| Tag | Content |
|---|
EnhancerAtlas ID | HS044-13017 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr8:125685490-125686340 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2C | MA0497.1 | chr8:125685813-125685828 | TGCTATTTTAAGCAC | - | 6.18 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_05555 | chr8:125684683-125686801 | Brain_Cingulate_Gyrus | | SE_10199 | chr8:125684875-125686959 | CD19_Primary | | SE_10859 | chr8:125679883-125697394 | CD20 | | SE_20175 | chr8:125685036-125686607 | CD56 | | SE_33465 | chr8:125684767-125689850 | H2171 | | SE_62452 | chr8:125604945-125703109 | Tonsil |
|
| | 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 |
| GH08I124672 | chr8 | 125685003 | 125686851 |
|
Enhancer Sequence | GCAGGCGCCT GTAATCCCAG CTACTCGGGA GGCTAAGGCA GGAGAATCGC TTGAACCCGG 60
GAGGTGGAGG TTGCAGTGAG CCTAGATCGC ACCACTGTAC TCCAGCCTGG GTGACAGAGC 120
AAGACTCTGT CTCACAAAAA AAAAAAAAAA AATCACTCTT TAAGAGTACT GCCTGCACGT 180
GGAGTAAAAG CTGGTCACAA GCACATGCAT GACCCAGATG TGGTGCCAAG GGAACCGAAC 240
CCACAGCCAC CATTCCAAAA CCCTGCGTGA AAGTCCCCAG GGGAGGTGGA AGAGTGAGAG 300
TTGCTCTCAG CCACTCCACC CTGTGCTATT TTAAGCACCA TGACTTCATT CTTGTTTGTT 360
CTGAAGCAGC ACAGATGGGC CGCGTCAATT TATGTTACTA CAAGAAGAGA AGGAGACCCA 420
GATTCAAAGC TGCACGTTTC TCTTGCCTTG TGTTAGGGCA TCCTGAAGCT GGAACTGTGG 480
TGTGTCGAGC AGAGGAAAGC ACTATTTCTT TTTTTTCCTT TCTCTTTTTT AGAAGCCTAA 540
GAGTATTTCA CCAACGTGCC CATATTTCAT GGAACCAACA GCCAGATCTA CCTGAAAAAT 600
GGCACAAGGT GAGTTGCTAA TAAAGCCATC GAGCCTTTGC AGCTTTGTCA GTGCCACCCA 660
ACTGTGAAAT CCATGGCCCT TGCTCCAGAC ACAGGAAGGG TCCTCTTCCT CAGAGAGCAG 720
GAGACAGGGT CAATGATCCA AGCTGCAGCA TGATCCAGGG TGGAAGGGGC TCCAAACCAC 780
ATCTCACCCG GTCACCTCGG AGGGCACAAG GCTCTTCCCT GAACCTTTCC AAGAAACTTA 840
ATGAACCAGA 850
|
