| Tag | Content |
|---|
EnhancerAtlas ID | HS129-11847 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr14:70354260-70355290 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr14:70354923-70354934 | CATGAGTCACT | - | 6.14 |
|
| | 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 |
| GH14I069888 | chr14 | 70353970 | 70355470 |
|
Enhancer Sequence | CTTTGCATGT GAGGTCAAAC AAAAAGTCCC AGAGTAAGGG ACTCCTTTCT TGCCACCTTC 60
TGCTTCCTCC CCACCTTTCA AGATGTGCAT GTGGCTCTAT CTAAAATAAC CCCACTGGGG 120
AGTGATTTTG GCTTCTAGAC CCAGAGCAGA CCCAGGCCCT GGCATAAACG TCTGCATCAG 180
GTGGCCTAAG GGCTCATTTG TAAAGCTAAG CTGGCAGTGG GCAGTCTTCC CTTTTCCTTG 240
CTCAGGGTGA TTCACCCTGC AGAGTGGAAG TGTTCATGAG CTGATGCATG GGTCAGAAAC 300
TTTATTTGCC AGTGGGGCCT GTGGGTGGAG GTAGTGTCTG GACTAGGGGA AGGCCTGTTT 360
CTAGTTTGAT GCCTGTCTTT ATTCCAACCT CCCCTCACCG CCTTTTGCAG GAGCTGGGGG 420
TGGGATGCAT GGTCCTGCTT AGCAGGTACA GGGCACCCTT TCTCTCTGGG CCACATAGAG 480
ATTTATTGTT TAGGCAGCCA AGTCCTGGTA TTGCTGCTAG TGGTAGAGGA TGTCAGTGTG 540
GAGGGCCCCC TCCTTCCATG TTTGGGGAGG ACAAAGGTTG AGTTGCGGAT GAGAAATAAA 600
TCGGAGCTGC TTGTGAGGCC GCCAAACAGG GTTAGATTTG TACAGTATGT GCTCTGCATG 660
GGTCATGAGT CACTGAGAGG TTCAGAGATT GGATTGCCAT GAATCACTTC CAACTGTCCC 720
CATGAAGACC CCAAAGCAAC ATAGGTGACT ATAGGGTTTT CTTTTGCATC CAACATCATT 780
CGGAATTCAG TTGCTAGATC ACAAAATAAT CTTACCTTTG GCCACATCTA AGCTTGTTAG 840
GTATGGAGCT CTGCATACTT CCTGGACGTC ACCTTGGTTG ATTTCAGCAT CCTTTTTTTG 900
AGTCAGAATG GGGCAGCCTC TCTAAGACAG GAAAGGTAGC TCTCATCTCA GTAGAGCCTT 960
TCCCACCACC AGGGAGCACT GGGACTGAGC AAAGTTCCAT GAGGTCAGGC ATAATGTGTT 1020
TTGAAACCTG 1030
|
