| Tag | Content |
|---|
EnhancerAtlas ID | HS050-20082 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr14:35816470-35817490 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TCF7L2 | MA0523.1 | chr14:35816776-35816790 | GGAGATCAAAGGGA | + | 6.75 | | ZNF263 | MA0528.1 | chr14:35816784-35816805 | AAGGGAGGAGGGGGTGGGGAG | + | 6.61 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_23298 | chr14:35816257-35817251 | Colon_Crypt_1 | | SE_24327 | chr14:35816552-35817140 | Colon_Crypt_2 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr14 | 35816661 | 35817200 | | chr14 | 35816552 | 35816667 | | chr14 | 35816709 | 35817157 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH14I035346 | chr14 | 35816026 | 35817319 |
|
Enhancer Sequence | TCATGTGCGG GGCGCTGTCC TAAACACTTC ACATGAATTA ACAAATTTCA TTCTCATAAC 60
AGCCTCTAGG ATCAATATGA TTATTGCTGG GTGTTCCAGA TCTTGATGCC TAAGGATACC 120
CAGGTAGTCA ATGGTAGACC TGGGCTGTGC ACCCAGGCAG GCTGGCCCCT CAGCCCACAG 180
GCGTGACCAG AGGTCATCCC TCCTCTCCTC CAGCTTTGTG CCCTGGAGGA GCTGCTGTGT 240
GCACTGCATG GACGCCACCC TTGCCCTCTG GCCGCCTTTT GGTCATGGCC AGTGAAGAGC 300
CTAGTGGGAG ATCAAAGGGA GGAGGGGGTG GGGAGTCTGC ATTCATTCCC CTGCAGTCCT 360
CCCCGCAGGG TCGCCCAGGC TGGGTTGGAC CTAAAAGGAA GGTCACGGCC CCACTCAGGC 420
AGCCTCTGTC CCACAGGGTT CTGGTGCGGG TTTCTGGTGC AGGTGCTGGT GCGCAGTGTT 480
CCTCTTGCTC GCATCCGCCC CGCATTGCTG CACAATCCCT ACTTCTACGC CCCTCGTGGT 540
TTTGTAAATA GTGTCATTGT AAATGAGCCA GCCACTCCCC CATGCTGCCT CTCAGCTGCA 600
GGCTGAGCAA AGCTTAGCTT GTCCTTGAGC CTTACCTGCT TACTGTGTAA TGCCCAACCT 660
CATTTTTACC AATCCTGTTT TTAGACTCTC CCTTTCCTTT AATCACCCAG CCTTGTTTCC 720
ACCTGAATTG ACTCTCCCTT AGCTAAGAGA GCCAGACAGA CTCCATCTTG GCTTTTTCAC 780
TGGCAGCCCC TTCCTCGAGG ACTTAACTTG TGCAAGCTGA CTCCCAGCAC ATCCAAGAAT 840
GCAATTAACT GATAAGATAC TGTGGCGAGC AATATCCGCA ATTCTCAGGA ATTCGTCTGA 900
TTGATAATGC CCAAAGCCCC AAGTCTATCA CCTTGTAATG GTCTTAACGC CCCTGCACCT 960
GGAACTGTTT ACTTTCCTGT AACCATTTAT CCTTTTAACT TCTTGCCTAC TTTATTTCTG 1020
|
