| Tag | Content |
|---|
EnhancerAtlas ID | HS073-07987 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr19:57780660-57781850 |
Target genes | | Number: 11 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| POU2F2 | MA0507.1 | chr19:57781438-57781451 | ATCATTTGCATGT | + | 6.1 | | Pou2f3 | MA0627.1 | chr19:57781065-57781081 | TTTTATTTGCATACTA | - | 7.22 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_10624 | chr19:57780937-57781428 | CD19_Primary | | SE_59521 | chr19:57778061-57795685 | Ly3 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr19 | 57780905 | 57781379 | | chr19 | 57781316 | 57781665 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I057269 | chr19 | 57780529 | 57781665 |
|
Enhancer Sequence | GGTCAGGAGA TCGAGACCAT CCTGGCTAAC ACGGTGAAAC CCTGTCTCTA CTAAAAATAC 60
AAAAAATTAC CCGGGCATGG TGGCACATGC CTCTAATCCC AGCTACTCCA GAGGCTGAGG 120
TGGGAGAATC GCTTGAACTC AGGAGGAGAA GGTTGCAGTG AGCCGAGATC ACGCCATCAC 180
ACTCCAGCCT GGCGACAGGG CAAGACTCCG TCTCAAAAAA CAAACAAAAA CATAAATCAG 240
ATAACATCAC AGCTCTGCTC AAAACCCCAT GATGGCTACC CATTTCACAG TGTATTAGCT 300
ATATTTTCTT ATTTTCTGCA TTGTTGATGC TATGGAATTT GGGACCTTGC CATTTAGAGT 360
TAACTGATTC TTAGAGATTG CAAATGACTC ACTCTGAACC ATGCCTTTTA TTTGCATACT 420
AACAAATCCA GAGTACCCTA ATGTGAATCA TCTCCTCTGT CTGGCTCTTA CACTACAGGA 480
GACAATTTTT TTTTTTTTTT TTTTTTTTTG CTCTAATGAC TCCAGGGCCA GGTACTAGGC 540
AGACAGGGAC AGCTCCTAGA CCCCAAAGTC TACCAACTTT ATTCAAACCA GCAAATCCTC 600
TTCTGGTTAC CCAGCCCTGC CTTTCTTTTC CTGTGGAAAA CAATAAAGGA TCTGGCCTCT 660
GCTTTCTCCT CTGCTTCTGC TTCTTATACC ACCCTGGTGC TTCTCACATA GCCCTGCAGG 720
ATGTGTTTTG CCTACTGTTT CTAAAACTCC GTGAGTTGAA AGTTCTTCCT TCCTGGCAAT 780
CATTTGCATG TCCGAGTTTC TTATCAGACC ATACTGCAAA AAACCCCAGG TACATTTTTG 840
AACACACAGG AACATATTAC AACCTCTCTA CGCTGGCATA AAAGACTACA CAATTTGTTT 900
CCATCTATCT CTCCAACTTC CATGCACATT CAGTTCCAGC CGCACTAGGC TTCTTGGTGT 960
TCCACAAACA CCCAGGATGC TCTGTCAGTT CCATTGTCCT GTGTGTTTTC TCTGAGTGAT 1020
AACACTGTTT CCTGAGATCT CCACTTGATG AGTCTTTAAT TCCTCCAAGT CCATGCTAAA 1080
ACATCACTTT TTTTTTTTCT TTTGAGACGA AGTCTTGCTC TGTCGCCCAG GCTGGAGAGC 1140
AGTGGCGTGA TCTCGGCTCA CTGCAACCTC TGCCTCCCGG GTTCAAATGA 1190
|
