Tag | Content |
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EnhancerAtlas ID | HS159-01661 |
Organism | Homo sapiens |
Tissue/cell | Pancreatic_islet |
Coordinate | chr13:22054970-22057770 |
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) |
IRF1 | MA0050.2 | chr13:22054972-22054993 | AAAAAAAAAAAGAAAGAAAGA | - | 6.25 | JUND(var.2) | MA0492.1 | chr13:22056767-22056782 | AATGACCTCATTTAA | - | 6.01 | POU4F2 | MA0683.1 | chr13:22057337-22057353 | ATGCATATTTAAGGAT | + | 6.11 |
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| Number: 1 | ID | Chromosome | Start | End |
GH13I021480 | chr13 | 22055125 | 22056010 |
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Enhancer Sequence | AAAAAAAAAA AAAGAAAGAA AGAATATGTT CCTTCCCTGC TGCCCTCCAA CAGTGCAGGG 60 ACATGGCAGC TGCCGTGTTG GTATAGACCC TGCCCTCCTG GCTGCAGTGG ATTGGTCTGG 120 AATAGAACCT GGTTCAGACA GGGCAGCCAA TCAGCCCCTT TCCCAGAGAT TTTTGACTCT 180 TAGGGAGAGC ATAGTTAGAA TTTCTCTGGT GTACATGCAG TAAAAGAGAA TGAAATTGCT 240 ACCCAGATCG AAGTAGAGAA AAGCCTGGTG AGAGTTCCGA GGGCTTCAGG TCCTCAGTTG 300 GAGTTTTCCT ACGTCCCAGC TGCTCCCCTG ACCTCCCCAG GTTTGACCCT GTGACACTCC 360 TGTAGACCTT TCCTATCAAC TCCTCTTTTG TCTAACCCAT TTCGAGATGA CTTTCTGTTG 420 TTTCTGTCCA AGAGTCCTAA TGATTACATA TGGAGAAACC TGTATCAAGG TCCCAGCTTG 480 GCCAGGAAAG ATTCGAGTAC CAAAGAGTAT TCCTTCCCTG TAAGCAGATG ATATGGAAAC 540 CAGATTATCA GAAGGTTGCT CGGAGACCGT AAAATCAGAA CAAGGTGTAC TAACATAATA 600 ACGTGATTAA CAGCAACAGG CTCTGCTAAT CTAACGTGCT CATCTTTAAA TAGAAATAGA 660 TCTGTCATGA AAGGAGAATG CTTCGTTGCT AGGGCTCCCT TTATTTGGAA AGCTCTTGGA 720 TGACCACTGC ATTGCTTGTT TCTGTGGCCT CTTTTCTATG CTTGCATGAC TGACTCAATG 780 CTCTTTGTGA TTTATTTATT TGTTCAGGGA TTCAAAAATA TTTATTGGAC ATCTACTCTA 840 TGACAGGTGT TGTTTCAAGT TTCAAGAACA CAATGGTGAA TAAAGAAAAA TTCCTGCTGT 900 AGTCCCAGCT ACTCGGGAAG CTAAGCCAGG AGGATTGCTT GAGCCCAGGA GGTCTGGACT 960 AGCCTGGACA ACATAGTGAG ACCCTGTCTC TAAAAAGGAA AAAAATCCCT GCTTTTATGG 1020 AACTTACATT CTAATAGGAT AAGCAGATAT AAACAGATAT ACAAATATAT GTATATATAC 1080 ACATTTTAAG TTGATGATCA AGTTCTAGTA AGAAAAACAA CATAGAGAAA GAGGGTGGGG 1140 TACAATGGGG ATTGGTTTGT TATGGTCTTT TTTTTTTTTC TCCTTCCAGT TTATTTATTT 1200 TTCTCTCTAA GACCAATTTA CAGTCTATTA GCACTGTGTG AGCACCTGTT TCACCACATA 1260 TACAAACCCC TCCAAGACTA TAAGGATATC ATTAGGCTTT ATATCAGTGT CAGGTAGTAA 1320 ACATAATTTT GTACATACTT TGCATTTTAT TTCTCCTGAG GTTCAGTATT TTCCATGGGT 1380 AAACAATAAA TATGTTAGAA CATATTTATT CAAGATGAGA CATTTGTCTC CTGGTGAGAC 1440 ATCTTGGTCT AATGCTGACT CTGGGGACAT TTGGTTGTTG ACTGTGAGGT GGCTATCTAC 1500 ATGTGGAGTG GAGGAGTCCT GGCCTTGGAT TGAGGAGAAC AAGGTCAACT TCTCACCTCA 1560 CTCGTTTCTG GCTTTTGCGA CCTTGGATAA GTTTAACTTT CTCTCTCCTA GGTTTAGTTT 1620 TCTTGTGTGT AAGTGCTGCC TTCTCACTGT GAGCTCACAC AGCCTTTCCT CAGTGTGTGT 1680 GTGCAGAGAT CTCTCTCTTC CACTTTTTTT AAATGAATTA TTTAATTTGG AGGACCAAGT 1740 GCAGAATCTT CCTCTACTTA TAAGGCCAAA AATCCTATCC AATTAGAAAC TCATTCTAAT 1800 GACCTCATTT AACCTTAATT ACCTCTTACA AGTCCTGTCT AGAAATACAG TCATATTGGG 1860 GTTTAGGGCT TCAATATACG AATTTGGGGG GATGGGGAGA CAATTCAGTC CATAGTAAAC 1920 ACTTTCTCGA AGAGTAGTTA CAATGTTTAT AAGAGACAAT GTAGGTAAAA GTAGTTTCAG 1980 TTACCTGCAG CTAAATGCAG TTTATTATCC CTTCAGAATC CTCTGCAGAA GAGGCACCTA 2040 ATAAATATTA TTTATTTGGA CTTAACCTAA GGTATTATTC TTTATATAGT GCCTTCCCAT 2100 GGAATGATTG AAATCATGTT TATCATTTTG CAGCACAGTT TATTTCTTAT AGGGTCATGG 2160 CTAATAAAAA ACATGGGAAA ATGACCCTCA CTAATAGAGT CATTAATTTA AATAAGGAAA 2220 TGTAATTTCA AATTTTTTCT TTTTGGGGGC CTATTACGTT AACAATGCTT TTAAAAATTT 2280 ATTGTAAATA TGAGTGTTAT AAAACAGAAA TTTCCACATT ATGTTGGGAT TATAAATTGG 2340 CATGCTCCTG AATAGCAATT TTTGGCAATG CATATTTAAG GATCTTAGAT AATGTTTTTC 2400 ACTTTTGATT TAGTATTTCC ACTTCATGAA TATCCTTAGG AAATAATATT TGAACAAAGA 2460 TTTATGTACA AAGATGTGTG AGCTGTATGA TCTATAATGC ATAGAAATGG GAATCAATTG 2520 AAATAGTCCA TAATGAAGAA CTAATTACTT ATCAATATAT CCATAAATTA TGCATCCATT 2580 AAAAATTATT TCTAAGCATA TTTAGTTATC TAAATATATA TATAGCATGA CACCTAAGTT 2640 TATTTTATAT ATATGGGATA CATGATGTGA GATATATGTA TATATGAATG TGAATATATA 2700 TGATATACAT ATAAAAAGAA TAGGAGATAC TAGGAGTTAT TTTAATTTTG TCTTTATGTT 2760 TCTCATTTCA TAAATTTCTA TGAAGAACAT TTTAATTGTT 2800
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