| Tag | Content |
|---|
EnhancerAtlas ID | HS048-02776 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr1:174143300-174144180 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Mecom | MA0029.1 | chr1:174143928-174143942 | TTTTATCTTATCCC | - | 6.05 | | NR2C2 | MA0504.1 | chr1:174143848-174143863 | TGAGGTCAGAGGGCA | + | 6.95 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 174143601 | 174143847 | | chr1 | 174143509 | 174144047 |
|
Enhancer Sequence | ACATGATAGC AATGAAGAAA TTGGAAAAAA AATACACACA CACACACACA CACACACACA 60
CACACACACA CAACTGAATA AGTCATAGAT AATACAAGGA AAACATCCTT GGACAACTAA 120
ATTAGCTTTA AGGGTATCAA ATGTATTTGT AATACTATAG AATAATAATG AAAGTTTGCT 180
GTGCTCTCTG TTACCAAGAA GACATGAAAT ATATGTCCTG TATAGTATAT ATATTAGTTA 240
GGATTCTTCA GAGAAACAGA ACCAATAGGA TAGCTATGTG TAGATACAGA TCTGTTGGAA 300
TTGGCTTACA CAATTATGGA GGCTGAGAAA TCCCGTGATA GGCCGTCTGC AAACTAGGGA 360
ACTAGGGAAA CCAGTAGCTC ATTTCAAGTC CAAAGGCCTG AGAACCAGCA GAGCCAACAT 420
TGTATTAGGT TGGTGCAAAA GTGATTGAGG TTTTTGCAAA ATAACTCTCA ATTCGAGGCT 480
GAAGGCTGAA AAACTAGGGG GCTGCTGATG CAAGTCCTGG AGTCCAAAGG CTGGAGAACC 540
TGAAGTTCTG AGGTCAGAGG GCAAGAAAGA CAAATGTCTG AGCTCCAGAA CAGAGAGTGA 600
GTGAATTTGC CCTTCCTCTG CCTTTTTGTT TTATCTTATC CCCCAGCAGA TTGGATGGTG 660
CCTGCCCACA CTGGGTAAGG GTAGATCGTT CTTACTCAGT CTATTGATTC AAATGGCAGT 720
CTCTTTGGGA AACACCCTCA TAGGCAAATG CGGAAATAAT GCTTTTACTA GCTATCTGGG 780
TATCCCCTAG TTTAGTCAAG TTGACAACTA AAACTAGCTA TCACAGTAAA TTTATGAAGG 840
TGTCAAAGTA TTTATATTAC TAAGATTTTT AAAATATGAA 880
|
