| Tag | Content |
|---|
EnhancerAtlas ID | HS190-05696 |
Organism | Homo sapiens |
Tissue/cell | Treg_cell |
Coordinate | chr17:73530660-73532070 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RUNX1 | MA0002.2 | chr17:73531239-73531250 | CTCTGTGGTTT | + | 6.14 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_23798 | chr17:73530683-73532839 | Colon_Crypt_2 | | SE_28701 | chr17:73529621-73533284 | Fetal_Intestine_Large |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr17 | 73530852 | 73531780 | | chr17 | 73530757 | 73530846 |
|
Enhancer Sequence | AAGTGATCTT CCCACCTCAG CCTCCTGAGT AGCTGGGACT ACAAGTGTAT GCCACCATGG 60
CTGGCTAATT TTTAAGTTTT TTGCTGAGAC AAGGTCTCCC TAAGTTGCCC AGGCTGGTCT 120
CGAACTCCTA GGTTCAGTGG ATTCTCCTGC CTCGACCTCC CAAAGTGCTG GGATTACAGG 180
CATAAGCCAC TGAGCTTGGC AAAGGACTTG GACTCTTGAC TGTTTGAGCT TGGGGCCACT 240
CTGAATCGAT CACTTCATAA GTAATTGTAA GAATTAAATA AGGTGAATGT AAAGTGCTAA 300
AGTCACATCC AGCCATAGCT AGCTCTCAAT CCCTTTTACT ACTTAATTAA CAACAGCGGG 360
GACGACAGTC CTCCAGTCAT GCCCCCATTC CCTCTGGTTT GTGTTCCCCT AGATCCCACT 420
CCATGGAACT GCCTTTCAGC CAAGGTTTGG TTGCTAAGCT GCTGGCCAGG GACCTGCCTG 480
GTGCTTCTGG GAGACTGGGC TTCCCAGGGC GACATGGGCA CTTGCAAAGC GGCTACAGGC 540
GTCTGAGTTG GCACAGATGC CGCAGGGGTC AGCAGCTGCC TCTGTGGTTT AGATCCCTGC 600
CCACCAGTGC CATCAGAGTA GGAGGTGCAG GGGCGGATTC ACATCCGTCA AACAGGAGGC 660
CACAGCCACA CTCAGGCCTC ACACAGGATG TCGCAGAGGG GAAGGCAGCT TCTTAATCAG 720
CAGCGGGCTG TGGGGAGCAC GAGCGAAGAG GAGAGGAGAG CATGGGACAT CAGGTGGCAC 780
GCCCTGAGAG CAGGCAGCTG GCGCTGGGTG CGGCCCGGGG GCCCTCTCTG GTTTCGGCTG 840
GGTCTGGAGT CCTGCCGCTG GGTGTGGACT CTCCCAGCAG ATCAATGAGA TCAATGGAAC 900
TTCCCGAGCT ATGGAGGGAG TTTCTTGAGG GCTGGCCCCT CCCACATCTC CAGGCCAGAG 960
GGCTGGCTGG GCTTGGCCAA GCCTTGGTCT CACAGGGACA AATTAGCCCA GGTGCCCCAA 1020
ACAGTGGCAG GGTGGGAGAA GCAGTCTGGC CTGGGGATCC CCTCTCCTCC GAGGCACAAT 1080
CGCATCTGCC ACTTAGAGCG AGGGGGGCCC AAGGCAAGTC CACCCCGTGT GGTTATTCTC 1140
TCTCTCTGCC CCCACTGGTC TCTTTCTTGA GCTCTTGAGA TGGAAGGCGG GCCAGGGTGT 1200
GGATTTTGTG GCCTGTCACC AAGTGGAGAG CTCTCCTGTT CTTTCCAAGT GGGTGTCCAG 1260
GTGTGTGGAC ACCTGTCCTA GACCCAGAAA TATTTTGCCG GCCAGGTGCA GACGTGGGTG 1320
AGTGGAACAG TGAGGAGGGA AGGAAACAGG TCGATCAGCT GCCCACAGGG AGCTCTCAGG 1380
CTGGTTCCAC ATGCAAGGCA CAGACTTGGG 1410
|
