| Tag | Content |
|---|
EnhancerAtlas ID | HS098-21388 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr16:21199250-21200360 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr16:21199703-21199714 | GATGAGTCACC | - | 6.32 | | JUND | MA0491.1 | chr16:21199703-21199714 | GATGAGTCACC | - | 6.62 |
|
| | 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 |
| GH16I021187 | chr16 | 21199161 | 21200521 |
|
Enhancer Sequence | CAAAGTGCTA GAGGCATTTT TTGTTATCAC GATATGCGTG CCTGTGTTGG GTGCTGCTGG 60
CATGTAATGA GTAGGGGCCA AGGATGCTGC TCAACATTTT ACCAAGCCCA GGACAGGCCT 120
CCACAACCAA GAATTATCTG GGCCCAAATG TCAACAGTGC CAGTCTTGAC AAACCCTAAC 180
CTCAACAAAT AATAAGAATT AAGAGAATTA GGCCAAGCAA GAGCACAGCT GGTGGAGAGG 240
GGGTCAAAAT TGACCAGGTC TGCCCCAGAG TGACCAGTGG CAATCGTGGC ATCATGGAAA 300
CACACAAGTT CACAGTTGTG AAATGGTTCA GGTTGTCAAA GAGTTTTCGT ATCAGTTACC 360
ATCCTTACCT TTCATAACAG TCCAGAGACG TTATTCTGCT CTCATTCCCA TCCCCTACTC 420
TTCAGCTGAT GGAAGAGGAA AGCAGGGTTA ATGGATGAGT CACCTGTGGA AGTTCTCAGA 480
GTCAGCAAAT GACTAAGCCA CAGAACCCGG TTATCGGCCT CCTAGCCCAC GTGCAGATCC 540
TTTCCTCCCC CTTCTGCTGC CTTTTTTGTT AAAGCAGAAG TGACAACGAC GAAACGTTCG 600
GAAGATGGAC TACAGTGTCC CATGGCAGTT GGGAGTCAGC CATCCAGGGG GTCCATACAC 660
TGCAGAGGGC ATGCTCCGTG TATGGACCTC CAGGCTGGAG AGGACATGCT CCGTGTATGG 720
GCCTCCAGCA GCACACATTG TTTGTTCATG TTTCCAAAAC TCAGGAGGAG ACTCAAGCCC 780
CAGCCACATG CTCTAGGAGT CTCTATGCCC CTGTTAGGAG CTCCCGTGCT GGAGTTTCAA 840
TCCCCAGCTG GAAACCTTAG AAAAACCATC AGAAGGAAAC GCAACTGTTT CCTAATGAAA 900
GCGTTTCATC TCTGAGCCAG TAGAGGGAGC GCACATCCAG GCCATCCGAA GCTGGCTCAG 960
CCGAGACTTC AATAGCACCG AGGGCTGGAA GAAGCATTCA ACGCGCGATC CTTGAACTTG 1020
AATGAGCCTA TGCATAGGAG CCTGTTAAAA GCCAAATTCG CGGGCGGATC ACGAGGTCAG 1080
GAGATCCAGA CCATCCTGGC TAACACAGTG 1110
|
