| Tag | Content |
|---|
EnhancerAtlas ID | HS073-10009 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr22:50153890-50155280 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr22:50154040-50154058 | AGAAGGAAGTAAGGAGAG | + | 6.04 | | Myod1 | MA0499.1 | chr22:50154538-50154551 | TGCAGCTGTTACT | + | 6.62 | | Myog | MA0500.1 | chr22:50154537-50154548 | CTGCAGCTGTT | - | 6.02 | | TP53 | MA0106.3 | chr22:50154114-50154132 | GACATGCCTAAACATGCC | - | 6.8 | | TP53 | MA0106.3 | chr22:50154114-50154132 | GACATGCCTAAACATGCC | + | 6.95 | | 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 | CCTCCATGGA GAGATCATGA TGGCTGACAG GCACAGATAG TATGTACCTC TTCCATGGAG 60
AGGAACAAAA TAGTAAATAG ATGTGCACAT TTTGAACAGA CCATCCCAGA GAGAATGCTA 120
GGATTCACCA GAGATGAGAC AGGAAGCACC AGAAGGAAGT AAGGAGAGGG CTCACGGCAG 180
CTTGCCCAGC CAGGAACTGA CAGCCTCCAG GTGGGAGTCT CCTGGACATG CCTAAACATG 240
CCTCGGGCCC GACATATGGA GCTGCCTGAA CATTACACAG AGACGTCACT CCAGAAAAGG 300
GAACCCACAA AGAACCTCAC AGGCATTGAA ACCTGGAGCA GCCTCAGCTG AGGCCGTTTT 360
GAGAGCCTCA CTACCAGGGA TCTAACAACA TGGCTGTAGC CACTGCACTG CTCCAAGGAG 420
ACAGGGGAGA CTGGGCACTA CCACACACTC CTGGGAGGTG CCCTGTCACC TTGCTGTGGT 480
CTGCTGTTGG GACCGATGCA TGAGCAGACC ACACTCCACA CAACTTCTTA CCCAAGCTGC 540
TTGCCTAGGA GAAACCCCAC CCACTCTGGT CTCAGGCCCA AGGCACCAAT TGGAGAGTTG 600
AGCACTGAAC TGCACCCTGA CCTCGGCCTG AGCTTGGGCT GAAACCACTG CAGCTGTTAC 660
TCAACCAAGA AAAGACAGGG AAACTAGGCT ACCTTATGTA TGTCTAGGAC AAGACCCACT 720
GCCCTGCAAT AGGTTGCCGT GAGACTGAGA TCCAACCAGA CCACACTTCC TGCAGCGTCC 780
TGCCCATGCT GTTTGCCTGG GAGGAGCCCC GCCCTCCCTG GTCTCAGGCC CGAGGCACCA 840
ATTTTAGAGT TTAACGCAAA GCTGTGCCCT GCCCTCAGGC CAAGTTTGAC TTGACATGGC 900
TGCAGCTGCT GCCCAGTCAA GGAAGGACGG GGAAGCTAGG CTCTCCTACA CATACTCAAG 960
ACAAGACCCA CTGCCCTGCT ATGGGCAGCT GCAGGACTGG GGACTTCCCC TACCCAACCC 1020
ATCGCAGCTT CCAGCAACAA GAACACAGAC TGTTTGGATC CCAGTGGGTT GCTTCACCAC 1080
CACTGCCGCC ATCACCCAAA CCACAGCAGC TGCCCCGTTG GTAGCGATGG GGTGAATGTG 1140
CTTATTTTTA GGCTCTAGAG CAGCTTACAC TGGCTGCAGC GTTGGTGGGT CCTGGGGCTG 1200
ATTCTTGGGC CTCCAGGTGG CTTGCTTAGA AGCTAGTAGT GGGAGCAGTG GGCCCAGGAT 1260
GTGGTTTAGG TGAGGGTTGA AATATTACCT ATTGGGTACA GTGTTCACTG TTCTGGTGAT 1320
GGGTACACTA AAAGCTCTGA CTTCAGCACT ATGTCATGTA TACATGTAAG AAACCTGCAC 1380
TTGTATCCCC 1390
|
