| Tag | Content |
|---|
EnhancerAtlas ID | HS076-04736 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr1:182667930-182669820 |
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 | GCTTATCATC ATTTTGTTTA ACCTTGAAAT AATTCTTACT TCGTAAGCAC AGAATTCACT 60
GCATAAATTA GACCAAGGGG AATTAGAACA ATGTGTGTGT GACTGTGTGC ACACATGTCT 120
CCGTAATGAA TGTGGAGTTA CATATATTCA GCACGTCTGT GTAAGCGCCC AGAGACTTAT 180
TGTATGCCTG AAAAATAGAG CCCAGAGAGG CATAAAGCTA TTTATTTGGA AGAAATTAGA 240
CTGTTTTTTA TGATTCTGAA AAGGTTAAGG CAGAAGATAG GTGGCTGCGT AGAGGGAGTT 300
ATGACTTGCG CATTTTGATT CATCTTTTCT TATTAAAAGC CGCCTCTCCA GCTGCTGTAC 360
TTTCATCACC CTGCATGCCT CCATCCCTGG GCCAGAGGGG TTTCCACATC ACCACAGAGG 420
CAGGCCTTCC TTCATTTTAT TTATTCCATT TGGGATTAAA CACATTGAAA GGGGGCCATG 480
GCTAAATGGG TGTTTCTCGC CTGGCTCGGT ACTTAGAAAT CAAAGAAGGA GCTTCATGGT 540
GTATGTGGAA GGGGATGGAG TGTAGAGAGG AGGAGGTGGT TTCTGCAGAC AGGCAGCTCT 600
TCCCATCTTC CCAGGAGCAA AGATTAGTTC CCTGGGCCCA GGCCTCAGTG GCAGGGGGCC 660
AAGGAAAGCA GGCCCAAGGC CTTTCCTAAC TCTTAGCCCC CAGGGATTGG CACATGCCAC 720
GGGGAAAGTG AAAAACATTT TACAAAACAG GCTAGACACG TGCCACATAG CTGTGTCCTT 780
AGAAACTTCC ACACAGATCC CTGTTGGAGG CTCTTCTCCC TGTGCTGTGG CTCCCCAAAG 840
CCTGCTTCGT TGCTGCAGGG ACCTTAAGAA TCCGAGGGGA TTCACAGAGC CCTGGGGATT 900
GCAACGGGAT TACCGGGGAG GGATACAGGC AAAATCCCCT GAGAGGCCTG CAATGTGCTG 960
CAGGCCTGGG GCCTTCCTGG CAGGATGGAT ATCTCTATTC CTGGAGCCAA AAGTTCTGGG 1020
ATCTGCAGAA AGGGATCCCT CGGGGACTAT AATGAATGCC GTGTTCCAGC AGTGCCAGCT 1080
CGGTTCAGCT GCTTGATTAA TGACATATGA GAGGTCTCAC GGCAAATTTA ACAGGAGGGC 1140
GCACCCTCAC ACAGTGCCTG CCCTGGATAA GATCCGGCAC CTCACACCCT GCAGGAGACT 1200
GGAGGGGCTC ACAGAACTCC TTCCCGAGCT CGGGATCCAG GGCGAAGCCT GTGAAGAGCC 1260
CGCCTGGGTC TCAGGTTCTG AGTCTTGAGT GCATAACAAT GCGCCCCAGA GCCCGCCGAG 1320
GGGAGAACTA GCTCCATCTG CTCCTTCCCA ATTCTCGGCT CCGGCGAGGG GGAGGGGGAT 1380
CCCTCGGCGG TTAGGCCGGG TCCTGCACGG TTATTGGCTG ACACATTTTC AAAGCTACTC 1440
TCAAAGGCTT TTATGAAAAT GCTGTTGCCG GGCAGCAGCT GAAGCCATTT GCCCTAGAAA 1500
ATGGATGGAA GCAGGTGTAA CCACTCACCC CAACATGACC CCCAAAACAT TCCCCGCGAC 1560
ACACACGCTA GTCTACAGTG TGTTACTTTG TCCCTGTATA TTTCAATAAG CGCACCAATC 1620
TGACACCTCA GCATTCCTCC CCGAAAACGT AACCATGAGC ATTGTTCTTC CTGGTTTCTC 1680
TTTCAAGAGA AAGGAGGTGC CAGTCCAGGG TGGTATTCCA AGAGACACCC CAGGTTCAGC 1740
CTCGGGCTGC CTCTGGCGGC AGAAGACACA GGGTGCATCT TCCGTCTTCT AATTCCCATA 1800
GCTTTCAGGA GATAGCAGAA TTGCTGGAAG TCATGAGTGT CTTAGAAAGA CTGAATGCTT 1860
TTTGTTAGAG TTCTCATTCT ACTAAGTACA 1890
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