Tag | Content |
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EnhancerAtlas ID | HS098-31230 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr2:113888830-113890230 |
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) |
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 | CTGGGTAGTT CTGTTCCATG TGGTGGAACA TGCTGGGGTC ACTTTGGAAG CTGCATTCAG 60 CAGAGTGCCT GGCTTGCGCT GGGCATCCAA GGTGGTCCCT CATCCTCCAG GCTCTCTTTC 120 CATGTGATCT CTCAGTGTTT AAGAGTTAGT TGGAGCTTCC TTACAGCATG GCGGCTGACT 180 TCCAAAAGGG ATTATTCCAA AAAGAGCCTC AACATGCAGG CGCTTATTAT GACTTCTGCT 240 TGCATCATCC TATTGGCCAA AGCCAGTCAC GTGGCTAAGT CTAGCCCCCT GTGAGAGGAG 300 ACTGCATAAG AGTGTGAACA CCAGGAGACA CGGTCACTGG GGGCCACCAC TGTAACCATC 360 TACCACAGGA CCTGAATCTC TGTGTGCTAC TCCCTTGCTC AAGGGCCCCC CTACCCACGC 420 AGACCTGCTG TCTTCTAGCA AAGCCCATCC TCAGGACCTT TCTCTTCCAA TCCTTATTGA 480 CTCAAATTGA TTAGTTGGTG CTCCACCCAG AGCCCTGTGC TCCTTTATCT CATGTAATGT 540 TAATGGGTTT CCCAGCCCTG GGAAAACATG GCTTTGTCTC AGGGGCTTGC TGGATGCAAG 600 CTTAACCTCA ATGTGAGTGG CCATACTGTG GCACTGTCCC ATCCCTCACC AGGGACACTG 660 TTCTGGAGGG TGACTGCCTG TTCTGTGAGG AGTGGGGATG GCTAGGACAT TGCATGGAAC 720 ACACCACCAC CCCATCTTCT CAGAGCTCAA ACCCTGACAG AACACCAGCT CCACAGGCCT 780 TGGCTTCTGC TGATGGTGCC GTGTATTTAC CAGACTTAGT GGTCCAAGGC CAGAGTGGCC 840 AGATTTCCCA AAGTCAAGGT GTGACAGTGG GACAGCCTCT TTGTGTCTTT GCTGTCCTAA 900 GAAACCTGGG CCAGGCCAGG CGCAGTGGCT CACGCCTGTA ATCCCAGCAC TTTGAGAAGC 960 CAAGGTGGGC AGATCACGAG GTCAGGAGTT TGAGACCAGC CTGGCCAACA TGGTGAAACC 1020 CTGTCTCTAT TAAAAATAGA AAACATTAGA CAGGTGTGGT GGTGCATGCC TGTAATCCCA 1080 GCTACTCAGG AGGCTGAGGC AGGAGAATCG CTTGAACCCA GGAGGTGGAG GTTGCAGTGA 1140 GCCGAGATTG TGCCACTGCA CTCCAGCCTA GGCGACAGAG CAAGACTCCG TCTCGGGAAA 1200 ATTAATTAAT AAATAAATAA ACCTAGGTCC CAGAGTCCCA CAGAATGGCA GACAGGAGCA 1260 CCTGGGGGCT TTTAGGGTAT GGCATTTCCC CTGTACTAAC TCTGGGCTGT CCAGAGGGCC 1320 ATTTCATGGC GTGGAGTGGA GAGGGAGGCA GCACAGGACT TCCTAGGCCT CAGCTCTCAC 1380 CTGCCCATCT TTTGATTTCC 1400
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