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EnhancerAtlas ID | HS082-08735 | Organism | Homo sapiens | Tissue/cell | HCASMC | Coordinate | chr12:89261730-89262280 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
JUN | MA0488.1 | chr12:89262016-89262029 | ATTACATCATCAT | - | 6.62 | JUND(var.2) | MA0492.1 | chr12:89262015-89262030 | AATTACATCATCATT | - | 6.12 | TBXT | MA0009.2 | chr12:89261898-89261914 | TCACAACTATATGTGA | - | 6.11 | TBXT | MA0009.2 | chr12:89261898-89261914 | TCACAACTATATGTGA | + | 6.1 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GGCTTATAAG TAACTCAATC TCAAATATTC CAGTGCTAAG CATATTTGCT CTTTCCTATT 60 CTACTACTCC TGCCAATCCC ACACAAGGTA AGAGAGCTGT GAATTGAGCA TTTACTAAGT 120 GCCAGACATG GTGCTAAGTT GTTCACATGT AATATCACTC TATTATTCTC ACAACTATAT 180 GTGATGAGGA CTATTAGTAT CTTAAATTCA CAGACATGGA AAATAAGGAT TAAGATGGTA 240 ATAGCTTGCC TGGAATTACA CTGTGGAGCA GATGTTTCCC ATCTCAATTA CATCATCATT 300 ATCCAATCAG TTGAGCAAGC CAGAAACCTA ATTCTGTCTC TTTCTCCCCC ACCTCCAGCC 360 TTGAATCAGT CATTAAGCCT TGCCAAACTT TCCAATATTT CTGGACTCCA TCATTTTCTT 420 TTCATTCACT GTCACTGCCA AGCTCAAGTT TTACCATTTT TGTCCTAAGG AGAACAATAA 480 TCTTCTATTT GGTTTCCCTA TTTCTTGTCT CTCAGACTCT AATCCTTGAA CCACTCTGAT 540 ATTTCCTTCT 550
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