| Tag | Content |
|---|
EnhancerAtlas ID | HS048-06698 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr11:61334610-61335180 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF16 | MA0741.1 | chr11:61334809-61334820 | GCCCCGCCCCC | + | 6.02 | | KLF5 | MA0599.1 | chr11:61334809-61334819 | GCCCCGCCCC | + | 6.02 | | REST | MA0138.2 | chr11:61334821-61334842 | AGAGCTGTCCAAGGTGCTGAA | - | 10.37 | | REST | MA0138.2 | chr11:61334861-61334882 | CTCCTTGTCCTTGGTGCTGAA | - | 6.33 | | SP3 | MA0746.2 | chr11:61334808-61334821 | CGCCCCGCCCCCC | + | 6.11 |
|
| | 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 |
| GH11I061566 | chr11 | 61334424 | 61335705 |
|
Enhancer Sequence | GAAATGGATA GAGAGACCAC TGCGGATCTG AATCCTGTTC TGTCACTTCC AGTTGTGTGA 60
CCTCAGGCTA CTCACTCAAC TCTCTGGTCC TAAGCCTCCT GGCTGGAATG CAGGGTCTAA 120
GATTCCCTCT ACGAGATGCC GTTCTATCAT ATTCAGGGGT ATCATTTACA CGGCAAATAT 180
TAGGATGGAG CCATTGAGCG CCCCGCCCCC CAGAGCTGTC CAAGGTGCTG AAACAGCTGT 240
CGGCCACGCG GCTCCTTGTC CTTGGTGCTG AAACAGAACT CAGTCCTGGG GCTGCGCCCT 300
CTTCCAGGTC GCCCTTTGCG CAGCTCCCAG CGAGCAGGAT CCGAGAGACT GTGCATAGTG 360
ATTCCGCCTT CCTCTGCCAA TGCCTCCCTG ATCAACCCTC AGCTGAAGCT ATGGCAGCAC 420
CCAGTGACCT CAAGAGCCCC CTTTCCTCGA GTTAGGTCCT CGGATGCTGA AGACCCCAGT 480
CCTGACTCAG GACAAAAAGG GCCGCCCCGC GAACGTGGTA AATACCACGC CCCATTCCCT 540
CCCGGGGGCC CGCCGCACTG CCTCCTGGTG 570
|
