| Tag | Content |
|---|
EnhancerAtlas ID | HS187-17282 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr3:63863480-63864700 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr3:63863733-63863751 | TGAAAGAAAGAAGGAAGG | + | 6.56 | | EWSR1-FLI1 | MA0149.1 | chr3:63863737-63863755 | AGAAAGAAGGAAGGATGG | + | 6.73 | | EWSR1-FLI1 | MA0149.1 | chr3:63863741-63863759 | AGAAGGAAGGATGGCAGG | + | 6.75 | | EWSR1-FLI1 | MA0149.1 | chr3:63863745-63863763 | GGAAGGATGGCAGGCAGG | + | 7.46 | | TCF7L2 | MA0523.1 | chr3:63864572-63864586 | GCTCTTTGATCTTT | - | 6.04 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr3 | 63863794 | 63864299 | | chr3 | 63864575 | 63864655 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH03I063878 | chr3 | 63863677 | 63863876 |
|
Enhancer Sequence | CAAGGTATTT AGAGACTCCC AGGTGATTTC AATTAACATC TAACCTCAAA TCCGGTCTCC 60
TTGGTAAGAG AAAAATCCAG AGAAGGAGCT CAAAGCAGAT TATGGTATAA GCATATGCCA 120
GTCCTCTCCT GTGGAAAAAG AAAAGTGCTA ATCTGGTCAG AACTGTTAAA GAGACAGGCA 180
AGGCTGAGCA CAGCAGAATT CTCTCATCCT GTTCATCTTT TGCATTAGTG CAGAAAAAAG 240
ATTTATCTCA GGATGAAAGA AAGAAGGAAG GATGGCAGGC AGGTGGCTAG TAATAGGAGA 300
TGGTTGGTTC TCTTCCTCTC TGCCTGGGCT AGTGGTAAGC AGGTCCTCAG GTCTGAAAAA 360
CTAGTAAAAG TGAAGTGACA CACAGGGCAG CTTCCCCAGG CAGTGATACA ACTTGTTGGT 420
ATTCAGTGTG AAAATACAAA GCTGACTTTG ATTCCTTGCC ATCAGCCAGA GGAAACCCTG 480
GAGAAGTAGG AGGCAGTGGC ATCTCTTTGT AAACATTTTA TTCTTGACAA GTAACAGACT 540
CCTACCTAGA GAATTGTAAG CGTTGGCCCC TCCATTCTGC CAGCTGTCTT TCAAGAGCAC 600
TCTCAGTATT CTCCTGCACT GACCAGTTTA AAAGGTGTCG TTTCTGCTCC CATGCAGTGC 660
TTGGTGTGAA GGAATTAATT TGCAAGATGA ATAACCATTG TGATAACTGC TCACATGCAA 720
AGGAGAGAGA TTGCTGATTT TACAGGTGTG TGGTTTGCTT TCTTAGATCT GGCAGGAAAC 780
AGAGTCCAAC TCAGATGGTT TAAGAGACTT TAAATGAAAG AATTATTTTC AGAAGGACGG 840
GCAGAGTTCA GGATGACATG GGTTTCTGTC ACCTAGAAAC TAATAGGAAT GGCAAGCTGT 900
TATCACTGCT AGATCTGAGG GAGCAAAGAG AAGAAATAGT GTTACTGGAG TCTAGTGAGA 960
GCTGGTGCCA TAGTGGATGG GCTGTTAAGA CAGGAGCTAT AGTACTAGAG GCATTCAGCC 1020
ACTGCCAGAA AAGGGAGCCC AGAGCAGGGA GGGAACAAGG AGGGAATATT CTCCTCTCTG 1080
ACTTTTTTCT TTGCTCTTTG ATCTTTTTCC AGTGCCTTCT ATTGGCCAGA CTCACCTGGA 1140
AGCTGGCCAG CAGGTGAATC TATGATGCTG CCCATAGAGG TCAGCCTCTT GGGACTCAGC 1200
AGGGCCCAGT ATGGTGGAAA 1220
|
