| Tag | Content |
|---|
EnhancerAtlas ID | HS128-18235 |
Organism | Homo sapiens |
Tissue/cell | MCF-7 |
Coordinate | chr5:138897130-138898390 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr5:138898206-138898218 | GTTTGTTTGTTT | + | 6.32 | | Foxd3 | MA0041.1 | chr5:138898210-138898222 | GTTTGTTTGTTT | + | 6.32 | | NHLH1 | MA0048.2 | chr5:138897574-138897584 | CGCAGCTGCG | + | 6.02 | | NHLH1 | MA0048.2 | chr5:138897574-138897584 | CGCAGCTGCG | - | 6.02 |
|
| | 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 |
| GH05I139517 | chr5 | 138896810 | 138898710 |
|
Enhancer Sequence | AAAAATAAAT AAATAAATAA ATAAAATAAA TAAATAAATT TCCTTCCTCC AGCTGCAGGG 60
CAAAAAATGG GTTGAAGAGC CGGACTGGTG GTAACTGGTG TGGCCATCCA GCCTGGAGTC 120
GATGTTGGCA TGAATGAAGA CACAGGCAGT TGGGACAGAG AGAAGCGAGT GGGATGTGGA 180
GGTGACCCGA TGAAATACTG GCCCGGAGAT ATGAGGCATG AGGCGGGGAG CACGAGGGTG 240
TCGAAGGGCC AAAATGTGGT AAGAGAAGCC GGAGGAGTGT GAGGACAGGT GGAAGGGATC 300
CAATGTGGGA TCTAAGGGGT CTGAGACCAC CGTGGCCGCG GGAGGCAGGA GAAGGTACCG 360
CAGAGCTCCC GGTGATGTGT CAGGAGGCCC TACACTCGCG CGTGCACTGG CTCGCAGTTT 420
GGACAGAGAC CCTACAGGCC AGGCCGCAGC TGCGCCCAGA CCACCCCCAG CGGGTGAAGA 480
CTGCCGCGGC GGCGCAGTTC CCGGCATGCC TCCGGCCGGT GACTTCATCC GGCCCGGGGC 540
CAAGGCCCGG CCTCCGCTAG AGGGCGCTGC TCTCAGCAGC CGCGCCGCCC GGATGGACTC 600
GCGCCAGAGT AGGACAAGAG AGGCAGGCGG CGGCTGCTCC GTGCGGCTCC CACGCCTCTC 660
GGGCGGCAGG TCCTGCCTCG GACCTGGGAC CACTGGCTGG CGCCTGTGGC TCACATCTCC 720
ACGCCTTTGC CCGCTCCTCC CAGGAGCCCG AGTCAGAAAC CTGTGCTTCA CCCTCGAGAG 780
CGCTGCCATC CTCCCCCTCA ACCAGACGGG CATGGCGTCT GGTTGTCCGT CCTGTCTTCT 840
CATCGTCTCA GAGCCCTTCC CTGACCCCTA CCCTCTCTCA GACCAACAGG ATGATGACAG 900
GAAGAGGATC CAGGACCAAC TCCTAGCGGT GACCTTGAGA AAACAATCTC ATACCCCAGT 960
TTCCCTTACA ATGCAATGGA AATAATACTA ACAACCCTGG AAGAGTGTTG GAAGGACTAA 1020
ACGAAATCAT CTTTTTCAGT ACTAAGCAGA GGCTCAGTGA GCATCAGCGT TTTTTTGTTT 1080
GTTTGTTTGT TTTCTTGAAA CTGGTTGGAG CCCAGGCTGG AGTGCAGTGG CATGATCTTG 1140
GCCCACTTGA GCCTCAATTG CCTGGGCTCA AGCCATTCTT CCTCCTCAGC CTCTGGAGTA 1200
GCTGGGACCA CAGTTGCATG CCACCACGAC TGGCTACTTT TGTTCATTTT TTTTGTAGAG 1260
|
