| Tag | Content |
|---|
EnhancerAtlas ID | HS078-13798 |
Organism | Homo sapiens |
Tissue/cell | H2171 |
Coordinate | chr5:179603910-179605230 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myog | MA0500.1 | chr5:179604506-179604517 | CTGCAGCTGTC | - | 6.62 | | Tcf12 | MA0521.1 | chr5:179604506-179604517 | CTGCAGCTGTC | - | 6.14 | | ZNF263 | MA0528.1 | chr5:179604095-179604116 | GGAGGAGGACCAGGGTGAGAG | + | 6.51 |
|
| | 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 |
| GH05I180176 | chr5 | 179603796 | 179605111 |
|
Enhancer Sequence | ATGACTGCTG CGTGGTGCCA GCCGTCAGGG TTGGGCAGTG GTCAGTCCTG CCCATGTCTC 60
CCCCTGGCAT AACCCAAGAC AGGGCCCCTG GCCTGGCCTC CAACTCCCAC CCAACCTTGG 120
TCAACCTCCC AGAGGAGAGG GCTGCAGACG AGGGGTTTCC AAGGGACGGC AACTTTTGCC 180
AGCATGGAGG AGGACCAGGG TGAGAGGTGA GACTCTCAGA GCCTGACGGA GGGGCTGGAT 240
GAGGGGCAGT GGGATGGGGG GCTGGCTGGG CTACTTCCAG AAACGTCCAG CCGAGTAGAG 300
GATGCATTCA AACCATGTGC ACATCAGCCC CTCAGCCCCG AAGCCAGGGG CTGCTTTCCC 360
TTTCCGGCCC CACCTCCCCA CCCAGTGAAG GGGCTGGCCT GCCCGGCTCA CCCAGCAGCT 420
TCCCCAAAGA CACAGGCTGT TCATCGGCTC CATTTTTAAC CTTCCTTAGT CCCAGCAGCC 480
CCAGCAAAAG CTCTTCGGTG AGTGCCTGCG CAATCTGCCC GGCTGGGCCG CAGCAGTCCA 540
CGGGCAGGGC AGAGCCCCGG GCTTCCTTCC GGGACCCCTG CCAAGGCTCA GCCCTGCTGC 600
AGCTGTCCAA GGCCATGGCC TCTGCGGCTT CTGCCTGGCC AGCATCTGTT CTTCCCTCTG 660
AAAACAGAGC CCATTTGTCC TTCCTCTCCT GCCCGTGGTA GGAGGACATG GCCCTGGTGC 720
CACTTGGGGA AGGAGTTGCG TTGGTCTGTG ACAGTTGGGA TGGCATGTGA TCCAGGCCCA 780
GCCACTCAGT GCCTTTCATC TCCCTGGCCT CTGGGATAAA TCCATGGGCA GGCATGTCAC 840
CTGGGTGGGC CACCAGACTC AGTTCGTGGG ACATTTATTT GAACTGTCTG AGCAGAGCCT 900
CTCTCTCTGC TCAGGGCAAG GTAAGGACAG GAAGTAAGTA TGGAGCTGGT GGGGGCTTTC 960
TTGTGAAAGG GGCCCACATG GAGGAAACGG AGCCAAGACT CACAGAGACC GAGACCATGT 1020
CCCACATCCA GCCATGCCTG AAGCCCACCT TGGGCTTTTT TTTTTTTTCT TTTTGAGGTG 1080
GAGTCTCGCT CTGTTGCCCA GGCTGGAGTG CAGTGGCATG ATCTCGGCTC ACCGCAACTT 1140
TCGCCTCCCA GGTTCAAGTG ATTCTCCTGC CTCAGCCTCC TGAGTAGCTG GGACTACAGG 1200
CGTGCACCAC CAAGCCTGGC TAATTTTTTT TTTTTTTTTG TATTTTTAGT AGAGACAGGG 1260
TTTCACTGTG TTAGCCAGGA TGGTCTCTAT CTGGCCTCGT GATCTGCTTG CCTCAGCCTC 1320
|
