| Tag | Content |
|---|
EnhancerAtlas ID | HS012-12066 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr12:121394200-121395320 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr12:121394714-121394735 | TTCTTCCCCTCTGCCTCCTTT | - | 6.23 | | ZNF263 | MA0528.1 | chr12:121394711-121394732 | CCCTTCTTCCCCTCTGCCTCC | - | 6.28 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_23495 | chr12:121393664-121395727 | Colon_Crypt_1 | | SE_24673 | chr12:121394214-121394869 | Colon_Crypt_2 | | SE_27808 | chr12:121394154-121395346 | Fetal_Intestine | | SE_28751 | chr12:121393913-121395686 | Fetal_Intestine_Large | | SE_53251 | chr12:121394016-121395312 | Small_Intestine | | SE_56873 | chr12:121394293-121394781 | VACO_400 |
|
| | 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 |
| GH12I120956 | chr12 | 121394180 | 121395668 |
|
Enhancer Sequence | TGAACTCAGG TGATCTGTCC ACCTCGGCCT CCCAAAGTGC TAGGATTACA GGCATGTGCC 60
ACCGCACCTG GCCTAAGAGC TACATTTTTT ATCGCAGTCT CAGCCTTTTC ATTTCCCCAT 120
ATCCCACTCA TTCCTATAAG GGCCAAATGC AATAAAACAG ATGTGTATGT GCACTCACGC 180
TGTGGAGTGA AGATGCAAAT GACTGTGATG ATCCAAACCC TGGCAGGAAG GTGGCAGCCC 240
CGTAGGGCAT GGGGATCAGA GGTAACTCCA CTGTGTGTGC CTTCCGCTGT GTGTGCCCTC 300
CACTGTGTGT GCCCTCCGCT GTGTGTGCCC TCCACTGTGT GTGCCCTCCA CTGTGTCTGT 360
CCTCCGCTGT GTGTGCCCTC CACTGTGTGT GCCCTCTGCT CCGCTGTGTC CACAGTGACA 420
GCATAGATTA TCCCAGGGCT CAATCAGTTG TTCCAGCTAA CTTCCTGCTA AACAGAGCTG 480
GTCACCAGGA GCCAGGCTGA CACCTTTGAA CCCCTTCTTC CCCTCTGCCT CCTTTCTCAG 540
AAAATATAAA GTGCAAAATG GTCCAGAGGT GGACAGTGTG GGGAGGGAGG GGACATTGAG 600
TCTTGATGAC CTGCAAATTT ACACCAGTTT CTGCATAATC CTATATGGGC TTTATCTGAT 660
CTTAGAGGCA CCCATCCCTT TGCAATAAAA GATTGCATCT GTTTTTATTT CCCCTTTCTG 720
TTGGAAGCTG ATAAGCCAAG AATGTACTCT CCCCACCTGC TCTCAGCTTT GATTCCCATT 780
AACACAGGGG CATTCCCAGG AAAGGGTTGG GCTCCCCAAG GTGTTTGCTG GAGAACCTGC 840
TGTCACTCTG CAGAGATGTA CAAGTATTTA CTGAAAGAAG AACTTCTCCA GGAATATTGT 900
GTAAGCAGAT TACACCGGAT CTCCCTGCCC TTGGACAAAT ATATATGGTG AAGCTCAAAG 960
AGGGGAATCC AATGCACAGA AACCTCCATG CTTAAAAAAT ATCTTGTGGC CGGGCACGGT 1020
GGCTCACGCC TGTAATGCCA GCACTTTGGG AGGCTGAGAT GGGAGGATCA CTTGAGCCCA 1080
GGAGTTCGAA ACCAGCCTGG GCAACATAGG GAGACCCCCA 1120
|
