| Tag | Content |
|---|
EnhancerAtlas ID | HS049-04322 |
Organism | Homo sapiens |
Tissue/cell | Fetal_spinal_cord |
Coordinate | chr2:1858340-1859450 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RFX1 | MA0509.2 | chr2:1859214-1859230 | GGTTTCCATGGAAACG | + | 6.47 | | RFX1 | MA0509.2 | chr2:1859214-1859230 | GGTTTCCATGGAAACG | - | 6.47 | | RFX2 | MA0600.2 | chr2:1859214-1859230 | GGTTTCCATGGAAACG | - | 6.88 | | RFX2 | MA0600.2 | chr2:1859214-1859230 | GGTTTCCATGGAAACG | + | 6.91 | | RFX5 | MA0510.2 | chr2:1859214-1859230 | GGTTTCCATGGAAACG | + | 6.5 | | RFX5 | MA0510.2 | chr2:1859214-1859230 | GGTTTCCATGGAAACG | - | 6.63 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_68228 | chr2:1839057-1874755 | TC32 |
|
| | 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 |
| GH02I001854 | chr2 | 1858495 | 1858644 |
|
Enhancer Sequence | TTTTTCATCA TGAAAACAAA CAAAACTATA TTGATTTAGC TCATTTTTAG AGCTTTCACT 60
GTACTGAGGA AGAAAAAAAT CATTGGAAGG AGGCTTTTCT CTCTTAAAAG GATTGTTCTC 120
ATTTCCAGGA TTTCGAGTTG GGCGGGTGGG GCGTTCATCC CAGGCGTGCC ACTTGCTAGC 180
CGCGTGAATG AATGTGGGGA AGCTGTTTGG CCCGAGAAGG CTCACAGTCC TCCTGGGCCT 240
GACGTCGTCT CCTTCTCTTG AGACGCCTCT CCACCCGCCT GCATAGGTTC CTGTGAACGC 300
CACAGTTCAG GCTGCCCTCA ACGTCCTCAC TAGCGCCCAG AGCAGAGACA TGCTGGAAAC 360
ACTGGCTGTG TCTCCCTGAG ATAACCAGCC CCCGGTTTTC GGGGGTGGTA ATTCAGCTTT 420
TCCGTCTTTA GGTGGTGCTT CTAGACCACA TAAGGCAGCC CAGAATGGCT TTTCAAGGGT 480
TCCTCCTTCC AACCGCTCTT GGTATCCATT TTTATGTTAC TGTTCAAGAA TTTAAGGCTC 540
TTTAAAAACT CATAGATTTA CATACAAATT TCCTAGCTTT AAGAAATCTC AACATTAAAA 600
AAATACAATG TTCTGAAGTC GATGGATGGG GAAGTGACTG TTCATCTAAC AAAAGGGATC 660
TTCGCCTCTC AAACGGAGTC AGCTCCAGGA TCCTCGACCA CGGGCGTGGC GTGAAATCGA 720
TTTACAAACA CGCGATTTGT ATCTGCCCAT CTAGGAGCAT TGCCTTTTCC ACGAAGGAAG 780
CCCAGGTGGG ACAATCAGCA TCCCCCGTGG ATAGAATCAG ATGGCAGCCT GTGCTGCACA 840
GCTTGGGTTT GGAAATGGCA GAAGAGATTG ACTGGGTTTC CATGGAAACG GCCTCTCAGC 900
TCCCTTTCAG GGAGGCTGCG GCTCTCAGCG CTGCAGCACT CAGGCTGCTG GGGAGCAGAG 960
TGGGGTTGGA AAGAGCACCA CTCACCTAGC GCCCCGCCTG CTTTCCTGAC AGTTACCACG 1020
AACAATAACA GCAAGGCTAT TTTAAGTTCC TGTAGATGGT TAAGGTGTAA ACTTGCATTA 1080
AATAAAACGC TTGGTTATAT ATACATATGT 1110
|
