| Tag | Content |
|---|
EnhancerAtlas ID | HS150-02885 |
Organism | Homo sapiens |
Tissue/cell | NT2-D1 |
Coordinate | chr12:31129290-31131490 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TFAP2C | MA0524.2 | chr12:31130386-31130398 | TGCCCGGGGGCA | + | 6.02 | | TFAP2C | MA0524.2 | chr12:31130386-31130398 | TGCCCGGGGGCA | - | 6.37 | | ZNF263 | MA0528.1 | chr12:31130546-31130567 | TCCCCCTCTCCGTGCTCCTCC | - | 7.79 |
|
| | 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 |
| GH12I030978 | chr12 | 31131431 | 31132370 |
|
Enhancer Sequence | TGAGCCACGT TTTTCTAATT TGCACCTAAG CACTAGCAGC CATCCAGCTA GAGCCAGCAT 60
GTGGTGGAGC CTGGACCCAA CCCAAGTCCA CTGACATTTC CCCCAGCTTT CCTCAGTGTT 120
TGGGCCCTGC TTCTCAGAGG CTCCTCAAGC AGGAGGACCA TCCACAGACG CTCTCTTCAG 180
CCTCCTGCCT CAGCTTACCC TGCATACCAC TCAGTACCAC ACGCAGACCC AGGCCCCTGT 240
CCTGAGGCCC CCTTCAACCA CACTCCTCCC CAGGGAGTGG AAAGTCCGTA GGGCAGAGGG 300
AACATCCCCT TGTGGAATCT GCAACTCCCT CCCGCCACTT CCTGACCTCC TCCCAGGGAC 360
CCAGGAGAGT GAATCCTCTG TCCAGACAAC CTGTGCCTGC AGGCAGCATC TGCAAGCATG 420
TCCTGAGGCT GACTAGACCC CTGGCATATG TGCCCCTAGC CTGCACCACA CCCAGCCCTC 480
TCCACACACC TCCCATCCCG CAAGGGGCAT CTGACCCTGG GGGAGGGGCA CACAGAGCTG 540
GAGGTTTTTC CTGATGCAGC GAAGAGCCTG GGGTAGGAAA GGAAGGGGCA GGGACCTTGC 600
ATTTGTGCTC TTGGCCTCAG GCCCCACAAA TGATGGGGCT AGGCCTGACA CTGTTATTCT 660
GAGACTGGAA ACTCTGTGTC CCTGATGCTG GGAGCCTATA GGACACAGTA AAATTGCAAT 720
GAGGAGGTGG GTAATGCACT TCATTTGAAA GGAAACCTTG CTCTTGGACC ACAGTTCTTT 780
TCCTGTGAAA AGAAATGGCC CCTCTCCCGT ATTCCTTAAT CCCTGCCCAT GCCAGGCTCC 840
CTGCTGAGTC GTGCAGGAGA TGGTTGGGCA AGGCCCATGG GCCCATGGAT TAGCATTGCC 900
TCTGAAATGC TCTGTCTATC CTGGGCACCG CCCCCGCTCC GCCGCCACCC GCCACCGTAT 960
CCCCCCTGCC CACACTCCTT TCCCTGCTGG GTGAGCCCTA GAGTCTCAGT CTCACCCACA 1020
GGCTGGGCCT TCCCTAGAAT CCAGCCATCC CAGTGACCAC GGGTAGCTGC CCTGCTGTGG 1080
CCAGGTGGGC GGGCAGTGCC CGGGGGCAGC CTGGGTGGCA GGTGCTCATG AGTCTGGCTG 1140
AGCTTCCCCA CAGTGGGGCC AATTTCCATC AGTAGTGCTC CCCCTCTCTC CTCTCTTCTC 1200
TATTCTCTCT CCTTGTCCCT GTCTGTGAGC TCCGTGGCTG CCTGTAGCCA GCTTCATCCC 1260
CCTCTCCGTG CTCCTCCAGG GTGGGGAGAG AGGGAGTCCC AACATGCCTT CTAGGCCTGT 1320
TGGCTCCTGC AAGCAGAGTT GGTCGAGCAG GGTCTCAGGA GCCCTCCTGA CTGTGCAAGC 1380
CAGGTGGGAG TGAGAAGGAA GCAGGGCCCA TGTCCTTCTA CAGGTCACAC TGAATGCACG 1440
GCTGGGAAGC CAGCAGCAGC AACAGGGCTG TGAGGTGGGA GAAGCAGTAA TGAGAACCCC 1500
TGCAGGGCCA TGTAGAACAG GAAATGGGCA TCAGGGCTGA AAGACAACAC AGGAATCACC 1560
TTCCCCTGGA CCTCTGATTT GCTTTTTCCT GAGCCTTGGT TGTCACAGTC CACGCTGGTC 1620
CCTGCATTCC AACTACAAGG GCACTCTCCA CTCCCTGAAC ACAAATGCCC CATGCTTCCT 1680
GCAGGCTCCA GGCTTTTCAC TTGTTCTCCC CTCTTCCTGG AATGTGCCTC CCTCCTTCAC 1740
TTAGCAAATG CCTATTCAGT CCTTAAAGAT GTTACTTAGG CGTCACCACC TCCAGGAAGC 1800
CTTCTCTGAC TGCCCACCCT ACCAGGAGCC TCCCACCATT TCTAGAGCTT ACCCTGTAGT 1860
TGCATTTGTA ACACAGCATT GCAGTCACTC ATCTGTCTTC CCACCATCAA TAACTTTGAG 1920
AGCAATAGTT GTCTTACTTA CGCTACCTGG CATCTGGCAT ATGGCATGTA TTTAATACAT 1980
ATTGGATGGG TACATGCCGT ACTGAATTGT CAGCAGACCA AAGAGGGAAG GAGTAAGTGG 2040
GGAACTTGGT GCCAGCAGCC AGTGAGGCTG GTACATCCAG GAGGAAGATG GCATGGATGA 2100
TAGGGGTCCC AGCAGGTATC TCTACCACCC CCACCACTGT GGGGAAACAT TTGTCATAGC 2160
AGCAACCCGA TCCCAGTGGT GACCGTCCTC TCTCTTTGCT 2200
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