Tag | Content |
---|
EnhancerAtlas ID | HS182-06080 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr13:111860620-111861860 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXP1 | MA0481.2 | chr13:111861657-111861669 | GTCTGTTTACTT | - | 6.52 | FOXP2 | MA0593.1 | chr13:111861658-111861669 | TCTGTTTACTT | - | 6.32 | HES2 | MA0616.2 | chr13:111861484-111861494 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr13:111861484-111861494 | GGCACGTGCC | - | 6.02 |
|
| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_01877 | chr13:111860875-111861465 | Aorta | SE_06513 | chr13:111860350-111871107 | Brain_Hippocampus_Middle | SE_58333 | chr13:111804891-111869905 | Ly1 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr13 | 111861497 | 111861547 | chr13 | 111861587 | 111861645 |
|
| Number: 2 | ID | Chromosome | Start | End |
GH13I111208 | chr13 | 111860876 | 111861465 | GH13I111209 | chr13 | 111861635 | 111865651 |
|
Enhancer Sequence | AGGTGATCCA CCAGCCTCTG CCTCCCTAAG TGTTAGGATT ACAGGCATGA GCCACTGCGC 60 CTGGCCTCGT TTCTTTCTAG ATTTCAGCTT TCCTTGATTG GCAAACAGTA AGACAACTGC 120 AGCAGCCACA GTTACTGTGG ACATTCTTGG GAAAATTGTC ATTGTCTTTC TGCTTCTGTC 180 TCTTAAAATC ATATGTGTTC TCAAGGCATT TAGTTGACTG TAACTGGCCT TTTAATTGGA 240 TAGAAGAAAG CTTGGTGATG GGGAAGTACA GAATGTCTTC AGGATGGCCC TCCTTGTATG 300 AGAATTTCCT GGAAGGCTGT GGCCAGCAGA GCACTGCAGA CCATGGCCGG GAGCCCTGTA 360 GAATTTGCTG GAAATGCCCT TTTAGCTGGT TTTGTGCTGC GGGTTGCCTG AGACCCCTGT 420 GTTCTCAAGC AGAATGTGCT CTATAGAGAT TACTCGTAAC CTGCCCTCAG CAGGTCCTGG 480 GAAGTGTAGG GTGAGGGGGT GACCTGAGAA GAATTTAAGA TCGTTGGAGT AGCAAGCCCC 540 CATCTGTGGG GTCAGGCAGG TGGCGTGAAG GGAGGAGCTG GATGGAAGGG CATGGGTGCT 600 GGGTCCTCTC AGGACAGCCC CTGCCCAGCT CTGAGCCAGC TTTACCTGAT GGGATATAGA 660 CCTGGTGTGG CCACATCCTA AATGTGTCAA GAGCAGTGGG GAATCTGGGT TTTTGGTGAT 720 ACCTTCAGAC TTTTCGATGT TGACCGTTTA ATTCAGAATT TTATAAGATA CGTGCAAGCC 780 AATCCAAACA CCTGGGAGGA AGCTGGGACC TGGAGACTTA GGGTTGCTTT CATGGAAGCC 840 TCCCTGGAGT TTAGGACATG GCCGGGCACG TGCCTCTCAG AACAGCGATT TTCCCAGCAA 900 AGTTTTTCAC AGCCTCATTC TCTCTTTTTT TTAATTGAGT CACTTTTAAG AATAAATTGC 960 TATTATTTAT TTGTTGGATG GCCTGTGTGG AGTGTCTTAT GAAGGGAGAT CCAGAGAACA 1020 GAACTAAGCC TCTTACTGTC TGTTTACTTT GATTCTGTCA GCAACTTCAT GAGGTGAGTA 1080 GAGCCTGTGC TGCCTTAGTG TTGGGGAAAT AATCCTCACA AGGTTCTCTC TGGCTGAAAA 1140 ATACACTGGA TTTTCTCTTT TAAATAAGAG TCTTTTCCTT CTGTTGCTTA TTGCATGACA 1200 CATCGTCCTG GAAAAGTGGG CATGTGGTGG TGATGCTTTG 1240
|