| Tag | Content |
|---|
EnhancerAtlas ID | HS051-21134 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr4:101014330-101015220 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr4:101014728-101014747 | TGGCCACTAGGGGTCCCCA | + | 6.01 |
|
| | 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 |
| GH04I100093 | chr4 | 101014221 | 101015466 |
|
Enhancer Sequence | CGTCTCCGGG AACAGATCTA AGAAGTGGGA CCTTGTATGC AGTCACTGAG ACAGCTGTTC 60
CCATGAAAAT CAGGGCTCAT GGAGGACATG CAAATGCTTC TCTGTCAGTC TTCAGCCTGC 120
TTGCTCTGCC TTCTGCTTTC CTGGTGAGGA TTAAAAGAGG ATTTCAGAGC TCTCCTTCAA 180
TTTGATGCCA TCATTTTGAT GTCTATGCCA CCCGTAACTC CAATTTCTAA ACTTGAGAGC 240
TGTACAGGCC TGTTACAAAG TGGTTACCTT TTAACCACTA ACTTCCGAGA AAAAACTTGG 300
ATCACTGAGG AGAGAACGAA GACAAATACA ATTGAAGCCC CAGGTAGTTT TCCTGAGGCC 360
TCATGATTTC TTTTGGCAGA GAAACCTATG ATAGCTGGTG GCCACTAGGG GTCCCCAGAA 420
GGCTTTTTTA ATGAACAAGA GGCACCCGCG CTCCTCACCC CTCCCTTTCC TTCCCACAAA 480
TGCCAGGGGT AAAAACAACT TTAAGCTCTG ACGTCAGCCA GCCAGGGGAG CCACCCTGTT 540
GTGCCCATAG GTATAGCTAA GCTTCTGAGA ACTGGGGCCT GGTGCTTTCC CTGGCAGCCC 600
AATTTTCAGC TTAAATCATT GCCTTAATGT TATTTTAATG TGCTTGGGGT CCCTGGGGGA 660
CAGAGTGGGT GGCAGGGGAA CAGCATTTAA TTTCCTTTGG AGTTTGGAAT GTGCCTGACA 720
CTTCTTAAGT ACTTGAGTGA ATATGAGAGT CTGTAATCCT TGCAAGAGCA AGCAACTTTG 780
GGGGCCTTCT TATTTGGCAA GCTTCAAGAC AAAGTTAAAT TTTTGCTAGG AGAGAGGGAA 840
AAAAGGAAAT AAACATGTAT TAAAAGTCTG ATATATGCCA TGGGCTTTAC 890
|
