| Tag | Content |
|---|
EnhancerAtlas ID | HS048-02436 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr1:155194450-155195060 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NKX2-5 | MA0063.2 | chr1:155194801-155194811 | ACCACTTGAG | + | 6.02 |
|
| | Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
| SE_27291 | chr1:155194552-155195090 | Esophagus | | SE_68020 | chr1:155161591-155248159 | TC32 | | SE_68021 | chr1:155161591-155248159 | TC32 | | SE_68022 | chr1:155161591-155248159 | TC32 | | SE_68023 | chr1:155161591-155248159 | TC32 | | SE_68024 | chr1:155161591-155248159 | TC32 | | SE_68025 | chr1:155161591-155248159 | TC32 | | SE_68026 | chr1:155161591-155248159 | TC32 | | SE_68027 | chr1:155161591-155248159 | TC32 | | SE_68028 | chr1:155161591-155248159 | TC32 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GAACCCGGGA GGCGGAGCTT GCAGTGAGCC AAGATCGTGC CACTGCACTC CAGCCTGGGT 60
GACAGAGCGA GACTCCATCT CAAAAAAAAA AAAAAAGAAA AGAAAACTAA GACTTAGAGA 120
AGTTAAATAT GTGGCAGAGT GAAGCCTAAG CTCATATCTG TCCTAATCTA AATTCCAAGC 180
AGTTCTGAGT CATCAGGTCA CACAGACTGC TTCTCACATG CTTCAGGAAT GCCTTTTCAG 240
TCTTCCTTAA AGGTTGCAAA CAGTTGCAAA GCAAATTTCA TGGTTCCTGT TTCTTCAAAA 300
TCTCAAAGCT CTTCATTCAG CCAGGCATGG TCGCTGGAGC GTGTATATTC AACCACTTGA 360
GAAGATGAGG ATCTTTTGAG CCCAGGAGTT TGAGACGAAC CTGGGCAACA TAGGGAAAGC 420
CCTGTCACCT AAAAAAATAA ATAATACAAC CAGCTCTTCA TTTAGAGGCA AGCACAAAAT 480
AGGTGCTCAA TGTTTGTTGA ATGAGTGAGT TGTTACCAAC CATACCCCAT TATTCAAGGT 540
CCTGCTTGTC AGTGTTTCAG GAAGTGTTCT TGGCAAAGGA GTGGTGAACT TCAAGAAGAA 600
TGATGCTGAC 610
|
