Tag | Content |
---|
EnhancerAtlas ID | HS060-10649 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr14:89896810-89897850 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr14:89897773-89897788 | TGAACTCCTGACCTC | - | 6.22 | ONECUT3 | MA0757.1 | chr14:89897008-89897022 | TTAATTGATTTTTT | - | 6.22 | ZBTB33 | MA0527.1 | chr14:89896974-89896989 | AAGACATCGCGAGAG | - | 6 | Zfx | MA0146.2 | chr14:89897798-89897812 | CCCGCCTCGGCCTC | + | 6.01 |
|
| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_02219 | chr14:89897002-89897996 | Aorta | SE_09185 | chr14:89894205-89899234 | CD14 | SE_27314 | chr14:89896960-89897446 | Esophagus | SE_30170 | chr14:89893751-89897921 | Fetal_Muscle | SE_43326 | chr14:89896920-89897880 | Lung | SE_52261 | chr14:89893861-89897676 | Skeletal_Muscle_Myoblast | SE_64066 | chr14:89893835-89897783 | HSMM |
|
| 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 |
GH14I089425 | chr14 | 89891558 | 89899105 |
|
Enhancer Sequence | TTTCGGTTTC CTGTTTAATA TTAAATAAAG AATTTTAGCT CTTCTGTTTT TATAAACTGT 60 GCTATTTGCT ACTACTGTCA CTACTAAAAG CATTATGACT GGGTGGATAA GTAGTCCTAT 120 GATTTTCAAG CCTTCTTTTT TCTTTAATCT TAGTATCTAT TTTGAAGACA TCGCGAGAGT 180 TAAGAGTCTC AAATCTGTTT AATTGATTTT TTTATTTTTA AAAGGCCCAA ATAAGTACTT 240 CCGTTAGCTC TTAGATCTCT GAACATTATG TATTTTTAAA CCACTTTGAA TACTTTGAAA 300 AGGGCCACAG AAAACACTCA TATTCAAATA CCACCAGACG GAGGTTCTGC CTAACCAAAA 360 GTAAAAGCAG AAAAGTTTAA AGCTGAATTG TGCCCTGCAC ACACCTTGAG ATTGTAGGGG 420 TGAAATGAAT GGTCTTGGGC CGGGGATCTT GCTAAAGGCA TGATAAATCA TGCGTTGCAG 480 GCAAATTAAG ACCCAGGCTC TAACTTGAAC CTCAGACTGT GCCAAACTCC ATCTCCATTT 540 AAGGAAAATG GTTTTCTCAG TTTCTTGCAC ATGACCTAAA GGCTTGTCCA GTCATTTCCG 600 TTGTCTGAAA TGCAAAGCAA TCTTTCTTTT TTAAGTAGAG AAAGAAGAGT CCTGAAATAT 660 TTATAGGAAA GTGCTTCACT ACCTACTGAC AGCAATGTGG TTGGTCTCTA CGTGTTTAGC 720 ACATTTTTTT TTGTTTGCTT GTTTCTTTGA GACAGAGTCT CTCTCTCTCT CCCAGGCTGG 780 ATGGAGTGCA GTGTTGTGAT TTCAGCTCAC TGCAACTTCT TCAGCTTCAC TTGAACCGGG 840 TTCAAGTGAT TCTCCTGCCT TAGCCTCCCA AGTAACTGGG ATGACAGGCG CCCACCACCA 900 CACCCGGCTA ATTTTTGTAT TTTTGGTAGA GACAGGGTTT CACCATGTTG GCCAGGCCGG 960 TCTTGAACTC CTGACCTCAG GTGATCCACC CGCCTCGGCC TCCCAAAGTG CTGGGATTAC 1020 AGGCATGGGC CACTGCGCCT 1040
|