| Tag | Content |
|---|
EnhancerAtlas ID | HS098-12096 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr12:1921770-1922700 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr12:1922201-1922216 | AAGGGTCAAAGGCCA | + | 6.85 | | NR2C2 | MA0504.1 | chr12:1922201-1922216 | AAGGGTCAAAGGCCA | + | 6.19 | | Nr2f6 | MA0677.1 | chr12:1922202-1922216 | AGGGTCAAAGGCCA | + | 6.26 | | Rxra | MA0512.2 | chr12:1922202-1922216 | AGGGTCAAAGGCCA | + | 6.19 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr12 | 1921843 | 1922000 | | chr12 | 1922000 | 1922400 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I001810 | chr12 | 1918961 | 1923200 |
|
Enhancer Sequence | GAGTGTATTG AATCCCACAG CAGGCCAGTC CTATTATTAT TCTGACTTTC CAAGCTGAAG 60
AAATGGAGAC TTTTCAGAGT CACATGGCTT GCCCAAGTCA CCAGCTTGTT AATCACAGAA 120
GCAGGACTGC AGCCTGGGCC TGTCTCTCCC TGAAGCTGCC TCCTCTCTGG ACCTGGACTG 180
AGTCCTGGTG ATCGGGAAGG AGCGGCGGGC ACAGGCAAGC CGCTGTCTGC TCAGGCTCGG 240
GTTTCCTCAT CTGTGAAACG GGAACGGATG TGGCTTCTTA ACCATTACGC TGTGTCCGTC 300
ACAGTCATTC TCACTTCTCG AGTACCCAGT TGGTGGGAGT TCCAGTATGG CACAGAGATA 360
CAGGATTGTG TTTTTGTTTT TTCACTCTGG AATGATCTTA GAGAAATTTG ATGGGAAAAA 420
TGAGAGCAGG GAAGGGTCAA AGGCCAGAGG TCCAGCCCTG CATTTTCCAG GGTTGTGATC 480
TTTGCGTTTC GTCTCCTCAG CTGCAAGATG AGTCACGGTT CTACTTCCCC TGGAAGGGCA 540
GAAGTTGCAT AAGATTGTTG AGGCTCAAGC GAGATAATGT GTGAGGCTGT TACTCCAGAC 600
TAGAGCCTTG ATTTTTAAAC TTCAGCGTGC ATCAGAATCG CCTGGAAGGT TTGTTAGAAC 660
CCCGCCCCCA GAGTTTCTCC TTCAGGGGGT CCAGGGTGGG CCTGAGAGTT TCTGAAGTGT 720
TCCCAGGGGT TGCCGATGCT GCTAGTCCAG GCACTATATT TAGGGAACCC CCGTCCTAAA 780
GCCTCACCAA TTGAATCTCC TAAGATGATG AAGATGGCCT ACATCTGTGC TGTCCTAAAC 840
GGTAGCCAAC AGCCACACGT GGCTACTGAG AACTCGGAGT GTGGCTAGCA CGCCTGAGGA 900
CCCGAATTTA AAAAACAGTT AATTTTAATT 930
|
