| Tag | Content |
|---|
EnhancerAtlas ID | HS051-27190 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr9:35847230-35848750 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MSC | MA0665.1 | chr9:35848376-35848386 | AACAGCTGTT | + | 6.02 | | MSC | MA0665.1 | chr9:35848376-35848386 | AACAGCTGTT | - | 6.02 | | MYF6 | MA0667.1 | chr9:35848376-35848386 | AACAGCTGTT | + | 6.02 | | MYF6 | MA0667.1 | chr9:35848376-35848386 | AACAGCTGTT | - | 6.02 | | NEUROG1 | MA0623.2 | chr9:35848069-35848079 | GACATATGTC | + | 6.02 | | NEUROG1 | MA0623.2 | chr9:35848069-35848079 | GACATATGTC | - | 6.02 | | SOX10 | MA0442.2 | chr9:35848656-35848667 | TTCTTTGTTTT | - | 6.62 |
|
| | 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 |
| GH09I035847 | chr9 | 35847359 | 35849309 |
|
Enhancer Sequence | CAGCTGTTCC ACACTCTGTC CACCCTGAGG GCTGAGGGGA CCTTTACTCA AATCATGGGC 60
CAAGAAACTG GCCTAAAGTA TGGATTTGTG TCTGCACAGT CACCATGTTC TCTGTATGGG 120
GGCAGGAAAT CTATGCTTTC CCCCACACCT CTGCACACAG TGTCTTCATC TTCACCACAT 180
TCTTCCATGA TATGAGAGCT AGCTAGCTAC TCTGAGCTCC CCTTCTCCGT CGCACTGGGG 240
ACCTGCACAT CGTTAGCACG TTCGTTCCTG TGGTCTGAAA TGGCGTTCCC ATTCAGTCAC 300
CATGCCACCT TGATTTCTCA TGAGAACTTT GGAAAGATAG AGGGGATCTC TCTATTGGGG 360
GATTATAGGA CAATCTGACT CTCAGAGTCC TGAGAAGCTT TACAGACTCA ACTATGTCCT 420
GAGGCATTGT CGGAAGTGGC AGTGTCATAT CACATCCCAG CTCAAAGGAG TGCATTTTGA 480
TGAAGATTAA TATAGTTTAA AACCCCTCCA TTCCCATTGC AGAATTGCCA CAATCTCTTT 540
CCTGTGTTTT CCTCACTCCT CCATAATCAG AAAAGTTCAT TATAAGCAAG CGTCCAGAAA 600
CTATAAGGAA AGGTAGAGAA GTGAGCCTGC TAATGTTACT TAACCCCCAA GTAGACTTTT 660
TACCCCTGAA GTGTCACATC TGGGAATCTT TTCAACTCAT CTCTAGGCTC TTGGCACCAT 720
GTGACATGCA TGTGAGCACT GCAAAAACTC TTAGATGGTT TCAGACTGCT CAGGCCTTGT 780
CAGCAAGGAT ATCACAGAAA GCAAGACAGG CCTTCCTGGC ATCCTGCATT ACTAGGTCAG 840
ACATATGTCT AAATTAGAAA AATCATAGTT CTCATCTGGG AGAAAGCAGG GGCAAATGTG 900
CTGAAACTGA GGGGCCTGGG TCCTCCTGGA GATTCATCCA GAGATGAGGA AGAAGAGTCT 960
GCAACCATGC TGCAGAGAGA GATCTTGGCC CTTTAAGCTG GGTGAGAAGC ATATACCCCA 1020
GTTTTGCTTG ATTGGCCCCT TTTTAGGCCT GCCCCCACAG TGCCTCATTC TATTTTTATG 1080
TTAGACACTG TTTCTCTTTC GTATTGCCAG ATGCCCTTTC TACTGTGGCT CACCAAATCC 1140
TCCAGCAACA GCTGTTCTAC CAGCCCACTC TCGGCTACAT GCAGATCGAA TGTGATTCAT 1200
AATTAGTAAG AATACCTAAG TGTGTCAGGA GCCTGAAGCA TGTAGGGAGA GCATATTCAC 1260
TCTCTGGACT TGACACAAGT ATCCTGATTG GCTCCAGAGT GTTCAGTGCT AGATGACTCT 1320
TCCTTATCTG GATACAGTGG CTGTCAGCCT GAAAAGACCT TCCCTGTAGC AGGAGTACTA 1380
GGAGAGCCTC AAGTGCCTGG CACCACATAA AAAGCTCCCG GTTTCTTTCT TTGTTTTTTT 1440
TCTTTTTTTT TTTTTTTTTG AGACAGAGTC TTGCTGTGTT GCCCAGGCTG GAGTGCAGTG 1500
GCGCGATCTT AGCTCACTGC 1520
|
