| Tag | Content |
|---|
EnhancerAtlas ID | HS175-02663 |
Organism | Homo sapiens |
Tissue/cell | SK-N-MC |
Coordinate | chr1:203021010-203022110 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr1:203021869-203021887 | CCTTCCTTCCTTCTCTAC | - | 6.73 | | EWSR1-FLI1 | MA0149.1 | chr1:203021865-203021883 | GCTCCCTTCCTTCCTTCT | - | 6.82 | | EWSR1-FLI1 | MA0149.1 | chr1:203021861-203021879 | CCTGGCTCCCTTCCTTCC | - | 7.55 | | Myog | MA0500.1 | chr1:203021124-203021135 | GACAGCTGCAG | + | 6.62 | | Tcf12 | MA0521.1 | chr1:203021124-203021135 | GACAGCTGCAG | + | 6.14 |
|
| | 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 |
| GH01I203051 | chr1 | 203020347 | 203021868 |
|
Enhancer Sequence | GGGGTGGAGG GATCTCCTCA GGGAGTTTGG GGTCAATTCG GCCGCGTGCC TGGCTCCAGT 60
TACGCAGACG GCTGGTGTGT GGGGCAAATC CTTCCCCTTC CCTCCCGTGT CAATGACAGC 120
TGCAGCCCTG GGGTTGAGGC CATCGTCAGC TGCAACAGCT GTGCCCCCCC CCCCGCTTGC 180
CTTGGCCTCC TGGTGGGCAA GAGGTGGGGG CTGGCAGGCA GCCAACAGTC CCTGAGGCCC 240
CACTGAAGTG TGTGTGCGTG TGCCTGGGCG TGCAGGCGTG TGTATCTGGT GGTCGGGCGT 300
GGGGGGTGGG GGAGCTTCAC GGGTAAGATG GAATTGGCAG ACTTTCTGGA ACAAAAGCTG 360
TGGTTCATGG CGGAGACGAG GGAGGGATGA CAGGTTAACT GGCCCTTGGG ATGGCACCTG 420
GAGTTTTCCG AGAAGCAGCT GTGAGTTCAT GCTGTCTGAG TCTGCCTAGG GAGATTAGGG 480
GAGAATGAGG AAAGATATGG GGCAGAAAAA TGCCGAGTTT GATCTTTTGG GAAAGTGCAA 540
TTATTCGTCA TGCTCTGTCC TGAATCCAGG TCCTCTAAAT ATCATTTAGA GCACTGGGGT 600
ATTAGAAGAT ATAGATGGAG AAAGAGGGAA CTCCTAGTCT CAGGGGAAGA TTCACTCTGC 660
CCTTAAGAAA TCCTCAGTCC GATGGGGGAG TCACAGTCTG AAGGTGCCTC TTTTTCTTTC 720
TCCCCCGACT TCTTTGCTCT TTCTGTTTAT AAGAATATAG CAGCTATCCA GGAGCTGAGA 780
GGCTGCAGGA GCCTGAAGGG GAGCTAGGGG GCTTGGGTCA TAGAGGATGG GTGTTAGAGT 840
ACCTTTCTGT CCCTGGCTCC CTTCCTTCCT TCTCTACTCT TCTGTTCTCC ACCCTCCCCT 900
CTTCTGGGCC TTTGTCCGCT GGATAGGTTT GTAGGATGAT TTCAGAGAAG CTGCCGCCTC 960
TCAGGGTTGA CCAGACTGTC CTGTGATGAT CTGAAACTCT GCAGACTGTC TATTCAGGCC 1020
TGCTTGGCCT TTCTGTTCTC TGGGTGTAGT CAGCCTTTGA GTTTGTATGG ATGGAAACTG 1080
ATAGCATTTA TGTAGTGCTT 1100
|
