| Tag | Content |
|---|
EnhancerAtlas ID | HS051-18376 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr22:24999740-25000950 |
Target genes | | Number: 21 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXH1 | MA0479.1 | chr22:24999829-24999840 | TGTGGATTGGG | - | 6.14 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GCTCTGGAGT AGAGCCAGAG CTGTGATGGG GTTGGGGGAC CCTGTGTCCT TGGGCCATGC 60
TTGCCTCGCT CCTGGGTTCT GTTTGTGGCT GTGGATTGGG GTGGGGCAGG GCCGGTTGTG 120
CGAGGGGTCA TTGCCCAACT CCAGGGGGCG CCTGCCACCT CTCAGCTATA TATATAGGGA 180
TATATATAGT TCTTTCGACA GGTTTCCAGC AGGTAGTGGT TATTAAATCT TACTGAAGGG 240
GTGTTTTTTC TGATTCTCGG CTCTGTGCCG CAAGGGTGGA AACTGTGAGA GACAGATTCC 300
AACTCCACGT CTGGGTAGTA AGCATCCAGT CCAGGGCTGT AGGCAGTCCT GGGGAAGACG 360
CCAGAGATCT GTGCATTCTC ATATCGAGGG ATAGCGACTC CAGGCTGGGG GCTGGCAGGG 420
TAAGGGGTGG GTGGGTCCTG GGCTTACCCG CAGGTCTGCA GACTTCCTGG GGCCAGCTGA 480
CCTCGTAAAA TCCCTTTTGT CTAAGCTTCA GTTTCCTGCC TGTGAATGGG GTTGGGGCTG 540
TGCTCTGGTT TCACCCTTGT GGCTCTGGGG TTGTGGTGAC AAAGCCATCA AGCTGGGTTG 600
AAGGATTAAC CAGGAAACTT CAGACTGGCT GCCGTGTCTA CCTCTTCCTC ATACTCCTCT 660
CTCTGCTGCA TCCTGGGAAG CTGCTCTGCT CAGCCTAAAT GAGGCTCAGT TGTGTGTGTG 720
CGCACGTGCT TGCACGTGTG TTGGAAGTGG GTGATACTGA CACCAGAGTC TGTGTCTCTG 780
GGTGAGTGAG GCTTGCACAT TTCTCGGGAC AGGGAACTCA CTACCTTATG TGCCCAGGAC 840
AAGAGCTGTG GGGTCTGGAG AAGACTTCTA GGCCAGCCCC TGCAGTCCTT CCTCAGGTGA 900
CATGGCTTCC CCAGACCCAC TTCCCCCTAG GTGCCCTCTC TGCATTCAGG GGGTAGAGGG 960
CTGACTGGGA CAGAATGTGA CACACTCAGC ATGTGAGGAA AAGCCTCCTT CATTCTGTAG 1020
GCCCTACCTC TATTAACATG TCCTTTGATA AAGTGCCTCC CCTCCTGTCT CCCCTCTCTG 1080
GAATCCTCAG CTGCTGCCAG GCTTCAGCTG TGCCCCATTG AAGGCAGCTC TGTCTCCCTA 1140
CTTTCCCCAG CCCAGGGTTT TCCTTTTGGG GTCAGCTGCA GGGATCTGGG CCATCCTTTG 1200
CCCACTCAGA 1210
|
