| Tag | Content |
|---|
EnhancerAtlas ID | HS110-01302 |
Organism | Homo sapiens |
Tissue/cell | KATO3 |
Coordinate | chr14:100905220-100906420 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr14:100905708-100905719 | GGTGACTCATC | + | 6.32 | | JUND | MA0491.1 | chr14:100905708-100905719 | GGTGACTCATC | + | 6.62 |
|
| | Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
| SE_23539 | chr14:100904693-100908815 | Colon_Crypt_1 | | SE_24202 | chr14:100904835-100907247 | Colon_Crypt_2 | | SE_25594 | chr14:100904556-100911740 | DND41 | | SE_33398 | chr14:100898204-100917685 | H2171 | | SE_34657 | chr14:100900599-100909087 | HeLa | | SE_50425 | chr14:100904779-100908202 | Sigmoid_Colon | | SE_65652 | chr14:100904764-100908513 | Pancreatic_islets | | SE_66879 | chr14:100898204-100917685 | H2171 |
|
| | 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 |
| GH14I100435 | chr14 | 100901862 | 100909591 |
|
Enhancer Sequence | AGAGCTGGGA TTTGAACTCA GAACTGCCTG GCTGCAAGGC CAGAGTTCCT TCTAGAACCC 60
CTCTAGGGGT CTGCACTTCC TTTAGCACAT GGCCAATTGA CCACCTGCCC ACAAAAAATG 120
GCCTGGCCCT GGTGGCTAGG GCACCCTCCT GCAGATGGAG GCAAGGAGCA GTAGGGAGTG 180
GGGCTGGGCA TCAGTTGCCC AGGTACTTCC TAGCTCTATG CCCTGGGCAA GTGAAGTCCT 240
CCTTTCTGAC CCTCCCTGCA CCCACTGGTG ACTGGTGGCA GAATACCCTC CTGGGTTATT 300
GTTAGGATCA CAGACAACAT GTGTGAGGCA CCTGGCACTT GGTGGGCACT CAGGAAGTGA 360
AGGACCCTGC CCTTTGGCAT CTGTTGCTTG TCAGAATGCG TGGTGGATGG CTCTGGCCTC 420
GGTGACGAAG CTGCTGTTGC TTCAGCCCCC GGACTCCTGT GCATCACAGA GCTGATTCAG 480
TGCAGACAGG TGACTCATCT GATGGCATTT TGTGTGGCGT TGTGCAGTTC AGCCTGGTAC 540
AGCACGGCCC GCCCACAGCA GGTATTCAAG AGCCGTTAGT GTTTATGAAG GTGATAAAAT 600
TGCCTAGATG GAGGGAAGCC GTCAAAATAA GAGCCTTTGC CTGTCTTGTG AAAGTTAACT 660
TGCAAACCTA ATGCCTGTGG GGCTGCTGAA AAAGCGTCAC CTGGATTTCT CCTTGGAGAC 720
AGAACTCTCT GGAAGGACAG CTGGGCAGCC CCTGCTTGCC ATGTGGGGGT GGACGCTTTT 780
TATGTGACAG TGAGTTGGAG AAACTAACAG TGGTCTTCAA GGCATTGTGC TCAGCTTAAC 840
TCTTTGAATT GCCATAGCTT TAAAATGAAT ACTAGAAACA GTTATATATT TTTCACACTC 900
TCCATATTTT CTCCATTCAA TATAATAAAT GTTATCTTGA ATGTTTGAGG GTTTTATAGC 960
AAAAATTCCT CCCATTTGTA AAGCATGCTG CAGTGGATGG GAGTGAACTA GCTGGCAGCG 1020
CTCTCGTGTG ACGTGGCAGA GGCTGAGGGA GTTGCCCAAA CCCCACTTCC AGTTGGAGGA 1080
AGCCTGGGCC CTGACTTCCA GTGCATGTTC AGGTCCACTT GTCAAGGAAA GGATCCATTG 1140
TTAAGAAACA AACATGGGAA ACTGTCATGT GAGCGTCCCT AAAAGCAGCA TAGTCATTTT 1200
|
