| Tag | Content |
|---|
EnhancerAtlas ID | HS047-05855 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr11:45920530-45921680 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF16 | MA0741.1 | chr11:45921652-45921663 | GCCCCGCCCCC | + | 6.02 | | KLF5 | MA0599.1 | chr11:45921641-45921651 | GCCCCGCCCC | + | 6.02 | | KLF5 | MA0599.1 | chr11:45921652-45921662 | GCCCCGCCCC | + | 6.02 | | REST | MA0138.2 | chr11:45921027-45921048 | GGATCTGTCCAAGGTGCCAGG | - | 6.37 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_06398 | chr11:45919591-45927053 | Brain_Hippocampus_Middle | | SE_07614 | chr11:45920183-45927434 | Brain_Hippocampus_Middle_150 |
|
| | 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 |
| GH11I045898 | chr11 | 45920350 | 45923025 |
|
Enhancer Sequence | AGCCAGATAC GGTGTCAGGA GAGTGGTTAC CATAGGAGCG TGAGGTGTGC CTTGGGGAGG 60
GAGTACCTGT CTCTGTGTTG ACCTCCTGCT ACTCCCAGAG ACTCAGTAAG CTCTGCAAGA 120
GGAAACCAAG GGGTGAGGAT AATCCCCTAG TCCCCAGTAC CCCAACCTTC CACTCTCTGG 180
CCAGGCCAGG AAGAGGCAGA GGCCTCTAGA TTTGGGGAAT GGTCTCAGAG CCCTGACTTA 240
GCTTCTCAGA GGTCAGGCAC CTGTTCTGGA CTCTCACCCT GCCCTCTCCC CCAGCTGCAC 300
CAGCAGAGCC TTGGAGAGGG TTGCCTCCGA GCTAGGCAGG GGCCCCAGGC ACTACTGGCC 360
AGAGGTGTGC CCCTAAGGGG CCTCAGACAA GCTCCAGCGG GCTTCACACA CGTTCCAGTG 420
AATACTCAGC TCTCTCAGAG GCTGGGAGGC AGTAGTGTTA TCCCCACTCA ACTGATGAGG 480
GGGCCTGAAG GATCAGGGGA TCTGTCCAAG GTGCCAGGGA GTTGGCGGCA GAACTGGAGC 540
TAGATGGGGC TCTGCATCCT CAAGGCAGGC TCGTGGAGGA CCGATCTAGG GCTGGAGGGG 600
CCCCGGGCCA GCTGGCTTAG GGCGCGGCTG CCACCGCCTT GGTTCCTGGC CCCCGCTCGC 660
CCCTCCCCCT CGGCGTCTCC TTCCCATCCC TCTCAGGTCT CCGCCGTTCC TTGCTTGGCT 720
GAGCCTCAGT TTTTCCAGTT TTCCTCAAGA CCCCTTCAAA TACTATTTCC CCAACCCCCA 780
TCCCTTGCCC ACCCCACCCC GAACTCCTTG GCGACCACTG AGTCCCCATA GCAACAGCGG 840
TGACTTCACT CTGGGCTCGG CTTACAACCC CGGTGAGGTC ACCGGCCGTT GCCAGGGGAA 900
CGGGAGGGCG CAAGGAGTCC GGGGTGGGGA CTGTGGGGAG GTGCTGGCCG TCAGAGGCAC 960
GGCTGGATCG GGGAGGCGGC GGCCTCGCGC TTCCTCGCGG CGGACGGGCG AGAGCGCCCC 1020
AGTCTCCGGC GGCCCCTGCT CGGCTCCCCT CGTGCCCCCT TCGCGCCACA GAATGGACTC 1080
GCCCGGGCGG GGGGCGGTGC AAGCGGCCTC GGCCCCGCCC CGGCCCCGCC CCCTGACGCC 1140
CCTCCGTGCG 1150
|
