| Tag | Content |
|---|
EnhancerAtlas ID | HS051-19990 | Organism | Homo sapiens | Tissue/cell | Fetal_thymus | Coordinate | chr3:126217020-126218170 | Target genes | | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SP2 | MA0516.2 | chr3:126217536-126217553 | CTCAGCCCCTCCCACCT | + | 6.26 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AGCACAGATG CCTCCTCACC CTGGGCCCGC TGGCTTGTTG GGGGAGGGGG TGCAGGTGTG 60
AGCATGCCAG GGAGGAGGGC TCAGCATCCA GAAGTCAGGT GTGGAACCCC CTAAGCTGTC 120
ATTGGACAGA AAGTTCCAGG GGCCTCCCTG TCCCCTCTCT GTGTCCCAGT GCCCCCAGCC 180
CTCCATCCCT GCCTCCTGGC TGTACCATCT CTAGCTACAG GAGTGGGGAG CTGGGACCTG 240
GGCAAACAGA AATGACCCCA ATTGCTGTTA CAGATGACAA GAAAATCCAT CACCTAAAAG 300
TGACAGTCAC ATTGAGAGGA GAGTCAACCT GGGGCTGTAG CCTTGGGGAA CTCGCCCTAG 360
GTGAGCTTAT CTTCCCAGGA GCCAGGCTCC AGGACAGGGC TGTCCTGGGG GGAGGATGCC 420
GTGGCCTGGG CCCTCCCTGG GCTCCTGCAC TTGCTAGGCC AGGGGGTGCC TCCTCCTGGG 480
CAGCCCTCCC TCTCCGGAGA GTGCCAGCTG ACAGTGCTCA GCCCCTCCCA CCTCTGCACC 540
CCACAGTGAG CTTGACAGTA AGTGGCATTT GCCTTTCTCA CCTCCATCTC TCTCTCGTCC 600
CATGTGGCAC CCACTGAGGA CTGGCACATC TTCCAAAAGT CATGTGGTCC CTCCTGCCCC 660
CAGCAGAAAG CCCAGACTTC TCAGCTTGGC CCAGGCTCCT CTCTGGCTCC CGCCCTCATC 720
CCCTGCTTGT CCTGGGCTGC TGGCCTTCCC TAGACCTGCA CCCCCATGGC CAGAGAGGCC 780
CACGACCCCC AGGGCCACAG CAGGTGCTGG GCTTCATGAT CCAGCCATCA GCCACCCACG 840
AGGGCCTGTG AAGACATATT ATTCAGGTGC AGTTGTTTGC CAGGAAGTGG CCTCAGCCTC 900
TAGGCCCCGC AGCCCCCTGT TCTCACTGAG GCCCTGCAGG AGGCGTCTCT CGTCTGCATT 960
TCCTCCTCAC CTGCCTGTCT GTGGTGGAAA ACCCATGGAC AGAGCCTGGC CACTTTGGGG 1020
CAGTGTGGAG GTCTCAGCGC ATGACCTCAG GGGCGGTCAG AGGCTGAAGC TTCTCCAACC 1080
TAAATACCCA GGACGCAGAC CCTGAACGGG GCAGGGGTGG CACTGGGCAC ACTAGATGTG 1140
GCAGCCGCCC 1150
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