| Tag | Content |
|---|
EnhancerAtlas ID | HS099-01372 |
Organism | Homo sapiens |
Tissue/cell | HSMMtube |
Coordinate | chr1:150166080-150167560 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr1:150166345-150166356 | GGTGACTCATG | + | 6.62 | | JUND | MA0491.1 | chr1:150166345-150166356 | GGTGACTCATG | + | 6.02 | | RARA(var.2) | MA0730.1 | chr1:150167433-150167450 | TGGTCATGAGAAGGTCA | + | 6.09 | | Twist2 | MA0633.1 | chr1:150167427-150167437 | AACATATGGT | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 150166670 | 150167023 | | chr1 | 150166245 | 150166384 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I150193 | chr1 | 150165894 | 150167634 |
|
Enhancer Sequence | ATGTGCCACC ACGCCCAGCT AATTTTTTTG TATTTTTAGT AGAGATGGGG TTTCACCATG 60
TTGGCCAGGA TGATCTCAAT CTCGACCTCG TGATCCGCCG CCTCGACCTC CCAAAGTGCT 120
GGGATCATAG GCGTAAGCCA TTGCGCCCGG CCAACTCCAG CCATTTTTAA GCTATACTTA 180
AGATCTTTCT GTCTTACATT TCTGTAATGA GACAGCTAAT CACAACTAAG CGGGTTGGTT 240
ATAAAGATCT AAACCGGCCG GGCGCGGTGA CTCATGCCTG TAATCCCAGC ACTTTGGGAG 300
GCCGAGGTGG GCGGATCACG AGGTCAGGAG ATCCAGACCA TCCTGGCTAA CAGTGAAACC 360
CCGTCTCTAC TGAAAATACA AAAAATTAGC CAGGCATGGT GGCGGACGCC TGTAGTCCCA 420
GCTACTCGGG AGGCTGAGGC AAGAGAATGG CATGAACCTG GAAGGCGGAG CTTGCAGTGA 480
GCTGAGATCG CACCACTGCA CTCCATCCTG GGCGACAGAG TGAGACTCCG TCTCAAAAAA 540
AAAAAAAAAA AAAAAAGACC TAAACCGACA TTGTAAGCAA GACAATGCTA CAAAATATGG 600
AAGACACAAA GAGAGTTCCT ACCCTCCAGA GAATTTCCCT GAGACGAGTA CTGCCTTTCA 660
GTTTTCTCTG TTGTGGGGAC AGAAAGAATA ATGGTAAGAG GCTGAGTAAT GGCTGCATCA 720
TGAGGGTAGT CTAGACAAGC AACCCATGGA TATGCAAGAG AAAGACTGTC TCCAGGGGTC 780
CATGAAAGAG ACTGCCTGAA GGTGGGTGGG ATCTTGATGA GATGGAAAAC CTTCCAGGCA 840
GAGGGAAAAG TGTGAGCAAA GACAGAGAGA TTTGTGTATT CATTTCCCAG GGCTGCTGGA 900
ACAAGGTACC ACAAACTGGG TGGCTTAAAA CAGCAGAAAT CTCTCACAGT TCTGAAGGCC 960
AGAAGTCTGA CATAGAGTTG TGGGTGGGGC AATACTTTCT CTGAAGGCTC TAAGAGAGGA 1020
TTTTCCTTGC TGCTTCTTAG CTTCTGGTGG TTGCAGACAA TTCTTGGCAT TCTTTGGTTT 1080
GTAGACACAC ATCACTCCAA TCTCTGCCTC CACCGTGATA TGTTGTTTTC TTTATATGTC 1140
TCTCTGTTCA CATGCCCCCC AGCTCTGCGT CTGTATCTAT ATCTCCTCCT CTCATAGGTA 1200
CATAGCTTAT ACTGGATTAG AGCCCACCCA CCCACTAGGA CATCATCTTA ACTACATCTA 1260
CAATGACTCT ATCTCCAAAT AAGGTCACAT TCATAGGTAG GCATTAGAAC TTGAACATAT 1320
CTTTTTGAAG GACACAATTC AACCCACAAC ATATGGTCAT GAGAAGGTCA GTGTGGTCAG 1380
AAAGTAGAGT ATATCTAGGG AAAGAGTGGA AGTAACTCAG GAAGAAGGGG CTGGAGTATA 1440
GAGAACCTTG ATGAATAAGC AATGAGGGTG CACAGAATAT 1480
|
