| Tag | Content |
|---|
EnhancerAtlas ID | HS051-11690 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr17:37400150-37401330 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr17:37401167-37401186 | CCCTGCCCCCTGGTGGCCA | - | 7.81 | | RREB1 | MA0073.1 | chr17:37400258-37400278 | TGGAGGTGTGTGTGTTGGGG | - | 6.86 | | ZNF263 | MA0528.1 | chr17:37400523-37400544 | TCCTCCTCCTGCTGCTCCTCC | - | 8.06 | | ZNF263 | MA0528.1 | chr17:37400520-37400541 | CCCTCCTCCTCCTGCTGCTCC | - | 8.09 |
|
| | 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 |
| GH17I039244 | chr17 | 37401081 | 37401270 |
|
Enhancer Sequence | CCTGCAGCAC AAAGGAGCGG AAACTGAAAA TGGACCGTGA GAAGATGGAG AAACAGCCCC 60
TGCATGAGAG GGACAAGTAT CAGACCGCCT GCGAGAGCAC TGTCTTCTTG GAGGTGTGTG 120
TGTTGGGGCG AGAGCAGGAG GGGAGAGTTG GAGAAAAGAT CCTCACGGTA CAGATGGGGA 180
AATGGAGGCC TCCAGGGCTC TGACTGCTGC AAGCCCATCA CAGCCCCCTG GGGACTCCAC 240
CACTTCCTGC AAAGGACACT CTCTGCCCTG TCTGTGGTTG TTGAAGCTTC CAGGAGCTGA 300
CGCCCTCCAG GCTGCCTGTC CTACGCGGGC CATCGCCACC TCCTTCCTTG TGTGCTCCCT 360
CTGCCTGGCC CCCTCCTCCT CCTGCTGCTC CTCCTGGCCA GCTCCTCCAA GGCCCTTCCT 420
CACTGCCCCA GGCCCGCCGG GTGGTTAACT TCTTCCTTCC TGTGGAAACC CAGTCCACTT 480
GTCAGGCCCC TGGTCAGCTC TTAATATACA GGTGGAGAGA AGGGAGCAAT GACCAGCCTT 540
GCTGTGTGTT TGCCTGCAGT GTTCGCCATG GCCGGAGTCC CCTGCAAGGC CCCGGCCACC 600
TCTCAGCTCT CTGGCTCTGA CCTCTCCCCA CTCCTGCAGG CTCTTGTCCC CAGAAAGGTG 660
AGGCAGGATG AGCACCTCCT GTCAGCCCTT TGGGGTGAGA GTGAAGAAAA GAGCTCCCAG 720
CCCAGGCATG GAGCAAAGGG CAGGGCTGGG GATTGGTGGG GAATTTGTGG GGTGAGGACA 780
GGAGCAAGCT CTGTGTCCCA GGGCAGGCCT GGAGGAAGGG TGTTGGTGGA GGGAGACTGG 840
CTGTAATGCT CCGCAGAGTT CTTGAACCTT TGCTCCTCCT CATAGGCTCT GTTCCTCACC 900
ACCATTCGCT CTGGATACCT TGGGGTGTAG CCCAGTTGAG GTGAGCCTTC CCCTTCCCAC 960
TCTCCACTGT CCCAAAGCCT TCTCCGCAGC TTCATCTCAA GCTCCAGAAT GGAGTGGCCC 1020
TGCCCCCTGG TGGCCAGATG TGATATGGCC ATAGATTGTA ACTTACCTGA TAAGACTGGG 1080
CAGGAAGAGC CTCCCTTCTC AGACTTGGGA CCTCCCAAGG GAGGGGCTGT TTCCCTTTCT 1140
TGTTCTGTCC CTGGGTCCTG GTATTACCTG GACCATCCAT 1180
|
