| Tag | Content |
|---|
EnhancerAtlas ID | HS182-14454 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr21:39664970-39666030 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr21:39665911-39665926 | CAAGGCCAAAGGTCA | + | 6.36 | | Nr2f6 | MA0677.1 | chr21:39665912-39665926 | AAGGCCAAAGGTCA | + | 6.73 | | Rxra | MA0512.2 | chr21:39665912-39665926 | AAGGCCAAAGGTCA | + | 6.09 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_09241 | chr21:39660078-39666461 | CD14 | | SE_45623 | chr21:39660171-39665954 | Osteoblasts | | SE_55658 | chr21:39660110-39676088 | u87 | | SE_67472 | chr21:39660110-39676088 | u87 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr21 | 39665562 | 39666030 | | chr21 | 39664991 | 39665991 | | chr21 | 39665068 | 39665250 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH21I038285 | chr21 | 39657535 | 39666122 |
|
Enhancer Sequence | CCTAAGATAA AAAAATATGT ATTAATCGTG AAAATGTCTC TGTGGTCAGG TTTCACTAGG 60
TTTTGCCTTG TTAACAACTC TAAGAACTGT GTGGCTTACA GCAACAAGAA TTTTTTCTCA 120
CCTGTGTTTC AAGTCAGCTG TAGTTGAATT ATGGCTCAGT TCCAAGTTTC CTTCTTCCCA 180
CTTACCAGAA GGAAGGAACA GCCCAATCCA TGACCCACCC ACATGCAAGG CAAGCCATGT 240
GATGATCCCG ACACCTCTCT TCAGGCATGG TGTGGGTTAC TGCTGTTCAC ACTCCATTGG 300
CCAAAGCAGG TGACAGGGCC ACACCTGACA CAAGGGAGTA GGAAACACAC ACCCCACCCC 360
CGCTACGCCC GGGCAGGGAA AGTCCCAGTG AAGGATCCTT TGTGGAAGGA CCCAGCCGAG 420
AGGCACAGCA AATAGTTGGG AGCAACATAC ATCAACCACA ACCTCCCAAA TTGTCACAGC 480
TCTACCAATA GTTTCCAAGT TCAAACACAT CTTCCAAACA CAGGTCACTG AGAGGAAACT 540
AGCTTCCAAG TGTGCTGTAA TCTCAACTGG TGCTTCCCCT GAAATCCTGA TAATTCCCCT 600
GGAGGAGAAT GAGTGATTCT TCAGCCTCCA AGGAGCTGTC ATTCTTTCTG GGCCATCCTT 660
CAGTCCTCAG TAGTCTAAGG AAAAAGTGCT TTTGCAGAAG GAAAGTAGAA TTTCCTCAGG 720
AGATACAAAC CGAAGGATTG CCCTCTGGAA TCTGCTGAGA ATCCACTTTG TCCACCTTGC 780
TTGTTTTCAA TGAACATGTC TGTTTCTGAG GCCACTTGGC AAAGCTATCT GTGCCCTTGG 840
CTGGTATGGA TGAGTTAAAA GCTGGACTTT GTACAGTCAG ACCAGCCTTT AAAGCGGATC 900
CTTCACTGCT GCGTAGTGTA GGGAGGAAAA TGGCCCAAGG CCAAGGCCAA AGGTCATGGT 960
GCATGTGCTC CTGTGACCAC AGTCGAGGGA GCCCAGGGAG GAGAGCTAAG CCTTTATTCT 1020
CAATTGTTTT AAGCCTCCTG AGCTCAGTGA ACCCCAAGTA 1060
|
