| Tag | Content |
|---|
EnhancerAtlas ID | HS024-08385 |
Organism | Homo sapiens |
Tissue/cell | Cerebellum |
Coordinate | chr19:19760990-19762490 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myod1 | MA0499.1 | chr19:19761365-19761378 | TGCAGCTGTTGCT | + | 6.64 | | Myog | MA0500.1 | chr19:19761364-19761375 | CTGCAGCTGTT | - | 6.02 | | SPI1 | MA0080.4 | chr19:19761220-19761234 | CACTTCCCCTTTCT | - | 6.22 | | SPIB | MA0081.2 | chr19:19761220-19761232 | CACTTCCCCTTT | - | 6.07 | | Tcf12 | MA0521.1 | chr19:19761364-19761375 | CTGCAGCTGTT | - | 6.62 | | ZNF263 | MA0528.1 | chr19:19761993-19762014 | GGTGCAGGATGGGGTGGAGGG | + | 6.3 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr19 | 19761258 | 19761567 | | chr19 | 19761851 | 19761963 |
|
Enhancer Sequence | ATTAGAACCT GGGCAGTCTG ACCCCAGCTA AGCCATGCCC CCACCTCATG CAAGGCCCCC 60
TAACCTGAAA CACACAGAAG GGGGCTATTG CGCTCTCCTT GGGAAACCCC ACACCAGGCC 120
CTCACCTCAT TTATCCCTGC GCCCGTGGCC TCTCTGAAAT CCTGTTTTCT CGGGGCTGGG 180
CCCCCTCCCA ACTCTGACAG GGCCCCTGAG TTCTCAACAT CTTCTTGCTC CACTTCCCCT 240
TTCTTGCTGG CTGGCCCTGG CTTGGATGCT GGGCGCTGAG GATGGCCAAG GGCGGCCCGC 300
CAGCCCTCCT GGCACTGCCT GCTCACCCTG GACCATCTCA AGCTGAAGGG CAGCACACTT 360
CCACCTGGCT TGTGCTGCAG CTGTTGCTAG ACCAGCTTCG CTTGTCAATC AACAGTTCTG 420
CTCATCCGCT CCATGCCACC TGCCCACAAT CCCCAGGCCC TGGAAGACCC CGGTAGCTGG 480
GGCTGGGACA GGGGGAGGCC TGCGACCAAT AGAACAGAGG GAGGGCAGGG ACCGAGTCCT 540
CTGAGAGGTG GCCTGGAGGT TCCGGAAGCT GCTCTGGCCC AGACCTGTGA ATGTTTGCTG 600
CCAGCAGCCC TGTGGCAACA CTGCTCCATG TGGTTCTTCT TAGGGCCCTG TCAACACTCA 660
TGCAGGTCCT GAACTGCGTG CGCCCACAGG GGCTTCACCT CTAGCTCTGG GGCAGGTATC 720
TGGTAAGCCC CACACCTCTA GCTGGGAGGG GCTGGGTCTC TATGTCTGCC TCTTCATCAA 780
TCTGAATCCA GGGCATTGCT CAAAGAGGTC ACTGGGGAGA GGTTGGAGCC TTGAGCTCTG 840
GAATCAGGCT GTCTGGATTC CAATCCTTAG CCATGGATTG GAAGTGACCT GGGCAAGTGG 900
GTTCACTTCT GAGCCTCTGT CCCTTCTCTA CAAAGCAGGG CCCCGAGAGC TGACCCAGCC 960
AGCTTCCTCC TCTGTGGTGT GGGGAAGGCA AGCCACCCCG TGTGGTGCAG GATGGGGTGG 1020
AGGGACCAAC GCAGTAACAC GCACGGAGCG CTCCGCCTGG GGTCTGGTCA GGCTGAGCAC 1080
TGGGCAAACT GCCATCAACT GTGGCTGAGG ATGCCAGCAG TCCCTGTGCT CGGGAAGGGA 1140
GCACTCGGTA CATGGGCAGC TTGCCGGGCC AAAGAGGGTG TGAAATGAGG ATGACACTGA 1200
GGATGGGGAG TAAGCGTGGT AGGAGCAGTA TCTGCCCATG AGTGCACAGG AAACCCGAGC 1260
TGGCAGTCAG ACTATCGCCT CATTATGGTA AATAAACACC TACATGCCGC ACATCCTGGG 1320
ACCTGCGACC CAGTGAACGC TCACATGCTG TCCGAGGTGC CCAGTGGGCC AGGGCTGTGA 1380
TTAGTGGTGC CAGGCATTTG AAGACACTGT GCTGCTGAGG CCTGGTACAC AGGTGGGCTG 1440
TTGCGATGGG AGCTGTTCTT GGACTCAGGG TCCCCCTTCC CCACTGTGGG CCAGGCTAGG 1500
|
