| Tag | Content |
|---|
EnhancerAtlas ID | HS042-00331 |
Organism | Homo sapiens |
Tissue/cell | Fetal_brain |
Coordinate | chr1:6398040-6399490 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr1:6398642-6398655 | GAATGTTCTAGAT | - | 6.03 | | RFX1 | MA0509.2 | chr1:6398961-6398977 | GGTTTCCATGGTTACC | - | 6.24 | | RFX1 | MA0509.2 | chr1:6398961-6398977 | GGTTTCCATGGTTACC | + | 6.26 | | RFX2 | MA0600.2 | chr1:6398961-6398977 | GGTTTCCATGGTTACC | + | 6.41 | | RFX2 | MA0600.2 | chr1:6398961-6398977 | GGTTTCCATGGTTACC | - | 6.5 |
|
| | 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 |
| GH01I006338 | chr1 | 6398431 | 6399551 |
|
Enhancer Sequence | ACAGAGTGAG ACACCATCTC AAAAAAAAAA AAAAAAAAAA AAAGAAACCT GCTCTTCAGG 60
GCTTCCTCTG AGGCTATGGC CTCTGATGGA CCACAAAGGG GGCTTTCATG GCAGAAAATC 120
TGCAAAGCAG ATCCCTTCCT GGCATTTTTG AAGCCACCAA CTCCTGCAAT GACAAAGGGC 180
ACTGCTGACT GGGCCCTCAC AAGCAGGAAG GTCCTAGGAA GCAGGAGAGC GCGGCAGGCC 240
ATCCCTCCTC TCCAGGAAGG GGCCAAGGCT CCACCCCCAG CACAGTCGGA GAAGAGCTGC 300
GATCTCACAG GAGATGGCAG GGAACCCCCA AGGCCCCTAA AGTGGGGAAC CCACCCAGCC 360
CTGAGCCTCT CCCGAGTCGT GGGCGCTGCT CCTGTTGTGG GAGGTGCCCA TACACCCCTT 420
CCTGGGCCAC ATCCTGAGAC CAGCATCCAG GGTCCCTCTG ATGTCAGAGG TGCCTGCTGA 480
GGGAGCAGCA GGCAATGGGA ACGCAGACCA CCTTCCACCC CAGGCCCTTG CTCAGCTCCA 540
TCTGCCCACC TGCCGGAGCT GGGCTGACAC AGCCATTCTA ATCAACCCTG CTGAGGTCCT 600
CAGAATGTTC TAGATGCATA ATCGTGCTTG CTACCGGCCC GTCATGAGGA AGAGGACTCA 660
AGCCCCTCAA ATGGCTGTGA GCTGGCACTC CACGGGGCAG CCACTGCTGA GGAACAGGCA 720
TGGGGAAGAG GAGGAAACCG GCCCAGCCTC TCTGCATGGG AGGACTGGTG ACCTGGGAGG 780
TGGCAGGGAG AGGACCAGGG GCAGGGGAAG AGGCCCGCCT TCCCCCTCAC CTCCCGTCCC 840
CAGCCTGGGT ATAAAAAGAA GCGTGAGCTG GTGAACACTG GAGCCGCCCC CTCCTGCAGC 900
GCCCAGTGGG AAGGGGAAGG GGGTTTCCAT GGTTACCATG GCCAAGGAGG AGAATATTCA 960
GATGAAAGCA GAGGCAAAGG TTCACCCAGT GAGCTTCCAT CTGAGCCTGG TTTCTGGGGC 1020
TCCCAGGAGC AAGCACTGTC CTCTCTGGAG CCAACACCTC CCTACGCTTG AGGAGGGCAA 1080
GCAGGGCAGG GAGACCTGCA GAGGGGTGGA TGGTGCGTAC CGGCCTCACA GCCCGCGCCC 1140
AGCCCCTGCC ATGGATGAGC TGGCCACGGG CAGCAGGACA GGCAGCATGA TGTGCTCAGG 1200
CCGGACCCAG ACAGCAGGGT TGAGTCCTGC TCTGGGTAAC TGAACTCGTT TCCTAACCCC 1260
TCTGTGCCCC TTTCCTGTCT GCAAAATCAG GGCAATGGAC ATAGCTGCTC CCAGGGCCAT 1320
GGTGGGAGGT GAGAGAGGTC TCATTGGTGG AAAAGGGGCC AGGCCCTGGA GCGTCCTCTG 1380
CCCTCAGGAG GGAAGCAGCT GTGTAGCCAC GGCCCTTACT GCTCCAGTCA ACACTGTCGC 1440
TCCCAGAAGT 1450
|
