Tag | Content |
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EnhancerAtlas ID | HS177-09538 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH_RA |
Coordinate | chr17:59237620-59239950 |
Target genes | |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFAT5 | MA0606.1 | chr17:59237961-59237971 | ATTTTCCATT | + | 6.02 | NFATC1 | MA0624.1 | chr17:59237961-59237971 | ATTTTCCATT | + | 6.02 | NFATC3 | MA0625.1 | chr17:59237961-59237971 | ATTTTCCATT | + | 6.02 | SCRT1 | MA0743.1 | chr17:59238758-59238773 | GCCCACTTGTTGCAT | - | 6.11 | SCRT2 | MA0744.1 | chr17:59238760-59238773 | CCACTTGTTGCAT | - | 6.17 |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I061161 | chr17 | 59239121 | 59239270 |
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Enhancer Sequence | AACTTTATAA AAATAGTCTG AGTTAATTTT TTTTTTAATT TACTGGATAA CCTTGTAAAA 60 GTCCCTCCAC TAGTCATATA GTGAATATGT CACATTTAGG TAATTGCCAT TGCCGTGCTG 120 GATGGTTAAT ATACGGAATT TCCGAGCACT GATCTAATAG AACTTGCTGG GGCATCATGG 180 CAGACAAGTA TGTCTCCCCT CCCTGTGACT GCGCTCCTGC ATGGTATGCT TGGCAAGCTT 240 AGCAAAGCTT AAAAGTCAGC TGCATCTGTG TGATCCAACT TTGCTTTGAC TGGGAGCAAT 300 TGAGTACACC ATTTGTTTTT TCTAAATATC ACAAAAATTG TATTTTCCAT TTACTAGGGC 360 CTTTTAAGAA AAAAATGCCT AGGGCTGATG GTTTACCAAC TTTTTTACCA TCTATGCCTC 420 CAAAATATAA AAAAGGTCAT GGTCTTACTA CTGATTATAG TGGACCACAC TATGGTCACT 480 CTAGTTAAAA CTGTGACCTT GAAGCGGGGG TTGGGTAAGG AAGGCCCTAC TTGTGGCAGC 540 TTTCCTCCAC ATTTTGGAGC TTTGATGTGT TCCTGCAGCT GATATAAATG CAGGGAGGGG 600 GTGTCAGGGA GAGGCAGCTG GCTGGCAGCG ACAGATTAAA ATATTTCTGA CCCACAAATG 660 TAACCAAATG CCCATATTTC TTCATTTAAC ATAATTAATG CCTTGTATTT CCACTGACTT 720 TGATAAAGTG GCCTTCCTCT TCCCATCCCA TCCCCCTTCC CTGTGTCAAC TTTGGGACGA 780 CTACAAGAGA TCTATAGTTA AAATACTCTG CAGATGATGA AGGATAGCAT GTCTGAAAAA 840 AGCTAACATA AAAGTCTCAA TTAGGTTGCT GCCTAGCAGG AAGCTTATAA CCACATTAAA 900 ATGGAAAAGT TATTTCATTT TTAGTATACT GTATTTCAGC AGCAAGAGTT GCAATCTGAG 960 AGTAATATGA AACATTTTGG TTTGGCTGCC AAGTACATCC ACATTTTGTT ATAAATGTAT 1020 AATTACAGGA AATATGTGAA AAGTGTTAAA TATTTCTTAT CAAATATTGT TAAAGAGGTA 1080 TTCTGGTTAC ATTTGGAATT TAGAAAAGGC CTGGGATGGA TTTTGATCAT GTTACAAGGC 1140 CCACTTGTTG CATTTAATTT AAAGCAGTTG TCCCAATTTC ATTACCACAG AGCATAGCGT 1200 TTTCAAATTT ATTCTTTAAA AGACAGAGAT AGTGGCACAA AATGTGCTGT GGGTTTAAGC 1260 AATATTTGAT TGATCATGTG ATTCTATCAG TATCTTTTTT TTCTTTTATT TTGCCTCAGT 1320 ATACACATTT CTGAATGAAA AGATAGACGA TGTCTTTATT TTAAACAATC TAGTGGTGGT 1380 TGAAGAGGCC ATCTGGAAAG GTGATGTCAA CGGAGGGTAG GGTGGTTGCT GGTGGAGGGG 1440 AGTAGCCAGC GCCCCTCCCC TCAGCACACA TACCAGCCCC CGCAATTCCA GTTTCATGGT 1500 GCCTGAGTTG CTGTCTGGTT GGTTGAACTC ATTCTCCTCA GCTTATATTT AACTCGTCGC 1560 TTGTTCTGGA AAAGTAGTAG TACTGCCTTC TCTGGCCTTT ATAAACATGA TTGCTGGACA 1620 AAGATGAGCA GCACGGATTT GCTGCGATGG TCAGAATTCA ATTATATTAC TCTCTCTGAG 1680 GCAAAAAGCA CACATTTAAT AACTAAATTG GATTCCTTCT ACTAAGAGAT CCTAAATTCG 1740 TGTTTAATAG CCAGCTAAAT GTAGAGCTGA TTTATATTTA TAGGCTGGTT GTAGATTTGG 1800 TTGATAGAAT ATAAAGTTTG ATCTGTATGT GGATGGTTTT ACTACCCCAA ATGAAATGTA 1860 CGTATCCTGG TCCTGCACCA TGTTTTTCTT CAGTAAAAAT TGAAGATATT TTATTGGGAA 1920 ATATCCTGGG TAAGTAAACA GTGATTGCAA TGTGTATGGA GCCACGGTTC TTACAGGAGT 1980 GGGTATGGTT CACATAGGAA GTGGGAGCCT AGTTAAGATT CCGATTCTCT GTGGGATGGG 2040 GATAGGTAGG GAATCATTTC TCAGGAGAAG GAGAGCTTGC GAATGGAAGG GGTGTTCCTG 2100 CCAGCTGGGT TTCTTTGCAT TCCCAACAGA AGGTTGTTTC ATATGCATTT GCCTCTACAA 2160 GAATATTCTC ACACCATAGA TATAGAGAAA GGACAGGTAT ATACATCGTA TTTTATTTGA 2220 AGGTATCCTG ACAGAATTTC TGCCTATCTT TTTTCCTGCT ACAGTCTGTT GTACAGCAGC 2280 AAGACCAAGA TGATTCCAGT AATAAGCCTT ATTGGTATGG TTCACTGATT 2330
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