| Tag | Content |
|---|
EnhancerAtlas ID | HS010-01467 |
Organism | Homo sapiens |
Tissue/cell | B_cell_blood |
Coordinate | chr14:69821190-69822010 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RFX2 | MA0600.2 | chr14:69821750-69821766 | TGTTCCCATGGAAACC | + | 6.01 | | RFX2 | MA0600.2 | chr14:69821750-69821766 | TGTTCCCATGGAAACC | - | 6.12 | | RFX5 | MA0510.2 | chr14:69821750-69821766 | TGTTCCCATGGAAACC | + | 6.11 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_59418 | chr14:69802940-69828523 | Ly3 |
|
| | 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 |
| GH14I069353 | chr14 | 69820701 | 69823060 |
|
Enhancer Sequence | ACCAGCGCCT TCCTTTCTGC CTCCAGGCCT AGCCCTTCAG CACACCCTCC CCCGCCTCGT 60
GGGGAAAGTC CGGGCCTCCT TTCTGTAAAA GTGAAACTGA ACATGCTCAA GTCTAGCCCT 120
GTCCTGCACC TGGTAGCTTG CTCGTCGGCC TCCATGCCCT GTGGTGCCCC AGGAACTCCT 180
GACTGCTCTG GTGGGGGCCA ACAGGTGGCC CTACTGCAAG GGCAGGCCTT GGACCAAAAC 240
CAGGAATCAG CACAGGTCAG GTGGAGCCCA GGCTCCTGTG GCCTCATTAT GGGATTCTAC 300
TTGGGGCTTA GAAATGGAAA GCAAATTGCT TCTCCAAATA GGTATTGCCC TGCCGCCGTG 360
CTTGCCTTTA GCCAGCCCTC TCTCCTTCCC TGTGAGCCAG GCCTGTCCCC TCGGAGCTGC 420
CCTCCCCTGC TCTACCACAC AAGAAGGCAG TGGTACAAAT TCAGGCAGGA CATACTTCCT 480
GGGTAAAAAC AGCAAAATAA TTCTGAAAAG AGTCTTACCA GACCAGCTTT GCTTGATTGG 540
GTAGCAGATG CTCTGCCTAA TGTTCCCATG GAAACCAATG GAAAACCCCC ACCATGTCTG 600
TGATCAGAAG CTGAACCTAC CCAGGTAAAA ATAAACGCTG CTTCAACATA CATATGAACT 660
GCAGCTGGCA GGCCAGCACA CCACTAGCCT CTCCTGGACG CAACCATTTC TGCCCTCAGC 720
CCCACTTTGC CGTGGGGCTG CTGATCTGGA GTTACCCAGA ACTTCTGACC CCTGGGCCTG 780
AGGAGCCTGG AGCAAAGCCC TAGCTGGCTG CAGAGAATAC 820
|
