Tag | Content |
---|
EnhancerAtlas ID | HS029-03922 |
Organism | Homo sapiens |
Tissue/cell | CUTLL1 |
Coordinate | chr12:132336450-132338060 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
REL | MA0101.1 | chr12:132337947-132337957 | GGAAATCCCC | - | 6.02 | Znf423 | MA0116.1 | chr12:132337201-132337216 | GCCACCCAGGGTGCA | + | 6.09 |
|
| 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 |
GH12I131852 | chr12 | 132337401 | 132337670 |
|
Enhancer Sequence | TCGCATTCCT CCTTGTTCAT CAGCCCGTCC CGCGCTGTCT CTTCCAGTCC TCGTGCCCCG 60 AGGAGTCCCC ACGCCCCTGT CACAGATGGG AGAGTTGAGG CCCAGCGGGG GATGAGCCTC 120 AGTGCTACAG GCAGGGGCAT CACGGGCGGG CGGGGCGCCA GCTGGCCCAG TGAGATCTGA 180 GTGTGGGAGG TGCCCGAGGA AAGGCATCAG TTGTTGGGTG AGCCACTTGG GACGCTGTCT 240 GCCCCGCAGC ACTAGACCAT GATGCCCGGC CGAGCACCGG GACCTGGGTG CGCCCAAGAG 300 GGAGGGTAGG TGCTCCCTGC GCAAGAGGGA GGGAGGGTGC TCCCTGCAAG GGGCTGATTC 360 TAGCTCCAGC CACTCTGTCA CTTGCTCCCT TTGCTCCCAG CCTCCAGATC CACAGCGGAG 420 TCCCTCAGCC TGCCCCCACT CTGGCCGGCG AGTGACGCGT CTGTCCTGCA GTACCCTCTT 480 GTTCAGAGGG TGCAGCCGAT GCCACTCTGC AGGGCCCAGT CCTCCCGCTG GTGCACAGTC 540 CTCTGGTCTC TGCGGCACAG ACGCACCCCG GGCCACAGGT TCGGGGCCTC AGGCTCTGGC 600 TCACCAGCAT CTGCCCTGGG CTGTGGAGGG CCCGGGTGCC CCCTCAAACG TGACTCAGTG 660 AGGATGAGGA GGTGGCCGTT GGACTGTGGG GGATTCACTC CCACATAGCA GGAAGTTCCT 720 GACCACAGGC CCAGCATAGG GAGCGGCTGG GGCCACCCAG GGTGCAGATG AGGCTTCCTG 780 GCACCCAGGA GCCAAAGCCC ACAGCCCCCT TGTCCCATCC CAGGGATGGC ACCCATCCCA 840 GGATGAGGCT GCCAGGGCCG GGCAGGCAGG CCCCAGGCCA GGCCTCATGG AGCCGGGCCA 900 CCTCCCCGTG AAGAGAGGCC ACATCCTCAT GGAGTCCAGC CGTGTCCTCT GTCCCCCGCC 960 TGTTCACCAT CTGCTCCCTG GAGCAGGAGG AGTCCCTGCC TGTCAGACCA GTCTGTGGAA 1020 AGACCGACCT CCCTCCTGTC TGTCGGGGAC ACTGGCTCTG CCCTGCACCA AGTGGTGTTT 1080 CCTCATCACG CTTTGTTGCC CAGCAGCCTG TGGGGTGAAT TCCCCCGTGC AGCTGGCCCA 1140 GCCCCGTGGT CCCCACGTCC TGGGTCGTGC CCCAGTGCAA AGCCGGCTGT GGGCCTTGTC 1200 TGCTGAGTCG GGCTCTCACG TTGGCAGGGC TCACTGCGGT TTTGAAGTCC AAACTCTCCG 1260 TCATAAGCCT CTTCTGCCGG TCCTATCTCT GGTGAAGAGG TGAACCGTAG GCGGGGCAGG 1320 GGGGCTGCTC TGAACTTGCC TCTCCATGCT GCAGCCCACC TCCCTCTGGC AGTGGGGTGG 1380 CCGTGCTGGG TCCTGGGGCA GGGCCTGGAG CCCCGCCAGC CCATGACGCA TTTCATGAGC 1440 CCCCACCTTT TGATATGCAC ATGCAGCTGA GGCTACCCTG ACCCCACATT CAAAGTCGGA 1500 AATCCCCAAA ACCCAAGACC TTTTGAGCAC TGATGGGCTC GGGGTGCACA CAGAACATTT 1560 GGGATTTCAC TTTTTTTTTT TTTTTTTTTT TTTTTGAGAC AGAGCCTGTC 1610
|