| Tag | Content |
|---|
EnhancerAtlas ID | HS187-23775 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr8:42520660-42521760 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXA1 | MA0148.4 | chr8:42520981-42520997 | TATTGTTTACTTAACA | - | 6.97 | | IRF1 | MA0050.2 | chr8:42521279-42521300 | CCTGAGTCTCAGTTTCACTTT | + | 6.07 | | IRF1 | MA0050.2 | chr8:42521285-42521306 | TCTCAGTTTCACTTTTTTCTC | + | 6.86 | | Myog | MA0500.1 | chr8:42521123-42521134 | CTGCAGCTGTT | - | 6.02 | | Tcf12 | MA0521.1 | chr8:42521123-42521134 | CTGCAGCTGTT | - | 6.62 | | ZNF263 | MA0528.1 | chr8:42520803-42520824 | GGAGCAGGAAGAAGGAGGGGA | + | 7.7 |
|
| | 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 |
| GH08I042665 | chr8 | 42521121 | 42521262 |
|
Enhancer Sequence | GGATGCAGCT AGAGGCCACT ATCCTAAGCA AATTAACTCA GGAACAGAAA AACCAAATAC 60
TGCATGTTCT CACTCCTAAG TGGGAGGTAA GCATTGGGTA CTCATGGACA TAAAGATATG 120
AACGATAGAC ACTGGGGTCA CCTGGAGCAG GAAGAAGGAG GGGACAAGGG CTGAAAAAAT 180
AACTATTGGG TACTATGCTC ACTATCTGGG TGGTGGGATC ACTCATACCC CCAAACCTCA 240
ATGTCACACA GTATACCCAT GTAAGAAACG CCTGAATCTA AAATAAAAGT TGAAATAATT 300
TTTAAAAAAT ATAAAAGGAT TTATTGTTTA CTTAACAATG AGTCTAGGCT GCTTAGAGCT 360
TGTTTAGTAG CTCAGCAATG GCATCAAGGA TCAGGTGACT TCAAACACCC TGAGTGTGTT 420
GACATCTCGT CCTCATGCTT GCTGACTCCT GGTCACAGAG TGGCTGCAGC TGTTCCAAGC 480
ACCACAGCCT CACACTGCAC CCACAGCAGG AAGCAGCAAG GAAGGATGTG GGCAGAAAAG 540
GGCTTTCTTT TTAGCAGACA GGAAAAACAT CTTCGCAGAA GGTCCCCCAT AGTTTCATTG 600
GCCAGAACTC AGACATGGCC CTGAGTCTCA GTTTCACTTT TTTCTCTGGC CTCCCAAACA 660
AGAGCATTTC TCTGAATTCT TCAGTCAAAC TTAAGAGGTC TTCTGTGTGT CCTCTCCGCC 720
TCATGTCTAC CCCCATCACA AAACCTAATG CTTTTCATAG CACCAGATGC CTTCCATTTA 780
TTCTTTTTTT TTGTAGAAGG AGTCTCGCTC TGTCGCCCAG GCTGGAGTGC AGTGGCACGA 840
TCTCGGCTCA CTGAAACCTC TGCTTCCCAG GTTCAAGCGA TTCTTCTGCA TCAGCCTCCC 900
GAGTATCTGG GACTACAGGC ACGCCCAGCT AATGTTTTGT ATTTTTAGTA GAGATGGGGT 960
TTCACCATGT TAGCCAGGAT GGTCTCGATT TCCTGACCTC ATGATCCGCC CGCCTCAGCC 1020
TCCCAAAATG CTGGGATTAC AGGCTTGAGC CACCACGCCT GGCACACCTA ATGCCTTTCT 1080
TCCTCAATAA ATGCCACCTT 1100
|
