| Tag | Content |
|---|
EnhancerAtlas ID | HS139-42075 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr4:148418820-148420280 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxa2 | MA0047.2 | chr4:148419299-148419311 | ACAATGTAAACA | - | 6.04 | | NEUROD2 | MA0668.1 | chr4:148419732-148419742 | ACCATATGGC | - | 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 |
| GH04I147497 | chr4 | 148418821 | 148420520 |
|
Enhancer Sequence | TCACACCATT CTCCTGCCTC AGCCTCCCGA GTAGCTGGGA CTACAGGTGC CCGCCACCAA 60
GCCTGGCTAA TTTATTTGTA TTTTTAGTAG AGACGAGGTT TCACCGTGTT AGCCAGGACG 120
GTCTGCATCT CCTGACCTCG TGATCCGCCC ACCTCGGCCT CCAAAGTGCT GGGATTACAG 180
GCCTGAGCCA CCGCGCCCAG CCTCTCTCGG ACTTTTTGAG ACCAAAGAAC ACAAAGATAC 240
TATTTTTAAT GTGAAATACC TCTAAAAATG TTCATTGAAA GTAGAAAGAT TGGCATCTTA 300
ATACAAGATT GCCAGGGTAG GGATGGTTGT CATAGAAATT TACCAAATTG GAACACATGA 360
AGACAGAGCT AAAAGAAAAA TTTATCTTAA TATCATCAGC AAAATTTGCA TTTGCAACAT 420
CCCAAAAAGA AATTTTATTT ATGAAAACCC ACTGACCACA TATGAAATGG AATCATCTTA 480
CAATGTAAAC ACTCCCAGGA AGTCATTCAG AACTCTGTGA AATGTCTGAG CACTGCATTT 540
TTGCAATCTC ATGAATAAGA GTTTAAATGT GAGTCATTGA CACTTTTCCT GCTTTTTGTT 600
CTGGGGAAAT AGCTTCACGG TAATATTTTC ATTAATTGTA TGGAGTGACT TCAGAATCAT 660
CTCCAGCTCC TGTACCATCA TAAAGGAAGT CAACCCAGAG GGAGTGGTAT GCACTAAGGT 720
GACCGTCCAG AGCCCACTTT CAAGCACTGC TGCTTGCTCC TGCTTGATTC GCTCACCCAG 780
GGCCCAGCAA ACTACAGCTA GTGAGCCAAA TCTGGCCCAC CACCTGTTTT TGTAAATGAA 840
GTTTTATTGG AACACAGCCA TACCTATTGC TTACGTATTT TCTATGGCAG CTTTTGAGTA 900
GTTTCAACAG ACACCATATG GCCCAGAAAG CCTAAAATAT TTACTATCTG GCCATTTATG 960
GAAAAAGTTT GTCAAGCCTG GTGGCATCTC ACCAACTGCC CTGCCCCTTC CTCTCATCCC 1020
TGGCTCTCAT CTACCTCCAT TTGGACCCAC AGGCAGTCAA AGCCCAAGAT CTGAACTTCA 1080
GAAATGTGAA TAAGGCTTCA TAACCTTTTT CTCTTTTTAA TAGAGATGGG GTTTCACTGT 1140
TTCCCAGGCT TATCTTGAAC TCTTAAACTC AAGCAATTCT CTTACCTCAA CCTTCCAAAA 1200
TACTGGGATT ACAGGCATGA GCCACTGCGA CCAGACACTT CATAACCTTT GATATTTTTA 1260
AGTGCCTAAT GCCTTAACCC CAAGAAGTAA ATGGGCATAA TCTCAAGAAA TCAAAATATG 1320
TTTTATTTTT TAAAATGGTT TGTCACTGAT CTTGAATAAA TCACTTGACC TCCCAAGTCA 1380
TTCTTTTTCT TTTTCTTCTT TTTTCGAGAA AGGGCCTCAC TCTACCACCC AGTCTGGAGT 1440
TCAGCGGCAT AACCACAGCT 1460
|
