| Tag | Content |
|---|
EnhancerAtlas ID | HS145-16982 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr3:46204630-46205540 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr3:46204896-46204907 | CTGAGTCATCC | - | 6.32 | | FOSL2 | MA0478.1 | chr3:46205159-46205170 | CTGAGTCATCC | - | 6.32 | | JUNB | MA0490.1 | chr3:46204896-46204907 | CTGAGTCATCC | - | 6.14 | | JUNB | MA0490.1 | chr3:46205159-46205170 | CTGAGTCATCC | - | 6.14 | | NFE2L1 | MA0089.2 | chr3:46205155-46205170 | ACGGCTGAGTCATCC | - | 6.09 | | NFE2L1 | MA0089.2 | chr3:46204892-46204907 | ATGGCTGAGTCATCC | - | 6.36 |
|
| | 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 |
| GH03I046161 | chr3 | 46203463 | 46206226 |
|
Enhancer Sequence | AGTGACCCAA ACAGCAAAGG TGGCAGCCTG CCCCTCCTAG TGGTCACTCT GTCCTAGGGA 60
GAAATTTGAA CTCTGTCAGC CATAGGATAT GAGTTGGGGT GGCTGAAGGT CCTGGATGGG 120
AGGTCCTGCC CAGTGAGGAG GAATGGATCA GGGTCCCGCT TAAAGAAGCA GTCTGGCCAC 180
AATTTGGTAA ACCAGCTGTG GTATGCTGGG AGATCCCTTT CTTGTCTGGT CAGTTTGTAC 240
TCTCCAAAGC CCACAGGTTG GAATGGCTGA GTCATCCAAA CAACACAGGT GGTGGCCTGC 300
CCCTCCCCGC AGGCACTCTG TCCCAGGGAG AAATCAGAAC TCTTTAGAAT ATGGGTGAGG 360
GTGGCTGGAG GCCCCGGATG GGAAGTCCAG CCCAGTGAGC AGGAGTGGAT CAGGGTCCCA 420
CTTAAAGAAG GAGTCTGCCC ACATTTTGGT AAAGCAGCTG TGTTGTGCTG GGCGAATCCC 480
TTTCTTGTCT GGTTCATTTG GACCCTCCAA AGCCCACAGG CTGGAACGGC TGAGTCATCC 540
AAACAAAAAA GGTGGCAGCC CATCCCTCCC CCAGGAGCTC TACCCTGTCT CAAGTAGGTG 600
CTACCCTGTT GCTGGTGGCT GGCTGGAATT CCAAGCCAGT TGATCTTATC CTGTGAGGTC 660
CCTTGGAAGT GGGGCCCACA GACTGACGCT GCTCTGCTTC CTGGATTCAG CCCTCTTCCT 720
AAGGGTATGT ATGGACCTCT TGTCTTGCTT AAGTTGTAGT CATGTTTGCC AAAGATCCCA 780
GAGTAGATTA TGTAAAGCTC CTGGGCCTCT GTGCATGCCT AAGCAGCTGC TCTGCTGTGA 840
CTCCACACAG CTCTGTGTGT CAGACCCAAG GCCCTGGTGG AGTGGGTTCA TGAGGGGGAT 900
CTCCTGATCT 910
|
