| Tag | Content |
|---|
EnhancerAtlas ID | HS091-33957 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr3:38044800-38045740 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr3:38045022-38045041 | TGGCGACCTCTGCTGGCAG | - | 6.66 | | EWSR1-FLI1 | MA0149.1 | chr3:38045374-38045392 | CCTGGCTTGCCTCCTTCC | - | 6.43 |
|
| | Number of super-enhancer constituents: 11 | ID | Coordinate | Tissue/cell |
| SE_07845 | chr3:38040618-38048908 | Brain_Inferior_Temporal_Lobe | | SE_23094 | chr3:38042553-38048483 | Colon_Crypt_1 | | SE_23776 | chr3:38044399-38046929 | Colon_Crypt_2 | | SE_24926 | chr3:38044398-38046088 | Colon_Crypt_3 | | SE_27673 | chr3:38043997-38047377 | Fetal_Intestine | | SE_28599 | chr3:38043966-38047307 | Fetal_Intestine_Large | | SE_31470 | chr3:38041929-38048199 | Gastric | | SE_41818 | chr3:38045015-38046770 | LNCaP | | SE_50214 | chr3:38043706-38047988 | Sigmoid_Colon | | SE_52525 | chr3:38044805-38046603 | Small_Intestine | | SE_57893 | chr3:38045349-38046277 | VACO_503 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr3 | 38044835 | 38045358 | | chr3 | 38045185 | 38045543 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH03I038001 | chr3 | 38043099 | 38047783 |
|
Enhancer Sequence | AGAGGTAACA GGGTTGGGAG GAGAGTGTTC TTACCCAGAG GAGGAATTGA GGCCCAGAGA 60
GGAGGGTGGG TGACTGGGAT TCACACAGAG AGCTGGCAAG ACGAGACTAG AACCAAGGAC 120
TCTCAGTTTC CCACTCACAG AGGCTCCCAC AAGTACAGCC CACGCTTCGC TCCCAGGCCT 180
GGGTAACTTG CGTCTCTCAG ATGCTGGGGA GAGTGGGGGC AGTGGCGACC TCTGCTGGCA 240
GCATCCCCTC CCTGCATTGT CCTGGTCCTG GGCCAGGGGA CAAAGCACCC TTCCCCACCC 300
TACAGTCCTC AGGGATCACG GTGCCCAGTG TGTGTGTATA CAGTGTCATA TGATGTGTGG 360
GTATACAGTG TGTGTGGATG TGCAAGAACA GGTGTATTCA GGGTGTTGTG TGTGGTGTGT 420
AAGTGGACAG GGTGTGTGTA GGAGGTAGGA GTGAGGCCTC AAGGGGAGGA GGGAGCTGAG 480
TCCTGGTCGC TCTTGGTCTG CCTGTGGGGC TTGGTTTATG TGCTGCACTC CCCACAATTC 540
TCCTGAGCTC AGTACTCCCG TCTCCTTCTC CCAGCCTGGC TTGCCTCCTT CCACTTTGGG 600
CCGGAGACCT ACTCTCTGCC AGGGGTGGGC TGAGGAGCTC CTCCCATCCC AGGGAGGGCG 660
AGACTCCAGC TCAGGCCCTC CCCTACCCCT GCAGCCCTCT CCTAGGGAAA TTCATGGGGC 720
ACCTTGCGTC ACAGCTGGGT GGGGCGAGAG CTTTCTCCAT GAGCAGAGAG GGACCCTGTA 780
CCCAGAGCAG AGCGGAGTGC TCGGGGAGAA ACCACGGGGC TCAGAGGAGG GCCCAGGGCT 840
CCCACTCCTG AGAAGTGGCT TCCCAGGCCC TGGGGTGGGG CACTTGTGCC ATGGGCTGGG 900
GTGCCCCTCT GGGTGGCTCA CAGCCTTGCT GTCCGTGCTG 940
|
