Tag | Content |
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EnhancerAtlas ID | HS105-45059 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr2:113888740-113890230 |
Target genes | |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Lhx3 | MA0135.1 | chr2:113890028-113890041 | AAATTAATTAATA | + | 6.37 | POU6F1 | MA0628.1 | chr2:113890030-113890040 | ATTAATTAAT | + | 6.02 | POU6F1 | MA0628.1 | chr2:113890030-113890040 | ATTAATTAAT | - | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_10086 | chr2:113877616-113889890 | CD14 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I113132 | chr2 | 113890157 | 113891161 |
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Enhancer Sequence | ACATGCTTTG GATCTCAAAT CACCCCAAAA CCCAGTGGCT TGAAACAACC AAAATTTTTT 60 CTTATGATTC TGTGGGTTGA CCAGGATTAG CTGGGTAGTT CTGTTCCATG TGGTGGAACA 120 TGCTGGGGTC ACTTTGGAAG CTGCATTCAG CAGAGTGCCT GGCTTGCGCT GGGCATCCAA 180 GGTGGTCCCT CATCCTCCAG GCTCTCTTTC CATGTGATCT CTCAGTGTTT AAGAGTTAGT 240 TGGAGCTTCC TTACAGCATG GCGGCTGACT TCCAAAAGGG ATTATTCCAA AAAGAGCCTC 300 AACATGCAGG CGCTTATTAT GACTTCTGCT TGCATCATCC TATTGGCCAA AGCCAGTCAC 360 GTGGCTAAGT CTAGCCCCCT GTGAGAGGAG ACTGCATAAG AGTGTGAACA CCAGGAGACA 420 CGGTCACTGG GGGCCACCAC TGTAACCATC TACCACAGGA CCTGAATCTC TGTGTGCTAC 480 TCCCTTGCTC AAGGGCCCCC CTACCCACGC AGACCTGCTG TCTTCTAGCA AAGCCCATCC 540 TCAGGACCTT TCTCTTCCAA TCCTTATTGA CTCAAATTGA TTAGTTGGTG CTCCACCCAG 600 AGCCCTGTGC TCCTTTATCT CATGTAATGT TAATGGGTTT CCCAGCCCTG GGAAAACATG 660 GCTTTGTCTC AGGGGCTTGC TGGATGCAAG CTTAACCTCA ATGTGAGTGG CCATACTGTG 720 GCACTGTCCC ATCCCTCACC AGGGACACTG TTCTGGAGGG TGACTGCCTG TTCTGTGAGG 780 AGTGGGGATG GCTAGGACAT TGCATGGAAC ACACCACCAC CCCATCTTCT CAGAGCTCAA 840 ACCCTGACAG AACACCAGCT CCACAGGCCT TGGCTTCTGC TGATGGTGCC GTGTATTTAC 900 CAGACTTAGT GGTCCAAGGC CAGAGTGGCC AGATTTCCCA AAGTCAAGGT GTGACAGTGG 960 GACAGCCTCT TTGTGTCTTT GCTGTCCTAA GAAACCTGGG CCAGGCCAGG CGCAGTGGCT 1020 CACGCCTGTA ATCCCAGCAC TTTGAGAAGC CAAGGTGGGC AGATCACGAG GTCAGGAGTT 1080 TGAGACCAGC CTGGCCAACA TGGTGAAACC CTGTCTCTAT TAAAAATAGA AAACATTAGA 1140 CAGGTGTGGT GGTGCATGCC TGTAATCCCA GCTACTCAGG AGGCTGAGGC AGGAGAATCG 1200 CTTGAACCCA GGAGGTGGAG GTTGCAGTGA GCCGAGATTG TGCCACTGCA CTCCAGCCTA 1260 GGCGACAGAG CAAGACTCCG TCTCGGGAAA ATTAATTAAT AAATAAATAA ACCTAGGTCC 1320 CAGAGTCCCA CAGAATGGCA GACAGGAGCA CCTGGGGGCT TTTAGGGTAT GGCATTTCCC 1380 CTGTACTAAC TCTGGGCTGT CCAGAGGGCC ATTTCATGGC GTGGAGTGGA GAGGGAGGCA 1440 GCACAGGACT TCCTAGGCCT CAGCTCTCAC CTGCCCATCT TTTGATTTCC 1490
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