Tag | Content |
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EnhancerAtlas ID | HS177-18067 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH_RA |
Coordinate | chr5:92414050-92415120 |
Target genes | |
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) |
ONECUT3 | MA0757.1 | chr5:92414746-92414760 | CATAAATCAATAAA | + | 6.17 |
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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 |
GH05I093076 | chr5 | 92412575 | 92416893 |
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Enhancer Sequence | CTCATTTTCA GTTTCGACCT AGCATTATCT TAGGCTTAGT AGTAACAAAT GATAAAATGA 60 CAAATAAATT CTGACATTCT CTGCATAATC TACATTCTTG GCCATCGAAT CTTCATTTTA 120 CCAGCCTCTT AAGAAATGTT TAAGAAAAAG AAAAAAGAAA ACCTCAAACA TGACTGCCAA 180 TCTAACCCAT TCCATTCTGT GTGTCATGCT GCCGAAGCAG CACTTGGAAT CTAGAAGTAC 240 CAAGTGCCAC AATTCGTCTC CTTGTGACTC ATGGCACCAG ATGACAAGCA ATCCTCTGTC 300 CTTCAGCAGC ACCAGAAACA GTGGAGGATC CGTGTGGGTG TTCACAGCGT TGTGAATAGA 360 TCTAGTGGGA GGCAAGAGTC CAAGGCTCAG GCTTCCTGCA CGTACCACCA TCCTGACAGA 420 TGGCATATTC TTGGCCAGAA TCCAAGGACC TTGGTCACCG AGTGAACTTT CCCTGACTCT 480 GTGCTATGTC GATATCCCAG ACACACAGGG ACACAGGCCT TGCTTATGAA TCATTCTGCT 540 AGAAGCTGCC TCTATGTGTG TTTTCTGAAT GAATGTTCAT AAAGGTATTT TGCCTAAACC 600 AAGTAAGACT GTTCAGCACT TTGTCACACA ATTACCGTGG GTTGTATCAA CACAGAAAGT 660 GTGTTTTATA ATTTAGTCAT AATGAATTTT TTGACCCATA AATCAATAAA CCTGTTACAG 720 ACTGAATAAT AATATTTGCT TCCTGAAAGC ATGTATGATA TCAACAAGGT CGCAGTTTAC 780 TGTCATTTTT AATAGGGAGA AAAAATCTGT ACTCAAGGGG CATTTAACAT ATTTTGACAA 840 GGTGACCCAC AATTATCCAT TAACACTGTA TTTGTCTAAG CCCTACTGCA TTGATATGCA 900 GGGACCATGT AATAGTTCAT TGATGTCCCA CTTGGGGGTG GAGCATAAGG CAAGTGGGAC 960 CTTTCCAAGG TCTTTCACAG CCAGAATGCA TCTTGCTATT GCTGTATTGA TTAAACATTT 1020 GGATAGTTAA TCAAAACAGC TCAGCCCTGT TAACCTGCCA CGTGCAGTAT 1070
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