| Tag | Content |
|---|
EnhancerAtlas ID | HS187-16002 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr22:17717620-17718800 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxq1 | MA0040.1 | chr22:17717766-17717777 | TATTGTTTATT | + | 6.62 | | IRF1 | MA0050.2 | chr22:17718040-17718061 | ATAATGAAACTGAAAGTTGAG | - | 7.24 | | IRF8 | MA0652.1 | chr22:17718043-17718057 | ATGAAACTGAAAGT | + | 6.32 | | IRF9 | MA0653.1 | chr22:17718042-17718057 | AATGAAACTGAAAGT | + | 6.43 | | PLAG1 | MA0163.1 | chr22:17717687-17717701 | CCCCCTTTGGCCTC | - | 6.95 | | RREB1 | MA0073.1 | chr22:17718113-17718133 | GGTTGGGTGGTGGGGAGGGG | - | 6.09 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_59002 | chr22:17686269-17740590 | Ly3 |
|
| | 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 |
| GH22I017236 | chr22 | 17717486 | 17718819 |
|
Enhancer Sequence | TTAGTAGAGA CGGGGTTTCT CCATGTTGGT CAGGCTGGTC TCAAACTCCC GACCTCAGGC 60
GATCCGCCCC CCTTTGGCCT CCCAAAGTGC TGGAATTTCA GGTGTGAGCC ACCACGCCCG 120
GCCAGAAATA GCTCTTAAAT CTATTTTATT GTTTATTAAA GCCATGGTTT GTGCTTTCCT 180
GGTCTTCCCA GAGTTCTAGG CCCTGCCTTG GCTTCTCAGT TTGCTTCTCC CCAGCCCCTG 240
AACCCAGCCT GGGGGACAGC CCTGGTTCTC TGGATGGATG GATGTCTGTC TGCTGATGAA 300
TGTGCAGTCA CTGCCCACTG TGAGTTTTTT GCAGTGGTGA TAGAAGGCTT GGAGGGGTGG 360
GTACTTATCC CCAGTCAGTC ATCAGAGAGC CCTTCAGGAG ACGTCACTCA TTTCTGTCTC 420
ATAATGAAAC TGAAAGTTGA GACCTCTACG GAATAAAATA GGAAGGACAG AAAACTTCTG 480
GTCCTGGGGC TGAGGTTGGG TGGTGGGGAG GGGGCAGGAA ATTGGCTGCA GCCAAGACCC 540
TTATTGTGCA TGCCTTGAGA GGCCAAGCCC TGCAGTCAGC TGAGCTTGCT ATTTTAGGTG 600
AGGAGATCAG CCTTCAGAAT CAGCTTATGA ATCTTCAGAC ACCTGACGAC AACCCAGAAA 660
ACAGGAGAGG AGGAGGGACT GGCCAGGGAG CCGGAGGCCT CCAAAGGGCC AAAGGAAAGG 720
GCCCTTGTGG GCAAGAGCAT AAACACCACC CAGAAGATGA GCGGGGATGA CAGTTCAGGC 780
CCCGCAAGAG GAATGTCCTC TGGTCAGAGT GTCAAGGCCG GTGGGTGCAG GGGCTTGGGG 840
CCGAGTGGCA GCTTGCCCAT CTGGTGGCTG CACCTGACAG GCACCGTTCA CATGGACTGG 900
GTTGGTGTGC ACTGGGGCTG ACCAGTGTCC TACAGAAAAG CTGAGAATGC TTTGGCAGCA 960
CTGAGACAAC ATTTAGGTTC GGCAATGACA CAGATTCACA GATTTAAGCA AAAGCCTCCA 1020
TTTTGTGGGC CATCAAACTG CCCATGGACA AGTTGTGTAC CCACAAGAGA CTGTTACCAC 1080
CCCAACTTGC CTCTAGCCTT AGAGATGTTA GAGTAAAAAA CAAAAATCAG TGGTCACATG 1140
TAAGCAATGT GTGTGTATGA AGTTAGCACA GGTGGCTACA 1180
|
