Tag | Content |
---|
EnhancerAtlas ID | HS051-13568 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr19:7710190-7711130 |
Target genes | Number: 18 | Name | Ensembl ID |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GATA2 | MA0036.3 | chr19:7710869-7710880 | TTCTTATCTCT | + | 6.32 | Gata1 | MA0035.3 | chr19:7710869-7710880 | TTCTTATCTCT | + | 6.32 | Gata4 | MA0482.1 | chr19:7710870-7710881 | TCTTATCTCTT | + | 6.02 | ZNF263 | MA0528.1 | chr19:7710666-7710687 | TCTCTCCCCCATCCCTCATCC | - | 6.09 | ZNF263 | MA0528.1 | chr19:7710770-7710791 | CCCCTCCCCTCTCCGTCCCCC | - | 6.5 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr19 | 7710196 | 7710278 | chr19 | 7710620 | 7710829 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH19I007643 | chr19 | 7708106 | 7712061 |
|
Enhancer Sequence | GGGTACGCCA GGAGCGGGCA TGGGGGGACC CTGGGAGAGG GTGCGGATCA CAGCCGGGGC 60 TCTGCAAGGC AGAGGGCCAT TGGTGCACAG GCACGGTGTG GTTCCTGGCG TGGTGTGGTT 120 GCTGGGAGGC CAAAAGCAGT GTTTCGGGTC TGGTCTGGGG CCCAGAGGAC ACTGGGGCCT 180 CTCCCAGTCC CAGCTTACAC AATAGGCAGG GGAAGTGAGA CATGGTCGCT GCCAGGCTGG 240 TCCTGGCAGT GGTGCAGTTG GGAGCGGGTG GTCTGAGTGC TAGAGGCAGG GAGTAGGGTC 300 CCCAGCATGG GGGCTACACC ACATTGTCTA TCTGGGCTCC CAGGGGTCTC TGAGGGTCCC 360 CCGCACCCAT CCAGCACCCA CACACAGCCA TGTGTGTGCT TGACTCTTGG GTCAGCCTCT 420 CCTGTCTCTC TCTGGCCCTG TGCGTCCCCC TCCAGGGTGC CCTCACCCCG TCCCCATCTC 480 TCCCCCATCC CTCATCCATC TCGCTGTGCA CTGTTTCTCC ATATCTCTCT CTCTCACCCT 540 TCTCTCTGCC TTCCCCTTTC TCTCTGTTCT CTGTCTTGCT CCCCTCCCCT CTCCGTCCCC 600 CTTCTGTCCC CATCTTCCTC TCTCTGTTTC CTGCTTCATC TCTTGTCTCT CTCTTTGCCT 660 TCATACTTTG TCTCACTGCT TCTTATCTCT TTGCCTATCT CTGCCTCTGT CTTTGTCTTT 720 CTCTGGCTCG CTCTCTCTCC CTTTGGCTTT CTCTCTCCGT CTCTCTCTGG CTCACTGTTT 780 CTCTCTCTCG CTTTCTTGCT GTCTCTCGCT CTCTCTCGCT CTCTGTTCCA CTTCCCCATC 840 TTTGCCTGCC ATCCCCCACC CTACCAGCCA CACCAGGCGC AGCCCCTCTG TGACCAGCCT 900 CCTTCCCCTC AATCCCCCTG CTGCCCTCCC TGCCCTGCCT 940
|