| Tag | Content |
|---|
EnhancerAtlas ID | HS187-00361 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr1:24476210-24477230 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr1:24477126-24477145 | CGTCCAGGAGGTGGCAGCA | + | 6.27 | | HLTF | MA0109.1 | chr1:24476873-24476883 | AACCTTATAT | + | 6.02 |
|
| | 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 |
| GH01I024149 | chr1 | 24475961 | 24479769 |
|
Enhancer Sequence | CAGATGGTCC ACTAAGCACC TGGAGAAACA GACTCAGAGT GGGGTGGGAT ATGTCCCACC 60
CTGGAGGCAC CGCCCTCCTA GAGAGGGGCC TCTCGCCATA TGCTGATGGT TTTGTCCACC 120
AGGACAGGGC ACTCCTCGTG ACCTTATCCT CTTCATCCAC TTAAATAAGC AGTTGGGGGA 180
AATAAAAAGA CTCAGCTTAT ATAAAGCCAT CACACCTCCA TGTCATGTAT CGTCACACGC 240
CAAGGGTGGG GCTCCCAGGG CTGGAACCGG TCCTGGTGTC AACCAGTATC TCTTGAGGAA 300
CTGACTCATG GAGCTGACTC ACGCATTTAG ATATAACTTC TAGTCTGTTT TCTAGAAAAA 360
ACACCCCCAA CCCTCATTAC TTCAGCCCCA CTTTATGCAC ACAGGAATGA GCTCAGGGAA 420
GATGCGCAGG CAGCCATTGA TCAAAACCTA AATCACATGG GAAACAATCA ATTACAGAAT 480
AATAAGTCCC AGACCAAGTG TTAAGGTCCT GTTCTGTCTC CCGCGTACTC CCTCCAACAT 540
CACTATGCTC GCTGAGCAGC ACCAGTGCCC CCTCAGAGCA GATGCTGGGC GAGGGAGGAC 600
GGGCACCGAC GGGCAACGGG AATTTGGGAT CAGGATGGTA TCATCGCATG CGAGAGCTCC 660
TGCAACCTTA TATGTAAGTC AGTCACAGCC GTCCACTTAC TGACTCCAAT TCATACGCCA 720
ATTCACTCAC TTATTCTTTC ATTCACTTAC TCAATCCCAA GCTTCCACTC TGTGCCAGGT 780
GCTGGTGCCA AGAGGAAAAG CAACCCCTTT CCTAAAGGAA GTTTTCAGGG CGTCCATTAC 840
CCCAGCCCTC CCCTCTCCAG GTTCCCTGAG CTCGGTTCGG GTAAGACCGC GCCCAGCCGC 900
CCTGACATAC CACCACCGTC CAGGAGGTGG CAGCAGACAG GTTCGGAGAA GCTCAAGGGC 960
GGCGACCCAG CAGTAGGAGG AGGAGGAGGG CGGGCGGGTC ACCTGGAGAG GACGTCCTTC 1020
|
