Tag | Content |
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EnhancerAtlas ID | HS146-03362 |
Organism | Homo sapiens |
Tissue/cell | NHDF |
Coordinate | chr12:13328040-13329460 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFIC | MA0161.2 | chr12:13328921-13328932 | TGTGCCAAGTA | - | 6.32 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_00070 | chr12:13322001-13329284 | Adipose_Nuclei | SE_26715 | chr12:13324024-13328761 | Esophagus | SE_26715 | chr12:13328797-13330070 | Esophagus | SE_36302 | chr12:13324133-13329267 | HMEC | SE_45692 | chr12:13323910-13328954 | Osteoblasts | SE_55863 | chr12:13323889-13330257 | u87 | SE_64909 | chr12:13324369-13329500 | NHEK |
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| 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 |
GH12I013171 | chr12 | 13324128 | 13329500 |
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Enhancer Sequence | TTGATATTCC AGTTAGTACC CAATTCAGTT TATATATGTA TAAAATTACA CACCCTGCAT 60 CAAAAACATC TTTACATATT TTTATACTTA AACCCAGTTC AAATTGATTT AAGGCTTAGG 120 AAAATAAGTT AGGTTTAGTT CAGTATGTGG TTTAGAAAAT GTGTACACTT TATTCTGGCT 180 TCCAACTAAA ACTGTGGTGT GTTTCTTGCC TCTGAATTGG ACAGATTTCT ATGTTTGGCC 240 TGTATTGTGG CAATGGTGTA TTATTTTGTT CTTGTCAGTT GCATTCATCA TTATTTTAAA 300 AAGATTCCAG AAAGCCTGGT GTTACAGTTA GCCCACCTTG ACCCTAAATG CTGCACTACT 360 GCATTTTGAC CAAGCATTGG GATCATAAAA ATTATCCACC TTCTGTTTCT AGGCTTTCCC 420 CACAGCTTGC AGCCCAGAGT CAGGAGAAAT GGCGTTTTAC TTCATGTGCT TCCCTAGAGT 480 GAGCAGGGCT ATCCAGACTG AAGGGAAATG GCATTTCTCC TTCTGCAACT CAGGACCCTA 540 CTGGATTAAT TCTTGCCTAA GAGGGCATCT CAGCCATGTG TTCTCCAGCT CATTAATCCT 600 CAGCAGTGAC TAACGCTGAA AACCCAACCC TTGTCTTTGG CTGCCAAGGG TGTAATTTCG 660 CTTGGAATGT TGCTTTCAGT TGACTTGTTC TCTACCTTTC TTTTCACCTG TCTGTTATGC 720 TTAGCTCTAC CCTCCTGCAC GTGTTAATTC TAATCCTTTG GTGATCTAAA CTAAAGAAAA 780 TGCCTCAGGA ATAAACTTTT TATGGATAAG GTTTTTTTTG TGTGTGCTAT GACACCTATA 840 CCTCTAATAT TAGTTTAAAT CTACCATTTC TCGAATGCCT ATGTGCCAAG TAACTTACAC 900 GTATCACATT TGTTGTTACT AACAACCCAA TATAGTGTTG TCCCCATTTT TTAGATGAGA 960 AAACTGAGGC TCAGAGAGTC TGAATGCCTT GCCCAAGGCC CTGCAGCTAG AAATCAGATT 1020 AAACCTCGTC TGTCTGACTC CAAAGTTTGT GCTTCATGGA CTTCCAGCTC TGGTTCATGT 1080 TACCCCAGTA GAGCCCTGTG ACTTCAAGAA TTTCTCAAAT GTCCAAAGCA ATCTATTTTA 1140 ATTCACTTTA TTAATAAAGA TAATAATTCC TGTCTGTCTC ACAGGTGGTA TAATGAAGTG 1200 AAAGGAAGCA GAAGAGAGTG TTATAGTTGG AAAGGTGGGA AATCACCCCC TCCATGCTGA 1260 AGGGAAGATT TCAGGTTCCA AATGACACGT TTCCCTCAGA ATGACTTTTG CTGTAGGTAT 1320 GTGAACCTGC CACCACCCTT TGAATTTGGT GGATTGATTT AACGCTGTAT CTGAACCTGA 1380 CTGAGGAGAT TCCTTCCTGG TTCATGACCC CGCTCTTGGA 1420
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