| Tag | Content |
|---|
EnhancerAtlas ID | HS148-07151 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr17:8601450-8602760 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EGR1 | MA0162.3 | chr17:8602168-8602182 | AGTGCGTGGGCGGG | - | 6.71 | | EGR2 | MA0472.2 | chr17:8602170-8602181 | TGCGTGGGCGG | - | 6.32 | | EGR3 | MA0732.1 | chr17:8602168-8602183 | AGTGCGTGGGCGGGA | - | 7.44 | | EGR4 | MA0733.1 | chr17:8602167-8602183 | AAGTGCGTGGGCGGGA | - | 8.08 | | ZNF263 | MA0528.1 | chr17:8602147-8602168 | AGAGGAGGAGTGGAAGTGGGA | + | 6.35 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_01600 | chr17:8598052-8603111 | Aorta |
|
| | 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 |
| GH17I008695 | chr17 | 8599201 | 8602804 |
|
Enhancer Sequence | TGCTCTGCCT TGTCCCCAGC ATCCACACCT GATGCATGGC TGCGTGCACC ACCCTGCAAG 60
GGAGCTCCCA CTCTGGGCCA GACATTGTGC AGGAGGCCAG AGGAAGGTGA CAGTATAGAG 120
CAGATCCTGG CTCTCACGCA GCGTGTCCTG GATGAGGCAA TGGACTGCTG CCATACGGGG 180
CATCCAGCCA GACACAAGGG CTCAAGGAAG CTTCTGGGAG GAGGCGACAC TTGAGCTGAA 240
TCTTAAAGAA CAAGCAGTAG TTAGCCTAAT GATGGATGGG GATTAGAACC GGAAACCCCG 300
GGCTGAGGAG AGAAAGCGGG GGAGAGAGAC CAGATGGGGC TGAGTGCCTC CAGGTGTGGA 360
GAGACGTGAG GCTGGAGGTA AACAGGGGCC AGAGCATGGA GCCTTTTTCT AGGAGATGTT 420
AAAGGGACTG GGTCTCTGTC ACCATCTCCC ACTCCCAGCT CCCAGCCTTC TATCTCACAG 480
CTCAGTCCAC CACCGCGGAG CATGGGTCAG GTCAGGCACG TGTGCACGCG CGCGCGCGCG 540
CACACACACA CACGAATATG CCCGGAAATG TATACTCAAT GCCACATCAC ATAAGCAAGG 600
ACATTTAGCA AAAGGGAAGA AAAGAAGAAA AATGATGTTC AAATGAGAAC CAGGGAGAGA 660
CGGCAGGCCT GGGGGAGGGC ACTCAGCCAG GAAGGGGAGA GGAGGAGTGG AAGTGGGAAG 720
TGCGTGGGCG GGAGAGCCAG GAGGCTGTTG ATGGAAAGGG AGCTGGAGAA TGCTCTGGGC 780
TCTCCGCAAG GGGAAGACAC AGACAGCAGC GGAGACAGCT GGTCAGCAGA GGTGGTGGGA 840
GTGGGGGGCG AAGCACAGAG TCTAGAGCCC AGCCTCCCCC ATCCAAGGCT CAGCTCGGAT 900
GTGTGTCCCC TCACGCCTCG CCCGCGGGAA CTGTGGCTCC TCCTTTAGCT GACCACAGTG 960
GTGGGCATTG GCTGCAGGAG GTCCCTGAGA AAGCCCTCCA GTGTGGTCCA GGAGGGAGAT 1020
AGGGCCTGGG GATCTGTCTG ATGCTCCGCT TTAGTGTGGA TACATTGATC AGATGTGTTC 1080
CCTGGCATCC TGGAGGGTTC GAAAGCCTGT TCTGAAGGGT GAGTGTCCTT CATGGCACAT 1140
GCCTCAGAGA CCTGTGTTCC CTGTGCATTC AGAGGGGAGG ATCATATTTT AGGACTCAGC 1200
CGAGGCTTTG CTTCCACCTC CTTGGCTCCT CAGGGCTAGG CCAGGGACGT GCCTGTGTAT 1260
TCGTTTGGAA ATCCCAATGC AATGCAGTGG GACATGCTTA GGGCAAGTGA 1310
|
