| Tag | Content |
|---|
EnhancerAtlas ID | HS051-09891 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr16:1439120-1440630 |
Target genes | | Number: 20 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| E2F6 | MA0471.1 | chr16:1440567-1440578 | GGGCGGGAAGC | + | 6.02 | | HES2 | MA0616.2 | chr16:1440129-1440139 | GGCACGTGCC | + | 6.02 | | HES2 | MA0616.2 | chr16:1440129-1440139 | GGCACGTGCC | - | 6.02 | | SP2 | MA0516.2 | chr16:1440505-1440522 | GAGTGGGCGGGACCAAG | - | 6.5 | | Znf423 | MA0116.1 | chr16:1440612-1440627 | GAAACCTTGGGGGCC | - | 6.6 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CCTCCTGTGA GTGGAATCAC GCAGGTTTTG CCTTTCGGTA ACTGGCTCAT TTCAGTCAGC 60
ACAGTGTCTT TGTTATGGAC CAAACGTGTC CCCCCCAAAT TCCTACGTGG AAGCCTTGAC 120
CCCCGGTGTG ACTAAATTTG GAGATAGGGC CTGTGAGGAG TAATTAAGGT GAAATGAGTT 180
CTTACTCCAG GCGTGGAGGC TCACACCTGT AATCCCAACA CTTTGGGAGG TCAAAGCAGG 240
AGGATTGCTT GAGCCTAGGA GTTCGAGAAC AGGCTGGGCA ACCCCATTTC TAAAAAAATA 300
CAAAAATTAG CCAAGCCTGG TGGTGTATGC CTGGGGTCCC AGCAACTCAG AAGGCTGAAG 360
TGGGAGGACT GCTTCAAGCC TGGGAGTCCC GGGCTGCAGT GAGCTGGGAC TTGGCCACTG 420
CACTACACCT GGGTGACACA GCCAGACCCT GCCTCAAAAA ATTTAAGAAT CTGTAAAAAC 480
ACAACAGCAA CAATGAAATG AGGTGTGGGG GCAGGGCCCT ACGCAGCCAC TGTCCTCAGG 540
AAGAGACCCC AGGGATGCCC ACGCACAGAG GGGTGACCCC AGAGGACACG GAGGAGGCAG 600
CATCTGCACC CGGGGGGCCT CAGGAGCCAG CTCTGGACAG CTCAAGCTCG GACTCAGCCC 660
CCAGAACTGA GAGAGTCAAG TGCTGCTGCT TGGGGATTGG TTTTGGTTTG GTTTGAGACA 720
GGGCCTCACT CTGTCGCCCA GGCTGGAGTG CTTGGCTCAC TGCAACCTCC ACCTCCTGGG 780
CTCCAGCAAT TCTCTTGCCT CAGCCTCCCA AAGTACTGGA ACCACAGGTG TGAGCTACTG 840
TGCCCAACTA AAACTACCTC ATTCATTCAT TCATTCATTC ATTCAGAGAC AGAGTCTCAC 900
AGTGTCACCC AGGATGCAGT GCAGTGGCAC GATCTCGGCT CACTGCAATC TCCACCTCCC 960
GGCTTCAAGC AATTCTCCTG CCTCAGCTTC CCGAGTAGCT GGGACTACAG GCACGTGCCA 1020
CCATGCCTGG CTAATATTTT GTATTTTTAG TACAGATGGG GTTTCACCAT GTTGGCCAGG 1080
CTGGTCCCGG ACTCCTGACC TCGTGATCCG CCCACCTTGG CCTCTCAAAG TGCTGAGATT 1140
ACAGGTGTGA GCCACCGTGC CCGGCAAGTT CTGCTGTTGG AACGGCCCCA TCTGCATCCT 1200
TCCCTCGCAG CCCAAAAAAG TAACACAGAT GGGCTCCAAA GGGCCCCTCT TATTTCCCCG 1260
AGCACGATGT TGTGGCTTTG TTTCCAAGGT ATAACACGAA CGTTTCAAAC AGACAAACAC 1320
GGGGGTACCA GGAAAGAGCT AATTCTACAA CAAGCGGACG TCAACCAGAT GGCTTTGCGA 1380
GCCGAGAGTG GGCGGGACCA AGGATGCATG AGCGCTGCCC TAACGCGATG CCACGGGTCA 1440
GGCACGAGGG CGGGAAGCCT CAGCCCTAAC GCGACATCAG GCACGAGGGT GGGAAACCTT 1500
GGGGGCCTGT 1510
|
