Tag | Content |
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EnhancerAtlas ID | HS042-17663 | Organism | Homo sapiens | Tissue/cell | Fetal_brain | Coordinate | chr16:56457530-56458980 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF16 | MA0741.1 | chr16:56458911-56458922 | ACCACGCCCCC | + | 6.14 | TCF7L2 | MA0523.1 | chr16:56458228-56458242 | AGACATCAAAGGAA | + | 7.34 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr16 | 56458785 | 56458895 | chr16 | 56457601 | 56458417 |
| Enhancer Sequence | TACATTATAA TCTTAACATG GCAAAAACAC TCTCCATATC ACTTTGTTTA CCTGCTAACT 60 CAAATGCAAA AACAGATTTG AAATTAAGCA AGAGATGTGA GTTGAGTTCT TTCGCTTCTC 120 CCTTCTTTAG GACTGTAAAG TTCAGCTTTA CACAGCAGTA GATAAACAGG AACTTCACCC 180 TTCACTGCCT TCTACTAAAC TCTCCATCAG AAGGACCAGG AGACTTAATC TACAGCCCAC 240 AGAGTCCATA AATCCCACCG CTTCCTGATG AAGCACAGTG GGACTAATTA TAACAAATGA 300 GTTGCATATC ATACTATCAA CTTGGAATAT TAATCTCTCA GTCATTTACA GCCCACTTTC 360 AACCCCAAAT GGGAACATGC AAGGAGACAA GATCCAAGAA GCCATATTAA ATCCAAGTGA 420 GGCTTTAAAT CCTGGAGAAA CTTTTCTGAT CACTGCGGGA TTTACATAAG TATTCAAGGC 480 CAAGATGAAA GCAAAATTCT CTAGCCAAAA TACCGTTGAT CTGATCAGTC TGAAATTATC 540 TGTTCTAATG AACGAAACCA GCATGTGTGC CTTATCAATG CTGCTTATCT CGCAGGGGCA 600 GACAACCTGG AAACTGTGTT AGAATAGATC CTCAAATAAG AAACATTCAG TTAAAATGAT 660 GGGCTGCCTC TTGACACTGT GAATGTTTTG CTGCGTTCAG ACATCAAAGG AAAACTGTCA 720 TGAACATCAG GTAAAGGCAG CAGAAAAGGA AGCACAGTTT GGTGTTTGTT TCATTACACA 780 GCTCCCAAAG GGGACAATCG AATACTAAGC GGCAAAAAAG TTGTGGGAGA CGGCCTCTCT 840 CCAACCGGAA TGTCCAAAGA CACCTGAGTG CCGAAAATTC CCCCATACTC AACGTCTGAA 900 TTCTCCCCTC TGCCCTCTCC TCTTCGTCGG AAGAAAATCC GCTAACAATC CCATGCCTGA 960 CCAAGTGGGA AAAGCTTTCA ACTTCACTCT ACTTCGTCCA ACCCTCGGGA TAACGCACTC 1020 CCAGATCCCG ACCTCCCCTT GAACCTGCCC TCTGAGATCT TCTAGTTTCT CCCGAGGGTC 1080 CCTCAGAAAA CCCAGCCCGT TCCTCCCCAC TGCCCCTTAA CCCCTTCCCC TGCCCCAGGC 1140 CCCGTCCGCG CCCCAGCGCA GACCATCACC CGCCGCCTCC CCGACCCCCT TCCCGGAGCC 1200 CTCAACGCTG GCCTGCCCCT CGGGGCCTCC TCCTCGCAAC CCCACGCGAT GTTCCTCCCG 1260 CCCGCGGCCC CCTCCCCCTC CCCGCGCCTC ACCACTCTCC CTCAGCAGCG CTCCCGCGAG 1320 CAAGGCCGCG CCCCCCAGGC GCTCGCCCTC GGGGGTCCCT GGCGGAGGGG CCCCTAGGCC 1380 CACCACGCCC CCGCGGATAA AGGGTGACGC AGCGGACCCC GCCCCTGCCC CGCGGGCCCG 1440 GCCGCCTCGC 1450
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