| Tag | Content |
|---|
EnhancerAtlas ID | HS098-52393 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr7:75795550-75796580 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GLIS3 | MA0737.1 | chr7:75796513-75796527 | CTTTGTAGGGGGTA | - | 6.51 | | NRF1 | MA0506.1 | chr7:75796011-75796022 | GCGCATGCGCA | + | 6.32 |
|
| | 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 |
| GH07I076162 | chr7 | 75791992 | 75796918 |
|
Enhancer Sequence | GTCTCGCAGG ATAGAGTGCT GTGATGGGAT CATAGCTCAT TGCAGCCTTG AACCTTGGGG 60
TTCAAGTATC TGGGAAGCTG AGGAGGGACT ACAGAGATGG AGTCGCGCCA TGTTGCCCAG 120
GCCGCTCTTT AACTCCTGGC CTGAAGGGAT CCTTCCGCCT CGGCGGAGCC CGGACATAGT 180
TTTCTAGTTT TGACCCACAG AAACACTGTG CTGGGTCGGA GTTTGTCAAC TACCCTTCTC 240
CAGCCAGCAA CACACAGAAC ATGGCGGGGA AGTCACGGTC ACCAGGCTCC AAACCGAGGA 300
GAAAACAGCC CAGCTCCAGG CACTGTAGCG TCACTGTGAC ATCGCCGAAG GCCGGCGCTA 360
TTACGTCGCC GGAAGGCCCG CGCCTGTGAC GTCAGCGGAG GCGCGCCCCT TCTGTAGAAC 420
CAATCGGAAC TCGAGGCGCG GCGGCTGGGT ATTCCAGGAG AGCGCATGCG CAGACGCGTG 480
GCCACAGACT GCCGGTCAGT GTCAGTAGGC GGCGGGTTAG TGTCCGCAGG CTCCGACTCG 540
GCCGCCGACA CCAATAAGCT ACAAGGACGA GCTTTACCAC TGCCTGTACT ACTGCTACCT 600
GCGCGACTTC CCAGCCTGCG GCGTAGGGCG CAGCAAGGGC CTGACGCTGA GCGAGTAGGC 660
GCTGCGCACC AAGCGGCTGT GGCCCGGAGG GCACTGTCGG GCAGAAGCTC CTCAGTGGCC 720
ACCACAAGCC CGCTAGCTCC GGCTACAGCC CTTGCCGCAC ACTCGCGTCA CCTGAGCCTG 780
TGTAGGTGCG CCCCCCCAAC TCCTCCCCCA GCCAGGTCCC GGGGACACCG GCAGCGTCCC 840
CCACCGCCCG GCGCCGCTCA TTCTGGGCAG GATCGGCCCC GTCTGAGGCT ACACCGCATT 900
AGGGAGCTGC ACCCCTCGGC TTGACCTCTC ATGGCCTTTG CAACAACATC AAAGCCTTTG 960
GAACTTTGTA GGGGGTACGA GGGGCTAGGA AACCAAGAAA ACATCTCTTT AAAAATATAA 1020
GCGATCGGGC 1030
|
