Tag | Content |
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EnhancerAtlas ID | HS176-32096 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr5:92413640-92415120 |
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 |
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| Number: 1 | ID | Chromosome | Start | End |
GH05I093076 | chr5 | 92412575 | 92416893 |
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Enhancer Sequence | CACATAGTGA ATTTTTAAAC TGAGATGCTT ATTCTATTTC ATTATAATGT GTAAACTGTT 60 ACTTTATACT CAACTACCCT GAGGTAAATT GAAGATGGGT ATACAAAATG AAACTATTCC 120 TCTAATAAAA TCACTGACAT GTTAAGAGGG TTCCCATTTT AGTTATTTAT GCTGTTTTCT 180 TTCATTTTTA AAGATGACAC TACCCTTTAT TACACATTCT GAATGTGTGT GTTATACTTG 240 TACGACACAT TTTCTTTCCA TGACCCATTA AAGTAGCATA ATGCTTTCTA TATTCATGCA 300 TCTCTTAGCA CACAACCTAT GGTTTTAAAT ATTTTTGCAT TCTTTCTCAG AAGGGAAAAA 360 AATGGGTTTC ATAGTGAAAG AAAAAACTTG GCCAATTATG TCATTTTTAT CTCATTTTCA 420 GTTTCGACCT AGCATTATCT TAGGCTTAGT AGTAACAAAT GATAAAATGA CAAATAAATT 480 CTGACATTCT CTGCATAATC TACATTCTTG GCCATCGAAT CTTCATTTTA CCAGCCTCTT 540 AAGAAATGTT TAAGAAAAAG AAAAAAGAAA ACCTCAAACA TGACTGCCAA TCTAACCCAT 600 TCCATTCTGT GTGTCATGCT GCCGAAGCAG CACTTGGAAT CTAGAAGTAC CAAGTGCCAC 660 AATTCGTCTC CTTGTGACTC ATGGCACCAG ATGACAAGCA ATCCTCTGTC CTTCAGCAGC 720 ACCAGAAACA GTGGAGGATC CGTGTGGGTG TTCACAGCGT TGTGAATAGA TCTAGTGGGA 780 GGCAAGAGTC CAAGGCTCAG GCTTCCTGCA CGTACCACCA TCCTGACAGA TGGCATATTC 840 TTGGCCAGAA TCCAAGGACC TTGGTCACCG AGTGAACTTT CCCTGACTCT GTGCTATGTC 900 GATATCCCAG ACACACAGGG ACACAGGCCT TGCTTATGAA TCATTCTGCT AGAAGCTGCC 960 TCTATGTGTG TTTTCTGAAT GAATGTTCAT AAAGGTATTT TGCCTAAACC AAGTAAGACT 1020 GTTCAGCACT TTGTCACACA ATTACCGTGG GTTGTATCAA CACAGAAAGT GTGTTTTATA 1080 ATTTAGTCAT AATGAATTTT TTGACCCATA AATCAATAAA CCTGTTACAG ACTGAATAAT 1140 AATATTTGCT TCCTGAAAGC ATGTATGATA TCAACAAGGT CGCAGTTTAC TGTCATTTTT 1200 AATAGGGAGA AAAAATCTGT ACTCAAGGGG CATTTAACAT ATTTTGACAA GGTGACCCAC 1260 AATTATCCAT TAACACTGTA TTTGTCTAAG CCCTACTGCA TTGATATGCA GGGACCATGT 1320 AATAGTTCAT TGATGTCCCA CTTGGGGGTG GAGCATAAGG CAAGTGGGAC CTTTCCAAGG 1380 TCTTTCACAG CCAGAATGCA TCTTGCTATT GCTGTATTGA TTAAACATTT GGATAGTTAA 1440 TCAAAACAGC TCAGCCCTGT TAACCTGCCA CGTGCAGTAT 1480
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