| Tag | Content |
|---|
EnhancerAtlas ID | HS091-32323 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr21:45724340-45725130 |
Target genes | | Number: 20 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr21:45725003-45725022 | TGCTGCCACCTGCTGGGCT | - | 6.27 | | TFAP2A | MA0003.3 | chr21:45724500-45724511 | AGCCTCAGGCA | + | 6.32 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_06363 | chr21:45720112-45726807 | Brain_Hippocampus_Middle | | SE_24343 | chr21:45723249-45725579 | Colon_Crypt_2 | | SE_25003 | chr21:45723294-45727311 | Colon_Crypt_3 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GGGCTTGGAC CTGTGGTGGG ACCAGGTCTG CAGGGAGGGC GAGGGAGGGA CGGAGGCTTA 60
GCTTCGGCCA GCTGTGGCTG AGTGGATCTC CCTCACTGCC CCCAACTCCA GTGAGGGTGG 120
GGGACAGGGC GCTGCACTCA CAGCACCACC TTGGACGCCC AGCCTCAGGC AGCAGGACTT 180
GGCTCTGCTG ACTGTTTTTG GTTGTCGGGT GCTTGGGGTG GCTCAGCTGT CTGGGGGGGG 240
CTCGGCTGTC TGTCTCGGGG GGCTTGGCTG TCTGCGGGGG GCTCGGCTGT CTGGGGGGCT 300
CGGCTGTCTT TCTGGGGGAG CTTGTCTGTC TGTCTGGGGG GCTTGGCTTT CTGGGTGTGT 360
GTGGGATGCT TGCTGGGTTC CCGCCCCAGT TTCAGCTGTA GCAGCCGTGC TCCCATCTAT 420
GTGGGGATGT GAGGGAGGCA CTGTTCCTTT AGAGACGGCG TTGCTTGCTC AAGTGGAGAA 480
GCTGCCAGTG TGGGCAGCTC CAGCTCCCTG CACGCTCTGT GCTCTGCCCA TTCTAACGTC 540
TGTGCCCCTT CTTCTGGATG GCTGCCGGGC TTGGCTCTGG CCCCCCTGTT GGATCCCCTG 600
GCTGCTGGGT GGGGAGAGGG CCACCTACTG AACCTGAGGG TGGGTCTGGG TGAGTCCTGG 660
CTCTGCTGCC ACCTGCTGGG CTCTGGAAGG TCCCTCACCC TCCCTCTGGG ATCTCATTGG 720
ATTCCTGTAG TGTGGGGATG GTGGCAGATA CTCTGGCTGC TACGTGAGAA CAGTGTGCCG 780
ATCCCTGGGG 790
|
