| Tag | Content |
|---|
EnhancerAtlas ID | HS095-07162 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr12:53821680-53822670 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr12:53822177-53822188 | GGTGACTCATG | + | 6.62 | | JUND | MA0491.1 | chr12:53822177-53822188 | GGTGACTCATG | + | 6.02 |
|
| | 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 |
| GH12I053427 | chr12 | 53821211 | 53822832 |
|
Enhancer Sequence | ACGTGGAAGA GCTCCCCACA ACTCACTTTG CCCTATTGTA AGTAGTTCAA CCTCCACCAC 60
CTGTTTCAGA GCCCAAATGC AGTGGCTCTT CCCTGAACTT TTTCAGCACC TACAGCTTCT 120
GTACTTCTGA AATCTTGAAT GATGGAAAGT CCCTTCTTTG ACCATATACC TCCTGGCCCA 180
GCTCAAAAAT CACTGTTTTT TTGTTTGTTT AATTTCTCTG ACTTCTCCAG GCAGGGTTAG 240
TCATTCTTGC TTTATGCCCC TTGGCACTCG GTTAATTTTC CTATCTTGGG GTTTACTGCA 300
TTCTTTATCT CTTACCTTCC CTGAGCCATC TTGGTGCCTG AACACAGTTC GTGGCCACCG 360
AAGGTGCTCG ATGACACTTG TTGAATGAGG GGTTCTATTG CTCCCTTCCC TCCAATTCCC 420
ACTTGCCCTC CACCTGCTAC TCTGTTATCT ACTGGCTCTG CCCGTCTATG TGTACACATG 480
CCTGACACCT CAGACAAGGT GACTCATGAA GGATGCCCCT GACTAGCTTG CCCTGCCTCC 540
TCTGTTACTG TCTTTGCCGC ATGTCTTCTG AGTCAGTATA AGGTGGTGGT TATTAGTAAG 600
TGATCCTGAG TCAGACTGCT TGGATTCAAG CTCCACTCCT GCCTCACCGA CTGACTTCAA 660
GAGAGTTTCC TTAGTTCTGT AAGGAAAAGC TCTTCATCTG TTAAATGGGG GTGTGACAGG 720
AGCACCTACC TTCTAGGGTT TTCACAAGGA TTACAGGAGG CCACATCCAC TGGGTCTGGA 780
CCACAGTAAG TGCCCAGTAC CCTTGATCTA GAGTTACTAT TTTTCATGTC AATTGATGCA 840
CAGTCTTACT CCTCTACCTA TTGTCTTGGC CAGCATCCAT CAGTGTGTCT GTCTGCTGGG 900
GAGATGCAGG GAGAAGACTG TCAATTGATC TCTGCTCCCT GGGATGGATC AGCCGTCTCC 960
AGCTTTGTGT ACCATCCTTT TCTCTCTGCG 990
|
