Tag | Content |
---|
EnhancerAtlas ID | HS003-16764 |
Organism | Homo sapiens |
Tissue/cell | A549 |
Coordinate | chr16:1407750-1408940 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
POU2F2 | MA0507.1 | chr16:1408804-1408817 | TTAATTTGCATTT | + | 6.25 | Zfx | MA0146.2 | chr16:1407757-1407771 | CCCGCCTCGGCCTC | + | 6.01 |
|
| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_01156 | chr16:1404853-1409582 | Adrenal_Gland |
|
| 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 |
GH16I001356 | chr16 | 1406640 | 1409035 |
|
Enhancer Sequence | TGATCTGCCC GCCTCGGCCT CCCACAGTGC TGGGATGACA GTCATGAGCC ACCGCGCCTG 60 GCCTCGACTT TATTATTAAT ACGGTAAAAC TACAGAGAGT TTGAAACATC AGTCTGGGGC 120 GTCCTCCTCT AACCAGTGCA CTTGCTGCTG CAGCGCAGGC CCTTCAGGGG ACGGGGATGG 180 GGGCCAGTCC CCTCCCTGCC TCCACGGCCC AAGCCCCAGC CTTCCCCACA GTCCTGGAGG 240 ATGGCCCGTG GCTGACAGTC TCGGTGGGCG CTGTGTTAAG GTGGCGTCCC CAGCCAGGTC 300 CCGACTCCCC AGCTTAAAGA ACAGGGTGGC TGCTGTGGCT TGACTCACGA GTTGCCACTG 360 GCCTTGATGT GTACACGCCC TTGCTCTAGC ACTGCCTGGG GCTGGCCTGG CTGGAGGGTA 420 GGGACGCTGC ACGCCTTCCC TCTTCCCCCA GGCGCTGGTG ACACTGCCCT GCAACCGTCA 480 GCACCATCAT CTCCACAACT TGCTCTGTCC CCTTCAAACC CTGACTCCCA GCTGCCCCGC 540 TCCCCCAGCC CCGGCACCCA CCATTCTGCT GTCTCTGAAC TTGGCTATTC ATAGACGTCA 600 CATAGGTGAC TCATAACTGT GTGCGACCTT TTGTGTCTGA CCAACTCCTC TTGGCACAGT 660 GTCCCCAAGG TCCCCCAGGC TGGAGGCTCT CAGTGCTTCC TTTTTATATG GCTGAGGACT 720 GTTCCACTGC AAGGACAGAC CACGTTGTTG TTTACCCGTC ATCTGTCCAT GGACACTGGA 780 GTGGCTTCCA CCCTCTGCCT GGGAATAGGC TGCTGTGAAC TTGGGTGTAA ATATTTGAGT 840 CTCTGCTTCC AATTTCTGAG AGTAGCTTTG CTGGATCTTA TTAGAATTCC ATGTTTAGCT 900 TTTTGAGGAA CCACCAAACT GTTTGCATAG TGGCTGCACC GTTTCCCATT CCAGCCAGCA 960 TTGCACGAGG GGTCCAGTTT CTCCACATTT TCACCAACAC TGTTTTTTGC TAACAGCCAT 1020 CCTAGTGGGT GTGAAGCGGT ACCTTAGGGT TGTTTTAATT TGCATTTCCC TAATGATCAG 1080 TCATGTGGGA TCTTTTCAGT TGCTTATGGT GTTTGTCCTT TTTTTTTTTT GAGATGGAGT 1140 CTCACTCTGT GGCCCAGACT GGAGTACAGT GGCGCCATCT TGGCTCACTG 1190
|