| Tag | Content |
|---|
EnhancerAtlas ID | HS051-04715 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr11:64333910-64334960 |
Target genes | | Number: 28 | 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) |
| Stat4 | MA0518.1 | chr11:64334872-64334886 | CCCTTTCCTGGAAG | - | 7.25 | | ZNF263 | MA0528.1 | chr11:64334445-64334466 | GGAGAAGGGAAGGCAAGGGGA | + | 6.34 |
|
| | 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 |
| GH11I064564 | chr11 | 64332189 | 64335552 |
|
Enhancer Sequence | TCAGAAGGAG TGCTCTCACT GCAAACACCC GGGACCAGTT TTTTTTTTTA AAAAAAAAAA 60
AAACCTTCCA GGATTCCTCA GTTCTCCCAG GGGCCGGCTC TGCAACCTTT GTTATTCAAA 120
TCAGAGGCTT TGAAGCTGGT GACCTTGTGG GTTTTCCTGT CTTGTTAACC CAGTTGTTAT 180
CTGTCCAAGG CTCCAGTGTC GGCCGCTTTG AGCACCAGCC CAGTGACTCT CACGTCACTC 240
ACATAAACTT CATGAAACAC CGCGGCTTGT GCGATTTTAC TCTGATGTTG TTGGGCTGGT 300
GTTGTCCGAT GTTTATTGGG TGATGCAATC AGGTGACGCC TAAGGGGAGG GCTGGGAGGA 360
GCATCTGGGT TAAGCAGGGA GAGCACAGAT TTTAAACGTG GCCGAGAAGA ATTTTACCTT 420
GCAGCCAGTT GTGGATCCAA ATCCCATCTC CAAACCATGA GAATTTAAAT ACCGTAAATT 480
CAGCTACTCG TGAGCCAGTG GGGTGGGGGA GTGGGCAGAA AGCAGACCCT GAGATGGAGA 540
AGGGAAGGCA AGGGGAGATG CAGCCACAGC CTGGGCCCAG CCCAGCCCCT GGGAGCGTGG 600
GAGCTGGGGC CTTTCTGGGT GGTCCCTCTG CCCCATGAAC CAGTCACAGG CTGCTCTCCC 660
CAGAGAAGGG GCAGCACTCC CAGGGGCTGG GGGACAGGCT CTCCATCCTG AATGTGGTCT 720
GGGCAATGCA GCCCAGGGTC TCCCGAGAGG CCCTGTCCTG CCATGATTCC CATCTTCCAA 780
GAGAAAGGCA CAGTGTGACT GGTTATCAGA ATCAAAGCCA GAGAGGGCTA GTCCGGAAGT 840
GAGGGGCAGC TCAGAGGCCC CCGAGGGCAG ACTTGGTCCC AGCCAGAGAG GCAACGCCCC 900
AGCGCATCGC TGCCCCTGAC ACAAAGCCTG TGTGTGAAGG GATGGTGGAG CCACCCTGCC 960
TGCCCTTTCC TGGAAGAGCC TGACGCTGGG GTTGTGTCCT GAGTTTGGCA GGCTTCTGGG 1020
ATCGCTGGCC GAGACAAGCC CAGGATTGTC 1050
|
