| Tag | Content |
|---|
EnhancerAtlas ID | HS098-04222 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr1:182668280-182669770 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HEY2 | MA0649.1 | chr1:182668684-182668694 | GACACGTGCC | + | 6.02 | | Npas2 | MA0626.1 | chr1:182668684-182668694 | GACACGTGCC | - | 6.02 |
|
| | 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 |
| GH01I182698 | chr1 | 182668125 | 182669832 |
|
Enhancer Sequence | GCTGCTGTAC TTTCATCACC CTGCATGCCT CCATCCCTGG GCCAGAGGGG TTTCCACATC 60
ACCACAGAGG CAGGCCTTCC TTCATTTTAT TTATTCCATT TGGGATTAAA CACATTGAAA 120
GGGGGCCATG GCTAAATGGG TGTTTCTCGC CTGGCTCGGT ACTTAGAAAT CAAAGAAGGA 180
GCTTCATGGT GTATGTGGAA GGGGATGGAG TGTAGAGAGG AGGAGGTGGT TTCTGCAGAC 240
AGGCAGCTCT TCCCATCTTC CCAGGAGCAA AGATTAGTTC CCTGGGCCCA GGCCTCAGTG 300
GCAGGGGGCC AAGGAAAGCA GGCCCAAGGC CTTTCCTAAC TCTTAGCCCC CAGGGATTGG 360
CACATGCCAC GGGGAAAGTG AAAAACATTT TACAAAACAG GCTAGACACG TGCCACATAG 420
CTGTGTCCTT AGAAACTTCC ACACAGATCC CTGTTGGAGG CTCTTCTCCC TGTGCTGTGG 480
CTCCCCAAAG CCTGCTTCGT TGCTGCAGGG ACCTTAAGAA TCCGAGGGGA TTCACAGAGC 540
CCTGGGGATT GCAACGGGAT TACCGGGGAG GGATACAGGC AAAATCCCCT GAGAGGCCTG 600
CAATGTGCTG CAGGCCTGGG GCCTTCCTGG CAGGATGGAT ATCTCTATTC CTGGAGCCAA 660
AAGTTCTGGG ATCTGCAGAA AGGGATCCCT CGGGGACTAT AATGAATGCC GTGTTCCAGC 720
AGTGCCAGCT CGGTTCAGCT GCTTGATTAA TGACATATGA GAGGTCTCAC GGCAAATTTA 780
ACAGGAGGGC GCACCCTCAC ACAGTGCCTG CCCTGGATAA GATCCGGCAC CTCACACCCT 840
GCAGGAGACT GGAGGGGCTC ACAGAACTCC TTCCCGAGCT CGGGATCCAG GGCGAAGCCT 900
GTGAAGAGCC CGCCTGGGTC TCAGGTTCTG AGTCTTGAGT GCATAACAAT GCGCCCCAGA 960
GCCCGCCGAG GGGAGAACTA GCTCCATCTG CTCCTTCCCA ATTCTCGGCT CCGGCGAGGG 1020
GGAGGGGGAT CCCTCGGCGG TTAGGCCGGG TCCTGCACGG TTATTGGCTG ACACATTTTC 1080
AAAGCTACTC TCAAAGGCTT TTATGAAAAT GCTGTTGCCG GGCAGCAGCT GAAGCCATTT 1140
GCCCTAGAAA ATGGATGGAA GCAGGTGTAA CCACTCACCC CAACATGACC CCCAAAACAT 1200
TCCCCGCGAC ACACACGCTA GTCTACAGTG TGTTACTTTG TCCCTGTATA TTTCAATAAG 1260
CGCACCAATC TGACACCTCA GCATTCCTCC CCGAAAACGT AACCATGAGC ATTGTTCTTC 1320
CTGGTTTCTC TTTCAAGAGA AAGGAGGTGC CAGTCCAGGG TGGTATTCCA AGAGACACCC 1380
CAGGTTCAGC CTCGGGCTGC CTCTGGCGGC AGAAGACACA GGGTGCATCT TCCGTCTTCT 1440
AATTCCCATA GCTTTCAGGA GATAGCAGAA TTGCTGGAAG TCATGAGTGT 1490
|
