| Tag | Content |
|---|
EnhancerAtlas ID | HS134-56919 |
Organism | Homo sapiens |
Tissue/cell | Mesendoderm |
Coordinate | chr7:107027080-107028520 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP1 | MA0481.2 | chr7:107028049-107028061 | AAGTAAACAGTA | + | 6.18 | | SPIC | MA0687.1 | chr7:107027325-107027339 | AAAAAGGGGAAGGA | + | 6 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH07I107386 | chr7 | 107026986 | 107028835 |
|
Enhancer Sequence | TTAAACAGCT GCTTGAAGCT AGTGGAACCT CGGTTTCACA GGCACAATTA AGGGACCTGA 60
TGCAAACTGT TGTAACCCAA AGCCCAAGGT TCCTGGAAAA AGGCATGCTA GACATAAAGC 120
TCTGGGAACA AGTAGGGAGA AATCTGAAAC AACATTATGC ACAAGGGCAA CAGGTCCCAG 180
CATCATCTTT AATGCTGTGG GCTTTAATTA AGGCAGCCCT GGCTTCGTTA TACAACAGAG 240
AGCCTAAAAA GGGGAAGGAG GAGGAAAGTC ACCTGCCTTA CCACCTCCTT TTCCCTCAGC 300
CCCACTATCA CCGGGCCAAA ATAACAAAGA GGAAATGGAG GTTTTGCCTG AACCCCCTCC 360
TCCAATAAAT AGGTAAAAAG ACAAGAGATA ACGCTGCAGC TACAAGACCC TGTCTTAAGC 420
AAGTGGCATT AGAAGGGGAG TTCTTAGCTT GCCCAGTAAT GCAAGATTGA CAAGGCAATC 480
GAGTATTTCT TTTAACACTT ATAAAAAGAT AAAGCATTAG AGGCCAGAGC CCCATGGTCA 540
AGCAGATGGT AAATTAAAAG AAAGGCTCTG CAGCGGGTAA GCTCACAAAC CCAGAGCCAG 600
CAAATGCTCC TGGGAACTCA GCCTGGACAG CAGAGGCAGC AACAGGAAGC CAGGCCAGGC 660
ACGCCAGAGC TGGCCTGCTG GGGAGGGGCA GGAGGTGCAA ACGGGAAGGT CCACCCAGCC 720
AGCAGCAGAA AAGCAGCAGC GCCTAAGCAA GTGCAAAGTG GCTGCCACCC TGGGGCCCAC 780
CTGCTCAGCT CTCCAGCTCC GCAGGAAGCC CAGGGCAAAA TTTCGTGTGT TCCTTGTATA 840
CAAGCAACAT CTCAGATTAT AATTTGCTGC TAAAATTTAA GTAAAATTTA AGAATTTGAT 900
AGACCTATTT CTGATGATGG CCACTGTTCT CTCTCTTACC CCTAATGTGA CTCTCTCCAA 960
ATCCAGTTTA AGTAAACAGT AACCTCTGAA GGGAAATTAA CAAAGAGCCC ATGAGTTAGT 1020
TAAGGAGCAG TTAAAAACCG GATGATAAAC ATGGAAAAGC AGCAGTCTGG TGGAGACCAC 1080
ATAACTCAAT CACTCGATCT GGGTTTACTA GCACTCAGAG AGCTGAGATC GGGGCTCTGA 1140
TACTGGCCTT GGAAACTTTT TCCACTCAGC CCATAAATAT CGTGAGTGAC TCAGCTTACT 1200
CTGTTTATTT ATTGCAGAAC CTTGAAACAG CCTTAATTAG GTACATTCTT GAGCCCACCC 1260
TGTGTGCTCT TTTTCTTCGA CTTCAGCAAT TGCTAGATCA ACATACACAA CCTATTTTTA 1320
TCACACACAT TCCAGCCCAT GGCTCTCTGC CTGGCCCATT GGCTTATGGT AATAATCAAG 1380
CAGACCTTCA GGTTATGACA TCACTGCTTG ACCAAGCCAC CCAATCACAT CAATTTTTCC 1440
|
