| Tag | Content |
|---|
EnhancerAtlas ID | HS017-08383 |
Organism | Homo sapiens |
Tissue/cell | CD14+_monocyte |
Coordinate | chr12:117571380-117572490 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NEUROD2 | MA0668.1 | chr12:117571981-117571991 | ACCATATGGC | - | 6.02 |
|
| | 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 |
| GH12I117133 | chr12 | 117571692 | 117572356 |
|
Enhancer Sequence | GCTGGGATTA CAGGCATGAG CCACTGTGCC CGGCCTTACC TGCCTTTTTC TTTGACAGCT 60
TCTACCCTAT TGATTTCAGC TATGAACACG GTGGTATTCA GAAAATTGAA GTGCTGTAAG 120
GTTCTATGAT AAAACTGGTT GATCCTCAAC ATCCAATTTC GTCTTATTTA GGATGCACTT 180
TTTGCATCAC TATTTTCTTA GGTATGATTG ATACTGTGCT TAGGTAGGGA AGTGCCCCTG 240
TTCTTAGGAG ATGCATGCTG AAATATGTAG GAAGAAGTTT CAAGCTGCTT GAGACATTTT 300
TGAATGGTTC AGGGAAAAAG CACACATACA CTAAGAGGGA GATAAAACAG AACAACTGCT 360
GAGTCTTGGT GGGTATCTTG GTTTCCACTA CACTATTTTT TTTCAATGTT TTGATGTTGC 420
TTAGACGTCT ATTAAAAGAG CACTGTTTAA ATGAACTTTA CAGTAGGGGT GAGGACACTA 480
CAGCCTGTGA GCCTAACCCA ATCCACGGCC TGGCTCTGGA CATAAAGGTT TAAGGAACTC 540
GCTCGTATTG CCTGTGGCTG CTTTCCCGCT ACAATGGCAG AGCTGAGTCA CTGCAACAGA 600
AACCATATGG CCCGCAAAGC CCAAAATACG CACTGTCTGG CCCTTTACAG AAAAAGTGTG 660
CCAACCCCGG CTTCAGAGGA AATCGTATTT TCAGAAGCAA CTTCCTTCAG AAGTCTTTGT 720
AGGCTTAGAA TAGGTTTCCC CCAAACTTCA AGAGCACACG TTACTGAGAT GGTGAAGGAT 780
AACATTTCCT CGCTTTCCTT CTACAAAGTA AATGTGATTG ACAAGAGACA GTGCTGTAAC 840
TGGCCAGGAG GCTGCCATGT ACAGTTAGTG AGAAAGAAAT AACAAAGCTT GGCAGGGCAT 900
GGTGTCTCAC GTCTGTAATC CTAGCACTTT GGGAGGCTGA GGCTGGTGAA TCACTTGAGC 960
CCAGGAGTTT GAGACCAGCC TGGGAAACAC GGCGAAACCC CATGTTTACA AAAAAAAAAA 1020
AAATTTAAAA AGTAGCTGGG CATGGTGGCA CATGCCTGTG GTCCCAGCTC CTCAGGAGGA 1080
TGAGGCAGGA GGATCACTTC AACCCAGGAG 1110
|
