| Tag | Content |
|---|
EnhancerAtlas ID | HS176-20343 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr2:43553240-43554000 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SP2 | MA0516.2 | chr2:43553574-43553591 | TGGGGGGCGGGAATTGG | - | 6.06 | | ZNF263 | MA0528.1 | chr2:43553456-43553477 | GGAGAATGGGGAGGAGGTAGA | + | 6.25 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_00553 | chr2:43550230-43553529 | Adipose_Nuclei | | SE_01936 | chr2:43553618-43555134 | Aorta | | SE_10147 | chr2:43553149-43555150 | CD14 | | SE_29749 | chr2:43550541-43554711 | Fetal_Muscle |
|
| | 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 |
| GH02I043326 | chr2 | 43553327 | 43562144 |
|
Enhancer Sequence | ATATACACAC AAACATATGC ATTAGGTCAT ATGTAAAAGC TGTTTCTTGT TGTCAATGTC 60
TGTCAAAAAA AAAAAAAAAA AAACACTTGA AAGCCACTAG TGTAGTTGGG AAAACACACA 120
ACCAGTCATG CTAGAGTATG ATGGGTGCCC CAAAAGGAGG GATTAACAGA GTAACTGTTT 180
GTCTGGGTGA GTCAGGAAGG GCCTTGGCAG AGAGTTGGAG AATGGGGAGG AGGTAGACCT 240
GGGCAAAGTG ACCACAACAG AGGAAGTAGC ATGTCCAAAG ACTTGGGGAC ATGACATGTT 300
TAGAGAATAA CAAGTGCTAA AAGGGACAAT GGTATGGGGG GCGGGAATTG GAATGGCAGA 360
GGTGGGTTAT TTTTATTTAA TTTATGTTTC CACATTTACA TGGCTTAATG TGGCCTCCAT 420
CAAAGAAGTA CCTCCTAACT CCTATCTACA AGATATAATC AAATATAAGG AGAGGCAGTG 480
TCTGGTCCAT GGACAGCTGT TACAATGATG TGAACTGCCA AGACTAGAAA GATGGCCAGT 540
GGGATTAGCA GGAAATGATA TGGGATGAGT CAACAGGGGC CCGAAACAGA AGTAGTCTTT 600
CAGAGCTCTA AAAGTTCCAA AGAATGAAGA CCCCAGTGGG ATCCCATAAG CTCAAGTCAC 660
ACTGGACAGC TGGGGTCCCC ACTCAATATT GTGAAGCCTT GGTGGGCTTC CTGGAAGAGA 720
GAGGGAATTC ACTTTGGACT TACCAAGCTC TACCAGAATT 760
|
