| Tag | Content |
|---|
EnhancerAtlas ID | HS105-72198 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr7:2102960-2105210 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TFAP2A | MA0003.3 | chr7:2103809-2103820 | AGCCTCAGGCA | + | 6.32 |
|
| | 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 |
| GH07I002063 | chr7 | 2102701 | 2104316 |
|
Enhancer Sequence | CCAGGCTGTG CCGGATCCCA GGACTTAAAC AGACACCATC AGGGAAGATC AGGGCTTTGA 60
AATAAAGGCA AGCCAGTGAC TTGAAGTGGC ACTCAGCTGG AGGAACAGCG GCCTTGTCTG 120
TGGCTGGGAC AGGCATGAGC TACATTAACC TTGTTGGGGT GGTCTCCAAA GTGGAAGCTG 180
CCCAAGCTGT ATGAACACAA AATAAACAAC AGCGCTTGCC TCTGCTCCAT GTCCCTTCCA 240
CCCACACGTC CTATGGGAGC AAAAACATGC ATCAGGTGTG TCTCCACCGT GCTATTCCAG 300
GAGAGATGAA AATAACCTGT TCAAAAATAA AAACACTCCA GCAACGTGGG CCCATTTCTA 360
AATCGCTGCG CAGCCTGGGC ACGGTGCCAG CGAGGCCCTG CCCTCTTCCC GTGGGCACCA 420
CACCCGCCTT TGTCATGGCC AGGGTGCGGC CACCAGAACA CACTCCTTCA TGATCCACGG 480
GCCACTCTGA CCCTGAGCAC CTGTGGCCTC AGCTCCCTCG GGGCAGCCAG CCTCCCTCGC 540
TCTGCCCTCA GCACACACAA TCCTGCAGAG GAGAAGAGAC ACAGTCAGAA GGAAATGGAG 600
GGGCCTCCTC AAACCCCAGG CCTGGGAGAA TCCCAGCGAG GACTGCACTG CCTTCCTAGG 660
ATGGACCAGA AGGGGGCCTG GAGCCTCTCC CGTAGCAGGC CGGCTCCACA GATGACACTG 720
AGCTTCAGCA AGGAACACGC ATGTCCTGTT CTGGGCCTGG CCTCGCGGCT AACCCTGCCG 780
AGACACTGAA TCCAAGGAGG CTGGGGATGC AGCCCAGCAA CCCCCTGGCG AGGGAGCACA 840
CAGGAGCCCA GCCTCAGGCA GCCGAGTGAA TACACAGGAC ACGAAGAGCA ACATGTCTTC 900
AAAACAATCA ACACCAATAT CCAGGCGGGC CCTCCACCAG AAAGGGCATG GGAGACTCCA 960
GCACAGCATC CTGGGCACAG AAACGACCCC CAAGAAGAGA GGAGGCCCTG GCAGAGTCAA 1020
CTGAGAACGC GCAGGGGTCC CTGAGCTAAG CCTGGCTCCC CTGCCCCAGA TTCCCTCGGG 1080
AAGGCACCAT AGCATGGAGA GGAGGCCTCA GGAAGCGGCT CTGGCCCCTG TAAGAGGCTG 1140
GGATGGCTCA GGCTCACAAG AGCTGCCTCT GGGCCAGGAA CATAGCAGGA AGAGAGCAGC 1200
TTCTCCGAAG AGGACAGAGG CTTCTCCCCG GAGGACAGAG GATTCTCCTA GGAGGACAGT 1260
GGCTTCTCCC GGGAATGTGG CAGCTTCTCC CAGGAGGACA GAGGCTTCTC CTGGGAGGAC 1320
AGAGGCTTCT CCTAGGAGGA CAGTGGCTTC TCCCAGGAAT ATGGCAGCTT CTCCCAGGAG 1380
GACAGCGGCT TCTCCCAGAG GATACCAGAT TCTCCTGGGA GGATGAGGAT GGCAGCTTCT 1440
CCTAGGAATA TGGCGGCTTC TCCCAGGACG GAGGCTTCTC CCAGGACAGC GGCTTCTCCC 1500
AGGACAGCGG CTTCTCCTAG GAGGACAGTG TCTTCTCCCA AAGGATGGCG GCTTCTCCAG 1560
GGAGGACGGT GGCTGCTCAT GGGAGGACAG AGGCTTCTTC CAGGAGGACA GCAGGTTGTC 1620
AAGGGAGGAC AGAGGCTTCT CCCGGGAGGA TGGTGGCTTC TTCCAGGAGG ACAGTGGCTG 1680
ATCATAGGAG GACAGCGGCT GCTCATGGGA GAGCAGAGGC TTCTTTCAGG AGGACAGCAG 1740
ATTCTCAAGG GAGGACAGAG GCTTCTTCTA GGACTCTCTT CTGGATGTGA GGCAGGAAGA 1800
ACATGGAACT CTTCTGAGGG GTCCCCCCTT GTACTTCCTG CATTCTGCCC CCTATTTAAC 1860
TGTTTCTTAA ACAGCAGCAG CCCCCGCCTT CTTGGGCCCA GTCTCCATCT GCCTTCAGCT 1920
GTCTCCTGGA TGGATCTGGC CTAAACTGCA CCCAGCGAAT ACAGACACCA GCTCTCCACA 1980
CTCTCCCATC ACTGAGGGTG GCAGCCGTGT CCAGGGTCCC AGCCCTCCTG TTAAAGCTCA 2040
TCCGCTCCCA ATCCCACAGC AGGCCCAGCC ACGTTGGTTT TGAGACCGTG GATCATCAGG 2100
AATGTTTGTG GACGGTTTTT TGATTGACAA AAGGAACTTT ATGGCAGTGG GCAGATCTGA 2160
TGCCCCAGGC AGCGAGGACG TGGGAGAGGG GAATGTGTGT CGTCACCAAC CCCAGCTTCG 2220
GAGGAGGTGG CCGAGGAACG TGCTCATTCA 2250
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