| Tag | Content |
|---|
EnhancerAtlas ID | HS145-05691 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr12:53821660-53822670 |
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 | GACTGTGTGT GTCTCTGTCC ACGTGGAAGA GCTCCCCACA ACTCACTTTG CCCTATTGTA 60
AGTAGTTCAA CCTCCACCAC CTGTTTCAGA GCCCAAATGC AGTGGCTCTT CCCTGAACTT 120
TTTCAGCACC TACAGCTTCT GTACTTCTGA AATCTTGAAT GATGGAAAGT CCCTTCTTTG 180
ACCATATACC TCCTGGCCCA GCTCAAAAAT CACTGTTTTT TTGTTTGTTT AATTTCTCTG 240
ACTTCTCCAG GCAGGGTTAG TCATTCTTGC TTTATGCCCC TTGGCACTCG GTTAATTTTC 300
CTATCTTGGG GTTTACTGCA TTCTTTATCT CTTACCTTCC CTGAGCCATC TTGGTGCCTG 360
AACACAGTTC GTGGCCACCG AAGGTGCTCG ATGACACTTG TTGAATGAGG GGTTCTATTG 420
CTCCCTTCCC TCCAATTCCC ACTTGCCCTC CACCTGCTAC TCTGTTATCT ACTGGCTCTG 480
CCCGTCTATG TGTACACATG CCTGACACCT CAGACAAGGT GACTCATGAA GGATGCCCCT 540
GACTAGCTTG CCCTGCCTCC TCTGTTACTG TCTTTGCCGC ATGTCTTCTG AGTCAGTATA 600
AGGTGGTGGT TATTAGTAAG TGATCCTGAG TCAGACTGCT TGGATTCAAG CTCCACTCCT 660
GCCTCACCGA CTGACTTCAA GAGAGTTTCC TTAGTTCTGT AAGGAAAAGC TCTTCATCTG 720
TTAAATGGGG GTGTGACAGG AGCACCTACC TTCTAGGGTT TTCACAAGGA TTACAGGAGG 780
CCACATCCAC TGGGTCTGGA CCACAGTAAG TGCCCAGTAC CCTTGATCTA GAGTTACTAT 840
TTTTCATGTC AATTGATGCA CAGTCTTACT CCTCTACCTA TTGTCTTGGC CAGCATCCAT 900
CAGTGTGTCT GTCTGCTGGG GAGATGCAGG GAGAAGACTG TCAATTGATC TCTGCTCCCT 960
GGGATGGATC AGCCGTCTCC AGCTTTGTGT ACCATCCTTT TCTCTCTGCG 1010
|
