Tag | Content |
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EnhancerAtlas ID | HS105-67124 | Organism | Homo sapiens | Tissue/cell | IMR90 | Coordinate | chr5:174773930-174774880 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr5:174774841-174774853 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr5:174774845-174774857 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr5:174774849-174774861 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr5:174774853-174774865 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr5:174774857-174774869 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr5:174774861-174774873 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr5:174774865-174774877 | GTTTGTTTGTTT | + | 6.32 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CATAATCAAA AACTGATGGT GGGGGATAAA GCATTCAGAT AGACAGCATG CCTCATCCAC 60 CAATACCAGG ACACCCTCCA AACATCCATC AGAGCCCTTC CTAAGGAATC ATGTCTCTGG 120 CTCGGCTGCT GCATCAGGAG GGACTCCCAT TCAGAGCTTG TCTTTGTTCC CATGCCTTGC 180 TGACAGAGGA CAGTGGCAGG CCACCCATGG GTAGACTGAC CCCCAGGAAA GCACATCTAT 240 CTTCTCTTCT TGCCCGCCCT TCTCTGCTTT TCAGCCACTC TTTGGGCATC ACAAAGAATT 300 TAAATAAACC ACTAGAGAAT TCACTTCCCC TCCCCTCTGA GTCATTAGGT ATAAATTAAA 360 TGAAACGTAA ATAAGCTTCC CAAGTGGACC CTGCTGAGCA GGTTACTAAT TCGATCCGAT 420 GAGTCAATGA GAAGCTGAAG CTTTTAAAGA AAAAGGAAAA GTTTATGCTT CATCCAAGGG 480 AACTAAGGAG AAACTCTCTC TTTTTCCTGC TGGATATTAA TGAAGAAGGA TGCTGATCCA 540 GGAACTTTTG ACCACCATTC TGGCATCCAC GACTGGGAAA AAGTCTGCCT AACTCTACTC 600 TCTCCAGGAA TAGTACTGAC AAGCAGAGCA TCCTCAGACG CGTGCTTCAG GTGAGCCTCA 660 GATCTCACCA TCTGGGAAAC TAGTTGCCCC TGGACTGTTT AGCCAAATGA CCCAGTGCAT 720 TTTATTTTAT TTTATTTTAT TTTATTTTAT TTATTTTTCA GACAGGAACT TTTTCTGTTG 780 CCCAGGCTGG ATTGCAGTAG CGTGATCATG GATTACTGCA GCCTTGACCT CCCAGGCTCA 840 ATCGATCCTG CCACCTCAGC CTCCCGAGTA GAGTAGCTGG GACTACAGGC ATGCGCCATC 900 ACAGCTGGCT AGTTTGTTTG TTTGTTTGTT TGTTTGTTTG TTTGTTTGTT 950
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