Tag | Content |
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EnhancerAtlas ID | HS002-02165 |
Organism | Homo sapiens |
Tissue/cell | A375 |
Coordinate | chr11:126412860-126414960 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF4 | MA0039.3 | chr11:126413364-126413375 | ACAGGGTGTGG | - | 6.14 | NR2C2 | MA0504.1 | chr11:126413894-126413909 | CGGGGTCAGGGGGCA | + | 6.53 | PBX1 | MA0070.1 | chr11:126413058-126413070 | GCATCAATCAAA | + | 6.32 |
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| Number: 3 | ID | Chromosome | Start | End |
GH11I126543 | chr11 | 126413753 | 126413870 | GH11I126544 | chr11 | 126414241 | 126414450 | GH11I126545 | chr11 | 126414521 | 126414750 |
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Enhancer Sequence | ACATTATCTT ACCTAATCCA CCTTCATAGC ACCCCGTGGA GCAGGTCCCA TCATCAGCCC 60 CCATGTAGAG ACTTGAATAT CACAGCTCCA AGCCAGATGT CCCCCGTGAA TATACCCTCC 120 CAATTCTGCC CTATTCTACT CCACTCTGCC TCTCCTGTCA CCCCCCAAAC AGAGGCCCTG 180 CAAAGCCTCA GCTGGTCTGC ATCAATCAAA GAGAACGAAG CAAAACTAAC TTGCCATTAC 240 TGCCCTAGTC TCTCTGATTG TTGGAAGTAG AGATGTTTCA AGGAGAGGTT TTGTGCTGGA 300 AGCCCCTTGA AAGGATGGAG AGGGAGTGTG AGGACTGCCG GAGACGCCCA GCCTAGGAGG 360 GGAAGCTTTC TGCTTTTCCA GCAGGACAGA ACTCCTTAGA AGCAGGTGTA GCCCTGGCTC 420 ATATCCACCA TCCTGAGAAA TAGAAAATCT TTCCCATTTT ACGGACAAGG AAACTCAGAG 480 AGGTTAACTA ACACATCCAG GGTCACAGGG TGTGGTAGAG GTAGGGTTTG AGCCATTTGA 540 CTCCAGGCCT GGCTTTTTTT CCCCCAACAG TAGCCGGTCA GCAGAGGGTG TTTGATCTGT 600 GTGGTTTCCT CTTCAGAAAG CAGAGACTCA CTACTGTGCC CCCTACCTGC CCCCAGCTGA 660 GCTCCAAAAA CAGCTATAAA GCTGATGGGA AGCCGATAGG ACAGCCCCTG CCCTTCCTGA 720 AGACCACGGA AACCTCTCCC ATGGTGCCCT TGGGGCTGAG ATCAGCTCTG TCACCAATAC 780 TTCAGGGCAA AAGTCGTTGG CACCACTTTT AATCCTAATC CTGTGTGGCC TTATTCAGAA 840 GCCCTTTGCA AAGGCCGATC CCTAGCCATA GCTCTCTCTG CTCGGCCTTG GGCTGGGTGA 900 ATAATGACTT CCATTTCCTG CCCTGCTGGA GCCTTGGGTC TTTGCCACTG CCACCGTGGT 960 GCTGAGCCAC TTATTTGTTG TGAGATGACC CAAGGAGGAC CAGCCGGTAC CTGCTAGGCC 1020 CTTCTGCTGG GGCACGGGGT CAGGGGGCAG CACATGGGCA TGTGGCCCCA CTCCTGTCTG 1080 CTCCCCAGGA CAACTCTATT TTCCAGCATG GAGTGCCCCT GGAGGTGGCG ACAGCTCCTC 1140 TAATAAGAGA GTTACTCATG GCTTCACTGG AGAGAAGAGA GCAGCTTTCA ACCCCCCTCT 1200 CCTAAACGCA ACGATATTTG GTAACATGCG GCATCTTGGG GAGAGCATTC ATGTCTGTAA 1260 TTAGTTACTG TATATCACGG TTAGTACTCT GCTCAGAATT TACGGGGCAA ATACCATTTA 1320 ACTGCACAAT AACTGCAGGT CCTTGCTGCT TATTGGGTAA TTTACTAAGG CTGGAAGAAC 1380 GGGGCAGGAG GGATTCTGAA TGGGAGGTAT TGTAACCCCT TGAATCAAAC TTTATGAGTT 1440 TGGGTTTGGC AGGGAGGCAG CTGCTTGCAG CCAGTTCTCT TCTCTTTGTT TTGCAGAGTT 1500 GGCTGGCAGA CTGCTTCCTT CCCTTGATTT ATTGCAGGAT GATAGGTCTG GGACTGGGGG 1560 TGGGACTGCC CGGGGCTACC TGGGGCTATG GAAGGGACTT TCCATAGAGG GTCTTTGGCT 1620 GAGAGTCTGC AGCAGGAACC CAGAGTCGGT GTCCTGGGGG CTCCATGCAG GACAGCAAAT 1680 GGGCCCTGTC ATTTATTTAC TCCCTCCACG GGGCTGCTTT TTGTATCTGG GCCAGTGGGT 1740 GGAGAGTGCA GGGAGCTGTC CTTGGTTGGC AGCATCAAGA TAATCGCCTA AGCCCTTTCT 1800 TCTCTTGCAA GTCCGTTGCT GCCTGGGAAG CAGCCATTCC TGGACACTTG GCCGACATTC 1860 CTGGCCTTAA TCTGCTTGAG CAAAGTCTGT CTTTGTTTGG CCATGCACTG TCTAAACTCC 1920 TCTAACCTAT TTAGGCCACA GAGAGGGGAG AAGACACAAT AATGAAAAAC TCAACGTGCA 1980 ACATTGCCTT ACGCAATCTA ATAAATTACT TGGTACCCGG CTGCCAGCTC AGACTAAGCC 2040 CAATATTGCC TGCAGTAATT ATTTGGATCA AATGCAGTTT ATCTGCTTCA TATTTGTGCT 2100
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