Tag | Content |
---|
EnhancerAtlas ID | HS047-29716 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr6:137289340-137291660 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SOX10 | MA0442.2 | chr6:137291482-137291493 | TTCTTTGTTTT | - | 6.62 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 2 | ID | Chromosome | Start | End |
GH06I136969 | chr6 | 137289381 | 137289550 | GH06I136968 | chr6 | 137289938 | 137291770 |
|
Enhancer Sequence | TTCATTAATT TTCGGTCTCA GGATTCCTAA TTATGGAAAC CAGCCAATAC GTATTTTCTT 60 CAGCCGTTCA TCCCTAAGTC CTTCCGGGGC TGGACAGAGG TAATATAACA ACTGTCGCCA 120 CACGGTGGCA GCAATATCTT CTTGGCTGTG CTCACCTAGC CTAGTGGGTG CTTTTTCTGT 180 AACTGCAGAA GCCATGGCTT TCTCCCCGCT GGGACTTGCT GTTTGAGGAG CTGAGGCGCC 240 TCACAGCACT TATTACAAAG AGTTTTCTTC ATGTTTTTCT TTTTCCTTAA ATGAATGCCT 300 TGGAAAATAT GAGGTTATGC ATTACCGGGT AACTTTTTGC TTTTGTTTTT GTGTTGAGGC 360 AGGGTCGCCA AAACAAAAAC TTGCTCACTC TGTCGCCCAG GCTGGAGTGC GGTGGCGCCA 420 TCTTGGCTGA CTGCATCCTC AACCTCCCAG GTTCGAGTGA TCCTCCCACC TCAGCCTCCT 480 GAGTAGCTGG GGCTACAGGT GTGCACCACC ACATCGGCTA ATTTTCTATT TTTTTTTTTG 540 TAGAGATGGG GTTCTCATGA TGTTGCCCGA GCTGGTCTCA AATTCCTCGG CTCAAGTGAT 600 CCTCCTGCCT CAGCCTCCCA AAGTGCTGGG ATTACAGGCT TGGGCCACCA TGCCTAGCCA 660 GCGGGTACCT TTCTGTCTTT TCCTAATGGC TAATAATTTA AATCTAACTA TATCTGTGAA 720 GCCAGTGGTT TTGCCACAGG ATGAGGAGGC GCCAGGGGAC GGGAAGGTGA CCAGATGTTC 780 TAATTGAGTC AGCCTTGGTT CTGGCAATGA GCAGGTGCTC TGGAAGAAGT CCCAGGCAAG 840 CTCTGCTGTG CCCCTTATCT GAACCGAGCT GATGAGCTGG CCCCCGTCCA GAGGAGGATG 900 ACCAGAGCAG AGAGGGATCT GGAAACCAGG AGTGACAGGG ACGTGTGGAA GGGAAGGGGA 960 TGTTTGCAGA GGAAGGGATG ACTTGAACAC TACAGTTAAA TGTTGGAAGG GTTGTCATGG 1020 AGAAGAGAGG TCGTTAGAAT CAGGTCGGAA GAACTAGAAC TAGTATGCTA GTTTGGAAGG 1080 GACGTTAGGA ATCCCATCAA ACACACTCCT CATTTTACAA AAGAAGAAAA TAAGGCTGAG 1140 AGAGTGACAC TTGTCTGGGG TCACGCCGTT GGCTGGTAAC AGACAGACAA AGGACTAGGA 1200 TACAGCCCTT TGATTATACC CAAATATGGT TGCCCATCAG GTTGTAAGCT ATAGGGTGGG 1260 TGAGGAGGGT AACGAAGGTG GTGGCCTCTG TTTAGTGTTG AAGCAGAAAC TGGGTGTCCA 1320 GAGAGTTCCT GAATTGCCCA GAGGGCTGGC CCCAGCCTAG TCACTGGAAA ACGTCTGCGT 1380 TTACCTCTGA CATACTCTAT CTCTGTGTGC CATATGACTC ACTTAATAAC TGCCAGGTAA 1440 TTCATGGTGA TGAAAGTTTG TGTGTAGCGC GTGGGGTGGA GGAGGGAGTT GGTGTCTGGC 1500 CTTAGAAAAG GCTGCTTTTA TGTGGCAGCA AATAGGAGGC TAGCAAGGTC TCTGGCTGGG 1560 GATTGCCTGG TGTCCTTGAC CTTGCAGAGT CCCCAGGCTC CATCTTGGGG AAAAGGGAGA 1620 CAGGAGAGGG AGTATTGCAG GCTTCCGTAG GCCCTCTGGG ACGGGAGCAG CACTATGGGG 1680 AGATGGGTGA GCTTGTGTGC TGAACATCGC TAACTTCATA GGGCTTTGCT CTTGTCTCCA 1740 TCCCTGAAAA ATCCTTCCTA AGCACTGTAT GGTATAAATA TTTTAGTATC TGTCCATGGA 1800 TTGGCTTGTT GTCTTTGTTG AGTTGCACGC ATGATCTGGG CCTGGTTTCA TCACACCTTG 1860 TGCAACTGCG ATCATTATCT GGATGACAAA GAAGTGGGTG CAGGCCGTTC CCTGGATACG 1920 AAATGCTGAG GCAATTAAGC ACATCTAATG ACTGTTTTCT TAAGATGAAT AGGAGTGATA 1980 GCAGTACACA AAGCAAAATG AGGTCTTATA GTCCATGCAG CCCAAGCATG GACTGGTCCT 2040 AGTAGAAGGA ATGATGTAAT TATGCTTCCC AAGTGTCACA CCTGTACCAT AGGTATTCTG 2100 AAATGACTTC ATGTGTGATG ACAAACATTT TCTTTTTTCT TTTTCTTTGT TTTTTTTTAG 2160 AGACAGGGCC CTGCTCTCCC ATCCAGGCTG GAATGCAGTG GTGGTGATCA TAGCTCACTG 2220 CAGCCATGAA TTCCTGGGCT CAAGTGATCA TCCTTCCTCA TCCTCCAGTG TAGCTGGGAC 2280 TATAGGCACA TGCCAGCATG CCCAGCTAAT TGAAGAAAAA 2320
|