| Tag | Content |
|---|
EnhancerAtlas ID | HS088-52241 | Organism | Homo sapiens | Tissue/cell | HeLa-S3 | Coordinate | chr8:145632950-145634390 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr8:145633983-145634001 | CCTTCCTTCACTCCTTTA | - | 6.02 | | EWSR1-FLI1 | MA0149.1 | chr8:145634193-145634211 | GGTAGGAAGGGAGGCAGA | + | 6.32 | | Spz1 | MA0111.1 | chr8:145634213-145634224 | AGGGTAGCAGC | + | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ATCCCAGCTA CTTGGTGGAG GGTTTAGGGA GCTGAGGCAC AAGAATTGCC TGAACCCACG 60
AGGCGGAGGT TAAAGTTAGC TGAGATCACA CCACTTCATT CCAGCCTGAG TGACACAGCA 120
AGACTCCGTC TCACCAGGAA AAACAAAAAA AAAAATTATT TGTAGAGATG GGGTCTTGCT 180
ATGTTGCTCA GGCCAGTCCT GAACTCCTGG CCTCAAGCAG TCATCCCACT TCAGCCTCCC 240
AAAGTGTGGG ACTATAGGTG TGAGCCAGTG CACCCAGCCT GAGATTCGGT TACAGGACTC 300
GCCGTGGCTT CAGTCTTGGT GGGTGTCTCA TTGTGAGGGA GGCTGCCATG TTGTGAGCTG 360
CCCCAGGGAG GGGCCCATGT GGTGAGGAAC TGCGGCCTCC TGCCAATAGT GTGTTAGGAG 420
CAGAAACTCC AGCCCTCGTC AAGCCTTCAG AGGACAGGAG CCCTGGCCAG CAAATACATA 480
TGTATGCCGG GGTAGGTGCC CAGGAGGGTT GGCCTCCTTT GGCCTGAGCT TCTGACCCAT 540
CTGCCTGCTG GGTCAGCCCC TATTCACAAC CCTCTTGTGG CTCCTCCCTG CTTTGTGGAG 600
AATAGTCCTG ACCACGGCCT ACCTCCCTCC ATCCCCACCA CCACATCCAG TCTATACCAC 660
GGCCACACTG TGCATGTCTC TCCACCCTCA ACTGCTTTGG GCCTGTGCAC AGGCTGTTTC 720
TTCTGCCTGG AACACCCTCC TCTCACCATC CCTGGGCCTG GGTAAGAGGT ACTCCTCCCT 780
TCAAGAGCAA TGGAGAAACT GCCTCTTGCA AGTTGCTTTC CTGGACCAGC TTTCAACCCT 840
CCGGCAACCA AAACACCACT GTATTTCCCA AACCCTTGAG GCGTGTGCCC CACTGTACCA 900
AGACTCCTGT CAACAGTCTG TCCCCATCCT AGACCTGGCC TTGTTCCTTG TGCTACCAAT 960
GTCCTTCCCC CGACAAACTC CCGCTCTGCC TCAGACAGGC TCTTCTGATC ATGCGACTGG 1020
AAATACACAG TCTCCTTCCT TCACTCCTTT ATTCCCGCAG CAGCACTTGC TGCAGGGGCA 1080
GGTGTGTTTA TTTAGATGTT CCCCTTCCCC AAGTGTCTGC AGGTGTGGTT CACATGGTAT 1140
CTCTGCTACC CAGCGCACAG TGGGCGTTCG CTCCTTCCGA ACAACTTGCT GAAAAAACGG 1200
AAGAGCAAAC AAGACGGCTA GGGCAGCGCG CCCTTCCCGG TGGGGTAGGA AGGGAGGCAG 1260
AACAGGGTAG CAGCTGTGAG AAAGGATCTG AGCACAAGAG ATTCAGGGTC ATGTCCTGGC 1320
TCCTCAGGCT GAGGAACGTT AAGCAAATCA CTCAACTTGT CTGGGGCTTG GCTCTTCCAT 1380
CTGCAACCGG GGGCGGTGAG AGCACCCACG TCGCGGACAG CGGGGAGGGC TCCCAGGGCC 1440
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