| Tag | Content |
|---|
EnhancerAtlas ID | HS101-08333 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr11:71211190-71212340 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myod1 | MA0499.1 | chr11:71212111-71212124 | AGAGACAGCTGCA | - | 6.36 | | Myog | MA0500.1 | chr11:71212114-71212125 | GACAGCTGCAG | + | 6.62 | | NR2C2 | MA0504.1 | chr11:71211746-71211761 | GGAGGGCAGGGGTCA | + | 6.26 | | Tcf12 | MA0521.1 | chr11:71212114-71212125 | GACAGCTGCAG | + | 6.14 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr11 | 71211627 | 71211690 | | chr11 | 71211465 | 71211936 | | chr11 | 71211998 | 71212187 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH11I071498 | chr11 | 71209802 | 71211346 | | GH11I071500 | chr11 | 71211761 | 71211910 |
|
Enhancer Sequence | GTGTGATCAG TGCACAACAG AGGCACACAC AGGTGCTGTA TGACCACAGA GTAGTAACCT 60
TCTAATCAGG AAGATGTCTT GAACTCTTCC TTAAGGACAT GAGGAAAACC CGCCTGTGCT 120
GAGCTAGAGG CCACAAGATG CCGCTTTATA CCTCATGATC GGTGACAGCA TCTCTGAGCA 180
GGTGGCCTGT AAAACGAGGG TGGATCAGTG GCAGGGGTTC TACATCTGGG ACCGTTGACC 240
CCCCGAGGAG ACATTAGGCG ATGACTGGAG ATGATTTTGG TTATCATGAC TGGGCTGGGG 300
TCTGTGCTCC CAGCATCCCG TGGGTGGAGC CCAGGGATGC TGCTGAATGT CCTACTGTGT 360
GCAGGATGGG CCCCTCCCAA CCCCACACCC AGCAGAGAAT TCTTTGTTCC ACGTGTTGGT 420
GGTGCCAAGG TTGAGGAATG CTGAACATTT GGGACTAGAA GACGTTTGGG GCTGCATGGT 480
TGTAAGGAAG AGATACTGTA TCTGGCTGAT TTCCGTGGAA AGGAACTTGC TCAAAGAGTG 540
ACTTAGAGGG TGGAAGGGAG GGCAGGGGTC ACAGGGTCTG GAAAGCTGGG ACTCAGGCCA 600
GGTGGCTGCT GCCCTATATC CCCTGCTGTG GCTGGACGGA GCCCACACGC CACACCCAGC 660
CTGGGCTGGA TGCCAATCTG CTCTGCCATC CCTGAGTCCC AGTGTCCCTG GGTCACCAGG 720
CAGTGGAGTG GCCAAGCCTC GGGTGATGGG CCCTGTCATC TGGCCACCCA GGGCAGGAGA 780
GGGAGCTGCC CCAGCTCTGG CCTCTGTAGT GGGAGGTGGG GGCTTGGCTC CCACCAAGAT 840
GTACTCAGGG GCGGGCTCCC CCAGATCAGG AAGGGGGTTC AGACACTATG CAGCCAAAAG 900
AGTGACGCAT GTGGGAGCAT CAGAGACAGC TGCAGGTAAA GGTGGAGACG CTGCTGTCAT 960
CTGCAGTGAC AGCTATGCGT GATCTGGACC CGCCCCTCCA GGCTTTTCCA GCACACACGC 1020
CCAGCATCTG GTGGGGACTC TGGTAATTTA CTTTTTCACC TCTGGGACTT GTGACCCGCT 1080
TTTGGTGCGT GCCAGTGTTT CAACAGCCCC ACAGTCCGTC TTTGCGGGGC TGTGGTGTCA 1140
CAGGCCTCTC 1150
|
