Tag | Content |
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EnhancerAtlas ID | HS051-11195 | Organism | Homo sapiens | Tissue/cell | Fetal_thymus | Coordinate | chr17:4651100-4652200 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NKX2-3 | MA0672.1 | chr17:4651570-4651580 | TTCAAGTGGT | - | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr17 | 4651269 | 4651456 | chr17 | 4651126 | 4651529 | chr17 | 4651126 | 4651672 |
| | Number: 1 | ID | Chromosome | Start | End |
GH17I004747 | chr17 | 4650751 | 4652095 |
| Enhancer Sequence | ATAGGCGTGA GCCACCGCAC CCAGCCCTGT TGATGTTACT CTTAAGTCTC TTTCATTTTG 60 TAACATACCT CCTTGGCTTT TATTTTTTAT TTCATGACAC TGATTTGACA AGACACAGAA 120 TCATTTGTCC CGTAAAATGT TCCTCACTCA GGAGCTGGCT GATTACTTCC TCAGGGTGTT 180 TTTTCATGTG TTCATTTATC TTCTTCAGTT CCTGTCAACC AGTAGTTAGA TCGAGATGAC 240 AAGGTTCTGC TGATGTGGTC CCTGCCAACC TCTGCAGGCT GATCTCATGC CATTTCCTTC 300 CCCTGTCAAC TCTGCAGCCA GATGCTTCTA AATAAAGACG CGCTCTCTCA CTGTGGAACT 360 TCCCATGTGT TTTTTGTTTT GTTTTGTTTT TGAGATGGAG TTTCGCTCTT ATTGCCCAGG 420 ATGGAGTACA GTGGTACAAT CTTGGCTCAC TGCAACCTCC GCCTCCCGGG TTCAAGTGGT 480 TCTCCTGCCT CAGCCTCCCA AGTAGCTAGG ACTACAAGCG CCTGCCACCA CGTGCAGCTA 540 ATTTTTGTAT TTTTGGTAGA GACGGGGTTT CACCATGTTG GCCGGGCTGG TCTCCAACTC 600 TTGACCTCAG GTGATCCACC CACCTCGGCC TCCCAAACTG CTGGGATTAC AGGTGTGAGC 660 CACTGCACCT GGCCAGAACT TCCCATGTTC TTGCTCAACT AATTCTTAGC CTAGGTGGCA 720 GCCTAAATGT CACTTCCTTA GGAAAGGAAG CATTTCCTGA CCCCCAGATG AGGTTAGACA 780 CCCCTCTCCC TATTAAGCCC TCATAGCACC TTGCATATGC CCTTTGATGA CCTTTATCAC 840 ACAATTTCTT GTCTACCCTT TCAACGGTCA ACCCAGAAGG GGTGGGTGCT ACCTCTATCC 900 CCCAGGGTCT AGCCTGGCCG GGCATATGGC AGCATACAGT AGGAGCTCGT TAACTGCTTA 960 TCAGATTGCT TTCCCCCCAT ACTTTCAACC CTCCCTCCTC ATCTTTTCTC TCAGCTTCAC 1020 CTCCTACAGC CAGAAAGGGG AAGCCTGGGT CTCTCGTGGA CTGAGGAGAA ATAGACCTTT 1080 TCACCACTCC GTTGGCCAAA 1100
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