| Tag | Content |
|---|
EnhancerAtlas ID | HS049-01982 |
Organism | Homo sapiens |
Tissue/cell | Fetal_spinal_cord |
Coordinate | chr12:121678670-121679500 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2C | MA0497.1 | chr12:121678901-121678916 | TTGCCAAAAATAGCA | + | 7.13 | | NFKB1 | MA0105.4 | chr12:121679359-121679372 | AGGGGAATCCCCG | - | 7.04 | | NFKB1 | MA0105.4 | chr12:121679359-121679372 | AGGGGAATCCCCG | + | 7.34 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_09417 | chr12:121675310-121679936 | CD14 | | SE_28089 | chr12:121673492-121679558 | Fetal_Intestine | | SE_28761 | chr12:121673137-121679628 | Fetal_Intestine_Large |
|
| | 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 |
| GH12I121235 | chr12 | 121673672 | 121679877 |
|
Enhancer Sequence | TCCTGCTCAC CGAACAGAAA ACCAACATTA AGACTCTGAG AAATGCCAGC GAGGCCCTGA 60
GCCAGCTGCT CCCACATCTG GGCCCCCTGC CCAAGTGGGC CGTCGCGCAC CCCCTGGAAC 120
GTGATCTACG TAACCCAGTC TTTGAGATCC TCTCCCCTTT TCCTTGCTCA CATAAATTTT 180
TCAAAGGAGA CTTTGCACGC AGCCCCTCTG TAAATGAAAG ACCAGCATCA TTTGCCAAAA 240
ATAGCAAGGA CCCGTACAAC AGTTCCAAAA CTATGTAACA CCAAAATTCA CTGCACAAAT 300
CCCAAGTAGA AGGCACCCCC CACCCCACGG CGCCTGTCAT ACCAGGTTTT TAGGTACTTC 360
GATCCCCCAC TTAGGCTATG AGCCCTTACA GGGAAGGGAC TGTGACGCTT GTCCTCAGTC 420
ACCAGATGTT GAGTTCCTTG TGTGTGGGGG TGATCAGAGC CTCCCCTGCC TGGCCTGGCA 480
CACAGCTGGC CCTCAAGAAA GGGCAGATGA CAACTGCTCC AGGGATCCTC CCGCCTCAGC 540
CCTCCTGCAG CCAGCCCTGA GGGAGGAGCA CCTCAGACAG AAGAGGAGGC CCCTTCCCTC 600
TTGGAAGTGG GAGGAGGAGA GCCCTTGTTT CCCTGAAGAG CCCAGGCTGG AGCCGCCGGT 660
GTGACAGCGT GGATGGCGTG ACAGGTGCGA GGGGAATCCC CGAGCCTATC CCCTCACCAC 720
CATCACACAG CTCCCCTGTT CTTAGGGAGG TCACTGGGCA TGCCACATGG GTTACTGTCT 780
GTCCTTCCCC CACAACAATC CGTGTCTCCT GTCCAGGAGG GAGACTGTCC 830
|
