| Tag | Content |
|---|
EnhancerAtlas ID | HS051-28700 | Organism | Homo sapiens | Tissue/cell | Fetal_thymus | Coordinate | chrX:136133960-136135010 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chrX:136134720-136134739 | CGGCGCCCTCTAGTGCCCA | - | 6.63 |
| | | 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 |
| GH0XI137052 | chrX | 136134160 | 136135359 |
| Enhancer Sequence | TCATGAACTC ATATGCATAT TTTTAGCTCC CATATTTCCT GCTGGTTTGA AGAAGTGTAT 60
AAGCAACCAT GTGGACAGCT GTGCTTCCCA TCAGTGAGGC AGTGCTGGGA AGTAAAAAGA 120
ACATGGGTTC CGTGTGAACT TGAGAGGTTC TACAACCCCT CTGAGCCTTA ATTTCCCCTT 180
CTGTAAGTGG GGAAAGTGGG GCTAACAAGA GTAACTCATG GGAACTATCT AGTGGGGCTA 240
ACTAGAGTAC CTCATTGTTT TAAGGATCAA ATGATTGGTG TGAAAGTGCT CACAGCAGCG 300
GATGGCAAGT AGTAGGTACT ATTGTGATGA TGATGGTGCA GTTCCGTGGC GTCCCATACA 360
GGTAGCCCCC TGCGGTGTAT GGGACCTCAG TATCTTCCAG GCGGGCATAC CTCCGGACAT 420
CGCCAGCTCT GGGTGATTGT GAGGTGCCGC ACGATGGGGT CTGACGGCAA TTGCTCATCC 480
TCAGCAGTTT AAAAATGACA TTTGGTTGAG TTGCCGTAGG TGTTATGGAT GCTTCCCCCT 540
CCTTCATTTG CGTTTTGCTG AGTTGTCGTC AGATATTATG TGGTCGGATG TTCCCGAGAA 600
GTGCAAGCCC CTCCCCGTGG GCCGCCCAGG GGTGGCCCGC GGGCGGTGCG GGCGACTAGC 660
GGAGGTTGGA GTGGGCTTGT AGACTCGCTC TTACTCCCAC CCTCTGGGAG GCCCCTAACC 720
CCGCCCTTTC CCTGCTCGCG GCGAAGGCAA ACTGCGCGCA CGGCGCCCTC TAGTGCCCAG 780
GAGCTGTCAC TGCGCGGGTG CCCGCGGCCC CAGCTCTCCC CGCCCCACCA AGGGTGTTTG 840
TGAAGATCCC TCGGCACGGC CGCATACCCC AATCTTCATT CCTGGGTGTC CTGACCATCC 900
CCCACAGACC CATAAGACGC AGATCCGAGA CCGCTTCTTG TTTGTTTATT TATTTATTTA 960
GCTAAAAGTT TACTAAAACC GGGGGGCTCT GTCGGTTCTT GACTTTGCGG CACCTGCCCC 1020
CGAAGGCGCC GTCTCCTCCA GAGAACAGCG 1050
|
| |
|
|
|
