Tag | Content |
---|
EnhancerAtlas ID | HS098-55187 | Organism | Homo sapiens | Tissue/cell | HSMM | Coordinate | chr8:71361270-71362640 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2A | MA0052.3 | chr8:71362245-71362257 | TTTATTTTTAGA | - | 6.07 | MEF2C | MA0497.1 | chr8:71362244-71362259 | TTTTATTTTTAGAAA | - | 6.28 | SREBF2 | MA0596.1 | chr8:71362276-71362286 | ATGGGGTGAT | + | 6.02 | ZNF263 | MA0528.1 | chr8:71361834-71361855 | CTTACCCTTCTTCCCTCCTCC | - | 6.22 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CCTTAAGCAA TCCTCCCACC TCAGTCTCCC AAAGCCCTGA AATTACAGGC GTGAACCACA 60 GCACCTGGCC TACCTTACAC TTTAAATTAA AAATAGATTT CTCAAAATGA AGTCAACTTA 120 TACATTAAGT GTAAACTGAA AATTTACAAG TTTCATGTCC CTTATCAAAA ATCTCTTCTC 180 TAACCAGGTA ATTGTCAAGG AAAACAAGAT GAAATAGAAG CACCTGCTCT CATTTATGCA 240 TTTATTAATT ATTCCACAAA TACTTGTTAA GCACCTTCTA AAGTTTTGGG CACTATGAGC 300 ATTTATATCA GTTACAGTCC CAAGAGTAAA CAGATGGCAC ATTCAAATTA CAATAATCCA 360 GAGGGAGTTT ATTTACAAAA GGGATTAATT TCAAAGGTGT GGGTAAAGCA GGATTATGCA 420 GGAACTCAAG GCTAGCACCA GCAAAACTGT CACCCCTTGT AGGTCCTGAA GGAGAGGGAG 480 CGAGCAAAGG AACACGACCA GGGAGAGAGC TGGCAGGATC AGGGAACCTT ACAGAAAAGG 540 AGCCAGGTGA ACCAACACCT TGATCTTACC CTTCTTCCCT CCTCCAATCT CTACCCAGGG 600 ATCCCCACTG ACTGAACTCA GCCAGCATCT GCAGAGACCT GAGCCCACTG GCTGAGTCTG 660 TGTGGGCAGC AGCCAGAGAG CAAAGGCAGA GAGCAGAGTG AACAGGAGGT CTGCAGGGGC 720 AGATCCAAGA CGTTCACATG GGACTAGACC AGAGAACAGG AAAGCACCTG TCCTCACAAA 780 GTTGACTTAT TTATTAGAAA GCATCGATGT CAACCTTTAG CAATAAAAGT GCTTTTAGGC 840 AAGTACAAAT TAAGGGCTAA TTTCCGGTTG GGACAGTATG AAATGCAACG AAGTAGCAAC 900 AGAATTGAAT CAATGTGCTC TGAATGGCTG CTGTGTTCTT CAAAAGCAGG AATGTAGAAT 960 AATATATACC TTTTTTTTAT TTTTAGAAAC CTTTCTCCTT GCTCTAATGG GGTGATAACG 1020 TAAGAGGTTG GAAAGAGAAG AACAAAACCA TTGTGTGAAA CACAGCCCTT ATTTTTCGTT 1080 CCTTCTCTCA GCATAGGAGC ATACAAGGGT GCTCTGCCCT TCTGGACTCC CTAGCACATG 1140 TCACACACAT GAGCTAGAGC TCTCAGTAAC TATTACATCC TGAACAAATT CATATGTTCA 1200 AAACTAACCC TCAATGTGAT AGTATCAGAA GGTGGGGCAT GTGGGAGGTG ATTAGGTCAT 1260 GATGGCTCCA CCCATGTGAA TGGGATTAGG GTCCTTATAA AGGAGACTCC TGAACACTAA 1320 CTAGCCCCTT TTACCATGTG AAGATATAGC AAGAAGGTAC CATCTCTGAA 1370
|
| |
|
|
|