| Tag | Content |
|---|
EnhancerAtlas ID | HS145-18980 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr4:1803750-1804640 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| REST | MA0138.2 | chr4:1804361-1804382 | GGCCCTGTCCAGGGTGCAGGT | - | 6.86 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_25282 | chr4:1794206-1804359 | Colon_Crypt_3 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | AGGTGGGCCA CCGTGTGCAC GTGGGTGCCG CCGCTGGGGC TCCTGGGCTG GCCCCAAGGG 60
TGCCCCTTGG CTGCGGGTTG CGTGAGGATT TGGGTCTAGG GGTTGGAGCT TCGGGGGCAG 120
AAGCTGTGGG GGTGCTTGTG GGGCCAAGTC TCAGCCACCC CACACCTCAG GGCCATAGGC 180
AGCTGCGTTG GGACCCGTTT CCGTGTCTGC AGAGGGCCAG CCTCAGCCAC TGAAGTCCCT 240
GACATGGAGC TGCCCACGGG CTTCTTGGGG GTGGGTGCGG CTTGGGCAGC AGTGGTGCCC 300
CAGGACAGGA GGGCAGTGTG GCCAAGCCCT CCAGGCCCCC TCTGGGCCTC AGAGGCGGTG 360
GCTGAGCCCC GACCTGGCCG ATTGGCTCTC GTCAGCTGTG TGCAGTGGGG CCCGAGCTCA 420
CTGTCTGCCC GCCTCCTGAA GCCCTTAGCT TTGTTCCCAT GGCTGCCGGG TGGGGGCCAC 480
TGAATTGGGA CGGTTGCGAC ACTCAAAGCC CAAAGAGAAA CATCTGTTCA GAGAGAAGAC 540
GGTCTCTTGG GGGCGGGGAG CAGGCGCAGG GCGAGGGTGG AGTCCAGACC CCGCCCAGAG 600
AGGCCGCCTC GGGCCCTGTC CAGGGTGCAG GTTCTGCAAG AGCCCGGGGG AGGGCAGGCC 660
AGTGACCAGA GGTTGTCTGA GGGTCTGGGC TGGGTTGTTG GGGTGGAGGC AGAGACGTGC 720
ATCCTGTGAA ACCACAGCCA CCGTGAAGTG CCTCCACGCC TCCTCCAGGC AGCCTTTGGG 780
GCTGACGCAG CCCAGCCTCG ATCTGTACCT TGGGGGTCTC CCACATCCTG CCTCGTGCCC 840
GGCGGGGCTG CCTCGGGGGC GTGCCTGAGC CGGGTCTCTT GTCCCCGCAG 890
|
