Tag | Content |
---|
EnhancerAtlas ID | HS154-08840 |
Organism | Homo sapiens |
Tissue/cell | Osteoblast |
Coordinate | chr17:1366040-1367210 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr17:1366284-1366305 | AAGCACTTTCTTTTTTTTTTT | + | 6.01 | NFYA | MA0060.3 | chr17:1366719-1366730 | GACCAATCAGA | + | 6.14 | Nr2f6(var.2) | MA0728.1 | chr17:1366494-1366509 | TGAACTCCTGACCTC | - | 6.22 | RUNX1 | MA0002.2 | chr17:1366643-1366654 | TTCTGTGGTTT | + | 6.32 | SPI1 | MA0080.4 | chr17:1366834-1366848 | CACTTCCTCTTTCT | - | 6.51 |
|
| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_42226 | chr17:1366443-1367195 | Lung |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr17 | 1366536 | 1367139 | chr17 | 1366143 | 1367043 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH17I001462 | chr17 | 1365452 | 1367261 |
|
Enhancer Sequence | AAAATGTAGG TGTGCGTACA GGATCGTGTC AAGCCCAAAA CACCACGTTG CGTGGTATCT 60 CCTTGTTTGA GAATCTCTGC CCCAGGTTTC AAATCTAAGC TCCTCAGGCA GCTGGCCTGA 120 CCCCGGGCCA AACCTGTTCT TGCCTCTAAG CTCCACATGC ACCGTTCCCT CCACCCACAG 180 CGCGCCGCCC TCTTGGAAAA ACTCACAGCC ATCTGCTGAC GACGAGCTCC GTGGTTGCAG 240 CTTGAAGCAC TTTCTTTTTT TTTTTTGCTC TGTCGCCCAG GCTGGAGGGC AGTGGCATAA 300 TCTCGGCTCA CTGTAACCTT CGCCTCCGGG GTTCAAGGGA TTCTCCTGCC TCAGCCTTCC 360 GAGTAGCTGG GATTACAGGC ACACGCCACC CTGCCTGGCT AATTTTTGTA TTTTTAGTAG 420 AGATGGGGTT TCACCGTGTT GGCCAGGCTG GTCTTGAACT CCTGACCTCA GGTGATCCAC 480 CTGCCTCAGC CTCCCAAAGT GCTGGGACTA CAGGCGTGAG CCACCGCGCC CGGCCCACTC 540 ATTCTCTTTC TTGTGGAGGC GACACTGATT TCATTTTGGC GAGTCATCTC CTCCCACTCT 600 TGGTTCTGTG GTTTCCGGTG TGGGTTCCGG TGTGCCCCTG GTAGCTCTGT CTCCAGGGGC 660 AGGCACTCGA TCCAGGCCTG ACCAATCAGA ATCTATTCCT CTCCCTGGCT ACAGTGATTG 720 GGTCAGGGTG GATGCCTCAT TCAAGGTGCT GCACTGAGAA TCCGCTCTGA GACTTCCACA 780 TTTTGGGAAA GAGGCACTTC CTCTTTCTGC CTCCAATGCT GAACTGACAG AATGAAAGCC 840 TGGAGCTGTG GGTGGCTGTT GCTGCCACCC CACCTCCAGG TGAGAATCTG CTTGGGAAAG 900 AAGCCACTGT AGAGGAAGGT TCAGCCAGGC GATGGTTCCA GACACATTCC TGACAGTGTG 960 TGAGCACCTG GAAGTAGCCT TACTCTGGGA CTAAGGTGCT AATGCTTATA AATATCCTTT 1020 TTTTGGCCCA AGCCAGTTTG GACTGGGTTT GTCACTTGCA ACAGAATTTG AACGAGAGGT 1080 GTCCGGGCAC GGTGGCTCAT GCCTGTCACC CCAGCACTTT GGGAGGCCGA GGTGGGAGGC 1140 ATCACCCAAG GTCAGGAGTT CGAGACCAGC 1170
|