| Tag | Content |
|---|
EnhancerAtlas ID | HS059-46652 | Organism | Homo sapiens | Tissue/cell | GM12878 | Coordinate | chr8:145633060-145634390 | 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 | TGACACAGCA AGACTCCGTC TCACCAGGAA AAACAAAAAA AAAAATTATT TGTAGAGATG 60
GGGTCTTGCT ATGTTGCTCA GGCCAGTCCT GAACTCCTGG CCTCAAGCAG TCATCCCACT 120
TCAGCCTCCC AAAGTGTGGG ACTATAGGTG TGAGCCAGTG CACCCAGCCT GAGATTCGGT 180
TACAGGACTC GCCGTGGCTT CAGTCTTGGT GGGTGTCTCA TTGTGAGGGA GGCTGCCATG 240
TTGTGAGCTG CCCCAGGGAG GGGCCCATGT GGTGAGGAAC TGCGGCCTCC TGCCAATAGT 300
GTGTTAGGAG CAGAAACTCC AGCCCTCGTC AAGCCTTCAG AGGACAGGAG CCCTGGCCAG 360
CAAATACATA TGTATGCCGG GGTAGGTGCC CAGGAGGGTT GGCCTCCTTT GGCCTGAGCT 420
TCTGACCCAT CTGCCTGCTG GGTCAGCCCC TATTCACAAC CCTCTTGTGG CTCCTCCCTG 480
CTTTGTGGAG AATAGTCCTG ACCACGGCCT ACCTCCCTCC ATCCCCACCA CCACATCCAG 540
TCTATACCAC GGCCACACTG TGCATGTCTC TCCACCCTCA ACTGCTTTGG GCCTGTGCAC 600
AGGCTGTTTC TTCTGCCTGG AACACCCTCC TCTCACCATC CCTGGGCCTG GGTAAGAGGT 660
ACTCCTCCCT TCAAGAGCAA TGGAGAAACT GCCTCTTGCA AGTTGCTTTC CTGGACCAGC 720
TTTCAACCCT CCGGCAACCA AAACACCACT GTATTTCCCA AACCCTTGAG GCGTGTGCCC 780
CACTGTACCA AGACTCCTGT CAACAGTCTG TCCCCATCCT AGACCTGGCC TTGTTCCTTG 840
TGCTACCAAT GTCCTTCCCC CGACAAACTC CCGCTCTGCC TCAGACAGGC TCTTCTGATC 900
ATGCGACTGG AAATACACAG TCTCCTTCCT TCACTCCTTT ATTCCCGCAG CAGCACTTGC 960
TGCAGGGGCA GGTGTGTTTA TTTAGATGTT CCCCTTCCCC AAGTGTCTGC AGGTGTGGTT 1020
CACATGGTAT CTCTGCTACC CAGCGCACAG TGGGCGTTCG CTCCTTCCGA ACAACTTGCT 1080
GAAAAAACGG AAGAGCAAAC AAGACGGCTA GGGCAGCGCG CCCTTCCCGG TGGGGTAGGA 1140
AGGGAGGCAG AACAGGGTAG CAGCTGTGAG AAAGGATCTG AGCACAAGAG ATTCAGGGTC 1200
ATGTCCTGGC TCCTCAGGCT GAGGAACGTT AAGCAAATCA CTCAACTTGT CTGGGGCTTG 1260
GCTCTTCCAT CTGCAACCGG GGGCGGTGAG AGCACCCACG TCGCGGACAG CGGGGAGGGC 1320
TCCCAGGGCC 1330
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