| Tag | Content |
|---|
EnhancerAtlas ID | HS184-25534 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr5:179598690-179600610 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2A | MA0052.3 | chr5:179599089-179599101 | GCTATAAATAGA | + | 6.62 | | MEF2B | MA0660.1 | chr5:179599089-179599101 | GCTATAAATAGA | + | 6.52 | | SOX10 | MA0442.2 | chr5:179598765-179598776 | TGCTTTGTTTT | - | 6.02 | | TFAP2A | MA0003.3 | chr5:179599644-179599655 | TGCCTGAGGCT | - | 6.32 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr5 | 179600051 | 179600423 | | chr5 | 179599206 | 179599298 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH05I180172 | chr5 | 179599066 | 179602192 |
|
Enhancer Sequence | GGCGTGTGTC ACCCACACCT CCTGACAAAC ACCCTTCGGC ACTCTGGAGA ACAGCGAATG 60
CGTAGCAAAA ATAAATGCTT TGTTTTCTCC CTGCGGCTTC TGGGAGTCAA TTCAAAGAGT 120
GGTCTTGGGA GGTAAGGCTG TGAGGGCCAG GACCTGCTCG GCAGCCAGGG TGTGGGCCCA 180
CTGGGGTCTC CTCCGCTGCC TGGCTGTGGG GCGGGCCCCT CAGCTGTCGG ACCTCAGCTT 240
CCACATCTGT AAAGTGGGCT CACGAGACCC ATGCTATAGG TGGGCCTACT GGGTTAGGGG 300
TGGGGTCAGT GGGTGCACTA AAGGCCGACA CCCGCAAGGA ATCTGCACTT CTACCCTTAC 360
ATTCATAGGA ATAAAAATAG TGTTTAAAAA GTCTCAATAG CTATAAATAG ATCTGTGTGT 420
TCTGCCCTGC CCATCTACCC TGTCCGATTC ACCTAAAGGT AGGCCAGGCA GGACGGGCAG 480
GGCCACCTTC CCTGTGATGA GAGCACAGTG GGCAACAGCA GCCACTGGGT GTCCCAAGCC 540
TGCCTGAGCA CTCAGGGCCC CAGCATGCCC AGATGGCTGG TGGTCCCTCC CACCTGCTCC 600
CCCAGCCCTT AGATGCCACC TCCAGGAAGG CTCCCATGCC TCCTCCTAGG CAGGAACGGC 660
CACCTGGCCT GGGATGCCCA GCTCTCTACT GCTGCGTGTG TTCCCCTGGC CTCTCTCCTG 720
CATGTGACCA GGGCCCAGGG GTCATGAGGC AGCCAAGGAA ATGAGGGCTG AGGGGCAGAG 780
GGACAGGGGG CACAGCAGCC TGACACGGAA TCTGTGGCAC ACTCCACTCC AGATGCTGCC 840
TGCCCGCCAC TTCTCTCAGA CCCTCCCACA AAGCCTAGCC CCGGGTGTCT GCCAGGGCCT 900
TCCAGCCCCA GCTGGCAAAG AGCCAGGTCT GTACTGTCCT TTCTCCAGAA TCTCTGCCTG 960
AGGCTCCACC CCAGAGCTTC GGGCTCCCAG CCCTTCTCTC ACGCCCAGCT CCCCAAGAGG 1020
GGAGGCCAGG CCACCTCTGC CACCTGCTCC CCACCTCCCT GGGCTCCTCT GTGCTCCTCA 1080
TCTCTGTGCC CCCTGCCTCC TGTACTCCCT GCCACCCTGC GCTTCTCACC TCCCTTGTCC 1140
TCTGCCTCCC TGTGCTCCTC ACCTCCCTGT GCCTCTCCCT GTGCTCCCGC CTCCATGCCT 1200
TTGCCCATGC TCTATCCTCT TCTGGGTTGC CCTTTCCTGC CAGTCTGCCA GCTGAGGCCC 1260
TGAGGGTCAA TGCATCTTCC TTTCCTCTGC CCCAACCTGA CCCTGGCAGC TGAGCACAGC 1320
CCTTGGGGCC CTTCTGTCCC CTGGCAGGAC CTGCGGCACC CTGCCTGGCT CTCCTGCCTG 1380
CTCCAGTTAA GTCACCTGCA GTTGACAAGC CGCCTGGGTG TCCTGCATGG GTTGCATAAT 1440
GCCCTTTTAG ACTGCGAATT TACTGGCCTT ATTTACACAC TGGGGCCTTT CAGGAGAATC 1500
AGTGCGTCTG CTTTCCTGCA AAAACTCAGA AGAGCCAGCT ACACAGGGCC TGCATTCCTG 1560
CCTGGTACTG TTTGTTGGCC AGAACCAAGG GCTGCCCCTC GACCTGGGGA TGCCACCACC 1620
TCACTGTCTC CGTCACCTGC TCCCTCTGCC CCACCTAAGC CTGCCACCCG GTTTCCAGAC 1680
CAAAGCCTCT GTGGCTGCCC AGGGTGTAGG CCATGAAGGG GACCCTGAGG TGGGGAAGGC 1740
AGATCCCACA CTGACTACAG CTGTCTAAGC AGAAGCAGCT ATGTGGACGT CACTCCCTGG 1800
GGCCATTTCC TTCTAGCTGG AGATGTATCT GTCAAGGTCT GGAAAATCTT AAATGACAGA 1860
GAAATAAGAA TTGAAAGAGA AAAGAATTTC ATTTCTCCCC TAAATTTCAA ATTTGGGGGA 1920
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