Tag | Content |
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EnhancerAtlas ID | HS060-14277 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr17:18078960-18080390 |
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) |
NR2F1 | MA0017.2 | chr17:18079156-18079169 | CCCATGACCTTTG | - | 6.48 | ZNF263 | MA0528.1 | chr17:18079171-18079192 | GCCTCCTCTCCCACCTCCCCC | - | 6.64 |
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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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Enhancer Sequence | CTGTCTGATA CTGAGGCTTT CAAAACCATG TCTACCATCA CAGCATCCAT ACTTCTACCT 60 CCTGCCCAGA CTACCTGAGC TCCAGGCTCC CTCAGCATCC CCCTTGGAGA CCAACAGTCC 120 TCTCCAGCTT TCCTCCCGAT CCTCCCAGGC ACTCAGGCCC CAAATCTGGG AGTCCTTCCC 180 ATCCCTGTCC CTTCCTCCCA TGACCTTTGT GGCCTCCTCT CCCACCTCCC CCATCTCTGC 240 TCATTCCTCC AGCCACCCTG GCTCCCTTGT GCTGAGCTTG TTCTCCCTGC CCTGGGCCCT 300 CTGCCCTCAC TGTCCTCTCC ACCTGGAATG CTCTTCCTTG ATCCATCACA GGGCCCATTC 360 TCTCCCTTTA TTTGGGTTTC AGCACAAATA TCACCTTTTT CTAGAAGCTT TCCCTAACCT 420 TCCTCCCTAA GAACTCACGA TCCCTGCCCC CATAGCCCTA CTTATGGCTT GGAAATCATT 480 TAGTTATTTG TTTATGTATT GTCTCCTTAT ATTAGTCTGT TTTACGTTGC TATAAAGGAA 540 TATCCGAGGC TGCATAATTT ACAAAGAAAA GAGGTTTATC TGGCTCACGG TTCTGCAGGC 600 TGTGCAAGAA GCGTGGCACC AGCATCTGCT TGGCTTCTGT GGAGGCCTCA CGAAGCTTTT 660 ACTCAAGGCA GGAGGCAAAG GGGAAGCAGG CACATCACGT GGCAAGAGAG GGAACAAGAG 720 AGAGAGGGCC CAAACAGCCG TCTCTCGTGT GAACTATTAG AGTGAGGACT CACTCATTAC 780 CTTGGGTAAC CAAGCCATTC ATGAGGGATT TGCCTCCATG ACCCAACACC TCCCACCAGG 840 CCCTGTCTCC AACATTGGGG ATCACATTTC TTCTCTTTTC TTTTTTTTAC TTTTCTTTTT 900 TTTTTTTTTT TTTTTTTTAC TACAGTGTCT TGCTCTGTTG CCTAGGCTGG AGTAATCTCG 960 GCTCACTACA ACCTCTGCTT CCCCAGTTCA AGTGATTCTT CTGCCTCAGC CTCCCAAATA 1020 CCGGGATTAC AGGCATGTGC CACCATGCCC GGCTATTTTT TTGTATTTTA GTAGAGACGG 1080 GGTTTCACCA TGTTGGCCAG GCTGGTCTCA AACTCCTGGC CTCAAGTGAT CCACCCGCCT 1140 TGGCCTCCCA AAGTGCCGGA ATTACAGGCA TGAGCCACCA TGCCTGGCTG GGCATCACAT 1200 TTCAACACAA GATTTAGAAG GGACAAATAT CCAAACTGTA TCATTCCCCC ATCAGAATGT 1260 CAGCTCCAAG AGAGCAGGAC CGTATCCATC TTGTTCATGC TGTGTCCATA ACTCAGCGCC 1320 TGGCACATAG TAGATGCTCC ATACATATTT GTTGGTTGCA TGGGTGGGTG GGTGGATAGA 1380 TGGATGGATG AAGGCCTCTT TGCTTTTCCC ACTTCCTTGC AGCACCACCT 1430
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