| Tag | Content |
|---|
EnhancerAtlas ID | HS007-01229 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr1:203037830-203039000 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF16 | MA0741.1 | chr1:203038890-203038901 | GCCCCGCCCCC | + | 6.02 | | KLF5 | MA0599.1 | chr1:203038890-203038900 | GCCCCGCCCC | + | 6.02 | | SPI1 | MA0080.4 | chr1:203038437-203038451 | TACTTCCTGATTTT | - | 6.02 | | SPIC | MA0687.1 | chr1:203038437-203038451 | TACTTCCTGATTTT | - | 6.83 | | ZNF263 | MA0528.1 | chr1:203038077-203038098 | CCTTCCTTTTCATCCTGCTTC | - | 6.69 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_30830 | chr1:203037394-203039627 | Fetal_Muscle | | SE_37852 | chr1:203030164-203044276 | HSMMtube |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 203038629 | 203038730 | | chr1 | 203038197 | 203038850 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I203068 | chr1 | 203037443 | 203039582 |
|
Enhancer Sequence | ACAAAGGCTT AGGTATCTTG GGGGGTGGGG AGCTTTTCTA GGGCCTATGC CAGAGGGGAT 60
CGCAATGTCC TCAATTCTCC AAGTGATCGC TGTGCATAAG CAAGCCCTCA TGGGAACACA 120
TGGCCTTCAC ATACAGAGCA CACCTAGCGT GGGCCTGGCA CACAGTGTGC TCTTACAATG 180
CGCATCCCCG TCCTGCCCTG GGTACCTCTA TCTCCTCCTA ACCCCACTTC ATAGCTGAGA 240
CTCTGAGCCT TCCTTTTCAT CCTGCTTCTC TGATCTGACT TTTCTTAGAG GGGAATGAGC 300
CCCAGGGCCC CTAGGGACCA GAGAGCCCAT ATCACCTTTG TCTACCACCC TAGGGATCTG 360
CTCCTGGGCC CCCAGCCTTA AAAAAGCTAA ATATACCAAA TTACACAACC CAGAGCCTCT 420
CCACACCAGG GCTTTGGCTC TCTGTCAACA GCTCAAATGA TTAAACATCT CATGAAATTA 480
CATTTCATCA TTTTTATGGA GCTGTCATCT AAGAATATAT CTAAATTCTC TTGAACCTAT 540
TTATATTTTT GGCCTTTCTA ACTTCCTGTG GGTAATAGAT TCTAGAAGTA CTGCTTGTTG 600
TGTAGAGTAC TTCCTGATTT TATTTGTCCT GAAAATGCCC CTGTCAGGCC CCTGGGGAAG 660
GAACTACCTC CTCTTGATGG TTTAGGTTTG GTAAGGATAT TTGTATTTAA CTAGTTCTCA 720
CCTTTTATGA TTTCATAAAC TCTGATTGTA TTGCCTCTGG GCCCAAGCCT TTGTCTCTCC 780
AGACGGAGTG TTCTTAATTC TTTTAGGCTT TCCTCATATA GACTCGCCTC TGTCCCCTGA 840
TTGTTTTAGC TGCCCTTGTC TGGACTGTTT GCAGCTGTCA GATCTCTTTT GAAATTCAGC 900
CACCAGAGCT GCACAGGCTA TTCTGGGAGC AGACACGTTT TGGCTTGAAT GAGGGTAGGG 960
CTGTGTTGTC TCGTAATTCT GGGCAGTGTG TTGGCCTTTT GGGGGTGGTG GCAGTGCACA 1020
GGGCCATTGT GTCCTGTAGG CATTCTGCAG TGACCCCCCC GCCCCGCCCC CACCCCAACC 1080
AGTCAAAATA GATAGGACAG ATCCCTTCAT TCTCCAAGAG GAGCCTGGAT TTTTCCCCCA 1140
AGTGCGTTCT CTCCACTTGC CCACTTCGGG 1170
|
