| Tag | Content |
|---|
EnhancerAtlas ID | HS052-15441 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr17:8601350-8602540 |
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 | TATCTGGGGG AACAAAATAG AATAAAATTT ACACACACAC ACACACACAC ACACACACAC 60
ACAATTTTTC TCTCCCCAAA CTTTCTTTCT TCCTTTCTTC TGCTCTGCCT TGTCCCCAGC 120
ATCCACACCT GATGCATGGC TGCGTGCACC ACCCTGCAAG GGAGCTCCCA CTCTGGGCCA 180
GACATTGTGC AGGAGGCCAG AGGAAGGTGA CAGTATAGAG CAGATCCTGG CTCTCACGCA 240
GCGTGTCCTG GATGAGGCAA TGGACTGCTG CCATACGGGG CATCCAGCCA GACACAAGGG 300
CTCAAGGAAG CTTCTGGGAG GAGGCGACAC TTGAGCTGAA TCTTAAAGAA CAAGCAGTAG 360
TTAGCCTAAT GATGGATGGG GATTAGAACC GGAAACCCCG GGCTGAGGAG AGAAAGCGGG 420
GGAGAGAGAC CAGATGGGGC TGAGTGCCTC CAGGTGTGGA GAGACGTGAG GCTGGAGGTA 480
AACAGGGGCC AGAGCATGGA GCCTTTTTCT AGGAGATGTT AAAGGGACTG GGTCTCTGTC 540
ACCATCTCCC ACTCCCAGCT CCCAGCCTTC TATCTCACAG CTCAGTCCAC CACCGCGGAG 600
CATGGGTCAG GTCAGGCACG TGTGCACGCG CGCGCGCGCG CACACACACA CACGAATATG 660
CCCGGAAATG TATACTCAAT GCCACATCAC ATAAGCAAGG ACATTTAGCA AAAGGGAAGA 720
AAAGAAGAAA AATGATGTTC AAATGAGAAC CAGGGAGAGA CGGCAGGCCT GGGGGAGGGC 780
ACTCAGCCAG GAAGGGGAGA GGAGGAGTGG AAGTGGGAAG TGCGTGGGCG GGAGAGCCAG 840
GAGGCTGTTG ATGGAAAGGG AGCTGGAGAA TGCTCTGGGC TCTCCGCAAG GGGAAGACAC 900
AGACAGCAGC GGAGACAGCT GGTCAGCAGA GGTGGTGGGA GTGGGGGGCG AAGCACAGAG 960
TCTAGAGCCC AGCCTCCCCC ATCCAAGGCT CAGCTCGGAT GTGTGTCCCC TCACGCCTCG 1020
CCCGCGGGAA CTGTGGCTCC TCCTTTAGCT GACCACAGTG GTGGGCATTG GCTGCAGGAG 1080
GTCCCTGAGA AAGCCCTCCA GTGTGGTCCA GGAGGGAGAT AGGGCCTGGG GATCTGTCTG 1140
ATGCTCCGCT TTAGTGTGGA TACATTGATC AGATGTGTTC CCTGGCATCC 1190
|
