| Tag | Content |
|---|
EnhancerAtlas ID | HS051-19955 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr3:121714140-121715040 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr3:121714563-121714582 | TAGCTCCCTCTTCTGGCCA | - | 6.92 |
|
| | 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 |
| GH03I121994 | chr3 | 121712875 | 121715130 |
|
Enhancer Sequence | AACGAGGTTA GGCCCCAGCC TGGCATTCTC AGTTCCTCCT TGCTTCCCTG GGCCCTGTGG 60
CCACCCCTAA AACAGCAGGG CCACGTACAG TAGAAGGGGG CAGAAAGCTG GCATCCTGAA 120
CACAGCCACA TAGGGTGTAG GGTTTGCCAA GGCCAGCAGC AAAGGGGTCA TCCAGTGGGC 180
TGCTCAGTGA TTCCAGTATG AAACTTCCAG CACAACAGGA AGTGGTTGTA ACAGAGTCCC 240
CAGAAATGTC CGGAGCTCCA ACCCTCAGTG TGAGTCACAG CCTAGCCTGG AAGAAATCAG 300
AGGCAAACTT GCAGCAGCTC CCCCAGCAGC TACACCTTCA TGCCAGCTGA TCACCTGGAG 360
CCTCCCTGAA GACAGGTCCA CAGGCTCAGC ACTGCCCTCT CCCTCTGCAG AGATGCCTCT 420
CCCTAGCTCC CTCTTCTGGC CACCACCAAC ACACATACTG GAATGCCCAG CCTTATACAT 480
GTAATTTACT TTACATAAGC TAACTAGTTC TCTGAAAAAT CTCTTCACGT GGGAATCCAA 540
TGAGGAAGCT GGGCTCAGAG AGATTACCTT CCCAGCCTAA GGTCCTACAG CTAGCGACTG 600
GCAGAGCCAG GGTGTGAACC TGTGTGACGC TCAAGCCTAC ACTCTTTGTG TGCCGCACCG 660
CCAAGTCCCC AGACTCCTTT ATTTTCTGTG ATGAAGCAAA AAACCTTCCC TGCAGGCACC 720
TCCTCAATTT ACCTCTCTCT AACTCGGCTC CAGACCTTTC AAAGTCCACT CCAGACTAGT 780
CTCTCCTTCC ATAGCCTCGG GACATCTGAT TCCAAGGAGA ACAACCCTAC CCACTGTACC 840
CCTTTAATGG AATCCTAGCT TCTTCCAGAT GGTCCTATTC CCATTTAGCC ACTCCTCCTG 900
|
