| Tag | Content |
|---|
EnhancerAtlas ID | HS064-12496 | Organism | Homo sapiens | Tissue/cell | GM18507 | Coordinate | chr5:150806840-150807910 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MNX1 | MA0707.1 | chr5:150807732-150807742 | TTTAATTACC | - | 6.02 | | SNAI2 | MA0745.2 | chr5:150806985-150806995 | TGCACCTGTT | - | 6.02 | | STAT3 | MA0144.2 | chr5:150807673-150807684 | TTTCTGGGAAG | + | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CTTGTCTGTT GGATACATTC TCAGAAGTGG AGATAGTGAG TGGGTCAAGG GTAAGTGCTT 60
TTAGAGTTTT GAGAGACATC GGCAAATTAC CCCCAGGGAG CTGTTTCAAT TGCTTCTCCA 120
CCAGCAGAGG GTGACAGGGA CTATTTGCAC CTGTTCTGGC AACCACCATG TGTCACACTT 180
TCTGTCCTGA GTCGCAGCTC CCTGTGGGGT TCATTTGCCT TTTGGGGCTT AGTTCCTTAT 240
TTTTCACTTT GTTAAGAGTT TTGTCAGACT GAAACCTGTT CAGAGGTGAG TTAAGTTGTC 300
AGGGGCCAGG AAACTATGTC TTAGGAGTAG AGCCTGAAAG GACTTCTTGG AAACTAGGAT 360
GGCCATACAT ACTCACACCC TGCCCCTCTC GGAAGTGCTG TCACTGGGGC GAGGGGGAGA 420
CAGTGCCATG CGTTCCAGTG GGGACCCCTG TGCAGCAACT TTCACCCTAA TCACAGCACT 480
CAGATCTCTC CAACATAAGG CGAGCTCCCT GCCACTCAGG GTATTCAGAC AGAGATGGAG 540
GGATGTGGGA TAGGGTTGAA GGACAGTTAC ATTATTTTGG TGTGCGTTCC TCTACTGCAG 600
AGGCTGGAGA GTGAACAGTT ACATCTCCCA GACTCCTGGA AGCTACAGTT CTAGATAGAA 660
AATAGGAAGG TCAAAATGGG TGTCCAGAGG CCACTGCAGC AGCAGCACCA GCAGATCCCT 720
GGGACACAGC TACAGCCTCG TGCTCCTGAC CCCGGTCCCC CAGGGACTCA GGCTTCAGCC 780
TCCCGATTGT GGTGGAGGTG GTGGCTCTCC CTGGCGGCAA CTCCAGAGAC ATGTTTCTGG 840
GAAGTCCAGC CTGGAATTCT CTCCTCCAAT CTTTCTAATG GCTATGTAAG CCTTTAATTA 900
CCATTCCTAA ATATATTTCT GATATTTTTC TGCCTCAAGT AGTATGTTTT CTACTCTAAA 960
TCCTGACTGA TAGGAGGCAG GGGTGTACAG GATGAGATGA CCTCCATGGT GTTGTCTCAC 1020
TTGCAATTTC TGTGACCTCA TGATATTGTC CCTCAGCAGA AAAAAAGCAG 1070
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