| Tag | Content |
|---|
EnhancerAtlas ID | HS050-04992 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:182667940-182669770 |
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 | ATTTTGTTTA ACCTTGAAAT AATTCTTACT TCGTAAGCAC AGAATTCACT GCATAAATTA 60
GACCAAGGGG AATTAGAACA ATGTGTGTGT GACTGTGTGC ACACATGTCT CCGTAATGAA 120
TGTGGAGTTA CATATATTCA GCACGTCTGT GTAAGCGCCC AGAGACTTAT TGTATGCCTG 180
AAAAATAGAG CCCAGAGAGG CATAAAGCTA TTTATTTGGA AGAAATTAGA CTGTTTTTTA 240
TGATTCTGAA AAGGTTAAGG CAGAAGATAG GTGGCTGCGT AGAGGGAGTT ATGACTTGCG 300
CATTTTGATT CATCTTTTCT TATTAAAAGC CGCCTCTCCA GCTGCTGTAC TTTCATCACC 360
CTGCATGCCT CCATCCCTGG GCCAGAGGGG TTTCCACATC ACCACAGAGG CAGGCCTTCC 420
TTCATTTTAT TTATTCCATT TGGGATTAAA CACATTGAAA GGGGGCCATG GCTAAATGGG 480
TGTTTCTCGC CTGGCTCGGT ACTTAGAAAT CAAAGAAGGA GCTTCATGGT GTATGTGGAA 540
GGGGATGGAG TGTAGAGAGG AGGAGGTGGT TTCTGCAGAC AGGCAGCTCT TCCCATCTTC 600
CCAGGAGCAA AGATTAGTTC CCTGGGCCCA GGCCTCAGTG GCAGGGGGCC AAGGAAAGCA 660
GGCCCAAGGC CTTTCCTAAC TCTTAGCCCC CAGGGATTGG CACATGCCAC GGGGAAAGTG 720
AAAAACATTT TACAAAACAG GCTAGACACG TGCCACATAG CTGTGTCCTT AGAAACTTCC 780
ACACAGATCC CTGTTGGAGG CTCTTCTCCC TGTGCTGTGG CTCCCCAAAG CCTGCTTCGT 840
TGCTGCAGGG ACCTTAAGAA TCCGAGGGGA TTCACAGAGC CCTGGGGATT GCAACGGGAT 900
TACCGGGGAG GGATACAGGC AAAATCCCCT GAGAGGCCTG CAATGTGCTG CAGGCCTGGG 960
GCCTTCCTGG CAGGATGGAT ATCTCTATTC CTGGAGCCAA AAGTTCTGGG ATCTGCAGAA 1020
AGGGATCCCT CGGGGACTAT AATGAATGCC GTGTTCCAGC AGTGCCAGCT CGGTTCAGCT 1080
GCTTGATTAA TGACATATGA GAGGTCTCAC GGCAAATTTA ACAGGAGGGC GCACCCTCAC 1140
ACAGTGCCTG CCCTGGATAA GATCCGGCAC CTCACACCCT GCAGGAGACT GGAGGGGCTC 1200
ACAGAACTCC TTCCCGAGCT CGGGATCCAG GGCGAAGCCT GTGAAGAGCC CGCCTGGGTC 1260
TCAGGTTCTG AGTCTTGAGT GCATAACAAT GCGCCCCAGA GCCCGCCGAG GGGAGAACTA 1320
GCTCCATCTG CTCCTTCCCA ATTCTCGGCT CCGGCGAGGG GGAGGGGGAT CCCTCGGCGG 1380
TTAGGCCGGG TCCTGCACGG TTATTGGCTG ACACATTTTC AAAGCTACTC TCAAAGGCTT 1440
TTATGAAAAT GCTGTTGCCG GGCAGCAGCT GAAGCCATTT GCCCTAGAAA ATGGATGGAA 1500
GCAGGTGTAA CCACTCACCC CAACATGACC CCCAAAACAT TCCCCGCGAC ACACACGCTA 1560
GTCTACAGTG TGTTACTTTG TCCCTGTATA TTTCAATAAG CGCACCAATC TGACACCTCA 1620
GCATTCCTCC CCGAAAACGT AACCATGAGC ATTGTTCTTC CTGGTTTCTC TTTCAAGAGA 1680
AAGGAGGTGC CAGTCCAGGG TGGTATTCCA AGAGACACCC CAGGTTCAGC CTCGGGCTGC 1740
CTCTGGCGGC AGAAGACACA GGGTGCATCT TCCGTCTTCT AATTCCCATA GCTTTCAGGA 1800
GATAGCAGAA TTGCTGGAAG TCATGAGTGT 1830
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