Tag | Content |
---|
EnhancerAtlas ID | HS182-22233 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr9:136127170-136128540 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
REL | MA0101.1 | chr9:136127794-136127804 | GGAAATCCCC | - | 6.02 |
|
| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_24494 | chr9:136126953-136128884 | Colon_Crypt_2 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr9 | 136127170 | 136128270 | chr9 | 136128302 | 136128371 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH09I133250 | chr9 | 136125724 | 136128898 |
|
Enhancer Sequence | AGCAGAGGGG CGGCCCCACC TCCACCTGGA AGATTCCTGC TCAGATCCTG GGTCACCTGC 60 CCAACTGATG ATGCCCCAGC TGCTCCTGCT GCGAAGCTGA ACCCAGAACC CACTCAGGTC 120 TGGTCCCCAC TCCGCCCCCA GCACCCCTAG TGCGGCCACG CGGGAGGATG GGGCCCGAGG 180 CTGCAGGGGA GGAAGCGGGT GGATCAAGGC AAGCCTCGCC TCGCCTCGCC TCACCCATGG 240 GTGTTGGTTT TTGTTTTTTA AACCAAACAG AGCAGAGAGG GGCAAGGAAG CAAAAATGAC 300 TCAAGCCCAC AGAGGCAGCA GCTCTCCCTG TGCTGGGCAC ATGCCCAAGG CTGGCTTTGG 360 GGACAAAGAA TAATCAAAGA TGACACTTTG GGGCTGCCCT CTCCCCAGCC CTCCTGGGCA 420 AAGTCGGTGC GTCCCAGGAG TCAGCCTGGA CTTGAACCTC TGACACCCGA TTGCTGCTGG 480 CCTGGTGCAG GGACCCGAGG GGCCCGAGGA CACAGGAAAG GGCCTGGAGG GAGAGAGCAG 540 CCGGACTCCG CCCAAGCAAT TTAGGCGCCT GCCTCATCTG TGGTCCCCCA CACCCCCAGC 600 TCACCAAGCA GCAGGACAAC CCCTGGAAAT CCCCCAGGGA GGCGGGGCGC AGGGATTGCA 660 GTGAGGCCCT GTGCCCAGGC TGGCTGTGCC CTACCTGCGG GAAGAGTCAC TCCAGTCCCT 720 CTGGGCTGGT CCAGGTGCAA CCACAGTAGG ACACAGGTCA ACTCCAGTGA AATGTGGAGG 780 GAGGAAGGGT GTGCCTGCCT GCTCCTTCCC CTCCCTTGCA GGGAGGGGCG GTTGCCCTCA 840 GCAACAGAAT GCCCACGTGG GATACTGGAA GCTTCAGCTT ACCCCACCCC ACCCCTCCAG 900 GCCCGGTTTG TCCTGGGCGC AAGGGGCTAC TTCAGAGCTG CCAGGCCTCC ACAGCAACAC 960 ATTAAATGTT CTGGAAACTA GGAGATGTGG CACTGCTGTA CAACGGTCAG GAATAGCCAT 1020 CCTGTCCTCC TGACCCGGTG AAAACCAGCT TCTGCTGGGA AGGAGCATGG GGTGGCGCCT 1080 GGCTTTTGGA GTCAGGAAGA ACCAGGCTTA AGTAATAGAA CTGCCTGACC TCCAGCTTGT 1140 CTCTTCAGCT CCCAGGTCTG TGCTCGATTT GGGATTATTG GGTGGGGCAC ATAAGAAGCT 1200 GCGTTCTGTG CTCTCAGGGT GCTGGACGCT GTTTCAGGTA CCAGTACACA CCAGAGGGAA 1260 GAGAGTGCCT GATGGCATGG TGATTGATTT TAGTGGAGAC AGCTAGACAC TAAACCAGGA 1320 GTTCTGTCAT GCCAGTTGGT GATAAATTGA TTTCTTGAAG ATTTTTCCAC 1370
|