| Tag | Content |
|---|
EnhancerAtlas ID | HS050-29996 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr17:73538030-73539470 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEOX1 | MA0661.1 | chr17:73539165-73539175 | GCTAATTAAC | + | 6.02 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_23798 | chr17:73538030-73540545 | Colon_Crypt_2 | | SE_28701 | chr17:73533670-73541102 | Fetal_Intestine_Large | | SE_47745 | chr17:73538648-73539543 | Pancreas |
|
| | 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 |
| GH17I075537 | chr17 | 73533691 | 73540100 |
|
Enhancer Sequence | CAAACTCTTG ACCTGAGGTG ATCCACCTGC CTCCGCCTCC CAAAGTGCTG GGATTACAAG 60
ACTGCCATTT TTTACAGTGC GATTTTGTAA AATCGGGTCA CCCTCCCAGC ACAGCAAGCC 120
CTCGGTTCCT CTGCCCGAAG ACACCCCCAA CTCTGCCACG CACGTTACCT ACCTTCTCCC 180
ACGCTGCCCA GATTACATGG GATCCTATCA TATGCAAAGT CCTGACCTGA TGGTTAATTT 240
TTGCCACCTC CCAAGAACGC GAAATCCTTC AAACCTCAGC TTAGATACCT TCTTCTCGAA 300
GGTATCTAAG CTGCCTCCCA CTTCGGGCCA GGTGTTCCCT CTCCCTCCTG CAGTCAAAGC 360
ACTCAACACT GGGCTGCCCT GTCTCTACCT GTCCCTGCCT GGAGCACGCG CCTCCAGGGT 420
GCGGCCTGGA TCTGCTTCCT TCCCCCATCC TGCTGGGAGT GGACGGAGCT GTGCCCAGGG 480
TCTGTGTTTC CCAAGGACGG GCCTTGCTGT CCTGTGGTCA GCAGGAGGCT GAGCTACTGG 540
AAGCCAGAAG CTGGAGCACA GAGGCTCCTT CCCCTTCCCC CAAGGATAAT CCAGAAATGG 600
TTTCCCCTTG GGCTGGGAAT GGATTCTATG GTGGGCGGAG AGTTTAGGGG CCTTGAGCTG 660
GTTTCTTTAT TGGGAGCAGA TTCCTCCTGA TTATTCTCCA CTAGGGCCCG TGGGAAAGAG 720
AACCTTTCTG AGCACAGCCC ATGAGCGCAC AGGGAAGCTG GACTGGGGCT AGCCAGAGAG 780
AGGGGAGGGG ACCGGCAGAG ACCCCAGGCA CGGTGGCATG GGCCAGCACC CCCTGACCGA 840
GTGCTCTGTG CCACCCGTGC CCACTTGAGT TTCTCATGGC TGTGGCTGGT TGGAGAGGCT 900
GAGGCCGAGA GTCCCTGGAC AGCCTTCCCC GAGGTCAGAA GGAGGAAGCA TCTGCCCGGT 960
GCCCTGGCCT GGAGTCACTG CAGGCCTCTC CCCTGCCCCG ACTTGGGCTC TGATCTGGGA 1020
AGGATGGCCT TGGTGTTTCT ACCTTCCACA AGACTTTGGA GGAAGAGGCT TGCGAAGTTT 1080
CCCTTTCTGC TTAGCTGGAG TTTCATGGTT TCTCAGAAAA CAGGTTAACA ATTAAGCTAA 1140
TTAACCTCAG GGCCCGCCGG CCCTCCTTGT GCTTATAAAG CCAGGCTAAA TGGCTTCCTC 1200
CCCCAGCTTT TCCTACCCCC ATTATAAGGC CACAGGTGGT GACAGCCTTC AGCCCTGAGG 1260
TGGGCCGGCC TCTAGATCTG AGCGTGGGGA AGCCAGGGTG CATGGGCGGT CACTGTGAAG 1320
CTGGCCTGGC CCCGGGGTGG CAGCCTACTG GACTTGGAGA GAGAGGCCCT GCTCCACCTG 1380
TTTGGGCCGG GCCTAATCGA TACCTGAGTG CCAGGACAGA CCCCTGCAGC TCCTTCTGTT 1440
|
