| Tag | Content |
|---|
EnhancerAtlas ID | HS187-15448 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr20:49094510-49095600 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr20:49094596-49094617 | GAAAAGAAAAAGAAACGAGAA | - | 6.07 | | KLF4 | MA0039.3 | chr20:49094989-49095000 | GCAGGGTGTGG | - | 6.62 |
|
| | 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 |
| GH20I050477 | chr20 | 49094401 | 49095408 |
|
Enhancer Sequence | ACCCGGGAGG CAGAGGTTGC AGTGAGCTGA GATCGCGCCA TTGCACTCCA GCCTGGGTGA 60
CAAGAGTGAA ACTCCGTCTC AAAAAAGAAA AGAAAAAGAA ACGAGAAAAT ACGTTTCTTC 120
ACAACAATGA AACAGTTCAT TGCCTTCATT TATGTCACTT CTTGATCCCT GTAGGCATTT 180
GAGTTTGCAA CTCCTGGACT GGTCCTTAAC CAAAAAGATG AGGAAACTGA GGTCCTCAGC 240
AGGTTAATGA TGAGTTAGGA GTGAATCCAC AACCTGGTCC CTCTCCCCGC ATTTCTAAGG 300
TACCAAGGCC TACGCACTGG CGAAGAATAT GGTTTCTGCA GCCAGACAGA CGTTGGTTCA 360
AACACTGGTA CTGACACAGG AAAAGTTCCC TTATCCTCCT CGAAGGGCAT GCGATGGGGG 420
TGTGGCTCAC TTCCTCAGTG CTTCGCTGCT CAAAACCCCT AGGGGGAGCA GGCAGACGGG 480
CAGGGTGTGG GACTCTGGCC ACGCAGCGTC TAGGCGTGAA TGTTTACAGC TCCTGAGGCC 540
CCAGTGGGCG TGTGTTCCAG GGTGCTCTTT TCGTTTAACC GTCCATAGAC AGCTTGTGTT 600
AGCTCAATTA GACCCCTTGC CTTATCTCAA GGACAGAGGG CTATCTGTAT CCTGGGGTTT 660
CTTGCCTTGG CGTACCTGAA GAACTGGATC ACACGTAGGC TTGGAGAATG AACGCAAGGT 720
TTTATTGAGT GGAGGTAGCT CTCAGCAGAT GGGGGAGCCA AAGGGGATGG AGTGGGAAGG 780
CGATTTTCCC CTGGACCTGG GCCGCTGAGT GGCCCAGGCT CTCCTCCCAC CACCCCAGCC 840
AAACTCCAAG TTGTTCCACC GGTCGATGGC CTGCTGGCAT CTGCCGGTGC CTGATGGTGT 900
GCTCTCATGC CAGTTCCTTC TTCTCCAGGT CTAGTTGCTT GTGTCTTTTT TTTTTTTTTT 960
TTTTTTTGAG ATTTAGTCTC ACTCTGTTAC TCAAGCTGGA GTGCAGTGGC ATGATCTGGG 1020
CTCACTGCAA CCTCTGCCTC CTGGGTTCAA GTGATTCTAG TGCCTCAGCT GGGACTACAG 1080
GCACCTGCCA 1090
|
