| Tag | Content |
|---|
EnhancerAtlas ID | HS130-07493 |
Organism | Homo sapiens |
Tissue/cell | MDA-MB-231 |
Coordinate | chr12:132969820-132971630 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr12:132970890-132970901 | CTGAGTCACCC | - | 6.02 | | JUNB | MA0490.1 | chr12:132970890-132970901 | CTGAGTCACCC | - | 6.02 | | Nfe2l2 | MA0150.2 | chr12:132970687-132970702 | TGCTGAGTCACCTGG | - | 6.02 | | Nfe2l2 | MA0150.2 | chr12:132970888-132970903 | TGCTGAGTCACCCGG | - | 6.46 | | Nfe2l2 | MA0150.2 | chr12:132970863-132970878 | TGCTGAGTCACTCTG | - | 7.73 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr12 | 132970087 | 132970237 | | chr12 | 132970628 | 132971029 | | chr12 | 132969905 | 132971000 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH12I132393 | chr12 | 132969946 | 132970585 | | GH12I132394 | chr12 | 132970628 | 132971029 |
|
Enhancer Sequence | AGTGCTGGAC ACAGAGCCTG GTGTACCTGG GAGGATGCTC ACCTCCCCAG CCCTGCTCTG 60
CTCTCCCAGT TCCAGTTTCA AACAAGCTGC CCCCATGGGG CAAGACGGCG GCAGAGGTTG 120
CAGCCAAACC CTCCTGGAAG TGGCTCCAGC CCAGGGTCAT CGGTCAGAAC TTGTGTTCGG 180
GAAGAGGCAA GGCTCTGGCC AGCTCAAGAG CAGAACATGA GGCCCCTCAA AACACCGGAT 240
GGGGAAGGGA AAGGGGCTCA GTTCTCAGTG ACAGTGAGAC ACAGAGACTG TGAGATGGCG 300
TCATGCAAAC GGACGGGGAC GGTCATCCTC AGGGTGGACG GGCGCTGACT CACCAGGGAG 360
CCACCCTGGA GAGATGGGAG GCGGGACTCA GAGCCAGAGG CAGGGACCGA GCCTCCAGAC 420
CAGACTGAGG ACTGACTAAA CAAGGAGAGG CGAAAGCACC TCCGCATGAG ACAGGCCACC 480
AGGGCCAGGT CCGTTTACCG TTGGGCGACC ACACCTTTCC ATAGCAACAA CCCCACGACC 540
CAGGAGTTAC CACCTTTTTC TGGAAATGTC TGCCTAACCT GCCCCTTCAT CTGCACGAAA 600
TTAAGCGTGG GTATAAATGA GGCTGCAGAA CTGTGCTGTG CGGCTGCCCT CGACGCCCTG 660
CCTATGGGGG GGCTGCAACC CTGCACCTCT GTAAACCTGC TTCTCCCACC ACCAGCTGGC 720
TCTTGAATTC ATTCCTGAGT GAAGCCAAGA AGCCTCCCGG GCTCAGCCCC AGTTTGGGGC 780
TCCCCTGTCC TGCATCACTG GGGGAGAGTG AAGGAGAAAG CCGAGTCACC CTGGGGAGGC 840
CGAGTCAGTC ATCCAAGAGA GAACGGGTGC TGAGTCACCT GGGACAGTGG GCGCCGAGTC 900
ACCCGGGGAC AGTGGGCGCC GAGTCACCCC GGGGACACTG GGCGCCGAGT CACCCGGGGA 960
CAGTGGGCGC CGAGTCACCC CGGGGACAGT GGGCGCCGAG TCACCCGGGA CAGTAGACAC 1020
CGAGTCACCC CGGAGACAGT GGGTGCTGAG TCACTCTGAG ACAGTGGGTG CTGAGTCACC 1080
CGGGGACAGC CACAGGCTCC ATGGATTAAG ACCCGAGGTC TTCAGAGGCC GTCACTGGCC 1140
TCCCACAGAG ACCTGTACTG GAGGTGATGC TGACCAGCTC TGACTAGTGC GTTGCAACCG 1200
GGGAGCCGCT TAGCTGTGCA CAGCCTGCAG TGAATCCTGA ACTCCATCCT TACGGCGTTC 1260
TACACACACA GACACACAGA CACGCCAGCA AACCCATATG CACATGTACA TACACACACA 1320
TATATGCACA CATGCACTTC CAAACACACT TCTACACACA TGCACACACA GACACACAGA 1380
CATTCCAGCA AACCCATATG CATATGTACA CACACATATA TGCACACATA CACATATATG 1440
CACACACGAA TACACATGCA AGCACATGTA CATGCAAACA CATCTGGACA CATGTAAACA 1500
CATGCCACAC ACATGTAAAC ACATGCCACA CACATGCTTG TATACACACA TATACACACA 1560
TGCCCCGCAT ACACACGTGC ACAGATACAG AGCTATACAC GTCCAGACAT GAACACATAC 1620
ATGTACACAT ATGTGCACAC ATACATACAC ACTTGCAAAT GCACATGCTC GTACATGGGC 1680
TGCATGTGTA TGCATAGATA CATGTGAGCA CGTACATATG CACACACATG AAGTCACACA 1740
TAGACATACA GACGTGCATG GATTGTGAAC ATACATATAC ACATGTGTGC ATGTATGTGA 1800
ACAAATGCAC 1810
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