Tag | Content |
---|
EnhancerAtlas ID | HS187-04051 | Organism | Homo sapiens | Tissue/cell | Th1 | Coordinate | chr11:3442980-3444750 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF16 | MA0741.1 | chr11:3443729-3443740 | GGGGGCGGGGC | - | 6.02 | KLF16 | MA0741.1 | chr11:3443822-3443833 | GGGGGCGGGGC | - | 6.02 | KLF5 | MA0599.1 | chr11:3443730-3443740 | GGGGCGGGGC | - | 6.02 | KLF5 | MA0599.1 | chr11:3443823-3443833 | GGGGCGGGGC | - | 6.02 | KLF5 | MA0599.1 | chr11:3444013-3444023 | GGGGCGGGGC | - | 6.02 | KLF5 | MA0599.1 | chr11:3444496-3444506 | GGGGCGGGGC | - | 6.02 | SP1 | MA0079.4 | chr11:3443821-3443836 | AGGGGGCGGGGCCTG | - | 6.75 | SP2 | MA0516.2 | chr11:3443820-3443837 | GAGGGGGCGGGGCCTGG | - | 6.63 | SP4 | MA0685.1 | chr11:3443819-3443836 | AGAGGGGGCGGGGCCTG | - | 7.5 | Zfx | MA0146.2 | chr11:3443822-3443836 | GGGGGCGGGGCCTG | + | 6.19 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ACTCACTCAT CCCAGTGAGC TCACCGCACA TGAATTACAA ATGGGGCCGG GTGCATTAAG 60 CCCCTCTACT GGCAGAAGGG AGGCTGCTGC CTGCCATGCG CCTGTGCTGA GAATGGCAGG 120 TCCCCAGGGA GACGAGAGGC CACCCCCTTC TCTGTCTCTT CCATCACAGG CGTGAGAACC 180 TCAGAGCATG AGCCGATTCT GTGCAGTGCT CGACATACAG ACGAGAACAC TGAGGCAGGA 240 GAGACAGCCT GTGACCTGGT CACTGCGCTC AGGAGGACGT GGTTACCCGT GGTCCTGAGG 300 GCGCTGACTT TTTAGAATGG GCGAGGGCAG CTCTGTCCCA GTGACCAGAA CGGTTACTGT 360 CTTTAAAAAG TCGTGAAAAT GATCGTGAAC TGTACCCCAC AACGAGTGCG CGTCTGCCCC 420 CCAAGACGGT GGAGAGGCCC CCAGCTTCTC CCGCCAGCTC GCGGGGCAGG AGGGGTGCGA 480 GCAACTCTGG CCAGGCCCCA GGGACGGGGA CCGGGTCGCG CGGACCTGAC CGGCGGGAGC 540 CCAGGCATTC ACGTGGCGGG AGCGCTGGAG GCTTCAGCAC GGAGACCCAT CCCGTCTGCC 600 CCTGGACTCC CGCGAGCCCC GCGGGCCTCT CCGCTCGCCC CGCCGCCCAC CTGCCAGGGG 660 AAGGAACGCA GTGCGCGCGC CGCCAGGAAG CGGCGCTCGA AACTCTGCAG CAAGAGTTCG 720 GTCCCCGCGT TCTCCTCGGG CACCATGACG GGGGCGGGGC CGCAGCGTTG CCGGGAGACC 780 GGGCGGAAGC CGAGCCTGGA CTGAAAAGGG GGCGGGCCCA GGGCAGTGCG CGGGGGCAGA 840 GAGGGGGCGG GGCCTGGGGG TAGGCTTAGG ATGAGAGTCG TGGGAGCGGC TCTAGGGCGG 900 GGCCAGGATG AGCGTTATGA GGCGGGGGCC TGGGGTGGGG CCAGAATGAG CGTCTTGAGG 960 GCGAGGCCTG GGGTAGGGCC AGGAGAAGCG TCGTTGGGGC AGGTCCTGGG GAGAGTTCAG 1020 GTTGGCGTGT CCTGGGGCGG GGCCAGGACA GGGCGATCCT GGAAGCGGGG CTTCGGAAAC 1080 ATCCAGGTTG GAGACGTCCT GGAGGCGGGG CCTTGCGTGG GGGCAGGATA AGAGTCCTGG 1140 AGGCGGGCGT TAGGGTGGGG GTAAAGGACG ATTGGGTTCA GGAGGCGAGA CTCGGAGCAG 1200 AGCCCAGGAG ACAGGTCCTA GGGCGGGGCT AAGGCCAGAC CCGGAGAACG GCTCAGGAGG 1260 CGGGGCCAGG GCGGGGCGTT GACTATGTCG TAGCACGTGG CCAGGCGCTG CTCGGACTCT 1320 GGGAGGCGGA GCTTAGGACG GGCCTACGTG GGGAGGGGCC CAGGGTCCGG GAGGCGGGGC 1380 CGAGTCCGGG CTGCTGGCTG CGCTCAGGAG GCGGGCCCTG GGAGGCGGAG CTTAGGGAGG 1440 GGCCGGTGTC GGGAGGGACC CAGGGACTGG GAGGCGGGTC GGGGCTGGGC TCAGGGGCCG 1500 AGAGGGAGCT GGGCTTGGGG CGGGGCCGAG ACGGAGCGAG GGGTCCAGGG TGTGAGAAAC 1560 GGGGAGGGGT TTGAGGAGGG GATTGGAGCG TGGCTCAAGT TCGGGAGGCG TTACCTGCGG 1620 AGAGTTTGAG GCAGGCCCAG GAGCGAGCCC ACGGTCTGCC GACGCGGAGC CAGGGACGGG 1680 CCCCAGGATC CGGAGCTTCA GGCGGGGCCG AGTCCGGGTT TGGGGCCCGG GAGTCGGGGC 1740 CGGTTAGGGC GAGGGTCCCC GGGATCGTCC 1770
|
| |
|
|
|