| Tag | Content |
|---|
EnhancerAtlas ID | HS047-35469 | Organism | Homo sapiens | Tissue/cell | Fetal_placenta | Coordinate | chrX:39680740-39681940 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chrX:39681873-39681891 | CCTACCCTCCTTCCTTCA | - | 6.63 |
| | | 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 |
| GH0XI039820 | chrX | 39679342 | 39681548 |
| Enhancer Sequence | GAGGCCCGCC ATTCCCTCGC TGGCTCGCTT GTTCGCTGGC GGTCCCAGGC GGCGCGCAGG 60
CCGCTGCTGG CTGCTGAGTA ATGATTTTTT TTCTAATTGG AGGCGAACAG CGGCCCTAAT 120
GGATGGAGCC GCTCTCGGCG CGTTCGCTGC GCCCGCCCTT CGATCAATAC GGCTCGCTGA 180
GACCGCCGGG CCGCGCTCCC CGGCCCTTTG TGGTCAGAGA TGCCTCGGGG GCCCCAATCC 240
CCGCCACCAC CACCGGCCCC CCATGCTGCC TCAGCCTCGC CCGGGGAGTT CCCAGCCCCG 300
CCACTCCGAG ACACCACCCC TCCTCCGGCC TACCCCCACC CCGGACACTC CAACCCCAGG 360
CTCCTTCCCG CACCCCCGCG CCCGAGTTCC CCTCTCGGAA CACTCTTACT CCAGCTCCCC 420
CAACACTGCC CCCGCGTGTC CCCGCCGTCC CGAGCCCTCC ATCCCTTCTT GTCCTCACAC 480
TATGCCCAGT AGCCTGGTCC CCGTGGCCTC TCAGACAGGG TGGGTTAGCA GGGAGGTGTA 540
CGGGAGGGCA GACCCGGGAT TGCCACCCTC ACCCCTTTTC CGTGACCGCG TTTCTGCCAA 600
GCGCCCCAGG CCGGGAGGAG AGCCGGGCAC AGGCGACAGC CTCCGAGAGT TTACGCCGGC 660
TGGTCCGGGA AGGGTTCGCT GAGTCCAATT AAATCCCCAC GTTCTTTCCT TCTTGAGCCC 720
ACTCCATCTC GGACTGGCTC CAACTGGGAC CCTCCGGCTT TCTGAAGGTA CAGAAACTTG 780
CGAGCACAGA CACACTCCCT GGGGGCACCA GTTTCCAAGA AGCCCTCTGG AATGTTTAGC 840
TCAGAAACCG GACAGCATGC ACAAGTCCTC CTAGGTCAGG GGTCAAATGT GCCCTCTGTT 900
TTGCAGGCCC TTCGTGCACT GCTTCTAACT AGCTGGTGAC CTTGGGCAAC GACTCAGTGC 960
CTGAGGGACT CTTTTTCTTA CACCTTACAG AAGTTTATCC AGCTCTACAA GCTAGGCGGC 1020
TGGGATACAA CATTAAAAGG AATGGTCAAA CCTTCCCACT CCTTCCTGCA GTTTAGAGAC 1080
TTTCCTCCTT CCACCCTGCG GAGAGCGGCT CCTGGGAGGC CCAAGCTGCT CCACCTACCC 1140
TCCTTCCTTC ATCTGCTTAC TTTCTGTTGC TGGCTGTGAT TCCTGCATAA CATTTAGCAT 1200
|
| |
|
|
|
