| Tag | Content |
|---|
EnhancerAtlas ID | HS076-43367 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr4:101014200-101015200 |
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 | AGCTTTATTG CTTATGTTCA CTGGGGTTTG GGAAATAAAG ACTCAGGAAG CAGAAACACA 60
CCAGCTACAA GAGTCTGACA TTTGTTTATG AGCAGGACAG CCTTGACTTA TTATTCTACT 120
TCTTCTCTTG CGTCTCCGGG AACAGATCTA AGAAGTGGGA CCTTGTATGC AGTCACTGAG 180
ACAGCTGTTC CCATGAAAAT CAGGGCTCAT GGAGGACATG CAAATGCTTC TCTGTCAGTC 240
TTCAGCCTGC TTGCTCTGCC TTCTGCTTTC CTGGTGAGGA TTAAAAGAGG ATTTCAGAGC 300
TCTCCTTCAA TTTGATGCCA TCATTTTGAT GTCTATGCCA CCCGTAACTC CAATTTCTAA 360
ACTTGAGAGC TGTACAGGCC TGTTACAAAG TGGTTACCTT TTAACCACTA ACTTCCGAGA 420
AAAAACTTGG ATCACTGAGG AGAGAACGAA GACAAATACA ATTGAAGCCC CAGGTAGTTT 480
TCCTGAGGCC TCATGATTTC TTTTGGCAGA GAAACCTATG ATAGCTGGTG GCCACTAGGG 540
GTCCCCAGAA GGCTTTTTTA ATGAACAAGA GGCACCCGCG CTCCTCACCC CTCCCTTTCC 600
TTCCCACAAA TGCCAGGGGT AAAAACAACT TTAAGCTCTG ACGTCAGCCA GCCAGGGGAG 660
CCACCCTGTT GTGCCCATAG GTATAGCTAA GCTTCTGAGA ACTGGGGCCT GGTGCTTTCC 720
CTGGCAGCCC AATTTTCAGC TTAAATCATT GCCTTAATGT TATTTTAATG TGCTTGGGGT 780
CCCTGGGGGA CAGAGTGGGT GGCAGGGGAA CAGCATTTAA TTTCCTTTGG AGTTTGGAAT 840
GTGCCTGACA CTTCTTAAGT ACTTGAGTGA ATATGAGAGT CTGTAATCCT TGCAAGAGCA 900
AGCAACTTTG GGGGCCTTCT TATTTGGCAA GCTTCAAGAC AAAGTTAAAT TTTTGCTAGG 960
AGAGAGGGAA AAAAGGAAAT AAACATGTAT TAAAAGTCTG 1000
|
