| Tag | Content |
|---|
EnhancerAtlas ID | HS184-18905 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr21:35917200-35918500 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SPI1 | MA0080.4 | chr21:35917721-35917735 | GAAATGAGGAAGTG | + | 6.22 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_02750 | chr21:35916566-35918720 | Astrocytes | | SE_09811 | chr21:35914742-35920153 | CD14 | | SE_29460 | chr21:35915039-35918724 | Fetal_Intestine_Large | | SE_41006 | chr21:35915863-35918362 | Left_Ventricle | | SE_46107 | chr21:35915787-35919758 | Osteoblasts | | SE_56471 | chr21:35916179-35919116 | u87 | | SE_67780 | chr21:35916179-35919116 | u87 |
|
| | 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 |
| GH21I034543 | chr21 | 35915834 | 35919761 |
|
Enhancer Sequence | TTAAAGACTG TATGACGTGA ACTCCAAGAT CTATCCTTGA AGGCCAGGGA GTGGTTGAAA 60
GATGGAGCCC TCTGATTTCT GACTTCACTT CTGCAAAGCC TACTGTGTCA TTTACTCCTC 120
ACCATCAGTG GAGCGAGAGC CTCTGGGACC ACGTCTCCCG AGTCCCATGC CTGCCATCAT 180
GGTGCGGGCT GGACCAGCCT TCTTAGTGGG ATATGTTCCC CATAGAAAGT AAACCAAGAG 240
GCAAAAGCAA AGCAAAGCTA CGAAAGCAGG CTCAGTGCCC CCGCCCCTTG TTTCAGTGTC 300
ACCTCAAGTT TGCTTCTTGC TCTCAGAGGG AGATCACAGC ATTGCACAAC GGGCAGTGTT 360
GACTATTTGC TGGCCCTTGT CACCCACCCT TCCAAAACTC GGGCAGAGGA CAATCTGAAC 420
ACCAGTGTGA CAGTTTCTAA CAAAAGGCTT TGCTAGTACA GTGCCTGAGT GTGGGTGTCC 480
ACTGAAAACT AATTTCAGCC CTGACTAAGA AAGGCATCTC AGAAATGAGG AAGTGTATTT 540
TGGGCTCCTG TGGTTTCTGA TGAAAAATGC TGCAATGTGG GGCATGGGTG AAAGGGAAAC 600
ACTGAGAAAA TAGATGTGAC CCCCAGTATG CTTCCTTGAA GAAGTGGGGG GCTGGCCAGG 660
CCAGGCACAA AGATCCTTTG TGTTCCCTGA GCCTGTGACT TCTCCCGCTG TTTCTCAGCA 720
GTTACACTAA CGACATTGTG GAGGAAACAG CTTCTCCTTG CATGGCCCTG CCCCTTGCAC 780
TCTAGACTGT TTAGCCTCCC TGCTGGTCAG TCCCCTCTCC CTACAAATGC CAGCAGCTTT 840
CCCCCAGTCC TTGCTGCAAC CACAAAGTCT CGCAAGGATT TTCAAATGCC ACTGGGAGGA 900
TAGCGGTGCC ACCCATGGAG AATAATGACC CCAGGCCCTA AAATGAAACA GGTTGCTCTA 960
ACATTCGAAG AATAGCCCCA GCACACCAAA TGCATTCACT TAATTTCTTG TTCAACAGAA 1020
AAGAATGACC TCTTTTAATA CAGAGCTGCT TTGAAACATG TCATTTCAAA CAGGTCCTAA 1080
GAAGATCCTG ATATTTGTCT GTATCTTAAC TGGATCTCTG TGGGTTGAAA AACGCTCATA 1140
GAAATGTTGA AGGACATCAG TCAATCTTTA ATAAGATGAG ATTTCTCAGA GATACAACAT 1200
GCTGTTTGAC CATCTGAAGG ATGCTAAAAG AAAGTGATTT ACTGAAATAA AATAGATAAC 1260
AAACATTTCA GTGACTTAGA AAATGGCGAG AAATCACGTC 1300
|
