| Tag | Content |
|---|
EnhancerAtlas ID | HS182-05378 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr12:110694350-110695280 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr12:110694620-110694638 | CCCTCCTTCCTCCCTCTC | - | 6.25 | | Nr2f6(var.2) | MA0728.1 | chr12:110694423-110694438 | TGAACTCCTGACCTC | - | 6.22 |
|
| | Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
| SE_23655 | chr12:110694542-110695202 | Colon_Crypt_1 | | SE_28268 | chr12:110694193-110695464 | Fetal_Intestine | | SE_29201 | chr12:110693988-110695645 | Fetal_Intestine_Large | | SE_29946 | chr12:110694606-110695326 | Fetal_Muscle | | SE_40866 | chr12:110694355-110696051 | Left_Ventricle | | SE_42743 | chr12:110694381-110695985 | Lung | | SE_48901 | chr12:110694395-110695394 | Right_Atrium | | SE_53187 | chr12:110694397-110696013 | Small_Intestine |
|
| | 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 |
| GH12I110256 | chr12 | 110693832 | 110695889 |
|
Enhancer Sequence | CTCACCACCA CACCCAGCTA ATTTTTGTAT TTTTACTAGA GATGGGATTT TGCCATGTTG 60
GCCAGGCTGG TCTTGAACTC CTGACCTCAG GTGATCCACC CACCTCGGCC TCCCAAAGTG 120
CTGGGATTAC AGGGATGAGC CACCATGCCC AGCCTTGAGT TTCAGTCTGG ATGAAGCTAC 180
TTTAAGGGTG CATCATGGAG GGGAAGAATG TTTTCAGATT CAGCATTTCC CGCAGAACCT 240
CAGTCTTAAT GAGGACTGTG TCCCTGTGGC CCCTCCTTCC TCCCTCTCAC CCGCAACCAC 300
ACTGTGTGGC TCTTGCAGAA TTGCCCCATC TCAGAGGAAA GGTCAGAGAT TGAGATTTCC 360
CTTAAACGGA AGCTCAAATG TGCACTGTCA AGCTGTCCTG GAGATAGTAC AGTTTTATTC 420
AGGAAGTACC AAACCAAGCC AGCCGGCCCA TGCCCTCTGC TTTCTCTTCT CAGGACACTT 480
ACATTCCTTT TTTCCTCAAG GGAGGTGAGA GTGGGACGGG GGCCAGAAGA AGAAACTCGC 540
TTTCCCGTGA GGCTTGTGGC AGAGGCGGCG TGGCCTTCCC TGCTGAGCTT CTGACTGGGC 600
TCCCCTGACT GAGGAGCCCT GGAGTCCTTG GAGCCAGCGA GGAATGCACT TTCATCTCTA 660
GGAGGCTACA CAATCACCTT TGTGTGCCTG GAGCATCAAG AGGGCAGAAG GTGTAGTCCC 720
CGAGCTGAGG AGAAGCAGGT GCTGGCCAGT TAGTCACTGC ACCCTCACTG CTGGCCCCAG 780
CTGTAAGGCT TCTCTCCAGG GACTCTCTCC AGGGCCAAAC TCGCTTCTAG GGACTCTCTC 840
CAGGGCCAAA CTTGCTCCCG TTTCCCTGCT TCCTCCACTT AAGATTTTTC TTTCTCTTGG 900
ATCTTTGGCC CACATACTGG ACATTCAGTT 930
|
