Tag | Content |
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EnhancerAtlas ID | HS184-02343 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr1:207413910-207415300 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOS | MA0476.1 | chr1:207414272-207414283 | TGTGACTCATT | + | 6.62 | PBX1 | MA0070.1 | chr1:207415240-207415252 | ACATCAATCAAT | + | 6.44 | TBXT | MA0009.2 | chr1:207414261-207414277 | TGGCACCAAAGTGTGA | + | 6.04 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I207239 | chr1 | 207413145 | 207418270 |
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Enhancer Sequence | ACTCCTGTAA CAGTCTTTGC AGCTGAACTA GGTAGGCAGG TCATTTTCAG GCCTTTCCCA 60 AAACTCATCT TCTTGTAGTA AAAATCAGCA TATTTATTAT TATTATATTA TTATTCAAGT 120 ATTATTTCCC ATGAATTATA ATTATGTACA TAAACAGCTT ATCTTTTACT GCCTTTTTTC 180 AGAGACATAA CACCAGGCTG AGTGTGGCTT TTGGCTGATT GAAAACCATG CAAGCATTCT 240 TCAGGTCTGA TGGAATCTTG CTGTCTGTGT ATGTTCCCAC TTGCAGCCAC ATGCTCCTGC 300 ATGCTTTTCA GTGCTTCAGG CACCACATTT CCCTCTTTTA ACAGACCAGA ATGGCACCAA 360 AGTGTGACTC ATTAGGTGAC TTAGGTAAAT CAGGAAAAAC AAAAAGGAAT GTCCCACTCA 420 AATATTGTCT GAGTAATTTT GTCAGGCCTG TCTGTATTCT TGAGGTTTTT TTTTTTTTTT 480 TTCCGTATTT CTCTTTCCCC CTCAGGCTTT AGAACTTTTG GAAGGAAATG TAACTTTCCT 540 CATCAATTTT GTTTTGTTTG TTTTTTAATT TCATCCTTCT GTTGGCAGTC CAAATTCATA 600 ACTGAAGCCA CACCTTGTCC TAAGTAGGCA GTGCTGCTCA GGATGGCTTT CTCTCACGCT 660 GTGATTTCCT GACTCGAGTG GATCTCACAC TCAGACTTAT CACACTCAAG GTTTGCTTTA 720 AGGGTGACTG AGCCTGCCCA CTCTGAACCA AAGTCCTTTT TTTCCATCCC TTATTTGTTT 780 TTTCACTCAA AAATGAATTA CTTACATTCC TAGATAACAA TCTCTTTTAA GTACAGCTCC 840 TATCCTGTAA GGAAAAGATT AGGGTTCTAT TGCTAAATGG CTTCAGAGTT CCACAAGGTT 900 ACTTACTCCT TGCATCAGAG CCCCTGATGC TAAAATTGAA GTTTTGAGTG TCCTTTGACT 960 CAGTTGATTC TAGGAACCCT GATTCCACCC TCTTGCCCTG AGCTCTTCCT TAATGCAGAG 1020 CTTGGTCTTG ACCTGACTTT GCCCCAGGGT GTAGCTGCTA CTGGCTATTG GACAGCTGAC 1080 CTCCAGTTTG GCAGAGGCTG CTGCTAGTTC TCTCTCTTTC CTTTAGTTGT TTCTAGGTGG 1140 AATCTGTGAC CTTCGGGCTT CTGTCAGTGC AGGTCAACAT GTACCATGAG GCCTGCGTCA 1200 GGGAGCAAAC CACCCTCCCA TCCCTGTATC TCATGCCTAT CCAGCCTACA CCGTGAGCCA 1260 GGCATTCCTA GTGCACAGGG CCCCAGGAAA GCCTGGGTAA AGTGCACAAT CAATGAAAGG 1320 AAGGTAGTTT ACATCAATCA ATTGCAAAGA TATTTATTCC ATGTTAGGAA TTTTATAAGT 1380 ATGGTCAAAT 1390
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