| Tag | Content |
|---|
EnhancerAtlas ID | HS051-18913 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr22:50154340-50155730 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myod1 | MA0499.1 | chr22:50154538-50154551 | TGCAGCTGTTACT | + | 6.62 | | Myog | MA0500.1 | chr22:50154537-50154548 | CTGCAGCTGTT | - | 6.02 | | Nr2f6(var.2) | MA0728.1 | chr22:50155388-50155403 | GAGGTCAGGAGTTCA | + | 6.22 | | Tcf12 | MA0521.1 | chr22:50154537-50154548 | CTGCAGCTGTT | - | 6.62 |
|
| | 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 |
| GH22I049760 | chr22 | 50153749 | 50155297 |
|
Enhancer Sequence | CTGGGAGGTG CCCTGTCACC TTGCTGTGGT CTGCTGTTGG GACCGATGCA TGAGCAGACC 60
ACACTCCACA CAACTTCTTA CCCAAGCTGC TTGCCTAGGA GAAACCCCAC CCACTCTGGT 120
CTCAGGCCCA AGGCACCAAT TGGAGAGTTG AGCACTGAAC TGCACCCTGA CCTCGGCCTG 180
AGCTTGGGCT GAAACCACTG CAGCTGTTAC TCAACCAAGA AAAGACAGGG AAACTAGGCT 240
ACCTTATGTA TGTCTAGGAC AAGACCCACT GCCCTGCAAT AGGTTGCCGT GAGACTGAGA 300
TCCAACCAGA CCACACTTCC TGCAGCGTCC TGCCCATGCT GTTTGCCTGG GAGGAGCCCC 360
GCCCTCCCTG GTCTCAGGCC CGAGGCACCA ATTTTAGAGT TTAACGCAAA GCTGTGCCCT 420
GCCCTCAGGC CAAGTTTGAC TTGACATGGC TGCAGCTGCT GCCCAGTCAA GGAAGGACGG 480
GGAAGCTAGG CTCTCCTACA CATACTCAAG ACAAGACCCA CTGCCCTGCT ATGGGCAGCT 540
GCAGGACTGG GGACTTCCCC TACCCAACCC ATCGCAGCTT CCAGCAACAA GAACACAGAC 600
TGTTTGGATC CCAGTGGGTT GCTTCACCAC CACTGCCGCC ATCACCCAAA CCACAGCAGC 660
TGCCCCGTTG GTAGCGATGG GGTGAATGTG CTTATTTTTA GGCTCTAGAG CAGCTTACAC 720
TGGCTGCAGC GTTGGTGGGT CCTGGGGCTG ATTCTTGGGC CTCCAGGTGG CTTGCTTAGA 780
AGCTAGTAGT GGGAGCAGTG GGCCCAGGAT GTGGTTTAGG TGAGGGTTGA AATATTACCT 840
ATTGGGTACA GTGTTCACTG TTCTGGTGAT GGGTACACTA AAAGCTCTGA CTTCAGCACT 900
ATGTCATGTA TACATGTAAG AAACCTGCAC TTGTATCCCC TAAATATATT TAAAACTTTA 960
AAATTTAAAA AAAAATCACC TGGGCCGGGC GCGGTGGCTC ACGCCCATAA TCCCAGCACT 1020
TTAGGAGGCC AAGGCAGGCG GATCACCTGA GGTCAGGAGT TCAAGAACAG CCTGGCCAAC 1080
ATGGTGAAAC CCCATCTCTA CTAAAAATAC AAAATTAGGT TATGGTGGCA CATGCCTGTA 1140
ATCCCAGCTA CTTGGGAGGC TGAGGTAGGA GCATTGCTTG AACCCAGGAG ATGGAGGTTG 1200
CAGTGAGCCG AGATTGCGCC ACCGCACTCC AGCCTGGGCA ACAAGAGCAA AATTCCATCT 1260
CAAAAAAAAA AAAAATCATC TGTACCCACA CCCCCTCACA TTTGTACACA CCCACACACA 1320
ATTTTGTTCT CCCAGGTGAA TGATTCAACA GCCAGCCCCA GACTGCGTAT GATGTTACCC 1380
TCCCATATTT 1390
|
