Tag | Content |
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EnhancerAtlas ID | HS101-02803 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:154422460-154423900 |
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) |
Crx | MA0467.1 | chr1:154423452-154423463 | GAGAGGATTAG | + | 6.02 | Nr2f6(var.2) | MA0728.1 | chr1:154423777-154423792 | GAGGTCAGGAGTTCA | + | 6.22 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_09189 | chr1:154422671-154430649 | CD14 | SE_18405 | chr1:154422817-154423718 | CD4p_CD25-_Il17-_PMAstim_Th |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I154450 | chr1 | 154422818 | 154423718 |
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Enhancer Sequence | GGACTGGGTA TTTTCATATT CCCAGGGTCC GAGGGACAGA AGATTTGTCT CTGCAGAAAG 60 TCCTTTCTTA TTTGGACATG TCGTCAGAGG ATCAATCACA GATCAATCGC AGAAATGTTC 120 TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG TGTGTGTGTT GGAGAGAGTC TTGCTCGGTT 180 GCCCAGGCTG GAGTGCCGTG GCATGATCTC GGCTCACCAC AACCTCTGTC TCCTGAGTTC 240 AAGCGATTCT CCTGCCTCAG CCTCCCAAGT AGCTGGGATT ACAGGCGCAT GCCACCATGC 300 CCAGCTAATT TTTGTATTTT TACTAGAGAC AGGGTTTCAC TATGTTGGCC AGGCTGGTCT 360 TGAACTCCTG ACGTTGTGAT CCACCCACCT CGGCCTCCCA AAGTGCTGAC ATTACAGGCA 420 TGAGCCACCG TGCCTGGCCA GAAATGTTCT TTTATTACTT TATATGTTGA ACTTTGATAT 480 TGTTAGCTAA GATATAATGA GGAGACCGTA AGAAAAGTGG GACAAATCAC TTCGAGATAT 540 TTGAAAAGTG AGATATTTCA CAGTTGGCCC ACAATACAAA TGAATGTGCT GCAAACAAGA 600 TTATTGGAGT CTGAAATGGA ATACCTGTTG AGGGAAATCT TTATTTTGGG AGCCCTTGAT 660 TTCAATGCTT TTGATTCCCT ATCCCTGCAA GACCAGGAAA GCTTACCAGT ATTTGAATCA 720 AGAAAGATCA CAAGTCCTGT GTTTGACTAG GTATATGGGA CTTATGGAAT CCAGACTCCA 780 GAGGTTCAGT AGTTGAGCAG CTCCCCTGAT GACTCTTGGG CTTCGTGAGG CAGTCCTTGC 840 CCTCGTTCCC CATCCCTGGG TGGATTCCTG CCTGCACTGA TGCTGGCTGC CTCTGCTACA 900 ACAGCCCAGG TACAAAGCCC TACCATGGTG CAGTGCACCT GTGGAGGACC TGCTAAATAC 960 CTGGGGCTGA GCTCTGCACA GTTGGGGACT CGGAGAGGAT TAGAGCCATC CCTGTTCTCA 1020 AGGAGGCTAC AGTCCAGGCT CTGACAAAGA GTAAATTGGT AACTGTGACA AAGACCAGCA 1080 TGTGAGATGG GCCAAAAGGG AGGCACAGAT AAAGCAAAGT GGAATTTAGA GATTTGAAAG 1140 AGTATATCAA GCTGAGCAGT CACAGAAAGC TCATGGAGGA AGTGCCATTT GAAATGGGCT 1200 TTGAATGGTA TGGGTGGGAT GCAAGAGGTT GGGTGTTCAA AGGTTGCTAT GGGCCGGGCG 1260 CGGTGGCTTA CGCCTGTAAT CCCAGCACTT TGGGAGGCCG AGGTAGGAGA ATCACCTGAG 1320 GTCAGGAGTT CAAGACTAGC CTGGCCAACA TGGTGAAACC CCATCTCTAC TAAAAATACA 1380 AAAATTAGCC AGGCGTGATG GCAGGTGCCT ATAATCCCAG CTACTTGGGA GGCTGAGGCA 1440
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