| Tag | Content |
|---|
EnhancerAtlas ID | HS051-11493 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr17:26669890-26671380 |
Target genes | | Number: 11 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr17:26670832-26670853 | CCTTCCCTTTCTCCTTCCTCC | - | 7.32 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_54210 | chr17:26668119-26675573 | Spleen |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GCAGCAGTGT GGTGTAGAAA CAGCTTGGGC TTTCGTGTTA GAATGCTGTT CAGATCTCCT 60
GTCTGAGCCA GGGACACAGG TGGGCACAGC ACTTGAGCCC AGGAGTTCAA GACCACCCTG 120
GACAACATGG TGAAACCCCG TCTTTACAAA AAATAGAAAA ATTAGCCAGG CATCGTGGCA 180
CATGCCTGTA GTCCCAAGTA CTCAGGAGGC TGCTGTGGGA AGATCCCTTG AGCCCAGGAG 240
TTTGAGGCCA GCCTAAGCAA AATAGCAAGA TTCCACTTCC AAACACTTTT AATAATAATA 300
AAATAAAATC TCCTTACTGG CCCCAACCAG CTGGGGGTTT CTGGCTAATC AACTTAGTGC 360
CAGGTACACA GGAGGCATTT GATAGGTGAC AGTCATCACA AACTCAGGTG GCCCCTCTCC 420
CCCAGGCTGC AGTCAGTTAC CCCAGAGAGT AGCTGCCTCC TGTGAGTGCA GGTCCTGGAG 480
ATGATACGCT GGGGTGGATG GCAGGTCATC CAGGAAGGGC CATGTGGGTG TGAAGAGCTC 540
AAAGTAGCCA GACTTGCCAA GCAACTTGTC GACCCCCAAA CTACTCCAGG TGCCTCCAGC 600
TGGGAGATCT GCAGAGGGTT TGGGGAAGGC CAACTTACAG GTGGCCCTGC TTCCTTCTGC 660
GGTTTTTGGT GTAGGGGTGG GAGGGAGGGC GACAGGTGGT TCCTGACCCT ATCGGTGGTG 720
AAAGGGTTCA GGGGCAGGTC TCCAGTGGCT GGTGATGCTG CGACGGAAGT GGCAGCGCAC 780
CTGGCATCTT CTTAAGTGTG TTGTCTTTCA TGAACTCGTG TGACCCCTCA CAACATGCCT 840
GTGAGACACG CAGGGCTAGA GCCACTCTCC CCATGTGACA GATGAGTGAA CAGAAGCTCA 900
GTCCAACAGA GCAGGTCTGG CTAGAATTCA GGTGCTTGAC TGCCTTCCCT TTCTCCTTCC 960
TCCAGGCAGG TCATGCCGGT GACACACTGC GTCAGGCAGG CAGAGAAAGG CAGCATAACC 1020
ACTCAGCATA GCAGCTGCTC TGTGTATGCC TCTGCTTGGT GGTTTGCTGT GTGCCAATCT 1080
TCTGCTAAGC AATCACATCT TTCCCGTAAT GTTGACAGCA ACTCTCAGGG GTTGAGCTGA 1140
ACCAACCTTT TGTACATATG GGAGCTGCAG CCCAGAAGGG TTCAGCCCAA GGCTCCACAG 1200
CTAGCAAGTG GTAGAGCTGT GTTGGGACCT AGCTCTGGCC CACCCTCTAT GCCCACTAGT 1260
CCCTTGGTCT CAGGCTGGGG CAGGGGTGTG GAGGATGTTG GTCTTCCCTG TCCTCATGTC 1320
TGTAGAGTAC ATCCCCTCAC CCCGCCTTCG GAGGGAGGCT GGCTTTCCCT GGAGACGGAC 1380
CGCCACCTGT TTTATGAGAG GTAGCGGAGG CCTTATGGAG CCTCAGGGCC AGCCGCTCTG 1440
ACGCATGGCT TCCTCTTGAA GATGAAACCT TGCTCCACCT TCTTCCTCCC 1490
|
