| Tag | Content |
|---|
EnhancerAtlas ID | HS129-32243 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr6:117879680-117880820 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr6:117880501-117880519 | TGAAAGGAGGAAGGAAGG | + | 6.84 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr6 | 117880291 | 117880401 | | chr6 | 117880579 | 117880766 |
|
Enhancer Sequence | GGTTTGCTAG GACTCATCAG ACTAAGCAAA GCTTTATTCA CAATTATGAT TTATTACAGA 60
GAATATAAAG CAAAATGAGG AAAGGGAAAA GGCATATGGG CACAGTCCCA AGAAAATCAG 120
GTACAAGCTC CAAGATTCAT TTCCCAATGG AGTCACACAG GACATGCTTA ATTCCTCTAG 180
CAATAATGTG TAACAATACA TCAAGTGTTG TCCACCTAGG AAGCTTGCCT GACTGAACCT 240
AGGAGTCAAG GTTTTAGGGA AGTCAGTGTA GGTACCCTCT GCCTAGCATG TACCAAAATT 300
CTAGATTCCC AGAGGAAAGT AAGTGTTCAA CAAAAATCCT ACTGTTTGTA CAAACACTTC 360
AGGCACAGTA AACCGCACTT ACCAGCAAGG GGATAATGGG AATACTCCTG ATATCCAAAT 420
TGCTGGACGC TAGCCAAGGT CCAACCTTGC AAGCAGACCT AAAGACAACA GGTTCAGGCC 480
TGTTCTGTTA ACTCTTTTCT GCACACCATT TGTGAAATAG CCACTGAGCC ATGATTTTGT 540
GCCAACGACT AGATAAACTA TACTCACCAA CCAGATGTCA CTGTCTTTAC CCTTTGGGTG 600
GGTTCCTAAT GCCCATCTTA TTACCTGTTT CCTCAAATCT CACTCATGGT CACTTGTGTT 660
AATCTAGCCT CTCTAAGAAG CAGACGCCAA CACCAAAAAG GGATCTGCTG TGCAACAGAT 720
TTATTAACGG CAATGCCAGT GAGGAAAAAT AGGTAGGAAG CTGGAGTTGA TTGGAGGCTG 780
GAAGGCAATG AGATCACAAT GGAGTTAAGA CCCAAGGTGA ATGAAAGGAG GAAGGAAGGT 840
TGGGTGAAAG CAACTTGGAC TACAATGTAA TCCTAAGGGA GTTTGGCAAG ACCATCGTGG 900
AGTGCTCCAG CTAAAGTTGA GGAGTCATCA TATAATATCC CTGTCATAAT CAGTCACTGA 960
CTGGCAGCAG CATGGAGGAG CATAGCCTCA CCATGTACAC AGGGATGGAT TTCAGACCAC 1020
AGCAGCTGGA CCTTCAGTAA GCTATGCTCC CTCCTGCACG AGAACTGACA GATGCATTCT 1080
CATGGCTGCT GCCGTGGTGA TTATAGCTCT CAAATCACAC CTGAAAAAGG TTCATTATTG 1140
|
