Tag | Content |
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EnhancerAtlas ID | HS101-05975 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr10:103475700-103477580 |
Target genes | |
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) |
MSC | MA0665.1 | chr10:103476759-103476769 | AACAGCTGTT | + | 6.02 | MSC | MA0665.1 | chr10:103476759-103476769 | AACAGCTGTT | - | 6.02 | MYF6 | MA0667.1 | chr10:103476759-103476769 | AACAGCTGTT | + | 6.02 | MYF6 | MA0667.1 | chr10:103476759-103476769 | AACAGCTGTT | - | 6.02 | Nr2f6(var.2) | MA0728.1 | chr10:103475819-103475834 | TGAACTCCTGACCTC | - | 6.22 |
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| Number: 1 | ID | Chromosome | Start | End |
GH10I101716 | chr10 | 103476661 | 103476810 |
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Enhancer Sequence | TGGGCTCAAG CAATTCTCCC CTCCCGAGCA GCTGGGATTA CAGGTGCACA TCACCATGCC 60 TGGCTGATTT TTGTATTTTT AGTAGAGACA GGGTTTCGCC ATGTTGGGCA GGATGGTCTT 120 GAACTCCTGA CCTCAAGTGA TCCGCCCTCC TCGGCCTCCC AATGTGCTGG GATTACAGGC 180 ATGAGCCACT GTGCCCAGCC ACCTTCTTCA ATTTCTTTCA TTAATGTTTT ATAGTCTTCA 240 GTGTACTACA TTAAATTTAA AATGTACTAT AAAAATTAAG GAATGGCGTG GTGGCTCATG 300 CCTGTAATCC CAACACTTTA GGAAGCCAGA CCCAGTGGAG ACCAGGAGTT CAAGACCAGC 360 CTGGGCAACA TAGCTAAACC CCGTCTTTAT AGAAAATACA AAAATTAGCT GGGTGTGGTG 420 GCATGCACCT GTAGTCCCAG ATATTCGAGT GACTGAGATG GGAGGATCAC TTGAGCCCAG 480 GAGGTCAAGG CTGCAGTGGG CCATGATTGT GCCACTGCAC TCCAGCCTGG GAGACCCTGT 540 CTCAACAACA ACAAAAATTA ATTTTTTTTA TTGTGGTAAA ATATACATAA CATAAAATTT 600 ACCCTTCTCA CCATTTGTAA GTATACAGCT CAGTAGCATT AAATACATCC ACATTGTTAG 660 TATGACCATC ACTAATATCT ATCTCCAGGA CTTTTTCATC CTCCCGGATA GAAGTTCTAT 720 ACACAGTAAA CAATGACTCC CTATTCCACC CCACACCCCC CAATCCCTGG TAACCACTGT 780 TCTACTTTCT GTATCTATGT ATTTGACTAT TTTAGACACC TCATTTAAGT GAAATCATAC 840 AATGTTTGTC TTTTTGTGTT TGGCTTATTT TACTTAGCAT AATGTCTTCA AGGTTCATCC 900 ATGTTGTAGC ATGTATCTGA TCAATCCCTT TAAAGGCTAA ACAATACCCC ATTGTATGTA 960 TTTAGCACAT TTTGTTTATC CATTCATCTG TTAATGGACA TTCAGGTTTT TCCACCTTTT 1020 GCCTACTGTG AAGTATGCTG CTATGAATAT TGGCGTACAA ACAGCTGTTT GAGTCCCTGC 1080 TTTCAGTTCT TTTGTGTACA TACTCGGAAG TGGAATTGCT GAATCATATG GTAATTATAT 1140 GTTTAATTTT CTGAGAAACC ACCATACGGT TTTCCACAGC AGAGGCACCA TTTTACATTT 1200 CCACCAGCAT TATACAAGGG TTTCTATTTC TCCGTATCCA TGCCAACACG CTGTTTTCCT 1260 GTTTTGTTTT GAGACAGGGT CTCACTCACC CAGGCTGGAG TGCAGTGGCA TGATCACGGC 1320 TCACTGCAGC CTCAACTTCC TGGGCTCAAA CGATCCTCCC ACCACAGCCT CCTGTAGCTG 1380 GGACTACAGG TGCACACCAC CACACCTGGC TAATTTTTTG AATTTTTTGT AGAGATGTGT 1440 TTTTGCCATG TTGCCCAAGC TGGTCTCACC GGCCTCAGCC TCCCAAAGTG CTAGGATTAC 1500 AGATGTGAGT CACAAACCAA GCCCTGTGTT TTTTTGTTTT TTGTTTTTGA GACAAGGTAT 1560 CGCTCTATTG CCAAGGCTGG AGTGCAGTGG TGCAATATAT GTCTCACTGT AGCATCGGCC 1620 TCCTGGGCTC AAGTGATCCT CCTGCCTCAG CCTCCCATGT AGCTGGGACC ACTGGCACAC 1680 ACCACCACAC CTGGCTAATG TTTGTGTTTT TTGTAGAGAT GAGGTCTCAC TTTGTTGCCC 1740 AGGCTAGTCT CAAACTCCTG AGCTCAAGTT CTCCTCCTGC CTTGGCCTTC CAAAGTGCTG 1800 GGATTACAGG TGTGAGCCCC CTGCCCACAT GTTTTGTTTT TATAATAATG TATGTGAAGT 1860 GGTTATATAC TTTTAAAAAT 1880
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