| Tag | Content |
|---|
EnhancerAtlas ID | HS098-51064 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr7:2102840-2104610 |
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 | AGTGAAAAGA AAGACTGGAC GTGGGGTGGG TGGGACCTCA CTGCGCCAAA ATCTTGCTCT 60
CTGATCCAAG AGTGGGCAGA GTCCTGGGCC CCTGGGAGTC CCTGGCTCCG CGTCCTCACT 120
CCAGGCTGTG CCGGATCCCA GGACTTAAAC AGACACCATC AGGGAAGATC AGGGCTTTGA 180
AATAAAGGCA AGCCAGTGAC TTGAAGTGGC ACTCAGCTGG AGGAACAGCG GCCTTGTCTG 240
TGGCTGGGAC AGGCATGAGC TACATTAACC TTGTTGGGGT GGTCTCCAAA GTGGAAGCTG 300
CCCAAGCTGT ATGAACACAA AATAAACAAC AGCGCTTGCC TCTGCTCCAT GTCCCTTCCA 360
CCCACACGTC CTATGGGAGC AAAAACATGC ATCAGGTGTG TCTCCACCGT GCTATTCCAG 420
GAGAGATGAA AATAACCTGT TCAAAAATAA AAACACTCCA GCAACGTGGG CCCATTTCTA 480
AATCGCTGCG CAGCCTGGGC ACGGTGCCAG CGAGGCCCTG CCCTCTTCCC GTGGGCACCA 540
CACCCGCCTT TGTCATGGCC AGGGTGCGGC CACCAGAACA CACTCCTTCA TGATCCACGG 600
GCCACTCTGA CCCTGAGCAC CTGTGGCCTC AGCTCCCTCG GGGCAGCCAG CCTCCCTCGC 660
TCTGCCCTCA GCACACACAA TCCTGCAGAG GAGAAGAGAC ACAGTCAGAA GGAAATGGAG 720
GGGCCTCCTC AAACCCCAGG CCTGGGAGAA TCCCAGCGAG GACTGCACTG CCTTCCTAGG 780
ATGGACCAGA AGGGGGCCTG GAGCCTCTCC CGTAGCAGGC CGGCTCCACA GATGACACTG 840
AGCTTCAGCA AGGAACACGC ATGTCCTGTT CTGGGCCTGG CCTCGCGGCT AACCCTGCCG 900
AGACACTGAA TCCAAGGAGG CTGGGGATGC AGCCCAGCAA CCCCCTGGCG AGGGAGCACA 960
CAGGAGCCCA GCCTCAGGCA GCCGAGTGAA TACACAGGAC ACGAAGAGCA ACATGTCTTC 1020
AAAACAATCA ACACCAATAT CCAGGCGGGC CCTCCACCAG AAAGGGCATG GGAGACTCCA 1080
GCACAGCATC CTGGGCACAG AAACGACCCC CAAGAAGAGA GGAGGCCCTG GCAGAGTCAA 1140
CTGAGAACGC GCAGGGGTCC CTGAGCTAAG CCTGGCTCCC CTGCCCCAGA TTCCCTCGGG 1200
AAGGCACCAT AGCATGGAGA GGAGGCCTCA GGAAGCGGCT CTGGCCCCTG TAAGAGGCTG 1260
GGATGGCTCA GGCTCACAAG AGCTGCCTCT GGGCCAGGAA CATAGCAGGA AGAGAGCAGC 1320
TTCTCCGAAG AGGACAGAGG CTTCTCCCCG GAGGACAGAG GATTCTCCTA GGAGGACAGT 1380
GGCTTCTCCC GGGAATGTGG CAGCTTCTCC CAGGAGGACA GAGGCTTCTC CTGGGAGGAC 1440
AGAGGCTTCT CCTAGGAGGA CAGTGGCTTC TCCCAGGAAT ATGGCAGCTT CTCCCAGGAG 1500
GACAGCGGCT TCTCCCAGAG GATACCAGAT TCTCCTGGGA GGATGAGGAT GGCAGCTTCT 1560
CCTAGGAATA TGGCGGCTTC TCCCAGGACG GAGGCTTCTC CCAGGACAGC GGCTTCTCCC 1620
AGGACAGCGG CTTCTCCTAG GAGGACAGTG TCTTCTCCCA AAGGATGGCG GCTTCTCCAG 1680
GGAGGACGGT GGCTGCTCAT GGGAGGACAG AGGCTTCTTC CAGGAGGACA GCAGGTTGTC 1740
AAGGGAGGAC AGAGGCTTCT CCCGGGAGGA 1770
|
