| Tag | Content |
|---|
EnhancerAtlas ID | HS051-07703 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr13:107569520-107570890 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr13:107570558-107570577 | CACTGCCCCCTACTGGCCG | - | 8.13 | | Gfi1b | MA0483.1 | chr13:107569857-107569868 | AAATCTCAGCA | + | 6.32 | | HSF1 | MA0486.2 | chr13:107569846-107569859 | GAATGTTCTAGAA | - | 7.52 | | RREB1 | MA0073.1 | chr13:107569784-107569804 | TGCGGGGGGGTGGGGGGGGG | - | 6.73 | | ZNF740 | MA0753.2 | chr13:107569796-107569809 | GGGGGGGGGGCGG | - | 6.64 | | ZNF740 | MA0753.2 | chr13:107569793-107569806 | GTGGGGGGGGGGG | - | 6.92 |
|
| | 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 |
| GH13I106915 | chr13 | 107567809 | 107573470 |
|
Enhancer Sequence | AAAAAACGGT GTACAATAAG AAATGAGACT TGAATGCGAG CGGGCGGGAG GCAGCGCTGA 60
AAGAGGCGGC CGTGGATGCC ACGGCGCTGG GTTCAAGTCC CGGTCCAGGG GGTTTGAGGG 120
GACCGGGAGA CAGTGGCCGC AGCGGCCATG GGGTCCCCGC AGACCTGGCC CAGAGTGCGG 180
AAGGAGTCGC CTGAGCCGCT GTTTTAATTC GTGAATTCAT TGAAAGACGA GAGGGCCCCA 240
GGGACTCCCT GGGAACGCTT GGATTGCGGG GGGGTGGGGG GGGGGGCGGT CAGGGCTTTC 300
CTACCCTCCC CGTTTCCCAT CCCTCAGAAT GTTCTAGAAA TCTCAGCACA CAGGAAGATG 360
CAGTGGCCGA GGCCCGTAGA AGGAAGCGGG CGAAGGGCGG AGGAGGACGC GCGGGGCCGG 420
GGCCGGGGCC GGGGCCGGGG CCGGGGCCGG GGCCGGGGCC GGGGTCGGGG ACGCGGGGCA 480
GGTTCGTGGC GCAGCCCGGG GAGACCTTGG GCGAGGCCTC CAGGCGGGGA CGGGAAAGGG 540
AACGGGAACG GGGACAGGGC GCAGGGCAGA GGGCCGGGAC GGAAACGGGG ACAGGGCGCA 600
GGGCAGAGCA CAGAGCGCAG GGGCGCAGAG AAGGGGACGA AGACGGGGCC GGAGGCGCCT 660
GAGGGGGGCT CCGTGCGGGA ATCGGCGGCG CCACCCAGCC CCGCACATCG CCGAGAGAGG 720
CCCGCGTGCT TCTGAGAGCG CCGCCCCTGA CGTTTCTGCT GCGCGCTGGG ACCGAACCTA 780
CAGGAAGCAA AACCCTAGAG GAAGAAGTCG GCGGCTTTTT GGCTCGGAGA CAAAATGGAG 840
CCCCGCGGAT GCAGCCTGGG CTCCCTCGGG CGCATCCCCA GAAGCTGCGG GTGTCCCCGG 900
AGGACTTGAA GTCCTCCCGT GCGTCTCGAT GCCACCAGTT TTTGTTTCTT TGGTGAGGAA 960
TCGGTTCACG GTGAAACTTC ATTCCTCAGC CGGTGGGGAG CCGAGGCTGG GCCGGGCGGC 1020
GAGGGTTGCG CTGGGACGCA CTGCCCCCTA CTGGCCGCTG CGCCGCGTTC CCAGCTGCTC 1080
GAGCGGGTGG TTCAGTGAAC TCGGATTAAT TTAAATACAG CCGTAGATTT GGCTTTTTTC 1140
CCTCCCGGGC GAATCTAAAT TTAAAAAAAA AACTAGGGAG AGTACCAAAC TTAAAATAAT 1200
AAACAGACTG AAGGATATTA TTTCTTAACC TTTATACAGC CTCCTAAAAG AGTGAAAATT 1260
TTATTGTGAG TAAAATCAGA GTTTGGCTCT CTGGTATCCC TTCTGCTTTA ATGTGCTTTG 1320
AGACTATTCT TATGAGACTA GAAATTCTTT GGTTAATGCA TATTTATTAA 1370
|
