| Tag | Content |
|---|
EnhancerAtlas ID | HS108-10999 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr12:132969170-132971470 |
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 | GCCACCCACT CTCCCCCGGG ACCCTCCGAC CACGTTGCTC TTCCCAGGGT TCTGGCACAG 60
CCCACAGGAC ATCGTGGGAA TGCCTGGACT GCGCCGCCCC TGGAGCCCAT AACCTGTCAC 120
TCTCATCTCA ACTCCTGTCA GCGAATTTCC TCTTTGTGTG TGTGCGTAAA CCACTTTGAG 180
GTGTGCTCTG TCCCTGTGAT TAAACACCTG GTGGATTATC AAAGCTGCGT GATGTCAGGG 240
CTGTGATGCC TTTGTAGCAA GGTGAAGTCC TCAAGTTTCT GAGTTCAGAT CCTCCGCGTG 300
GACCCTGGAG CGTGGGGGCC ACAGGGCCCA GAAAGTGCCT CAGCGTCGGA CGACCGTGGA 360
GCCGGCAGAT GGCGCCCAGC AGCAGGTATC CCGGGGGACC TACCGGCTCC AGCCTGGTCT 420
ACGACCCTCA CTGAAGATGC TCTTACCTGT AGGAAGGTGC CGGGGACCCA AATGACAAAC 480
ATCCCACTGA CTTGGGCTCC AGGAACCATG TGTGGTGCTG AGGTTCAGGC GGCGTATCCG 540
ACTGGACCAT CTTCACTGCG ATGGCAGCAG CTAACCTAGA CTGGCTTAAG TAGAAAAGGA 600
AATATGTTGA TTTAGGTCAG TGAAAAGTCC AGACGCTGGT GGGCTCAGGG AGTGCTGGAC 660
ACAGAGCCTG GTGTACCTGG GAGGATGCTC ACCTCCCCAG CCCTGCTCTG CTCTCCCAGT 720
TCCAGTTTCA AACAAGCTGC CCCCATGGGG CAAGACGGCG GCAGAGGTTG CAGCCAAACC 780
CTCCTGGAAG TGGCTCCAGC CCAGGGTCAT CGGTCAGAAC TTGTGTTCGG GAAGAGGCAA 840
GGCTCTGGCC AGCTCAAGAG CAGAACATGA GGCCCCTCAA AACACCGGAT GGGGAAGGGA 900
AAGGGGCTCA GTTCTCAGTG ACAGTGAGAC ACAGAGACTG TGAGATGGCG TCATGCAAAC 960
GGACGGGGAC GGTCATCCTC AGGGTGGACG GGCGCTGACT CACCAGGGAG CCACCCTGGA 1020
GAGATGGGAG GCGGGACTCA GAGCCAGAGG CAGGGACCGA GCCTCCAGAC CAGACTGAGG 1080
ACTGACTAAA CAAGGAGAGG CGAAAGCACC TCCGCATGAG ACAGGCCACC AGGGCCAGGT 1140
CCGTTTACCG TTGGGCGACC ACACCTTTCC ATAGCAACAA CCCCACGACC CAGGAGTTAC 1200
CACCTTTTTC TGGAAATGTC TGCCTAACCT GCCCCTTCAT CTGCACGAAA TTAAGCGTGG 1260
GTATAAATGA GGCTGCAGAA CTGTGCTGTG CGGCTGCCCT CGACGCCCTG CCTATGGGGG 1320
GGCTGCAACC CTGCACCTCT GTAAACCTGC TTCTCCCACC ACCAGCTGGC TCTTGAATTC 1380
ATTCCTGAGT GAAGCCAAGA AGCCTCCCGG GCTCAGCCCC AGTTTGGGGC TCCCCTGTCC 1440
TGCATCACTG GGGGAGAGTG AAGGAGAAAG CCGAGTCACC CTGGGGAGGC CGAGTCAGTC 1500
ATCCAAGAGA GAACGGGTGC TGAGTCACCT GGGACAGTGG GCGCCGAGTC ACCCGGGGAC 1560
AGTGGGCGCC GAGTCACCCC GGGGACACTG GGCGCCGAGT CACCCGGGGA CAGTGGGCGC 1620
CGAGTCACCC CGGGGACAGT GGGCGCCGAG TCACCCGGGA CAGTAGACAC CGAGTCACCC 1680
CGGAGACAGT GGGTGCTGAG TCACTCTGAG ACAGTGGGTG CTGAGTCACC CGGGGACAGC 1740
CACAGGCTCC ATGGATTAAG ACCCGAGGTC TTCAGAGGCC GTCACTGGCC TCCCACAGAG 1800
ACCTGTACTG GAGGTGATGC TGACCAGCTC TGACTAGTGC GTTGCAACCG GGGAGCCGCT 1860
TAGCTGTGCA CAGCCTGCAG TGAATCCTGA ACTCCATCCT TACGGCGTTC TACACACACA 1920
GACACACAGA CACGCCAGCA AACCCATATG CACATGTACA TACACACACA TATATGCACA 1980
CATGCACTTC CAAACACACT TCTACACACA TGCACACACA GACACACAGA CATTCCAGCA 2040
AACCCATATG CATATGTACA CACACATATA TGCACACATA CACATATATG CACACACGAA 2100
TACACATGCA AGCACATGTA CATGCAAACA CATCTGGACA CATGTAAACA CATGCCACAC 2160
ACATGTAAAC ACATGCCACA CACATGCTTG TATACACACA TATACACACA TGCCCCGCAT 2220
ACACACGTGC ACAGATACAG AGCTATACAC GTCCAGACAT GAACACATAC ATGTACACAT 2280
ATGTGCACAC ATACATACAC 2300
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