| Tag | Content |
|---|
EnhancerAtlas ID | HS062-00052 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr1:8042080-8043040 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr1:8042534-8042553 | TCGCCACTAGGTGGAGGCA | + | 6.92 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_45526 | chr1:8042303-8043138 | NHLF | | SE_45858 | chr1:8042312-8043591 | Osteoblasts |
|
| | 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 |
| GH01I007982 | chr1 | 8042389 | 8042967 |
|
Enhancer Sequence | GCTGAAGTGC AGTGACGCAT CTCGGCTCAC TGCAACCTCC GCCTCCCGGG TTCAAGTGAT 60
TCTCCTGTCT CAGCCTCCTG AATAGCTGGG ATTACAGGTA CTGGCCGCCA GGCCCAGCTA 120
ATTTTTGTAT TTTTTTTTTT TTTTTTAGTA GAGGCGGGGT TTCACCATGT TGGTCAGGCT 180
GGTCTTGAAA TCCTGACCTC AGGTGATCCA CCTGCCTTGG CGTCCCAGAG TGTTGGAATT 240
ACCGGCATGA GCCACTGCAT CCGGCTTCCC ATTGCTTTTT CTCTGAAGAG ACTTTAAGAC 300
TTGGAGTCTG GTTTAAAAAA AATAAAGAAA TAAAAATCAA TGCCTTCTGC TGGTTGAACG 360
GGAAGTGTAA AATCTGAATT CGCTATAGGG TCACAATCCC AGCCTCCAGT TCGCACAGTG 420
CCTTCCTGGT GCTGATGGGG TGCATGTTCT GTCTTCGCCA CTAGGTGGAG GCAGTTGGTA 480
ACCTTAAACC TTTTGCTTCT CGTGGTTAAA AGTCTGACAA GAACCGTAGA ACCTTTAAGC 540
ATATTTAACC AGTTTAAGCC CTGTTTGCGA TGTTTTAGCC ACAAAGATAC TGTTCAGTGA 600
ACCATTTACA GTTGTGCCTC GCGTTGTCCC ACTCTCAGCT GTGCATCTCA CTGTCGCTCT 660
GGAAGACCTA GCCCAGCCAG TTTCTAGGTT AGCATTTGAA ATGGTCTTGG CCTGGTTTAA 720
CCATCAGTAA ATGAGGCCAG ATTATGATAA ACCTTTTCCC CTCAAACTAG GGATCCTCTT 780
TTTCTCTACA ATAGTTAAAT TGGAAATTGT TTATGTACTC TATTCATTTA TTTTGGTGGG 840
TGACCTGATT TTTTAAATTT TTTAGATTAG TCAAGCACAG TAGTGAGAAG AGGAGAAAGA 900
GTAGAACAAG GTGTAACTGC CTGTGAACGA TCAATTGAGA TAACTCACTG CCTTCGACCA 960
|
