| Tag | Content |
|---|
EnhancerAtlas ID | HS034-09489 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr14:100798530-100799890 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myod1 | MA0499.1 | chr14:100799265-100799278 | AGCAGCTGTCACT | + | 6.64 | | Myog | MA0500.1 | chr14:100799264-100799275 | CAGCAGCTGTC | - | 6.14 | | Tcf12 | MA0521.1 | chr14:100799264-100799275 | CAGCAGCTGTC | - | 6.02 | | ZNF263 | MA0528.1 | chr14:100798637-100798658 | CCTCCTTCCTGTCCCTGCTTC | - | 6.15 |
|
| | 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 |
| GH14I100332 | chr14 | 100798484 | 100799410 |
|
Enhancer Sequence | CTGCTGGTGC TGCAGGCGGG CACTGGGGGC CAGAGGCAGG CCTGTTGCTT GCCAAGTGCC 60
GTCCTGGAGC AACGAGCTGT TCCACAGCCA CCCGTGTGCT CAGCCACCCT CCTTCCTGTC 120
CCTGCTTCCC CACCCAGTGC TGTTTTGTGT GCTTCTCAGG CACCATCTCC TTTCAGGCAG 180
GCTCAGCTGG TCTCTCCTCC AGGCTGGGGG CCACGGGACA GAGAGACTGA GCTGGGTTGG 240
CCCCACATCT GTCTGACAAG TGGACATTAC CAGCCAGAGC AGGAGTGCTC TTCCGGCAGA 300
GCCTCTGGCA CCACGGTGGT GCAGGCACCC GGCCTCATGC CTCATCCCCA AACACTCATG 360
GGGCCACTGC AACCTGTCCA TCCTAATCCA GACACGCCCA TGTCTTTCAG GGAACATTTC 420
TCTCAGAAAC CACTGGTTTT TAGCAAAACT GGGGAGGCTT GGGAGACATG TGGCTCCCCT 480
GTGTCCTGAC CAGCAGTGGC CTTGGGCAAG TCACCTGAGT ATTGGACCCA GGGCACCCCT 540
CCTAAGACCC TAAACAGGAG GCATCACTGC TTTTTACAGG GGAGGAGATG GAGGTCCTGG 600
GAGGTTAAGT GACCTGGCCA GAGTCACACA GCCGGTGAGG GGAGAAGCTG GTTGGTGTTG 660
GCTCACTCCT CCCTGGGGCC AGGGTCTCAC CAGGGCCCTG CCAATAGATG CTGTGGCTGG 720
GTGGACAATG ACAGCAGCAG CTGTCACTGA CTCCATTTGT CACCCCTCAT TGCACTTGCG 780
TCACAGGTGC AGTAGAGCGA CGAGGAGTCA TATTAGTTGC CCAAGGCAAC AGGCTAGTGA 840
GCTATGTGGC CTCTGTGGGT GGCTCACCCC CACTGGCCAT AGCCAGCCAG GTGAGCAGGG 900
GAGGGCAGGG GTGGGGCCCA GGCCAGCAGG AGTCGAGACC GGGAGAGGAA GCCTACTTGA 960
GGTCATGGTG CACCCGGGTA CCTGAGTGGG ACTCGAGCCC AGGCCTCCAG CCTCCAGGGT 1020
GGGAACCGTA GTTCCCTCAT TTGTAAAATG GTCCCTCTGT ATGTGTGTGG AAAGCACCAA 1080
GAGTCAGGAC AGACTCGCTG TATCAGAGTC ACCCTATGGC CTTGGACAAG TCATGTTCTC 1140
CTCTCCTAAG CCTCAGTTTC CCTACTTGCA AAATAAGGAT GGGCCGGTAG AATGAGCCCA 1200
GGGCTCCCTT GCAGCTCGGC CTCTGCCCTG GGCCTCATGT GAATGGGGCC CGACCTGGCT 1260
CCCAGCCTGT GCTCCCCGTC ACTACACAGC ACCACTAAGC ACCCCACGGC CAGCCCCTCC 1320
TCTGAAAAGC GAGGACAACC TCTGCTTGCA TTCTCCATCA 1360
|
