Tag | Content |
---|
EnhancerAtlas ID | HS095-01523 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr1:94566270-94567770 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myog | MA0500.1 | chr1:94567361-94567372 | GACAGCTGCAG | + | 6.62 | SREBF2 | MA0596.1 | chr1:94567632-94567642 | ATCACCCCAT | - | 6.02 | Tcf12 | MA0521.1 | chr1:94567361-94567372 | GACAGCTGCAG | + | 6.14 |
|
| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_33968 | chr1:94565292-94568811 | HCC1954 |
|
| 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 |
GH01I094099 | chr1 | 94565390 | 94573062 |
|
Enhancer Sequence | CTAAGACCCC AGGCAGAAAG GACCAGGAGG GGTATCCAGT CCTGATGGTA AAGGACACAA 60 ATCCATGTTC AATGAGCATG AGTGACAACA CAGAGGCGAG CTCCCATGTT GGACAGCGCC 120 CAGAGAGAAC GTTGCCATCG TGATGGACAG TTCTGGGAAC AGTGCTGATA AGGAGCCCCG 180 GAACTGGATG GAGGTGGAGA TACAGATCAG GAGCTAGAAG ACAGGTGAGC CCACAAGGCA 240 AAGCATCCTG GGAAGTGGGC AGGGAGGGCC GGGTTGGCTG GAACGTGCCT CTGCGAAGCG 300 CAGATGGCTC AGCGTTTGCT AATCAGCAGA GCATCAGCTC ATCAGAGCCA GCAACATGAA 360 ATAAAGGCAC AACCTGGTGA CCCCGGCCTC CATTCTCCAA CATGAAAGGC CTTGGCACTG 420 ATGCCAGAAG CACAGTACTA GAGATCTAAA TGTCACATTA GTAAGGAACT GGAAAGAAAT 480 TTCCCCGAAA TTCCTGTCCT TATCTTCATC TCCCTTTTAT TACCAACTGG AAGTCATCAA 540 GGCATTGTCA GGACTTGAGT TTTACGAGCT GAAGAGAAAG CAAAGGGGAA AATGAGCAAT 600 CGGTGCCGAC AGCACCCCCT CTGTGGGGGT GGGAGAGGAA GCTAAACAGG GCCTGGCCGG 660 AGCCGCACCA CCCAGGGCCT GGGCACTGCA GGCGCCAAGC TCACCCTGCC TCCAGGCTGA 720 CCCTAGGTTC CCCTTGTCTA GTTTCGGTGA AAACCTCAGG GTCTGAGAAG CCAGAAAAGC 780 AGGTATGAGC TCCTTCATTG TGCAGGGAAC CAGTGTGAGA ACCTGCTTCC AGGAGCTGGT 840 GCTGACCAGG TGGGGTGGGG TCCCTCACTC CTCTGGACTC AGACAGCACC CTGTGCAGAC 900 CTTGATCTCA GGGTTAACAC AGGCTCTGAA GTTCTGTTTA TGTCTCGTTC TCTCCTGGAG 960 TCTGGAGGAG GATCAGACCC AGCCAGGAGG GAGTCGGGAG GGTGTCTGGG ATATCAGCTG 1020 CTGCAGATCT AGCATTCTCG CTGTGTTCAT CACACTGAAG AAGCTGGGCG GGGAGCCCAG 1080 AAGGCCCAGA GGACAGCTGC AGCTCTCACA CCTGAGCCTG CGGAATCACC TGGAGGGCTT 1140 GTGAAGCACA GATTGCTAGG CCTTATCCCA GGGCTTTGGA CCCAGTTCAC CTGGAGTGGG 1200 CCCTGATAAT TTGCATTCCT AACAAGCTCC CAGGCATCGC TGATGCTGCT GGTCTCTGGG 1260 CTTTGAGAGC CACAGGACTG AAGTAAGAAA CACTGGATTA GGATTGAGAG GACCTGGATT 1320 CCATCTGGCT CTGACAATTT CTAGCCCTGT AACTGTGCAC AAATCACCCC ATCACCAGAC 1380 GCGCAAGCCT CCTTCTCTGA CCCATCTCAG GATTGTTGTG AGGAGTAAGG GAGCTAAGGG 1440 ATGTGCAAGT CGTGAGTTAG TGGTAAGAAT GCTCTGCATA AATAGAGGAG ATTATTTAAA 1500
|