| Tag | Content |
|---|
EnhancerAtlas ID | HS060-10747 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr14:95050780-95053420 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR1 | MA0112.3 | chr14:95051102-95051119 | CAGCTCAGTGTGACCCT | - | 6.1 | | INSM1 | MA0155.1 | chr14:95050883-95050895 | TGGCAGGGGGCG | + | 6.07 | | SP1 | MA0079.4 | chr14:95050887-95050902 | AGGGGGCGGGGTCTT | - | 6.21 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr14 | 95051064 | 95051267 | | chr14 | 95051288 | 95051671 | | chr14 | 95053234 | 95053306 |
|
Enhancer Sequence | CCAGGAGAGC CTAAGTGAAC CTGGGGCCCT CTCCAAACAG ATCCTGGGGG AGACTCAGTG 60
CACACCCGGA GAAGCAGCTC CTCCCCATCG GATCTCTAGT GCTTGGCAGG GGGCGGGGTC 120
TTGAGGGGGT GTCCACAACA CATGGCAGAC TGCAGATGAA GAAACTGAGG CCCAGAGGGG 180
GTGAGGCTTG CCCAGGGTGA CCTAGTAGCT GAATAGATGG GAGAATGGAG GCCAGGGCCT 240
CACTGAGACT CTCTGGTCAG CTGCCCCTGG GCTGTATCCA ATAAGGAAAC TCCCCTGCTT 300
CTGAAGCTGT TCTCGAAATT ATCAGCTCAG TGTGACCCTG TGGGGGGTTG AGCCACATTG 360
TTTCTTTAGA AGCATCTCCA TACATGGCTG GTTCCAACCC TTGGCAGGAG GGACCATATT 420
GTGCTGTAAA ATAGACTCAT TTAGAGAAGC CGGAGATTAA AGCACCCACC TATGTCCTTC 480
AAAGCTCTCC AGGCAAGTGC CATGGTGGGA ACAGGTAGGG AGTGTCAGTG GGGGGAAGCC 540
CAGACTCTGC TCACTCATTA TCTGCAGATT AGGGCTATTG TTGGTGGCTA CTAAGTCAGG 600
GATTTCAAAA TCAGGAAGAT GCAGCCAGGA AAAGAGGAGG CAGGACTCTG CAGAGGAGGC 660
AGGACTCTGC AGAGTCAGAG TGATAACCGA GTCTGAGTCC AAGCTTTGCC AGTGTTAGCA 720
AGCGACTCCA TCTCTCTGAA CCTCGGATTA CCCATCTGTA AAATAGAGCT AGCAGCAAGA 780
TGTACCTTTT TGGGTGGTGC AGGGCTGAAG GAGTTGGCAC AGTGCCTGAA AGAGGGTGCG 840
GGCAATGCGC CCAACTGCTG TGGCTGCTGG GTTTGGTGCC AGGTTCGATT CTGCAGGCAG 900
AAACTTCTAC ATGAGGCTCC TTCTCGGAAG GAGCTCAGGA CACAATTTGG AGGCTGGGCT 960
GGCAAGGGTG ACCTGCTGGA GCTATTCAAC TTCACTTAAA GACAGGCCTG CAGTCCAAGC 1020
CTGCCCAATT CCTGAGACCA TTCTCTCTCC ACTGCTGAGC CCCACGGCCA CTCTGCAAGG 1080
GATTTCCCAC CCACCTGTTT GGGGCCCTTT GGAGTTTGGT TTTAATTGGG TCACGGGATG 1140
CTGTGACAGG CTGCCCCTGC CTGGTGGGGA TCTGGGGTCA CTGATGACAT TGTGCCCATG 1200
GAGAGAGCCC AGCAGAAAGG GATTCCCTCC AAGGCGACAC ACAGGGCAAA GCTCACATCA 1260
GAAGCCAGGC AGGCCCTCTG CACCTGGTAA TTAGCCAGCC TGGGTGCTGT CAGGCTCACA 1320
CGTGTGTGTG TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG TAAAGCATGT ACCCTATGGT 1380
ACAGTTGAGA ATATGGAGGC CTCAGATGGG GCTTTTGCCA GAAACTGCCA TGCCTACTGC 1440
TCACACTTCC ATAGCACGTG CCCCCAAGCA CCCCATGGTG TAGGTGCTGT TATTATCACT 1500
ATCTTACAGT TATGGAGCAG TGGCTCAAGG TGTAACTGAC TTGCCCAAAA TCACACTACA 1560
AGGACACAGC AGGGCTGAGA TTTGAACCCA GGCAGTGGCT TCAGAGCCTG AGCTGTTTCC 1620
TACTGCAGAG GGAGGAGGCA AGACTTCTAC CCGTAGCCAG ATGGGGAGGC ATGGGCACAG 1680
GAACGGCTCT TGGGTGAAGT GGAGGGAGGA AGAGGAGGAC TGAAGGCCAA GGCCACGTCA 1740
GGAGTGATGG GAGACCCCAC AAAGGCCTCC CTGAGAAGAG CTAGAGACAA AGATGAGTGC 1800
CTCCTCATCT GGAAGATGAA AAGATGTCTT TGCCTGCATG GGCTGCTGTC ACAAAGTCCC 1860
AGGGGCTAGG GGGCTTCAAC AACAGAAATT TCTTTCTTTA CAACTCTGGA AGCTGGAAGT 1920
CTGAGATTAA GGCACCAGCA GGATTTGTTC CTTCCAAGGC CCCTCTCCTT GGCTCACAGG 1980
TGGCTGCCTT CTCCCTGTCT TCACCTGGTC TTCCCTCTGT GCATGTCTCT ATCCTGATCT 2040
CCTCTTTTTA ATTTTTGTGT AAGGACGTAG TCATATTGGG TTGGGGCCCA CTCTAGTGAC 2100
CTCATTCTAA CTCAGTCCCC TCTTTAAAAG CCCTATCTCC AGATATAGTC ACATTCTGGG 2160
GTATTGAAGG TAAGGACTTC AGCATATGCA TTTTGGGGGC ACAATTCAGC CAGAACAGGA 2220
GGACGGTGGG GATGTCCACA TGAAGAGGTT CAGGCAGAAT TCCTTTAGGA GGGGAAGATG 2280
TCTCTCTGTG GGACAAGGGT GGCATGGAGC AGCCCCTGGG GGAAGGAGAA GGGGACAGTT 2340
TGCATACTGG TATTCTGCCT ACCCCAGGGT GGACACTCAC TCAGCGTTTG CTGAATGAAC 2400
AGGGCAAGGC CAGCAGTGCT GATGGTCCCA GGCATGTAGC TGGTCTGAGT TCATAGAAGG 2460
ACCACAGCGC CCTGCCATGT GCCAAACCAG GACACCAGAG TGAAGGCCAG AAGCTCACAT 2520
GGAAGCAGCT TAGTTCCCTG GTAACCTCGA GATGCTGATG AGACAGAGCA GAGCAGAGGG 2580
AACCCTCTCC CTCCATATCC CATCCTCCAA AATGTGTCCC TTGATGTGGA TGGGTAGACA 2640
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