| Tag | Content |
|---|
EnhancerAtlas ID | HS051-20432 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr3:185976670-185977840 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr3:185977490-185977509 | CGGCCAGTAGAGGGCTCTC | + | 6.25 | | Mafb | MA0117.2 | chr3:185977828-185977840 | AAACTGCTGACT | + | 6.22 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH03I186260 | chr3 | 185976881 | 185977030 | | GH03I186259 | chr3 | 185977041 | 185978090 |
|
Enhancer Sequence | ACCAGACTGC CAAGGGGGTT CCTGGCACAA AAAAGTTAAG AACCTCTGCT TTAGAATGAA 60
TGTGCCCTGC GGACACCTTG GGGGTGGAAC TTGGGAAGCC TAAGGTCAAT ATTTCCAATC 120
TGCCCAGCCT GGTGGTCTGA GAAGAGCCCT GGAGCTTTCA GAATCACTGA TGCATGTGTA 180
GGCAAATTAA CATTCCTTCT CTTGCAGAAC TCTGCTCTCC GACGGGACTC TCCGACGGGA 240
AGTGAATTCT GAACAGACGC TCCCTCCAGC TAGGCAGCTT GTCTGATTAG AGAGTGACAT 300
GCGCATGAGA GACCCTCAGG GCGTATCAGC CCGGGAAGTA GCCACCTGGC TCGTCGTCTC 360
AGATGAAAAC AATTTAGAAT ACACGAGGTG AAGCTGGAGG ACTGTCTGCC AGTTTTGACA 420
GTGGGCTGGT AAAGGTGTCT GTGGGGGGCT GCTCCGTCAC AAGGCTGTAC TGTTCAGCAG 480
TGATGGCAAT CACGGTGACT GTGATGGCAA CTGCAGTGGT GTACAGAGGT GGGCTCTGTT 540
CTGAAATTAC TTTTACAGGT AAATCATGGC AGGTGTACTG AATCCGCACT TATGTTTCTT 600
TCTCTTTTTA ACTGGGCCTT GTACTACCGC TGCCATAAAC AATAGCTTTG GTGTCAGCCA 660
ACCAAAGACA GGGTCAAATT CTCTTTTCAG AGTCCTTACT CCAACCTCTC TGAGGGGTCT 720
AGCTGAACCC GGAGCAGAAA TCCTGGTTTG GAGGTTGGGC AAATGGCTGC GTGCTGGGCA 780
AGCCCAGCCC AGAGTATGCA GACAGCCCCG GGCCCGGGGC CGGCCAGTAG AGGGCTCTCG 840
AGCACCGGCC CGGACTGGGA GGAAGCCCAG GCTTTCCTGG CCTTCTAGCC CAGGTGCTGT 900
AGGGGCCGCA TCACAGAGAC CTGCAGCTCA CCATTAGCCG CAGACACAGG GACCACGCCT 960
CCCACCAGGC CTCTTTACAA CCCCATGCTA ACGAGAAGAG AATAGCCAAT GAGTAAGTGG 1020
CAGGAGGAGC AAAACAACCT CAAAATCGAA TGATTTAGAA AACAAAAGTG ATTCCATTGA 1080
ACAAGTAATT GTCTTGATCC TAAAATGACC CCACAACGGA ACACCAAGGC AGAACTCTGA 1140
GTCACTGTCT AGATTTCCAA ACTGCTGACT 1170
|
