| Tag | Content |
|---|
EnhancerAtlas ID | HS034-18252 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr2:242888650-242890110 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Arntl | MA0603.1 | chr2:242889814-242889824 | GGTCACGTGC | + | 6.02 | | RELA | MA0107.1 | chr2:242889991-242890001 | GGGAATTTCC | + | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 242888875 | 242889445 | | chr2 | 242889545 | 242889775 |
|
Enhancer Sequence | CCCCGTGCGC CCAGACCCCC ATGTCCCTAA ACCCCAGGGT GCACAAACCC CAGTGCCTAA 60
ACCCCAGAGC GTCTAAACCC CCGTGTCCCT GAACCCCGGA CTTAGCTGTT CTTTAAGCTT 120
CCCTATTTCA ACAAACTTCC AAACAATTTT AGTGGAGTTT TATATTTACA GGATGACGGA 180
GAAGAAGGCA GAGTCCCGTG GACCCCACGC CCACGTCCCC GTACTGGTGC CTGTGTCGTA 240
ACTGACCAGC CCACACTGAT CACTGATCCG TCATCATCGA CAGGACAATA TTTCATTCCG 300
CTTTCTTGGT TTTCTCCGTC TTTCTGTGCC AGCCCCGCCT CTGGGACTAC ATGTGGCGTT 360
TAGTCACCCG ACCCCTGGGG CTGCCCTTGG CTGGACGTTT CTCAGGCTTT CCTTGTTTCT 420
GACGACCTTG AGGGTTTTGA AGGGCTCTGT TAGGAACTCC GCGGAACGCC CCTCTTGGGG 480
TTTGGGTTTT CTCGTGCACC GACAGGACCA TCCCTGAGCC CGAGCTGGAT CACGTGCTGG 540
GCTCTCCTCG CCCGGCGGTA AATCTGTCCA GAGCTTCTTT CTGTCCCTGT GGACTTGCGG 600
ATGCTTCCGT TACACCTCGG GTTACCGCCC AGCGCTGCTC TGTTTTCCCG TTCAAATGGT 660
TCCAGCGTTG GCCTCGGGAG CGCTTTTCAC GAGCCCCGTG TCCTCGCGGC GAGCCCCGTC 720
GTTGTGGTGT GTGTTTGTGC ATCTCCTCGC TTTCTGACAC TACAGGTACT TCCAGTGTCT 780
CCAGCTCCGA TCCGTCGGTC GCCCCATGGA TCGTTCTGGC CCCGCCCTTT GCCCCTGCAG 840
CCCCACCCCC CACCTCAGTG AAAAACCCAC GCCCCCACCT GCCGTCCATT CACGTCGCCG 900
CCCAGATGCA GCGTCCACGG GTAGAGGTTT CAGAATTTCA CACGGTGTTT CCGTTTACTG 960
TTTGCACGTG TGTGTGACGC GGAGGCGATG GGAAGCATTC TGTTTATCTG TGGCCTGGGG 1020
TGAGGCTCCC CGTGCAGGGC CATCTGCCCG TGGGCCTGCC CAGACCTGGG CTTACCGTCC 1080
TGGAACGGAG AAAGGAATCA TGAGCAGTGG TTCCGGGAGG CTGGGAGGGG CGAGGCCGGG 1140
GAATGGGGCT GGGGCAGGGG AGGAGGTCAC GTGCTGTCTT CATAGGCTTT GGTATTTGAG 1200
GCACGTGGCT TGTTACTATT TGAGGATAAA ATTTGAAAAC CGTAGCACGA AGGACTTAGG 1260
TTAGACATCG GAAAGCACTT CCTGGCAGTG GCTACGGGGC AGCTTTCTGA GCTTTTCCTA 1320
AGCCACCCTG TCACTGTGAG GGGGAATTTC CTCAACCTGC CCTCCAGCGA CAGCCTCCAC 1380
CTCATGGCCA ACCCCCGAGG GCGGCTTCCG GGGCTTGCCC TGCTGTGGAT GAGGCCAGCT 1440
TTGCTCCCCA CTCTCTCTGG 1460
|
