| Tag | Content |
|---|
EnhancerAtlas ID | HS082-09392 |
Organism | Homo sapiens |
Tissue/cell | HCASMC |
Coordinate | chr12:133082830-133084240 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EGR1 | MA0162.3 | chr12:133083699-133083713 | TATGCGGGGGCGGG | - | 6.17 | | EGR3 | MA0732.1 | chr12:133083699-133083714 | TATGCGGGGGCGGGT | - | 6.23 | | Klf12 | MA0742.1 | chr12:133083601-133083616 | GGAGAGGGCGTGGCC | - | 6.34 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_06575 | chr12:133081509-133085747 | Brain_Hippocampus_Middle | | SE_24669 | chr12:133082856-133083153 | Colon_Crypt_2 | | SE_24669 | chr12:133083623-133083877 | Colon_Crypt_2 | | SE_32237 | chr12:133078546-133085188 | Gastric | | SE_41687 | chr12:133081655-133084777 | LNCaP | | SE_47660 | chr12:133082155-133084463 | Pancreas | | SE_65399 | chr12:133067333-133086073 | Pancreatic_islets |
|
| | 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 |
| GH12I132502 | chr12 | 133079421 | 133087879 |
|
Enhancer Sequence | CGGCAGAAAT CTTTATATTT TTTTGAAAGC AGAGTAACAC TAGAGCAGGT TTACAGAAAA 60
TGTGGTAAAT TTAAACAATT TGCCCTTGAC ACATGCGTCC TTCTGGCCAG CTGTGAGCAC 120
TGTGGCAATG GGGAGAGGTG TGGAGCGGGC CTGGGGGAGC GTCTGTGCCC CGAGGGTACC 180
ACCCGGTCCC GCCTCCTCAG ATCTGCCCTC TGCCTGTCCC CTCTGACTCT TTGCCCAGTA 240
GAAAGACAAA TCCCAGCACA GTGGTGCCCT GCGTGGCAGG CTGCCCTTGC AGGTTTCCTA 300
GTTACTGTGA AAGGTAACAC CTTGATTTGT TCCTGCTTTT GATCCAGCGC TGCAAACAGC 360
CGTTCTCTGG GCTGCAGCCT TTGATTCATC CAGGCTGAGA CCCTCAGAGC TCACTGGGAA 420
CCGTTTCTGC AGTGTTAGCA GATTGCGTCC ACAGCTGCCT GGGATGGGCA GCCCTGACAG 480
ATCCTGGGTG GGCGAGCAGG AACTCTGGAG GCCATGGGCT CTCGGGCTTG TGCAGGAGCA 540
GGCCGCTCAC AGCAGGGCTC TGGGCCTTGA GTGGTGGCTC TGCAGAGAGC ATATGGCGGG 600
AGCTGGGCCT CGGGGAGGCA AGGAGTCTTC CTGGAGCCGG AAACAGCAAA GAGTTGGAGT 660
GACAGGATCA GCCCTCGTGG GCAGGGGGCC CGGAAACGCT GCTGGGCCTC TCAGGGCCTC 720
CAGCTCAGAC TGGTGGGGGT GGCGCTTGTG TCATGGGGCG GGCGCCCAGC CGGAGAGGGC 780
GTGGCCGGCA CCACCATGGC TCTTGTCTCT GTCGTCTGCC CTTACCGGAG GGACAGCCAA 840
GGTCCTTCTC CCCAGGGACA CCATGGCTCT ATGCGGGGGC GGGTCCTCCT CGGGGACACT 900
GTGGCCCTCC GTGGGGGCGG ATCCTCCCCA GTGGCTTCCC AGGGTTCTTG GCAGCAGCTC 960
TGACATGGGT TCTGTCCTGG GCTTCACTGC TGCTGTTTTC CTCACAGCTG TGCCCTCCCC 1020
GAGAGGATTC TGTCCTTTCG TGGACGCTTC TCCCTGGCCG GCTGGCTCCT CTGGACCCTA 1080
AACTTGACGC GCCGTATCTG TCTGCACCAG CCCTGGTGCC AGGAGCTGAG CCAGCATACA 1140
GAAGGTGCTT ACTAGTGGTT TATCGAGTGT GGAGGTGGGG ACCCCAGAAC CTGGGGCTGC 1200
CCGATGTCCA CCGGCAGGGC GGAGGCTGGA GTGTCCTGGG GCTGTCCGCA GGCTAGAAGG 1260
TGCTCTGAAG GAGTCGAGAT GGGACGAGAG GGGACCAGGG GAGGCCAGCA GGTTTACAGG 1320
GGGCCTGGGG GTGTCCCCAG GGTCTGGTAG CCCAAAGGTG AACACGGGGA AGCATCTCTG 1380
TCCCAAATCC ACAGACCCGT CTGGGAGCAC 1410
|
