| Tag | Content |
|---|
EnhancerAtlas ID | HS088-14407 |
Organism | Homo sapiens |
Tissue/cell | HeLa-S3 |
Coordinate | chr12:109981890-109984020 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF16 | MA0741.1 | chr12:109982188-109982199 | GGGGGCGGGGC | - | 6.02 | | KLF5 | MA0599.1 | chr12:109982189-109982199 | GGGGCGGGGC | - | 6.02 | | Myod1 | MA0499.1 | chr12:109983668-109983681 | AGCAGCTGCCCCC | + | 6.03 | | SP1 | MA0079.4 | chr12:109982187-109982202 | GGGGGGCGGGGCTTC | - | 6.7 | | SP2 | MA0516.2 | chr12:109982186-109982203 | CGGGGGGCGGGGCTTCT | - | 6.7 | | SP4 | MA0685.1 | chr12:109982185-109982202 | GCGGGGGGCGGGGCTTC | - | 6.29 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr12 | 109981986 | 109982143 | | chr12 | 109982738 | 109983404 | | chr12 | 109982284 | 109982334 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I109544 | chr12 | 109982612 | 109983475 |
|
Enhancer Sequence | AAGAAGAGAG CGAGCTGGTT CTTCTGGCCC CAGCAATAAC AACAAAACAA CCTGGAGTAT 60
GGTCCCTGCA GCCCTTCCCA GACACAGAGT TCTCATTCTC CAAACGTGGA CATCCGGAGG 120
GACACACGGC CTTACGTGGC CACCAGCAGG CCATGGACGG ACATTGCCCA GCCCACGTTG 180
CTGCCACAGG TGGACACTCA GAGCGAGAGA GAGGGAAGTT GGGGTGCTGG TGGGAATGGG 240
TGTGGACTGG AATGTTCTAG AGGTATGGGG GGCCTGAGAC ATCTTGTGAA GTGGGGCGGG 300
GGGCGGGGCT TCTCCATGAG GCCAAAGGTG AGCAGGCCTC TGGGTGTTTC AGAAGAACTG 360
CCCTGGCAAC ATGCAAGTAC AGTTCTAGCA GAGACGCCAA ATCAACTGTC AAAACCGAGC 420
CACTGCCACC CCACAAAGCC AGGAAAAGCT TCTAACTGAC AATCTTGGGT AAGTCGGCCC 480
TCAGCCTCTG CATCTCCCAC CACAGACCAA GGCTCCCAGA TCCCCCCAGC CCATGCACTC 540
CATGTGGTCC CCTCTGTGTG CCTGGATACA TCGGGACTCT TGGGTGTCAC TGGGGATTCC 600
TGCCCTGCCA CATGGGGTAA GCTACTGGTA ATTACTCAGC TGTGGGAGCT CCTGGTCATC 660
AGCCTTCAAA CACAGAAACT CAGGTATTTT TCCCAGCAGA CCCTGACCAG CCTCTGTATT 720
TCTCCATAAC GCTGGTCGGC TGGGCACAGC GATCTTGGCA ACAGATTTTG CGAAATAAAC 780
TTGGTCAGTG GATCCCAGTC AACAAAATGT TTTTCCATCT GTTACCCACT TCCTCCTGCC 840
TGTGAAGGGG CAGTGCTCTC TCCTTCTTAT AGGTGAGGCT CTGAGAGGTG GAGTGAGTGA 900
CTTGCCCAGG GACTCAAAGC CAGGATATGA GGAACTGGGA TGTAAGCCCA AGCCTTTGAC 960
CAGGAAGGTG ACCTCACTCA CTCACTTGCC TTCCCTGATC GTCAGAGGCC TGGACAGAAG 1020
CCTTCTGTCT CCCAGAGGGG CTAGTCCCAC TGACTCTCCT GACCTGCTCC CATCCCACTA 1080
GGGACACTGT CCAGGGGAGG GAGCACACCC CATGTGGGGC TTGGTGTGAA GTCTGCTGGG 1140
TGGCTTTGTC ACATTGCAGA TGGTGCCAGA TGAGCCGGGC CCCGCCCAGG AAGCCAGACT 1200
GCCAGGGAGT TCAGACTCAG CCAACAAACA GACCCACAGG GCCTCCTGTG CCCCAGGCTG 1260
GGTGCTGAGT TACAGCCGTG CACACGGTGG ACGTGATCCC TGCCCTACAG AGCTCACTCT 1320
CTGGTGGGAA AGAGTCAGAA CTAATTCAAG GAGGAGGTGT ATGGCCACAT CCTGTGATCA 1380
GCGTCCCTGG CATCTAGTGC TGTGCTATTC TGATGCCCAC TCAAGTGGGG AAAGCTGAGG 1440
TCAGGAGCTG GTCATTCCCA TGCCCAAGGC CCCAGAGTCA GTTAAGTGGC AGAGCCAGGA 1500
TTCAAACCCT GGTCTGCCAC ACTCCAGAGC CCTCACTCGG TTTGAGCAGG CAGAAGAGGG 1560
GTGGGAGAAC ATTCTAGGCA AAGGGCTCAG CTTGAGCCAA GCCCCAGGGG CTGCTCTGTC 1620
CCTTATCTGG AGCCCGCTGC CTCCACTGCT TGTCCCACTT ACCCTTGCCG GGGATGCTGC 1680
AAACTGACAG ACACACCCAT TTTGCCAGTG AGTTCCCACA GCATTTTAAA GGACTTCTTC 1740
AGGACCCTAG AGCCCTGGTC TCCCCAAGGC TGCAGAGCAG CAGCTGCCCC CCAGGCACAG 1800
AGCTGAAAGG CAGAGCTGGA TTTCAGGGTG TGCTGAGTAA AGGGCCGATC TACCCTGCAC 1860
TTTGGAAGCT CACCGGGTAG AGGGAGGCCA GAGGAATTTC AGGGACTCCA CGACTTCCTT 1920
AGCTTATCAT TCATGTCCCA ACAGGCTGCA GCCTGTCTCC CTACCAGCTA AGGCAGAGTT 1980
GCAAGTGGGA CAGAATCAGT GCCCACTCCA AACATGGCTC CTTGGCTGCA TCTGGGAACG 2040
GGTTCCATTA GGTGGTGTGT GGAGGGTCTC AAACATCTTA ACAGTGATGG TGAATGCGCC 2100
AGTGCCTCTG CAGCAGGGGC CAGAGTTCCT 2130
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