| Tag | Content |
|---|
EnhancerAtlas ID | HS190-05478 |
Organism | Homo sapiens |
Tissue/cell | Treg_cell |
Coordinate | chr17:43465740-43467060 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr17:43466500-43466521 | AGGGGAGGAGGAGGAGGATGG | + | 7.35 | | ZNF263 | MA0528.1 | chr17:43466503-43466524 | GGAGGAGGAGGAGGATGGTGG | + | 7.88 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr17 | 43466361 | 43466922 | | chr17 | 43466933 | 43466997 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I045388 | chr17 | 43466059 | 43466248 |
|
Enhancer Sequence | TGGGGAAGGG GGCTGGGAGC TGCTGCAGGG TCCAGGCCGG AGATATTAAC CCCTTAGACC 60
AGGAAGGGGC CCTAGTGATG GAGAGGGGTG GATCAGACAG GAAGGACTAA CAGATACAGA 120
TCGGGCATGG AGGCAGGAGA GACAGATGAG ATGGAGGGAG CAGGCCACAT TCCCAGGTTT 180
CTGGCTCACC TGACTCGGGG GATGATGGAC CCTTTGCCTG GGACAGGTAA AACCCTGGAG 240
GAGTACAAGG TTTGGGGAAA ATCACAAATC CAGTCTTGGG CTGAGGACCG TCCCAGAGCA 300
GATGTCAGGT TGTCAGAGGA CACCAGGATT GGGAGCTTAG AGAGCAGTCA GGCCAGGCAC 360
TATGGATCAG TGAGTCACTG ATGCTGTGGG TGTAGCCAGT CTCATCCAGG GAGGGAGGAC 420
AGCAGAGGAG GGGTGGACCC CAAGGACTCT GCTTGTACTG GCTGTGCAGC AGAGAATGAG 480
ACACATGGCC CGAGGTGGGA GGAAAATGAG GGGAATCTGC AAGCCAAGAG AAAGGGAACA 540
TTTCCAAGAA TGGGGTGGTC AGCAGAGGAT AGGGTGCCAC TAAAAAGGCA ATTAATACAC 600
AGACCCCCAA ATATCCAGCA GCTATCAATG GGAAATCATC AGTGAGTTTA GGGGAAGAAA 660
CTCAGTGGTG TGATGTGGGC GGGGGGTGGG GTTGAGAAGC GAACAAGAGA AGCGGATGGA 720
TACCGTGAGT TTAGATGACT TCTGAGAAGT TTGGCTGCAA AGGGGAGGAG GAGGAGGATG 780
GTGGCAGCTG CAGAGAGACG TGGGGTTGTA GGGGGTTTCA GAGAGAGGCA CTTCAGCGTG 840
TTCCCGTGGC AAGGGGAAGT GGCCAGTATG ATGCAGTGGA TACCATGGGT GCTGCTCAGA 900
TGCCCTCTTC CAGCACTGAG CGATGATTTC CCAAAGGACA GGGAGGGTCA GCAGCCAATA 960
GCACTCATCT GAGCCTCTCT CCAGGATGTG TCCTGGGCTG AAGAGAGCTG CTCTGCCCAA 1020
ATCCATGCCC TCCCTTCTCC CACCTTACAA GGCAGCCCAT ATCCAGTGGC CTGGCCCCCT 1080
GGCCATAATG GGACACAAGA CTGAGGCTGT CCCAGCTCCA GGGCTTCCCA TGGGGTGGCT 1140
GAGGCCTTAG AAGGGGCTGT GCCCCAGCTC AGCTTCTCCC TCAGCCACTC CTGCTGGCTC 1200
CACCCCTCAG GCATTGGTCC CGAGATCACG CCCAGCAAGC CCCCTGCCAA CGTCTCTGTT 1260
TCCTGGGACA TTCAACCTGA GACAGCAGCT AAATAGCAAG AAGAGGGGCC AGTGATCATG 1320
|
