Tag | Content |
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EnhancerAtlas ID | HS047-02116 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr1:150867850-150868740 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFE2L1 | MA0089.2 | chr1:150868229-150868244 | GCATGACTCAGCCTT | + | 6.13 | Nr2f6(var.2) | MA0728.1 | chr1:150868038-150868053 | TGAACTCCTGACCTC | - | 6.22 |
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| 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 |
GH01I150895 | chr1 | 150867849 | 150868735 |
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Enhancer Sequence | TTTCTGTTGC CCAGGCTGCA GTGCAGAGAC GCGATCTCAG CTCACTGCAA CCTCCACCTC 60 TCAGGTTCAA GTGATCTTCC TACCTCAGCA TCCCAATTAT CTGGAATTAT AGGTGCGCAC 120 CACTACGCCC AGCTAATTTT TGTATTTTCA GTAGAGATGG GCTTTCACTA TGTTGACTAG 180 GCTGGTCTTG AACTCCTGAC CTCAAGTGAT CCACCTGCCT CGACCTCCCA AAGTGTTGGG 240 ATGATTACAG GCGTGAGCCA CTGCACCCGG CCATGAAGAA GTCTTTCTTC ACATGAATCT 300 GTCAGAAACA ATTCCCACTG CGGAGGCCTA GAGAAATCAA ATATTCCCTC TTCCACCCTC 360 TGGCAGCCAA GGTGTTAGTG CATGACTCAG CCTTGACCAG TCAGATGCTC TAGCCAGAGA 420 CTAGACTATT GAGTGACACA AAGATGACAC AATTTATAAT TCAGCCATGC CAGAGGCAGC 480 AGTATCCAAT GACAGTAGCA GCAGTGCTCG GCAACAGCAG TGTCTGGTGG TGGCAATGTC 540 TAATGCCAGC ATTGCCCTAA CCAGACTTTT CCTGTGCTCT CCCTGGCTAT GGTTCCTGAT 600 GGCTGGCTTC TCTTGATTTC TGTCTGTTTA TAAGACTAGT TCTCTTTCTG AGAGCTATCT 660 GACCTCTTTA CAATAAATAT ATTTTCTGTT TAACGGAGAA TCCGTTCCTG TTGCTTGCAA 720 ACAAGAATGT GTTCTTTTTT CCTCTGGAAA GGAGCAGGAG AGATGATAGG TAGGGGGAAT 780 ATGTGAGGTT TGAATTTGCT GGAGCCATTC TTGATACCGT AAGGGAAGCC AAACTGGGGA 840 TTAAATCAAC ATAGAAGAAA GGCAGGGTTA AGAAAAGCCA TAGACACATA 890
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