| Tag | Content |
|---|
EnhancerAtlas ID | HS026-14177 |
Organism | Homo sapiens |
Tissue/cell | CNCC |
Coordinate | chr17:46226560-46227180 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RARA(var.2) | MA0730.1 | chr17:46227007-46227024 | GGGTCATGGTAAGGTCG | + | 6.07 | | RFX1 | MA0509.2 | chr17:46226914-46226930 | CGTTTCCATGACAACC | + | 6.9 | | RFX1 | MA0509.2 | chr17:46226914-46226930 | CGTTTCCATGACAACC | - | 6.9 | | RFX2 | MA0600.2 | chr17:46226914-46226930 | CGTTTCCATGACAACC | - | 6.79 | | RFX2 | MA0600.2 | chr17:46226914-46226930 | CGTTTCCATGACAACC | + | 6.86 | | RFX5 | MA0510.2 | chr17:46226914-46226930 | CGTTTCCATGACAACC | - | 6.11 | | RFX5 | MA0510.2 | chr17:46226914-46226930 | CGTTTCCATGACAACC | + | 6.43 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr17 | 46226663 | 46227113 | | chr17 | 46226881 | 46226967 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I048149 | chr17 | 46226552 | 46227693 |
|
Enhancer Sequence | AGGACTCTGT CTATATTTTT AATTTTAGCT TAAAACCTTA GATTTTCTCT CCTTAAGTAG 60
AGATGTTGGG TGTCAGATTT CCACTGCCTT TCCCCACTTG ATTGCGCCAG ATTCAGCAAT 120
TTGGGTCTAG CTGGGGTGGG TTTTGGAGAA AGAGGGATGA CAAGTCACCA TGTTCCAGAC 180
CCTAGACAAA TGGAAGAGAG TTGCACATCA CCAAGAAAAT TAGGATTCCT TTTGCTTTGT 240
GAATTAAAGA AATGAATAAT TTAATCCTCA AGATTGTTCC GGCGAGGGAA AAGCAACGTC 300
CCAGTTGCGG AGCCCTACAG CCTGTCGGTG TGTTACATCA TCTGCACACA TAGGCGTTTC 360
CATGACAACC GCTTATAGCT TCATTTCCTG GATCCCTCTA GGGGGTGTCA CAGCCAGATC 420
CACCTGCTTT TCACCCTACC CTCGGTGGGG TCATGGTAAG GTCGCCAGAA TAAATGAACG 480
CGGGTACTAA TGATCTGTTT ACTGCTGTTT ATGCTCTGTG TGTGTCAGGG GCACGCACAT 540
TTAGAGAGCT CATTATGGTT GCAATTAGAA TGCACCATCG CTAGATATTT AACTCCTTTT 600
TCTTTTAAAT TAGCATTTTA 620
|
