Tag | Content |
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EnhancerAtlas ID | HS108-08644 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr11:117973970-117975400 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr11:117974094-117974106 | GTTTGTTTGTTT | + | 6.32 | Nr2f6(var.2) | MA0728.1 | chr11:117974315-117974330 | TGAACTCCTGACCTC | - | 6.22 | RREB1 | MA0073.1 | chr11:117974101-117974121 | TGTTTGTTGTTGTTTTGAGG | - | 6.45 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_29489 | chr11:117974955-117977386 | Fetal_Intestine_Large |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I118104 | chr11 | 117974956 | 117977386 |
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Enhancer Sequence | GAGTGCAGGG TCTGAGGCAC AAGAGAAGTG GGCCCAGCAG GAGGTCTGCT CAGGCCCCCA 60 CGGCCCACTG CATAGTATCT GCCCCCTACT TGTCACTTTT CATCCTTGTT GTATAAGGTT 120 CTTTGTTTGT TTGTTTGTTG TTGTTTTGAG GCAGAGTGCT CTGTGGCCCA AGATGGAGTG 180 CAGTGTCTTG GTCTCGGCTC ACTGCAACCT CTGCCTCCCA GTTTCAAGTG ATTCTTCTGC 240 CTCAGCCTCA TGAGTAGCTG GGATTACAGG TGCCAGCCAC CACGCCTGGC TAATTTTTAT 300 ATTTTTAGTA GAGACGGGGT TTTGCCACAT TGGTCAGGCT GATCTTGAAC TCCTGACCTC 360 AGGTGATCTG CCCGCCTCAG CCTCCCAAAG TGCTGGGATT ACAGGCGTGA GCCACCGTGC 420 CCAGCTGTGT AAGTTTCTTG AGAGCAGGAC CCTGTCTTGT CTACCTTTAA ATCCTAGTAC 480 TTAACACACA GCAAACAGTA ACTATTTGAT GACCAAATGT GAGCCAGAAA GGACAGGAAA 540 TTGTAACTGA GGCTGCCCCA TGCGTGCTGC GCCTGGTGGA TTTCAGGCAG AGGGCTAGAC 600 TGGGTGACCT TGGGGCATTC CTCCTTTCTA TGAAATTTGT TATTTCAAGG AGACTAGAAA 660 AGAGACTTCT CAGCCACTTC GCCAGCTATT GGTCCTTCTA TTCATTAGTG TTTGCTGAGA 720 CATGCTATGT GACAGGACTG AGCCAGGTCC TTTCAATGGA TAGGAGATGT TTTGAGCATA 780 AAATCCACGT TCTCTCTTGG GCTGGGCTCT TCTACCTTCT TCCCCCTGGT GCTTGGGCTC 840 TGAAGAAAAA AAGATAGGTA GGAGATGAGT GATGGGGCTT CTGAGGGCAG GGCTGAGTGA 900 CTTTCTGTGT ATTTGCTCTT TCTTTATCAG AAGTCAAATG CCCACAGGCA CCTGTCATCC 960 TACTGCCAGT AGGACTTCTC ACTCAACCTT CCCCTCTGAC CTTACTTGGA GAAGGACTTA 1020 GGTCCCTCTC TCAGACATTT CCCCAGGCTG GGCAAGTTGT GTGGACCATG GATGGGTATG 1080 TGGTCCATAC AATTTAAACA AGCTGTATAT GGTCGCTGGG TAGAGTGACC ACATAATTGA 1140 TCATCAAAAC TGATACCTGT AAGAGCAAAA GGGGGCACTA TTAACCATTG GGTCAGGGCA 1200 ACAGGTCAAA ATGGAGACCT ACCCTGGGAC TTCTGGTCAC ACTAGCTACT GTCAAAATGG 1260 GGCCCAAATA GACAAAGCCA AATGGAAGAA ATTCCCTTGA CATTGAAAGT GTTGGGGCTC 1320 TGTGGCACCC CCAGTTCTAG GTTGGGGGAG CTTGGGCTGG TCTCATGATG AGTTCTGAGG 1380 GGGATGGGCC AGTTGGGCCC CCCGTTCCAT CTAACTCAGG TTCCTTTCCT 1430
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