Tag | Content |
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EnhancerAtlas ID | HS193-02206 |
Organism | Homo sapiens |
Tissue/cell | U87 |
Coordinate | chr1:150867920-150868850 |
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 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I150895 | chr1 | 150867849 | 150868735 |
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Enhancer Sequence | GTGATCTTCC TACCTCAGCA TCCCAATTAT CTGGAATTAT AGGTGCGCAC CACTACGCCC 60 AGCTAATTTT TGTATTTTCA GTAGAGATGG GCTTTCACTA TGTTGACTAG GCTGGTCTTG 120 AACTCCTGAC CTCAAGTGAT CCACCTGCCT CGACCTCCCA AAGTGTTGGG ATGATTACAG 180 GCGTGAGCCA CTGCACCCGG CCATGAAGAA GTCTTTCTTC ACATGAATCT GTCAGAAACA 240 ATTCCCACTG CGGAGGCCTA GAGAAATCAA ATATTCCCTC TTCCACCCTC TGGCAGCCAA 300 GGTGTTAGTG CATGACTCAG CCTTGACCAG TCAGATGCTC TAGCCAGAGA CTAGACTATT 360 GAGTGACACA AAGATGACAC AATTTATAAT TCAGCCATGC CAGAGGCAGC AGTATCCAAT 420 GACAGTAGCA GCAGTGCTCG GCAACAGCAG TGTCTGGTGG TGGCAATGTC TAATGCCAGC 480 ATTGCCCTAA CCAGACTTTT CCTGTGCTCT CCCTGGCTAT GGTTCCTGAT GGCTGGCTTC 540 TCTTGATTTC TGTCTGTTTA TAAGACTAGT TCTCTTTCTG AGAGCTATCT GACCTCTTTA 600 CAATAAATAT ATTTTCTGTT TAACGGAGAA TCCGTTCCTG TTGCTTGCAA ACAAGAATGT 660 GTTCTTTTTT CCTCTGGAAA GGAGCAGGAG AGATGATAGG TAGGGGGAAT ATGTGAGGTT 720 TGAATTTGCT GGAGCCATTC TTGATACCGT AAGGGAAGCC AAACTGGGGA TTAAATCAAC 780 ATAGAAGAAA GGCAGGGTTA AGAAAAGCCA TAGACACATA AAGGCAGAAC CCTGATACTT 840 TGAATCACTG GATTCAGCCA TAGCTAAAGG TAGTCTCACT CTGGACTTTT TGGCCATATG 900 AGTCAATAAA TTCCATTTTA TTTTTAAGTC 930
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