| Tag | Content |
|---|
EnhancerAtlas ID | HS089-06048 |
Organism | Homo sapiens |
Tissue/cell | Hela |
Coordinate | chr17:73311780-73312600 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOS | MA0476.1 | chr17:73312170-73312181 | AATGAGTCACC | - | 6.02 | | ZNF740 | MA0753.2 | chr17:73311863-73311876 | GTGGGGGGGGCGT | - | 7.12 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_09177 | chr17:73302035-73320268 | CD14 | | SE_54131 | chr17:73311395-73312865 | Spleen | | SE_61022 | chr17:73284104-73345918 | HBL1 | | SE_62513 | chr17:73287335-73369120 | Tonsil |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr17 | 73312070 | 73312303 | | chr17 | 73311916 | 73312453 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I075311 | chr17 | 73307283 | 73317249 |
|
Enhancer Sequence | CCATCTCCTC CACACTCAAG TCTGAAGGTG AGCCTGTCAG GGGCTCCCAG CTCACTGGGT 60
GGAGGGAAGC GTGTCAGGGA GGGGTGGGGG GGGCGTGCCC TGAAGAGCGA GGCCATGCGC 120
CTACCTCCAG CTTTTCCCCT GACACACTGA GCGACTCCCG GCTGCACGCC GGCCACAGGG 180
CTCCTGTAAG ATGCTGGGAG GCTTCCCAAG GCACCCCGCC CAGATGTCTT CCCAGGAATC 240
CCGGATCCCT GAGGAGGGAG ATACCATCAC TAAGAAATCT GTGACCAAAC TGCTGATCAC 300
AGAAAAGGAG TGATTTTCCC ATTAATTCTG AAACAGTCAG TCAAACGCGA GGGAGGGGAC 360
AAATTGAGCA AAAAGCCTCA AATGAGGCTA AATGAGTCAC CACGCCCGGC CTTTTCAATT 420
ACATAGCTCC ATTTTGTAAA CTTCTGCTCA GCTTCAAGGA GGCCAGCCCA AGTGGACCAC 480
AGGACTAGCA GTCTTGACTC TTGCTGGGTC AAGATCCTTC CCACACATGA CTGCTGCAGG 540
GGAAGGTCAA AAACGTCCCA GGCCAGGCAC AGCTCACGCC TGGATTTCCA GCACTTTGAA 600
AGGCCAAGGG TGGGGGGATC TCTTGAGCCC AGGAGTCTGA GACCAGCCTG GGAAACACAG 660
ACCCCACTGT ACAAAAAAAA ATGAAATTAG CCAGGTGCAG TAGCGTATGC CTGTAGTCCC 720
AGCTACTTGG GTGCAGTAGC GTATGCCTGT AGTCCCAGCT ACTTGGGTGC AGTAGTGTAT 780
GCCTACAGTC CCAGCTACTT GGGAGGCTGA GGTGATCACT 820
|
