| Tag | Content |
|---|
EnhancerAtlas ID | HS034-16605 | Organism | Homo sapiens | Tissue/cell | ECC-1 | Coordinate | chr2:71785230-71786730 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr2:71786516-71786534 | TCCTCCTTCCTTCCTCTC | - | 6.35 | | FOSL1 | MA0477.1 | chr2:71785602-71785613 | GGTGACTCATG | + | 6.62 | | JUND | MA0491.1 | chr2:71785602-71785613 | GGTGACTCATG | + | 6.02 | | ZNF263 | MA0528.1 | chr2:71786464-71786485 | TCCTCCTCTTTTCTCTGCCCC | - | 6.04 | | ZNF263 | MA0528.1 | chr2:71786512-71786533 | TCCTTCCTCCTTCCTTCCTCT | - | 6.04 | | ZNF263 | MA0528.1 | chr2:71786526-71786547 | TTCCTCTCCCACCCCTCCTTT | - | 6.46 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CAGATTCACA CACCTGGTGA GTGGCAGAAC CCCCTTGCTG TGCTGCTCTG TAATGGACAG 60
AACCTGATGA TGGGGTGAAT ATGGGAGCCA CAGGAGGGTT CAGAATGATC CCCTGATCCT 120
GGCCAGGGGG GCTAGGTGGG CATGGGGGCT GTGCTCTGAG AGGGTCAGCA GGAGGAGGAG 180
CCAGTTGAGG GGGAGGTGAG GCATTCAGGA CAGGCTGTGT TGAGGTATCT GTGAGGAAGC 240
TGGCCTGTGG TCTGGAGGTG GGAGGACAGA GTGGGGTTGG AGGGGCACAT ATGGGCACGG 300
TCAGCCTGTG GTGGCTACAG CCACTGGGTG AGCTCCCCAG GGCATCCCCG GGGCCCCAGA 360
TCCCACCTGC AAGGTGACTC ATGGTGCCAT GTTGGCACCA CCTTGGGTGA GGTGGGTGGG 420
CCAGGACTCT GGGTTCTACC CGTGGCCCTG CACATGACCC CCGTGTTGTT TGTAGCTTGG 480
CAGGTCTGAG GAGCCTGGAA TATCTGAGAC CTGTGGGCCC TGAGTCCTTG GCTGCCCTCA 540
GTGACCTCTG CAGGGCTCTG CTCTTGGAGG ATCTGCCTAC AAACAGTTCT GGCGCCTTTG 600
AGTCACTCTC CTGGGGTTGG AAGAGTGGCT GGGCCTCCCA GCAGGGAGGC TGGTTCCAGC 660
TCAGGAGCTT GGGAGGGGAA CTGGGTTCCC GTCCTCTTGA GAATGCATAA TGCCTCTCTG 720
GGGGGGAATT CCAGGCAGCA GGAGCAATTC GCTCAGCTCC ACCTGAGGCC ACTGAGTGGC 780
CCAGCACCTC AGCTAGAGGG CTTCCTCCAC CTCTCACTGC AGTGCTGAGC ACCATCACAG 840
CTGATAGGCA GAGCAGCCGG GCATGGGGGC CCTGAGCGAA CTCAGGCCCA TAGCTGAACA 900
CAGCAGCTCA CCCTTTCTCC AGTCAGCCTG GCCCACTTCT CCAGCATCGG TGTTCCTCAT 960
TCCATCTCAG CCCTTTTCCC GGCTCATCTT CCGGGAGCCT CCCCCTTCCC CAGGGCTGGT 1020
GGTGTCCACT CTGTTCCTCC AGCCCAGCCC TCTTCTCTGA TCTCTAGACC TATGAACCCA 1080
AGGTGCTGGA CATGTCCACG TGGATGTCCC ACCAGCACCT CCGTGCTGCG TCTGGGGCTA 1140
CACATGTTGC AGACAGGTTT CATCACCTCC CAGCACTGTC TTTTCCTGGG TCCCCAGAAT 1200
CCACGCTGGA AACCTGAGCC AGCTCTGACT GCCCTCCTCC TCTTTTCTCT GCCCCAGCCC 1260
TGGTGGCTCT GCCTCACCCA TGTCCTTCCT CCTTCCTTCC TCTCCCACCC CTCCTTTAGT 1320
ATCCCCATCG TCTTCAAGCT GTGTCATGCC TGCCTCCATG TCAGCCCTGC AGTGGCTGCT 1380
GCTGCATCCA GGAAAAGCCC CTGCTCTCAT CCTGGTGGAC AGGCCTTTCT GTCCCCACCA 1440
CCTGCCTCAC GGAGCCCTAA CGCTTCTGAA GCTCTGCGCT AGTTTGTCCG GCCCTCAGCA 1500
|
| |
|
|
|
