| Tag | Content |
|---|
EnhancerAtlas ID | HS047-04211 | Organism | Homo sapiens | Tissue/cell | Fetal_placenta | Coordinate | chr10:69609090-69610540 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr10:69610504-69610516 | GTTTGTTTGTTT | + | 6.32 | | Foxd3 | MA0041.1 | chr10:69610508-69610520 | GTTTGTTTGTTT | + | 6.32 | | Foxd3 | MA0041.1 | chr10:69610512-69610524 | GTTTGTTTGTTT | + | 6.32 | | ZNF143 | MA0088.2 | chr10:69609212-69609228 | CTCCCATAAGGCATCG | + | 6 | | Zfx | MA0146.2 | chr10:69610076-69610090 | GAGGCCGAGGCGGG | - | 6.01 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CACACAAGAC AAGAGAAGAG AAGAGAACCA CACACACAAG ACACGGAGAG TCCGATGCTC 60
AATCCTAGGC CTTGGAGGCC TGTTCCTCCC TGCCGGGAAG CGTCTCTCAC CCGAGACTAC 120
AACTCCCATA AGGCATCGCG AGCATCGCGA GAACGGCGCC ACAGAGGAAC CGGAAACAAG 180
CCAGTTACTT TCATACTCAG GGACACCGTC CCCCCCTCCG CCCCCCGCCC TCCGTAAGTG 240
CTATTTTTAC ATCGAATGCC CTAGTCTGGA AGTAGGTAAA CTGAAACTAA GCTCAAATCA 300
AAAGGAGAAA GGCTGGAAAA CAAGAGGCTA CAAGCTCCAG AAGCTCCGAG CGAGGATGAA 360
AATTAGCCAG CCCACAGGTG GGCTCTGCGC GGCCCTGAAA GTCGCACTCT GACCTGACCC 420
TTTCCGCCTC TCGTTTTTCC TTCCAGCCTC GCTTCAAAGT TCTGTATTGC AGAATGAAAT 480
CGGCGCCTTT CCCCAGCGGT TTTTCCAAAT ACGAGCAAAG GAGGCACAAA ACGCAGGTTC 540
CAGAAACTGT GCCTGCAACC ATTCGTCCTT ATTTCCCGAC ACACGGGCCC CTGCTCCCCG 600
CTAAGGCTGG GGTCCTGGAC ACGAGTTTTG CGCTCTGATA GAAGGGCTTA GATTCCAGAT 660
TGACACTGGG CTCTCTAAAG CCTGCTCCTC AATCTACTGA TCCGGTCCAG CTTAAGATCC 720
AGTAGAAAGA AAACATAGCC TGCCCGGACC GTAACCTTTT TGTTTCAGAC CCTGCATTTG 780
TAAAATAGCC TAATAAAATC TCTCCCTGGC TTACAGAGCA AGACAGCGTC CTGGTCCAAG 840
AACCGGATGA GTCAAAAGGC GTTACTGTTG AGTCAGACAT AGAATACATG AATACCTAGA 900
AATTCGTAAA TGATTCTCCA AAGGCTGTTG AAATAGCGTT TTCAGGCCGG GCGCGGTGGC 960
TCACACCTGT AATCCCAGCA CTTTGGGAGG CCGAGGCGGG CGGATCACCT GAGGTCAGGA 1020
GATGGAGACC ATCCTGGCTA ACACGGTGAA ACCTCGTCTC TACTGAAAAT ACAAAAAATT 1080
AGCCGGGCGT GGTGGCGGGG GCCTGTAGTC CCAGCTACTC GGGAGGCTGA GGCAGGAAAA 1140
TCGCTTGAAC CCGGGAGGCG GAGCTTGCAG TGAGCCGGGA TCGCACCACT GCCCTCCAGC 1200
CTGGGCGACA GAGCAAGACT CTGTCTCAAA AAATGAAAAA AGAAATAGCG TTTTCAAGTT 1260
ATAATCAGGT GCGATGATGA ATGCTATTAA TGCCATTTTT AAGAATAGTA AGTGCAGGAT 1320
GTTGATAGGT TATTCTGGGA GGAAGGGAGA TGGGGTATGT GAACTCTGTA CTTTCCCCTC 1380
AATTTTGCTG TGAAACTAAA CTGCTCTAAA AGTAGTTTGT TTGTTTGTTT GTTTTTAAGT 1440
AACAATAAGA 1450
|
| |
|
|
|
