| Tag | Content |
|---|
EnhancerAtlas ID | HS051-26540 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr8:105337730-105339260 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myod1 | MA0499.1 | chr8:105338656-105338669 | CGCAGCTGTCTCT | + | 6 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr8 | 105337766 | 105338170 | | chr8 | 105338178 | 105338597 | | chr8 | 105338636 | 105338788 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH08I104325 | chr8 | 105337761 | 105338562 |
|
Enhancer Sequence | GCGTCAGGCA CACTTAGCAT CAATAAGTGT TGGATGTAAT TATTATTACT ATTAGTAAAC 60
ATTCCTGGGA GGATGGAGCT GCAGTCCCGA GCATGTCCAG CAGAGTGCGC CCTGCAGTTC 120
AGAGGCGCAG AGTGTTCAGG GGGTGGCCTC ACTGTGGGCT CCCCTGCATG CCGACTGCCA 180
GATACCCACT TAATGGATCC CATTGGACCA ATGGGTGCTT CCATCCCTTC ACAGGCTCCA 240
TCTTTATCTT TCTAAACCAT CGTGCCTGAA GACTCCTGGA GGTGACCTGT TTGTGAGGAA 300
GGCAAGAGAC CAGGAAGACA GGGAGGAAAT CACCTGGATT CTGATTCCCA ACCTCGGAAG 360
GGCTCAGTCA CTGGGCAAAA CCCTCACTAC TGGCAAGAGG CATAACGGGC ATTTTCATCC 420
ACACAGACTG GCTCTGAGGG TGCCCCCACT CAGCATTATG AGCCCTTTGG GGAGTGGTCC 480
TTTCGCCAGG GGCTGCTCTG TGCCATCCCA GGCTTTGGAG CGGCGGCTGG TGTGGATGAT 540
TCCACCAACA AATCTCTGAA ATCAGAAATG AGGCTGTTTC ATAATCTCCA AAGGCTGGAG 600
ACGTTCCAGG CAGTGGAAAG AGAAGCTGGC CTACTTTAAA GAGCTTCAGA GAATGAAATT 660
CCCAGCCCTC CGCAGACATG GGAAGAGCTG CCACCTTCAG GCCAAGTGTA GATGACAGGC 720
CTCTTCCTAA AATGCTCAGC CACCTGTTCA ACCCCTGTGG GACCCAATAG CTCACAAACC 780
TGTCTCCTGC CTGCTGGCAG GGAATTCCTA GGATCTAACC AGAGCCTGTG CCCTGCTCAC 840
TATCTATCTA CGTGGCCTCG CTTCTGGGCA GGTGTGGATA AATTTCTCTG TGCCCCCACT 900
AAATTAGGTC CCCAGGTAAG AGGACACGCA GCTGTCTCTG GCAGCCAGTC TCCACATTTG 960
CCTAACTTGC TTTGTGGCGC ACTGCCAGCT GCCTATGTTA GCGGCTGCTC CACAGCACAG 1020
AACGCAGATT AGAAGTCTGT GGACTCTGCA GGGGTCCAGG CTGCGCTGAC CTCCTGCAAG 1080
CTGGGTGGGG TAGGGTGAAC TCCAGGAGCG TGGGTCTCCT GAAGGCTGGG CTTGGGCCCT 1140
GGAGGTGGGC AGACCTCCAT GTCTGCAACC TGCCACCCAA CCCCTCCTTG GGCCTTCAAT 1200
ACCCTGGAGT CACCCATCAG AAAGGCCAGG CCTCTTGATT GCCTGTGATG ATCTATTTAG 1260
GCTCTGTTTA TATCACCTGT TTTAGGCTGA CTTTCCCTGG ATCAAGGGCC CACCAGTGTT 1320
GTTTCAAGTA GACAAGGTAG CCCTAGGTTG ATTTGAGAAG CTGCTGGTCT TTGGTGTCCG 1380
TCACTCCCCA GCCACAATCT CCTCAGGGCC TGGCTTTCCT GCGGTCTGTC CTGCCAAGCT 1440
CAGCAAATGT CAAGGATGTA ACCAGTTGGA GTGATGTGGG CCCTATAACA CTTCCCTGCC 1500
ATTCCCCTGC TATGGCTCCT TAACTGCCCT 1530
|
