Tag | Content |
---|
EnhancerAtlas ID | HS165-14854 | Organism | Homo sapiens | Tissue/cell | Ramos | Coordinate | chr8:10672880-10675390 | SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFIC | MA0161.2 | chr8:10672925-10672936 | TACTTGGCATA | + | 6.14 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AATTTCTATA CATTATATTC AAAATAATTA AGAGAGCACA TTCTTTACTT GGCATAGTTT 60 GTTCCACTAC ACAACACAAA GTTCATTCCT ACTATGCGCA CAAAGAAAAT TTACATTTTA 120 AGTAATTTTT TTTTGAATGA AGACTTTTAA ATGCATAGTC TTAGATTTTA AAGCTTCTTT 180 TTGGACCAAG GACACCTTCG AAAATCCAAT GAAAGCTCTG CACATGGGCC CACACATGTT 240 TTGCATGCAA TTTAAAGGAG GTCACAAACT CACTATAGTG AGTGTACCCT GAGATACTGC 300 CAACACCATG AGCTCTCCAA CACCAGCAGG CTACAGATGA CAAAACTGGT CACGATACCA 360 CTTTGTACTT ACATATCACT TCACAGTTTA ACATACCCCT GAAGTTATTA AGTAAATGAT 420 TTAACCAATT GGAGTGAACT TTAAAGACAT CAAATGATTT GATCTCTACA AGGAGTTCTC 480 TAAAGACTCA TAAAATAGAA AATAACACTG AGCATGGCTA AGTGCAGGAA GTAGATCATG 540 GAAACGACAA TCGGCCTTTA GCACTGGGTA GTGACCCCTG CAGATCTGAG CAGCCTCAGC 600 ATCAAACGGA GAGACCATGT GGTCTGTACA CACGATATTC CACTCCTAAT CAGACGATTC 660 TGTCGGCAGC TGTGATTGTC AGGGTCACGG GCGGTGTTGG AGGGGTATGC AACTATGATT 720 GGGGTTAGCA CAAGGGAGGC CTTGGTGGTA ATGAAATAGT TCAGGATCTT CACTGAGATA 780 ATAATGGTTA CACAATCCAC AAATGTGATA AAGGGGCACA GAGCTGTATG AGCAGATGGT 840 ACCAATGCCA ATTTCCTGGT TTCATCATGC TGTACTGTAG TTACGTAAGA TGTAACCACT 900 GGGGAAAACC AGATGAAGGG TACACAGAAC CCCTTTACTA TCTTTGCAAC ATCCTGTTCA 960 TCTATAAAAA GTTAAAGAAA AAACCCTCAT GACTATTAAT CAAGGGCTGC AGATGTTTCT 1020 TAGATATAAA TACATTCAGA TCATCCAGTT CAATAGAGAG ACGAAAAAAT ACACAAGCAA 1080 CACAACATCT ATGCTCCAGA TGCTCAAGCT CTTTCTTAAT TCAGCCTCCA GCCAATAAGG 1140 AAGTCAAGTC GTTCTTCAGG CTGGCCTGGA CACCTGGTCA CATGCTTGTC AACCCCTAAC 1200 AGCTCACCTC TGACTACAGG TAAGGTAAAG AAGTTTTGAA ATTTAAACCA TTATTTTCCA 1260 CAAAATAGCA ACAGCCAATC ATTTTCCCAC AAAGTTACGA TACAGCATCA ACCACTGGTG 1320 TCTCTGGTGA AGCTCAACAG AAGCTGCTAA GGCCTAACTA ACCCCCTTCA ATGTAGATTT 1380 TTTGTTAAAT GAGAAAGAGT TCATTAACTT CGGCAGGACT GCTGTATTAT CGGAGAAAGG 1440 CTGATTTTGG AATTGGACGG ACACAGATTT AAAAGCCCAC GTGTGCCATT TTGGAGCATT 1500 CTAACAATTC TCTCTGTGCC TCAGTTTCCT CACTGCTACA GAGGAGATAC TGATATTTAC 1560 ATGACGGGAT TGCTGTGAGG ATGAAATGAG AAAAATCCAG CACAGGGTTT GGCACACAGG 1620 TGCTTAATAA AATTGGAATT CTACGATGGC AGTCAGGAGC TGTAGAAATT AAAATCAGTA 1680 GGCTTCCCTT ATTGCAAGGG TGATGCTGTT ACCCAAGCCA AGAACATGGT TAACGCCAAC 1740 GTTCTGGAAC TCTGGATGCT GAAGACAGAT CAGCATCGGC ACCTAACTAG AGCACCCACA 1800 GAGCTACTGC TACCTTAGTG GCCCGCACTA CCACGGTTTC CAGGACTCTG GAGGGAGGTG 1860 ACCTCCAGCA ACACCTTGGC CTCTGCAATG CCAAATATAA ATCCAGACCG ACGGAGCTAT 1920 GAGAGTCAAG CGAAGCAACA ACATACAACA TTCCCGCCAA CTGAGGATGG GAGCCGAAAG 1980 AGGTTGTATT TTCAAACAAA TCTGATCAAA GTCCTCCTGC CTTTGACTAT AAGGGCTGTT 2040 GTAACTAACA AGGTTAAGGT TTCTTAGCAA TAGTCTACTC AAGGAAGGTA CCGGTATACC 2100 TCAATAAAAG CAAACTTAAC ATATGAACAT CCACAAGGAT GTCAAAGATA AATGTAGAGG 2160 TCATTTTGCT TTATAGAAAG ATACTCTGTT TGTCTTAAAT GTGATTACAT TTAAATAGAT 2220 TCTGTTTTCT GCACACATGC AGGCATGTCA AAAGGAAAAT ACTGCCTAGA CGCGACCTCC 2280 TCAGTGTGGC ACACAGGTCA GCAGCAGTAT CACCTGGGGG CTCCTCGGAT GGGGATGTAC 2340 AGGCTCTCAG CCCCCGCCCA GGCTTCCTGA GTTGGAATCT GCAGTTTGAC AGGGAAGACC 2400 TGTACACACG GCAGGACTTG AGGAGCTCTG TCCTCAGGGT TACTCACGAC CCGGAAGCCA 2460 GAAGCTCTCA GTACAGCTGC ATGGCAGGCT ATCCCCGTGT TCTCAACCCT 2510
|
| |
|
|
|