| Tag | Content |
|---|
EnhancerAtlas ID | HS187-16054 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr22:20960230-20961240 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR2 | MA0258.2 | chr22:20960358-20960373 | GGGCCAGGCTGACCC | - | 6.25 | | IRF1 | MA0050.2 | chr22:20960865-20960886 | AAACTGAAACAGAAAGAACAA | - | 6.97 |
|
| | 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 |
| GH22I020606 | chr22 | 20960382 | 20961659 |
|
Enhancer Sequence | TCTGGGCCAG AAGGGAGAGG GGACAGGTCA CCCACTGCTT CCATGAGAAA CCCATTCTAG 60
GGCCTGGCGA AGTTGAGCCT AGGAAGGGCT GGTCTGTGCT CCACTCAGCA GCAGCTGGGA 120
GAGGGCCAGG GCCAGGCTGA CCCCAGCACA GGCCGCTGTC TTGGCCTCCA CCCACTGGAG 180
CAACATTTGC CCAGGGGAGC CAGTGGCATG TGAGGAGAGG GGGCCAGGGC TCACCATTTC 240
TCAGACACAC TGGGGCTGGG AGTTGCTGCT GGCAGCCTGC TTGTCAGCTG CATACCACCA 300
TGGCTGCAGG TAGCTCAGCC ACACCTCCAG GACCTGTGGG GGAGGTGTGT GCTGAAGGCC 360
CAGTGGCTGG GGCCAAATCC TCTGATGGCC TGGAACCCAG GTACCCAGGT GGCAGCTAAG 420
TTGGCTCTTC CCACGTCCCC CAGAGGGCGC AGGAGAGACG CGCACAGCCC TGTGAGATTT 480
GGTTCTCTCA CTGCTCTTCA GAAGCCAGGG TCATGGGCGG GCTCTTCCCG GCCCACGGGA 540
CCCAGTGCTA CCTGGTTGCG TAAGAGTAGA AACCTGTCTG GCACCAGACA GGTGGGATGG 600
GGCAGGGCTT TGCTGTGCCT GAGGGTTGCC TTTGGAAACT GAAACAGAAA GAACAACGTG 660
GCCCTCCAAG GCCCCCTCCT CTCCAAGGTC TCTGTGACAA CACTTGTTCT CCTTCATCCA 720
CCCCAGGGGA CCTCCCTCAT TGGGGCACAC AGAAGACACA GGCACACATG TGATGGGGCC 780
GACACTCCTA GCTCTGAACA ATGCGTCCAA GGGCCAGTGG CCAAAGCAAT GCCGCAGGAA 840
GAGGTAGAGT TTCTGCTGGA CTAACCTCGG GACAGCGGCC TGCAGAGGAG GGGAGGGTCA 900
CCAGCCGCTT GCACAGTAAG GTGGCCCTGC TCACAGATGA GCCCGGGGTT CCCATTAGTG 960
AGGGTTGGCT CTGCTGGGAG AGAGCACTAG GCACTTCTGA GTGGTAAGAG 1010
|
