| Tag | Content |
|---|
EnhancerAtlas ID | HS060-29829 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr6:40687190-40688630 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr6:40688140-40688158 | GGAGGGAGGGAGGGAAGA | + | 6.16 | | IRF1 | MA0050.2 | chr6:40687499-40687520 | GGAGAGGAACTGAAAGTAAGA | - | 6.14 | | Nkx3-2 | MA0122.3 | chr6:40687581-40687594 | AAAAACACTTAAC | + | 6.06 | | ZNF263 | MA0528.1 | chr6:40688141-40688162 | GAGGGAGGGAGGGAAGAGGTA | + | 6.02 | | ZNF263 | MA0528.1 | chr6:40688137-40688158 | GAGGGAGGGAGGGAGGGAAGA | + | 7.74 |
|
| | 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 |
| GH06I040719 | chr6 | 40686943 | 40688858 |
|
Enhancer Sequence | CCCACTACTG CCTGCTATAC CTCCAGCTCC ACAGCCCCAC CAAGGCCCTT CTGCCTCTCC 60
TACTTTGAAT TCTTCTTTTT TTAGAGCAGT AAGCCCGGCA CTGAGAGGCA GTAATTGGGG 120
ATCTTTTGTT CCACACAGTC TCTGCCACGC TTGCTCCCAG GGTTGCAAAG TTGCTTTCTA 180
CTGCCAGGCA CATGGGGTTT GACCTTTTTC ATTTATTTGA ACACTTACCT TCCAAATAGG 240
AGAGTGGGGT GGAGCGTGGG GGGAGAAAGA GAGAGACAGA GACAGGGTGA TAGAGCAGGA 300
GACCTACAGG GAGAGGAACT GAAAGTAAGA TCAGAGCACT TAGAAAGAAA GAGGCAGGCA 360
GGCTCTGGGA AGGAAAACAG GAAGTGGGAA AAAAAACACT TAACTATGTA AGACTGAGAG 420
GCATCTGGAG CCCAGAGGAG CTGGAAGGAG ACACAGAGCC AGGGAGAGAT GGAGAGGATA 480
GACAGGGAGA TAACAGAGAG GAGAGCAGAC AGATGCAGAA AGAGAGCACA CATGGGAATC 540
CAAGCAAACT GGGGAGAGAG AATGAAGAGG TGGGAATGCC GAGTGAGGTG CCCTCTCAGC 600
TCTCAGAGTC CTGCAGTACG TGCACACCTA CCAGCCCAGA ATGTTAATTA CACGCTGCCT 660
TTAACAGCCT CCACTGCTGA GTCCCTGAAA GGGGGAGCTG GGATGCAAAC CTGCAGGCAG 720
CACGTAGCAG CCCCTTAGCC AACCCAGGGG CAGGAAGCAG AAGAACCTTT CAGTGTGATC 780
ACAGAGAGAG AGGCGCAGGA CAGTCTTGTG TGTCCCGCAG GAGTGGCCAG TGTCCCTCAT 840
AGACCTCAAG AGCCAGAAGA GAGGCTGACC AGCTGGGCTG GGGAGTGCCT GGATAGAGAA 900
AGCAGGGAGA GAAAGGACCC TGGGGAAGAG GAAGCTCGGG AGGGACAGAG GGAGGGAGGG 960
AGGGAAGAGG TACTAAGAGA CGAAAGATCC CTCAGGCCTC CCCACCCCCA CCTCACTTTT 1020
TGCAGACAAT AATCCCCTTC TGCCCCTTCT GTCCTGAGAT GAGGCAACCC CTCCCCCAAC 1080
TCCACCCACA GCATCCTTTC AAGTTCATCA GCACCATCTA TCACCACAGC CAAAAAGGTC 1140
TCAGTGCCTA TTCCTGCTCC CTGAGCCCTG ACCCAGCCCT GGCTTTCCAG CCAGCTGCAA 1200
GTGAGAAAAA CTTACTCTTC TCTTCAAGAG CATTATAAAA ACTGAGAATG CAACTTTCTC 1260
CTGAGTAATG AGAACTGTCT CTTTATGTCT AGCCCTTTCG TCCACCCCAC CGTCTCGTGC 1320
TTTGCCTCTC CAGATCCTCC AGCCAAGATC CATCTTCAGA TCAGGCATCC AAGTCAGATG 1380
GAGGAGGCCA GGCCTTGGCT GTGTAATCCA GGAGCTCCAA TCTCAGCTGT TTGCTCCCCT 1440
|
