Tag | Content |
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EnhancerAtlas ID | HS138-13555 |
Organism | Homo sapiens |
Tissue/cell | MSC_BM |
Coordinate | chr15:41550790-41552420 |
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) |
Nr2f6(var.2) | MA0728.1 | chr15:41552146-41552161 | TGAACTCTTGACCTC | - | 7.64 |
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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 |
GH15I041259 | chr15 | 41550594 | 41552606 |
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Enhancer Sequence | TTGTTCTTAA TGTGGGTTTT TCTAACATGA AACTAGTCTT TTGATATGCT TTACTACCTA 60 ATACACTGCC TTCACAGTAG TGAGTAAATA TTTACTGATT TGATTAGGTA CCTTTTCAAC 120 AATAAAACTT ACATATAAGC TTGTTTTAAG TAATTTCCTA AACAATCTAT TCCTGGTTTA 180 TATGGATAGT CTATGACCCA CAGGACTTCA AAATATTATA TGGGTGCCAG TTTTTAATAA 240 TGAGACTGTC AATGAGGACA CTGTCAGATA AAATGCCTGG AGAGGAAATT TTAGAACTCT 300 AAATTGAGAG CAAAGGAATT TGCTAGTTGA GAGGGTTGGG CATTCAGGAA ATGTGAGTGA 360 AAGTCAGAAG GGGAATTAGG TCGGGCAGTT AGTTCATGTA AAGATGGGAA TCAAATCACG 420 TTGACTATGA GGAATCTTAT GCCCTCTTTC ATTTTTTCCT TTCTCTCTCC TTGAACTGCC 480 CTGTTTGTTT CAGGTGTGGT TTTTATGCTG AATTCTTCCT TTTTTCTAAT TCCTCTTTTA 540 CCCCTGCAAA GCATTGAACC CTATCCAGAG ATAACTTTCA CAGCTATGCT TTGTATCCAA 600 ACCTTTTGCA ATGAAAAGTA AACCCAGGAG AGTCACTTTG CCAACTTTTT TTCAGAATTC 660 CTTAGTCACC ATTGATTACT TGAAGAAGCA GCTTGTGGGA AGCTGTTTTG TAAGACTAAA 720 CTACATTTGC TGTGACTACA ATATCACCTG TCATTCTGTC CACCAATCTA CTGCTAAGGA 780 AATGGGACAG AGTGCATATG AGGAAGTGGA GGGCTCTACT GGGCTGCACT GCTTAGCTCT 840 TAGCAAGCTG CGACTCTGCT TCTTGCTCTA ATCAGATAGA TATATTTGGC TTCTGGGTTT 900 TTCTTTCTTC CCTAGGCATA TGCACATTGG GGCTTTTTTT TTTTTTTTTT TAAAGAATGA 960 GATTTGAAAG TGGACCATGG TTATTCAATT CCCTTTTACC CAGAAACTTT ATGCTAGCAA 1020 TAATCATTAA TGTGTTTTTT CTAGCATATG TTTTAAACTT TACTCCACAT TACTTGATTC 1080 CTCAGATCTG ACATTTTTGA CCAGATACTG GTCCATTAGC AGTATAGATA CATCGAAGAA 1140 CTAAAAGGTC ATTCTTTTGT TTTGTTTTTT GTTTTTTTGA GACGGAGTCT CCCTCTGTCT 1200 CCCAGGCTGG CATGCAGTGG TGTGATCTTG GCTCACCGCA ACCTCTGCCT CCTGGGTTCG 1260 AGTGATTCTC CTGCCTCAGC CTCCCCAAGT AGCTGGGACT ACAGGCTCAC GCCACCACGC 1320 CTGGCTAAGG TTTCACCACG TTGGCCAGGC TGGTTTTGAA CTCTTGACCT CAGGTGATCC 1380 GCCCGCCCCG GCCTCCCAGA GTGCTGGGAT TATGGGCGTG AGCCACTGCA CCCAGCCAAG 1440 GTCATTCTTT TGAGTACAGA TGGCTCACAG GCTAGCCTTT GAACTCTGCC TTTAGAAGGG 1500 CTATGAACTG CATGTCTATA GAGCACAGAA GAGAACCTAC ATACCTCAGC TATTCGGTGG 1560 GGCACAGAAA GGCTGGGGTT TTTTTTTTTT TTAGGTAACC ACAGGAACCA GGCCATCTGC 1620 CTTAGATAAA 1630
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