| Tag | Content |
|---|
EnhancerAtlas ID | HS049-05354 |
Organism | Homo sapiens |
Tissue/cell | Fetal_spinal_cord |
Coordinate | chr22:41418260-41419010 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Arntl | MA0603.1 | chr22:41418636-41418646 | GGTCACGTGC | + | 6.02 | | CDX2 | MA0465.1 | chr22:41418489-41418500 | TTTTATGGCCT | - | 6.02 | | Klf1 | MA0493.1 | chr22:41418298-41418309 | GGCCACACCCA | + | 6.62 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_24366 | chr22:41417040-41419155 | Colon_Crypt_2 |
|
| | 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 |
| GH22I041020 | chr22 | 41416521 | 41419845 |
|
Enhancer Sequence | CGCAGAGGAC GACAATCCGG GCCGCCTGGG CTGGCTTCGG CCACACCCAG AGGCCGCACC 60
TGGGCCGGCG CCCTCTCTCG GCGCAGCCTC GCGCGCCCGG TCCCCGCCGC GCTCGCGTCC 120
CGGGGGGCGA GTGGGTCCAG ATCCCACGAA CCCCAGCCGG GACCCGCCCT CCCAAGCTCC 180
GGGGCCAAGG TGGGCCACCT CTCTCTCGGG CTCTTCTCTT TCTGATCTTT TTTATGGCCT 240
AAACTCGAGA TCTCCCCACC CTAGTGCCCC CACCCTGCCA CCCAACCCAA GGACTGAGTC 300
TGGAGGTCGA CCCTGAACCT TCCCTGATCC TCTACGACGT TCCGCGGCCG CAGTCCTCCC 360
GGGCCCCAGG GCTGCAGGTC ACGTGCCCGC GGTGGGGGCA GGGAGGGACG CGCAGCGGAG 420
TCTCCGGGCT GCACGTGCAA GGCCTCGGGG AGGGTGGAGC TCTGGCTTCC CGAGCTGCGC 480
TCGCTCCCGG CTTCCGCCGA GGTGCCCGGG GCGCCGGCCT GGAGCAGGCG GGGGTCTGGG 540
TGCCTGGGCT GCGGTCGGGA GCGCCTCCGA AGAAGCACTC GGTGCCTGCC CCGCTGGGAG 600
CGCAAGCATT GTTACCTATC AGCGCCGCAC TTAACAGTTG TTAATAGCAG TAAGCCCTCA 660
CTAAATTGTC ACTGCTGGCA GACCGCAGTA ACTCGGTCTG ACCTCAAGCA CCCGATAAAA 720
GAGTTCTTGT CCGTAAAGTC AGTTACGTAG 750
|
