| Tag | Content |
|---|
EnhancerAtlas ID | HS042-11914 |
Organism | Homo sapiens |
Tissue/cell | Fetal_brain |
Coordinate | chr12:133141790-133144060 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP2 | MA0593.1 | chr12:133141980-133141991 | ATGTAAACAAA | + | 6.14 | | Stat6 | MA0520.1 | chr12:133143170-133143185 | GTTTCTCTGGAAGAG | - | 6.54 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr12 | 133142336 | 133142390 | | chr12 | 133142593 | 133142924 |
|
Enhancer Sequence | TTACACAAGT GTTACCAGAA TGCAGTCTCC TTTATACAAA CTTAAAAGTA TGAGTTTAAG 60
CCTAGTCTCT TGTGCCCTCC ACCCCCGCCA TTCCCAGAGG GGACTGCTCT CTCCTGGTGG 120
ACACATTCTA CAATTTCACC AACATAGACG CCGACACGCG GGCACCTACG TAAACACACA 180
TGTGATGCTC ATGTAAACAA ACATCCATGC ACACACTGCC ACCCAGGTAC ACACACCCGA 240
GAATGTGTGT GTCCCTGTAC GTGAACCCGA GTGTGCCCAC GTACACGTAC CCAACTGTCC 300
TCATGTACAC GTACCCGAGT GTGCTCATGT ACACGTACCC GAGTGTGCCC ATGTTCATGT 360
ATCCGTGTGT GTACGTACCC GAGTGTGTGT ATGTGCCTGT GTGTACGTAC TTGAGTTTGT 420
GCCCATGTAC GTGTACCCGA GTGTGTGTAC GTGCCTGAGT GTGTGTACGT GCCCAAGCAC 480
AGGCACATTG TCCAGATCCA CATAACACTC CTTCTTTGCA GTTGCTTCCT CCACACACAG 540
AGTGTCCCCC ATCTCTCCAG GGTACACACT GCAGTGTGGG TGAACGTCAA AAGCCGTGCA 600
GTGAGAGAAG CCAATCACAG TAGGTCCGTG CCGCCTGACA GTGTTCACAT GGAAGTTCGG 660
AAAAGACGGC TCTGTAGAGA CAGACAGATT TGTGGTTTCC CAGGGTTGGG GGTGACGGTT 720
AGGAGTCAGG GTTTCTTTTT GGGGTGATGA TAATGTTCTG TAATGGATCG TGGTGACAGG 780
TGCATCACTG TGAACATACT AAACGCTAGT GAATTGTAAG CGTTAGACGG TGAGTTGGAT 840
GGTATGTGAT TTACATCTCA AGTCTTAGTC CGTGCGGGCT GCTCTGGCCC AGTTCTGCAG 900
CAGACATTCA CAGCTCACAG TGCTGGAGGC CGCAAGCAGG TCAAGGCATG GCAGAGTCCC 960
TGTGAGGGCT TCCTGGTCCA TAGAGGGTGC CTCTCCGCTG CGTCCTCACA TGGTGGAAGG 1020
GGCTAGGTGG CTCTGGGGCC CTTTATAAGG CACTGATGCC GCTCGTGAGG CTCCACACTC 1080
AAGACCTCAT GACCTCATCA CCTTCCACCT CCTGATCCCA TCACCTGGGG GTGAGGATTT 1140
AAACATGTGA ATTCTTGATA GACAGAAACG TTGAATCCAC AACTCAATGA AGCTGTTTAA 1200
TCAAAAAAAA AAAAAAAAGA AGAAGAAGAA ACTAGGAGGG AAATATCTAT TTAAGGTCAT 1260
TCTTATGAAG CTCATTCCTG GAAACTGCCG TGAAGTCCCC CAGAGCATGG GGCCCTCCGT 1320
CCACCCCTCC CCATCAGCGG CCACATTCTC GCCACCTGCT TGTGGCAGGT GGTTGAGCGA 1380
GTTTCTCTGG AAGAGATGGA GGAGTGGGGC TGAGCAATTT CTGCGATTGA CCCTCTGAGA 1440
GCTCCCCCAC ATAGCCTGGG ACACTCAGCT GCCTCTCAGC AACACTGGGC ACCAGGCCTA 1500
GAGCTTGGCC GGCCTGGGAG CATAGCGCAG CATTCTGTGG CTGCTGGGAG CTTGGCCGGC 1560
CGCAGGCACA TAGCGCGGTG TCCTGTGGGC TCTGGGCACC AGGCCTAGAG CTTGGCCAGT 1620
CCCCAGCACA TAATGCAGTG TCCTGTGGGT GCTGGGAGCT CGGCCGACCC CAGGCACATA 1680
GCGCGGTGTC CTGTGGGCGC TGGGCACCAG GCCTGGAGCT CAGCCGGCCC GGGAGCATAG 1740
CGAGGTGCCC TGCAGCCTTG CGGACCCACA TGTCCAGCCT GGTCGGTATC CTGGTTCTCT 1800
CACTTTCGCC AGGGCGCCTG TGCTGGGCAG TGGTTGGGAG CAGGAGGTGT GTCCCGGGGC 1860
TCTCCATCAT CCGCCTCTGG CCTGATGGGT GGGGGCCCAG CAGGGCCCAC AGCTACTGGT 1920
GCTGGTTCTC CTGGGAGGGG TGCAGATTTG CCAAATGCCG GCGCTCCCCC AGTCCACGCC 1980
AGCAGCAGCC TTGGTTCCCG ATCCCCCCAC AAACCCCGTC TTCACTCAGA CCCCCTCTAG 2040
GAAGCCTGCT GCTCTGAGCA GAGAGGGGCC TGTGTGCCCC CAGCGTGAGC ACATGTATAC 2100
ACATGCGTGG AGCTCAGGAC TAAGCGTGTT CACCTCGTAC ACGGGGGCAT CCACAAGGGC 2160
ACATCCCGCC TGGCCCTGCT GGAAAACCAC CCAGACTTGT GTGTGGGCAT TGGGCGCAAG 2220
GTCCACGAGG ATGAGGACCA CCCTGACTGC CCCTGACCCC CCTTCTCTCT 2270
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