| Tag | Content |
|---|
EnhancerAtlas ID | HS138-16614 |
Organism | Homo sapiens |
Tissue/cell | MSC_BM |
Coordinate | chr17:41773160-41774740 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2A | MA0052.3 | chr17:41774026-41774038 | GCTATTTATAGC | - | 6.32 | | MEF2B | MA0660.1 | chr17:41774026-41774038 | GCTATTTATAGC | - | 7.22 | | POU4F2 | MA0683.1 | chr17:41774511-41774527 | GTGCATAATAAATGTG | + | 6.77 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TGGCTTTTGA GGCAGTGAGT TCTACCTGAA GGTGGGAACA GCCCAGAGTG TCTGGGGACA 60
GAGTGGTAAA TTCTAATCAA GCCTTCCCAT GGCTTTGTGG ATGAGGATGA GTTTCTACCC 120
TGAAGCTCGG CCTGTTCAGC CATAAAATCA GGATAATGGT GGCTGTGCCT CCTTAGAGTA 180
GAATGAGAAT CAGAGCAGAA CAAGGGAAAG CTGCAGTGAC TTGTCAGGTG TCAACCTTCA 240
GCATGATGGG AGAGCCATGG GACCCTTCCC CTTTCCCTAA GAGAGCCAGC CCTCACAGCA 300
GGCCTGGGAT CCAATGCCCA GCACCCAGCT GGGAGCCCAG GGACCTTGGC CAAAATCTGG 360
TTCTGCTTCA ACTTGGTGCC CGGCCTTTGT CAAGTCACTT CCTCATTTGC AAACTGGGAG 420
AGTTTGGATG AAACTATTGA ATGAAATTAT TTTGGGGGTT TCTTTCTGGC TCTCACAGTC 480
CTCGCATGCT CACCATGTTC CCTTCAATTT CATTAGCACA GCCCAACAAA GGGTTAAGCA 540
GTGGCAGTTC CTCTCGTTCT TTGGTTAGGA CAGGAAGGTC AGGGGTGAGG CCAATACAAG 600
AGGTAGCCGC CACAGCTGAT GCTGGAAATG ACAATAGTTC TTTCCTAGAC TCATATTTGT 660
CCCCTCTCCC TGAAGCTTTG CCTGCAGTGC CCTTGTAAAG AAGTTGGCAA GAAGCAGGAG 720
TGAGGCTCAG CCCCTCTCTG AAATGGATAC GCCGGTTGCT CCCCCTCATG GCTGGTCTCA 780
TTTGCCTTCT TCATTTTTAG ACACATTCCA AACTTTTCAG CAAATTATAG TGTTTGCCAA 840
CTGGCCGTCT GGGGCCCAGG AGAGATGCTA TTTATAGCGA TGCTGGGATG CTGCCATCCC 900
AGAGCAGCCT GGTAAGAAAC GGAGCCAGAG TGCCTGGGAG TGGCGTCCTG CACCCTGGGG 960
AGAGGCCAGG GCCCTGGAGC AGGGTGGCAA AGCTGGTGGC CCGTGGCAAG GACCACTGGC 1020
ACATCCCCTG CCTGCCTGGG CCCTGGGGTC TGTGCCCATA CCCCACACGG GGGGCTGCTT 1080
CCGTGCTCCT TGGAGAGACG ATGGTGCTGT GGGGCCACTG AGCACAGTAA AGGCTAAGAC 1140
CCACCATAGG TCAGCCCTTG CTCATGCTGA CTGTTGCCCC ATTTCCCTTC ATTCTCTCAC 1200
TCGTTCATTC CTCAGAATCT GCATCCTGGT TTTGTCACTA CCTGGAGTTG TAAAGATACC 1260
ACCAAGCTCA CCTTGTGGTG TGAGCCTTGA TTTTCCCCAT CTGTGTAAAG GGTGGATCTG 1320
AGCTCCAAAG TTCCTTCTAG TCATATGCAG AGTGCATAAT AAATGTGTTT GTATTCCCAC 1380
TGTGCTCAGT GGGCACTGGG GCATGCAGAA GAGAAATTGG AATAAATGTG ACCCTTGTCC 1440
TCCAGAGGCT CAGTACCAGA CTGGAACCAG GACCCAGATG AGGGGCCTAC CCAGAGAGGG 1500
CAGCGTGCTC TCCTATTTGT GTTAGGCGTT ACCATTTACA AAGGGCTTTA CGGCTTTGAA 1560
GGTCCCCACA ACGCCCTGAG 1580
|
