Tag | Content |
---|
EnhancerAtlas ID | HS095-22082 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr4:1289950-1291860 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr4:1290422-1290440 | CCTTCCTTGCCCCCGTCC | - | 6.17 | HSF1 | MA0486.2 | chr4:1291737-1291750 | TTCTAGAACATTC | + | 7.52 | ZNF263 | MA0528.1 | chr4:1290024-1290045 | CCCCTCACCTGCTCCTCCCTC | - | 6.09 | ZNF263 | MA0528.1 | chr4:1291671-1291692 | CCTTTCTCCCTTGCCTCCACC | - | 6.16 | ZNF263 | MA0528.1 | chr4:1290039-1290060 | TCCCTCACCTGCTCCTCCCTC | - | 6.17 | ZNF263 | MA0528.1 | chr4:1290021-1290042 | GCCCCCCTCACCTGCTCCTCC | - | 6.28 | ZNF263 | MA0528.1 | chr4:1290422-1290443 | CCTTCCTTGCCCCCGTCCTCC | - | 6.44 | ZNF263 | MA0528.1 | chr4:1290036-1290057 | TCCTCCCTCACCTGCTCCTCC | - | 7.59 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TGCCCCCCTC ACCCACGTCT GCACTGCCCT CACCTGTGCT GCCCTCACCT GTGCCCCCCA 60 CCTGTGCCTG TGCCCCCCTC ACCTGCTCCT CCCTCACCTG CTCCTCCCTC ACCTGCTCCT 120 GCACCACCTT CACGTGCGCC CCCCACCTAC ATCTGCACCT CACCTATGCT ACCCTCACCT 180 GTGCCCCCCC ACCCGCACCT GTGCCCCCCT CACCTGTGCC TGTGCAGCCG TCACCCATGC 240 CATTCCTCAC CTGTACCCCT CACCCATGCC TGTGCCGTTC CTCACCCGTG CCTGTGCCCC 300 CCTCACCCGT GCCTGTGCCT CCCTCACTTG CGCTGTGCCC CCCTCACCTG TGCTGTGCCC 360 TTTGCCTTGT GGCTGCTCCT GCACTTGGTT CTCTCTCTGT TGGTCGGTTT TCCCATTGGC 420 TGTGCAGCTC CCTGGTGTGC ACGTGGCTCT GAGTCTTCCT CTCGTGAAAA CCCCTTCCTT 480 GCCCCCGTCC TCCTCCAGCT ACTACTCCCT GTCTCTGCCC CTTCATGTCT CTCTTCCTGT 540 TTTACCTAAA TCAGATTTTT GCCCCCCAAC ACTCCACCCA GATGTTCCTC TTGAGGACAG 600 GATGATGCTC CTGAAAGCGG TCAGTCCACA GCGGACCCCA CTGCCTCGAG ACGCTCCCAT 660 CACTCGGCTC CCGTGACACC ATCCTCTGGG CTCTCCCCAC CCCTCGCTGC ATGTCCTCAC 720 TTGCCTATGC TGTCTTCTCT AGTCTTGGAG GCCTTTTGTT TTATGTCACC AGCCAGCCCT 780 CCAGAGGTTG TGTGGCTTCA CAGACGGTCT CCAAGCTCCT GTCCCCACAC TGCTGCCCTC 840 CCCAGGCCTC TCTCCCTGAG GCCATCCCGT GTAGTCACCT CCCGGAGCTC TCTTCGCATG 900 TCTGGAAGGC AGTTCAAAGA TACGATACCA GGCGCAAAAC CAAATGCCGC ATCTCGGCCT 960 TGGGGCCCCA GACGAGCCCC AGACCTGCCT TACTAAGCCA CCCTTCCCAA GTCAGTTGAC 1020 AGCGATGTCC CCCGGCACTT GTTCAGTGAC AGCCGAGAAC TCGGAGGTTT TCTCGATTTC 1080 TGTTTCTCAC GTTTATCCTT GAGTCCACGA TGGCTGCTGG GGCTGCGGCC TTCGCGGCCA 1140 GGAGGAGGGT AAGGGGGAAT CAGTGCCGCC CTGCGTGGCC AGCTCCCTGC GTGGGGGCCT 1200 TAGTGGACAT CCTCCCAAGC GTTTACACTT CAGCTCATTC CCCAGAGCAC GGGGCTGGCC 1260 ATTTCTAGCT TTGGAGGAGC CTGAAAAAGT ACGTGCGTAT GTGTGTGTGT ATACATACAT 1320 ATAGAGAGAG AGCACGCGCT TGAGTGTGGG CTCATTGCTG CCCTAAATAA AATTAGGATG 1380 TGGTTCCTTT TGCCCTTTGT CCCTTGCCTG CCTGGTTTCC TTTGCAGCAC TCGTCACAGT 1440 CTGACGCGGT CGCCTGCATC TCTCTGTGCT TTGGTTGGGC GTCTCCTTTA GAGCGTCTGC 1500 TCTGCGAGGG CACGGGCCGT CCTTTGTCGT CGTTCACGTC ACACCCACGA GTGCCTGGCA 1560 CAGGAGTCAG TCAATGGCTG TTGGCCGAAC CAATTTCTCC CCCGTCTGTC TGGGAAATTC 1620 CTAAACTTCG CATCTCACTT TTGTCCACTT GCCGCATTCT AGAGTATGTC TTGGTCTCAT 1680 GGCCTGTGCT CTCATCTGGC TGTGGTCAGC CTCTTGCGTT TCCTTTCTCC CTTGCCTCCA 1740 CCCCTCGCGA TGTAGCCCCA TCCCCTGCCC TTCTCTGCTT CCCATTGTTC TAGAACATTC 1800 CAGCATGGAA ACCCCGCTGT GCAAGGCCCC TGCACTGGCC ACAGAAGCCG CACCTATCTG 1860 CTGAGGAACC CGGTTGCTGC CTGGAGTGGG TGTCGAGTAC TGCCTGGCAG 1910
|