Tag | Content |
---|
EnhancerAtlas ID | HS010-00680 |
Organism | Homo sapiens |
Tissue/cell | B_cell_blood |
Coordinate | chr10:90030730-90031700 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr10:90031426-90031447 | GTCCGGTTTCATTTTTATTTA | + | 6.25 | RARA(var.2) | MA0730.1 | chr10:90030796-90030813 | GGGTCATCAAGAGGTCA | + | 7.48 |
|
| 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 |
GH10I088271 | chr10 | 90030115 | 90032095 |
|
Enhancer Sequence | GAACTGCTCT TGGCGGGCTG GTGGCCTGTT TGATATTCTG AGGTCTAGCA AAGATTTAGC 60 TCCAGGGGGT CATCAAGAGG TCATGGTCTT GATCATTTCC TCTGTTATTT ATCTTTGGCT 120 TGTGGTACTG GAGCCTGCCT TTGATACAGG GCATTTCTAC CACAGCTGCA CAGAATCAAG 180 CATTTCAGTG ATTTGGTTTG AGGTGAAGGA GGCTTGGCTT CTAATGCTGC GAAAATGTCA 240 CTGGGTACAT CTGAGAATAT CTAGCTCTGT CCTTCACTGA TGAGCAAATT CATTTCTGGG 300 GGTTTACCAG TGGCACTTCC CAGACTTGGG TCAGGAAAGG AATCCTCCTG GTGAGGACAG 360 CAGTTTTCAG TTTGAGTAAT TCCATTTTCA GTTCCTTCTG AGACATTTTT CTTGCTCTGA 420 GCTGGAGATA AAAGCAGCAT GTCTCAGGCC TCTAGGGTGG ATCTCTACTT TTCAACACTG 480 TTTATGACTC ACCTGTGACT GCCCTCAGTG CAGCCAAGGG GACCATTTAT GCTGAATTAG 540 CCTTTGGATT TTTCTTCTTA GTGACAGCAA AACTTCCGTG ACAGCAAACA AGTAAACCAC 600 AGGAACATCC CTGGTCTGCT CAGCACAGCA GGCTCTTGGG TTCTCAGAGA GCCTGGGAGG 660 ACTTTTCAGC TTGTCTTATG TGGGTTTGTT CACCCCGTCC GGTTTCATTT TTATTTAAAA 720 CAATTGGTAT CTTTCATCTT GGTTGCCAAG TATGGGTTGC ATATGGTTTT GACCTGATAT 780 GAAGGGCCCA AATCAAATAC CCAGGACTTG GCCTGGAAAA TTGGTTGTAT AAGACCTGCT 840 CTCTTGTTCC CCTAAAAAGC AGCCTAGCAA ATGGAAGCAA TGGGTCCCAG GAGTTCGTTT 900 CTGTATGCGG CTCTAACTCT GCCACGAAGG CCAGGACAGA TAGTGTGCAG TGCTCTGTCA 960 TGTCTACCAG 970
|