| Tag | Content |
|---|
EnhancerAtlas ID | HS094-02983 |
Organism | Homo sapiens |
Tissue/cell | hMADS-3 |
Coordinate | chr1:181148700-181150010 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr1:181149515-181149527 | GTTTGTTTGTTT | + | 6.32 | | REL | MA0101.1 | chr1:181149149-181149159 | GGGGATTTCC | + | 6.02 | | RREB1 | MA0073.1 | chr1:181149927-181149947 | TGGTGTGGGGTGGTGTGAGG | - | 6.5 | | RREB1 | MA0073.1 | chr1:181149937-181149957 | TGGTGTGAGGTGGTTGGGGG | - | 6.99 |
|
| | 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 |
| GH01I181179 | chr1 | 181148337 | 181150297 |
|
Enhancer Sequence | CATGAGTTTC CAGCCTGCTA GCCTGCTCCA CAGATCTCAG ACTTGCCAGC CTCCACAACT 60
GTATGAGCCA ATTCCTGAAA TAAATTCCTT TATACATATA TGTAATATGT ACACATACAC 120
ACATCTATGT CATCTAGATT TAGAGCTAAT CTAGCTCCTC CTGGCTCTGT TTGTCTGGAG 180
AACCCCGACT GATACTGATG TGTTTATTTG CTTATCATCC TCCCTACCCC AGACGGAGGC 240
TCTCTAAGGG GAAGATCTTT TGTCTGTTTC CTTCATGCTG TGTCTGAAGT GACCAGGACA 300
GCAGCCGGCA ATAGGACGTG CTCAGTCGAT ATTGTACAAT GGATCTTCAT AATTCTTGCT 360
TATTTGTGTG GTTGTTATCT GTCTGAAATT CAAGAAAGAA GGACATGAGA AAAGAAAAGG 420
ATGAAAGCAC ACTGGTCTTA TCTGAGGCTG GGGATTTCCC CGTTGGGCCC AGTGTTGTGG 480
ATTCTGCAGT TGAGTTGTGT CTGTTTGCAG CTGAAAGAAA GCTGTGGCAG TGAGGAGAGG 540
TTGCAAATTT AGAATCAAGT TCAAGTTCTC CTAGCAACAT GCACACCCCC GCTGCTGGCT 600
GGTGTAATCC AAGCACCAAA CACGTGCAGC TGGGGCAGTG CGTGTTGCTA GGAGAACAAT 660
GACTCTCTTG CTTCCAGAGC TGGTAGGTGA CTGCGGTATT ACCAGGGGCG CACAAAGTGG 720
GTGTTGCCCT TTGTTTCCCA AGTAATTGTT TTAAAGCAAG GTGAGGAGGA GCCTGGGGAA 780
GGGTAGAATG AGAGAAAGCA TGAACCCTGA TTTGTGTTTG TTTGTTTAGG AACTAGAGGT 840
TAGTGAAAAG CCTCTTGTTT CAGAATGTGT CCCAAATGGG TTTACAATTA GTGACAGAGT 900
CTGTAGGAGC TTATGAAACA ACCAATTCCC CACACTGTTT GGCTCTCAGC ATCCACAGAC 960
CATCTGGATC AGCTGAGCAT GAAGTGTGGG GGCGTGCATT GGGGGTGGGG TCCAGAAACA 1020
AAAAAGATCA AGCTGGCATC GGTTGGGGCG GGAGAGGGAT TTGGGTTTTC AGATTTCCTT 1080
TCGCTTAATT ACATTCGCAG GCTGTCCTGA TCCTCATTCC CCTTCCCCAT TGTTTCTGCC 1140
CTGTCAGCGG GGTTGACTGG CTGAAAACAG ACCACCCGGG CAGCCAGAAG AACTGTGCCT 1200
GTCCCGGCAG CCCTGACTCT GGACAGGTGG TGTGGGGTGG TGTGAGGTGG TTGGGGGACG 1260
GGAGAACAGG GAAGCAGGGC CAAGGACAGT AATATCCCTG GCCACTCTTC 1310
|
