| Tag | Content |
|---|
EnhancerAtlas ID | HS047-30026 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr6:158375030-158376260 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Hnf4a | MA0114.3 | chr6:158375713-158375729 | CCTGGACTTTAACCCC | - | 6.7 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_23621 | chr6:158372548-158376467 | Colon_Crypt_1 | | SE_24200 | chr6:158373708-158376361 | Colon_Crypt_2 | | SE_28168 | chr6:158372423-158377079 | Fetal_Intestine | | SE_29030 | chr6:158372269-158377129 | Fetal_Intestine_Large | | SE_65268 | chr6:158373454-158376617 | Pancreatic_islets |
|
| | 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 |
| GH06I157951 | chr6 | 158372557 | 158376989 |
|
Enhancer Sequence | CTTTACCGCT GCACTCAGTC ATTATTTCTA TCTGATAGCT TAAAAAAAAC AAAATAGAAA 60
ACCACTACTC ATACCTGACC CCCCAAAATA TACTGGTAGC TGCTCAGAGG ACAGAATTAA 120
TTTTAAAAAT AATCTAAATT AGGCAAACAG AGCGTGAGAA GCCGATAATC ACGCAACTCC 180
CTCCAGAAAA GGAAGTGGAG CAGGCGGGCG CCCAGCTGCA AGCCCTCAGA AGGCTCAGCC 240
TCCAGCGCCA GGACCTGATT TTATTACTAA CAAGGTGCGG TCCTCATTCT TTGGGTCTGC 300
CACATGCCTC ACGGTAATTT TCCAGGCAAA CTATATCACA TGATACTGGC TTTACTGTCC 360
AAGCAATAAG CGCAGAGTCT CTGGCAGTTT GGACTTCTCT GAGATTGCAC TGCTGAGCAC 420
GTAGCTGCGG CGGTCACAGG AACTCACATG CCAAAGAACT GGGAAGAATG TTTTAAAAAC 480
CTGGAAAGAA CCGGTTTCCT TTTCTGCAGC CTAACAAATA CCTCCTTGAG GGAAGTAGGA 540
AGCTTTCAGA ACTCCCTCAC TATCCAGAGG CTTATCATTG TGTGAAGGAT CAGAGTTTGT 600
CAAGGCAAAG AGAATCAAAA CTATTTACTC AGGCTTGGAA TTGATCAGGT GCTCGGGAGG 660
CTCGGAGCAG GGGAGCGGCG GCTCCTGGAC TTTAACCCCC GTGTTTGTGG AAGCAGTGAC 720
TATGATGATG ATAGGAGAGC TGGCGCCCTC ACGCGCTTGT CACCTGCTGC GGGCATCAGT 780
GAGCGCTTGC TGCCGCCTCT GAGATAAGGA GGGCTCTGTA GAAACTCACC TGGGCCACCT 840
CCACTCGGAA GCCCTCCTTT CTTTCCTGCT AGACAAGAAG CGCCTGGAGC AGCCGAGGGA 900
ACACACCTGG TGGCAACGCC TGGTTCCCAC TTTCGAACCT CAGGATTGAG AGAGGGATGA 960
ACGCGGGAAG TCTGAGGACA CACTCTGTCC TGCCCTTAAC TGTGACTGTC CGAGCCACCT 1020
AGGGGGACAC GTGGGAGGCA GTCCCAGGGA GGCTGTACTA GAGAGGTGCT GCCCCCAACA 1080
GAAGCCGGGA GTCCCTGCCT GGGCCCAAGC TCCTGCCATT CTCTAAGTGA TGCAGAGAGG 1140
GCCCCACCGC CGGGAGGGGC TTTCTGGCAC AGCTGTTCTC GCCCCTGCAC TCTGAAGAAG 1200
AGTAGATACC TAGATACAGT AAGTAAAGGA 1230
|
