| Tag | Content |
|---|
EnhancerAtlas ID | HS102-06820 |
Organism | Homo sapiens |
Tissue/cell | HuCCT1 |
Coordinate | chr13:99126200-99127070 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZIC3 | MA0697.1 | chr13:99126699-99126714 | GACCCCCAGCTGTGC | + | 6.17 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_27318 | chr13:99125624-99126422 | Esophagus | | SE_32245 | chr13:99125599-99127531 | Gastric | | SE_45616 | chr13:99125684-99126805 | Osteoblasts | | SE_65772 | chr13:99126270-99131228 | Pancreatic_islets |
|
| | 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 |
| GH13I098473 | chr13 | 99125593 | 99126985 |
|
Enhancer Sequence | AGCAGCAAGG TTCGGCCTAT ATGCATATCT GAGTTAGGTA TTTGTTTGCT CAGAAACTTG 60
GAGCCCAGGA AAGCCAATTC TCCGTGGATC ATGTGGCCTT TTAACTGTGT ACAGGGTCCT 120
AAGAAGAGCA GACTGTGCGA ACTGAAGTTA AACCAGAGCC CTAGGAGGCA AAGTCCCGGG 180
ATTTTTTGTC CCATCTAACA GAGTTCACAA AAGTGGAGGG CAACAGAGAA AAAGAATATG 240
AGAAAAATTA GGAGAGTGTC CCTAACACAG GACAAGTAAA AAACAGTGGG AAGAAAGGGT 300
TAGGGTTTCA TCACATGTTG ACAAGGACAG GCTGGGAACG AGAATCCTCA GAACTAAAAA 360
TAATAGGAAG ACCCTGCAGC AGTCACTCAA AGCACTGTTC TTCCTCCATT CTCACGCTTC 420
CGTGGACTCC CTTTCTCTTG TGGGAGCCCC TTTCTCTACA GGCCCCTTCA AGGTTGCCGA 480
TTCCACGCAC TTGCACTTCG ACCCCCAGCT GTGCCCAGAC AGCAGGTGGA GCCCCTCTGC 540
AACCGCACAC GCCTCCACCC CTCACCACCA TGGCCCTTCA GTTCCTCCCA CCCCCCTCCA 600
AACCCGCTCC ATCCTGTGTC CCCGCTGCCA CCAAACAAAC ATAGCCTGAG TTAAAAACCT 660
CGATCATGGT GGGCTGGATC AGCACAGGGT ATTAAATGAT ACAGCAGGAG ACAGAGGAGA 720
AAACTGTTCA TAACCAAGGT TGAAGAATTA CCTTTATGAC CTACCTCAAG GTACCAGCTT 780
CGTTCCAACT TAGAAAAGCT ACCAGGCTAA AGAACAAAAG GCGGGAGCCC TCCAGGCCTC 840
GTGAGGCACG GCGCCGCCCT CACCCTCCCC 870
|
