACCACA AAAAAATAGC 900 TATAGAATGT ACATGAAAGG AAAGGAGAAA GGAACTTAAA CATTTCACTA CCAAGAAACC 960 AACCAAACAC AATTCTAAAT AGAAAACAAT ACTGCCCAGT CTGGGCCTAA TTAGGAGAAA 1020 GAAACCACAC AGTAATTTGA ACAAAAAAAG TTTAATATAC CAAAGGGCAG AAAAGAAACT 1080 GTGATGCCAC ACCCTCAGGA CTTGCTGGAA GTCTGCCCTG TAATGTGTCA GAGAAAACTA 1140 TTCATGAGAA GATGCCTCAC CTTTTGCTAC AAAACCATCC AAGAAGGGGA ATGCCATGGA 1200 AACTGCTGAG CTCTGGGCAC TGCTTGCCAC CATGCACTGC AGGAGCCAGG CACTGGAGAA 1260 GCCTTGCAAA ATGCCGGAGC ACATCAGAAC CAGGAAACAA AAGACCTTCC TCCTGTAATG 1320 TCTCTGCAGT GCTCTCTTCT GATAAAGCTT CAGTGCCTAC TGGCAAAGGA AAACTACTCA 1380 AAGCATCCCC ATTCATTTCT TTTTCTTTTT CTTTTTTTTT TTTTTTGAGA CGGAGTCTCG 1440 CCCTGCCACC CAGGCTGGAG TGCAATGGTG TGATCTCGGC TCACTGCAAT CTCTGCCTCC 1500 CAGCTTCAAG CGATTCTCCT GCCTCATCCT CCTGAGTAGC TGAGATTACA GGCGCACGCC 1560 ACCATGCCCG GCTACTTTTT GGATCTTTAG TAGAGATGGG GTTTCATCAT GTTGGCTAGG 1620 CTGGTCTTGA ACTCCTGACC TCGTGATCCA CTCACCTTGG CCTCCTGAAG TGCTGGGATT 1680 ACAGGCTTGA GCCACTGCTC CCTGCCATAC CCCCATTCAT TTTTACAGAG CAGGCCAAAA 1740 GGGTGAATTT GGAGCTAAGA GACAAAAAAA AATCAATAAC CATCTCGGGG TTGACCTCTG 1800 TTGATTATCT TTTCCCTTGA TAATTAGTCA TATTTTCCTG CTTTATGTGT GTGTTGAAGA 1860 CTTTTGGACT ATGTCCTAGA CATTGTGAAT GTTATGTTAT 1900
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