| Tag | Content |
|---|
EnhancerAtlas ID | HS182-00485 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr1:26002160-26003550 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myod1 | MA0499.1 | chr1:26002631-26002644 | AGAAACAGCTGCA | - | 6.29 | | Myog | MA0500.1 | chr1:26002634-26002645 | AACAGCTGCAG | + | 6.02 | | Tcf12 | MA0521.1 | chr1:26002634-26002645 | AACAGCTGCAG | + | 6.62 | | Znf423 | MA0116.1 | chr1:26002536-26002551 | TGCCCCCTGGGTGGC | - | 6.13 |
|
| | 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 |
| GH01I025675 | chr1 | 26002283 | 26003398 |
|
Enhancer Sequence | TGTTTTCCAT AGTGGTTGTA CTAACTTATA TTCCCACCAG CAGTGTAAAA GTGTTCACTT 60
TTCACCACAT CCATGCCATG GCTGCTTTTT ATTGAGCACA TATTATATAC GAGCCATTGT 120
GCTCAACACT TTACATCTGT TATTTACTCT TAGGGTTATT CTAAGGATTA AGTATTTCTG 180
TCCTTTTACA GATGAGGAAA CTGAGACTTA CAGGGGTTAA GTCACTCACT CAAGGCCACA 240
CAGCCAGTAA GGTGGCAGAG CCCTAGAGCA GCCTCTCAAG CTTCAATGTG CGTTTGAATC 300
ACCTGGGGCT CTTGTTAAAC TGCTGCTACA GATTCAGCAG GTGGGAGAGT GGAACTGAGG 360
TACTCTGTTT CTGACGTGCC CCCTGGGTGG CCCTACTCCT GGTCCCTGGA GCACTTTGAG 420
CAGCGAGAGT TTCTCTGCCT GTATGGCCCA CACTCTCGAC CCTGATGCCT TAGAAACAGC 480
TGCAGACAGG ATGCGATTCC TGAGACTGCT CAAACCTGAA ACCCCATGGG CAGGATGTGG 540
GTGAGCTGTC TGGACCTCAG GTGGGTGGGA GTTGTATCAT ATGCTCATTT CCCACATTGG 600
CCTTTCAATA GCTTGAGTAA ACCCGAAACT GAGAGGGTTG GAGGCAGCAT CTCCCCTTCT 660
ACTCCCCCGC TTCACCTCCC CGGGCAACCA AACCCCACCC GTGCCCAGCT TCTGAGCGAT 720
AGACCTGGGC TGTGTATTTG CAGGAGCCTC ACTGGGGTCA CCAACCAGGT CATGTTGTGT 780
TGCCCCAATA AATGGAACTG GATCAGAAAA TCCAACGTGG ATAGTTTTTA GGTGCCAAGC 840
TGTCAGCTCT TCCCTTGGAC TGTGCTGAAA GTGGAAGAGG AGAAAAAAAT CAACCCAATG 900
TTCTAAGCTC TCTGTCTACA TAGTCATTAG ATCCCAGGAT CGTTAGAGAC CAAATCCCTT 960
CCCACTTGGC CCCTGCAAAT GGGGCCAGGT GTCACTGCTG GGAGACGCCA GTAAGGCTGC 1020
ACGTCATGGT GTGAGCACTT GTCTTTAATG ACTGGGAAAA TCCATTTCCT TCCTTGGCAG 1080
CTTTGAATGT AGCAACTGTG GTTCTGGGTC ACTGCCAGAG CCAGCCTTGT GTGTATGTGT 1140
GTGATTTTTT AAAGTGGGGG AGAATGTCTC AATATTCAAT GCTCACCCCC TTCCTTCCAA 1200
GTTGTACCCC CAGAGAACTG TCCAACACAA ACTTTGGAGT TTTCCACTCT GGGAGTGGTC 1260
TGCTGGCACC CACGTGTCCT CCCCTCCTCT AATGCATCCT TTCTCTCTTG ATCTCATTGT 1320
TCTGGGGTCC TCAGCTGAGT GGGCATCTGT GCCTGGGTGA TCGATTCTAG TCTCTTTTCT 1380
GCAGGAGAGA 1390
|
