| Tag | Content |
|---|
EnhancerAtlas ID | HS047-14353 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr17:36101830-36103090 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr17:36101987-36101999 | GTTTGTTTGTTT | + | 6.32 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_23266 | chr17:36101321-36107651 | Colon_Crypt_1 | | SE_24029 | chr17:36101860-36106566 | Colon_Crypt_2 | | SE_25028 | chr17:36101208-36107357 | Colon_Crypt_3 | | SE_29293 | chr17:36100241-36108294 | Fetal_Intestine_Large | | SE_32396 | chr17:36101682-36107120 | Gastric | | SE_47579 | chr17:36101881-36106462 | Pancreas | | SE_65485 | chr17:36101485-36106876 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | AAAAAAAGCC CCCAAGAACC TTATAAATAA TGGCAAAACC TTTTAAGTCC GACTTAAAAG 60
AGTGAGGAGT AAGATGGCGC AGTTATACCT TCACAGCCCT CTGACCCCAA AATTCACGTG 120
TGTTCACCGG GAAGAGCCGG GAGAGCTGGT TATTTTTGTT TGTTTGTTTG AAAACACAGC 180
TCAGGTTCAG AGGTTCCCTA ACACGGAGAA AGGCACCGGT CCCGAAGAGG GCCTGCGGCC 240
ATTGTGTCCC AAGCGCAGGT GTCAAACGCC GGCCGCGGCG CCCGCAGGGT CCGTCCCGCA 300
CGCTCCTTCT CAAACAATGA CTTTGCTGCC CACGAGCAGA GAAGCCTGGA CTCCAGCGCA 360
GTCCGCAGCG CGTTCGTTAA GGAGCCCAAC TTCGGCTTCT TAGAATGCAG CCCACTTTCT 420
AGACGCCCCC GGCGCACCTG CCTCGAGGCC GCGAGAAAGG CCAGCTCCGG CCGGGAGCCG 480
GGGACCGGGA AGCGCGCAGT CCCGACCTTC CTCCCCTGCC TTTCTCTTCC AGGAGGTTTA 540
CTAGAACTCC AGGAACTCCA AAACGCGACT TTTCTTTCTC TTTGCTTTTC GTCTTAAGGG 600
AACACGGTGG GCAAAAGAAG GGAGTGCGTG TGCCCGAGGC TTGGGAGCCC CCTGTGCAGT 660
GACCTAGGAA CCGCTAGCGA TTTCTTGAAA AATTACTTTA ATCAAGTCCG GCGCTCCCGG 720
GAGCGGGGGA GGAAAGGCAG CACCCGCTCG GGACGGGAGA AAAAAGCCTC CAGGTCTGTC 780
CCGCGTCTCC AACTCGGCGA GGGTCTCCGG CTCCCCAGTC CCTCTCCCTG CCCTGCTGGG 840
GCCTGGGGCT TTGGGGAGGG AAGAGCGGGG CTGGGGTCTA AGGACCCTGG GCCGGGCCTG 900
GCTCTCCGCC GGCCGGGCCT GCGGGTGTCG GCGACCCGGG GGCTCCGCGG GCGGCTCGGG 960
CGCTCACAGA GCCCGCGTCC CGCGCCAGAG CGGTGAGGCC GCGGGGCCGC ACGGGGCGCC 1020
TGGCTGGGTG CGCGCTGGGA GCGGCGAGCA GCCCCGCGCC CGCGTTTTGA TCTCCTTCCC 1080
CCCTCTAAGC CGCGTTTACA ACTTCACCAA TGAATAACCC GCCTCTCTTT TCAACCTAAT 1140
CACGGCTCTT TGTGTATCTT TCTGTTGATG ATTTATAGAA ATAAATTAAT AACACCCCAA 1200
CTCCACGTGC TGCAGTTTAT GTTACGTCTC AGCTGCGGCC AGCCCGGCGC GGGGCTGGGT 1260
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