Tag | Content |
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EnhancerAtlas ID | HS159-01838 |
Organism | Homo sapiens |
Tissue/cell | Pancreatic_islet |
Coordinate | chr13:110487380-110489970 |
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) |
Lhx3 | MA0135.1 | chr13:110487795-110487808 | AAATTAATTAACA | + | 6.19 | ZNF263 | MA0528.1 | chr13:110489447-110489468 | TCCTCCACCTGCTCCTCCACT | - | 6.26 | ZNF263 | MA0528.1 | chr13:110489444-110489465 | CTCTCCTCCACCTGCTCCTCC | - | 7.75 |
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| Number: 1 | ID | Chromosome | Start | End |
GH13I109836 | chr13 | 110488541 | 110489815 |
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Enhancer Sequence | TTTTAAATAT CTTCCCAGTA GATATTTCAG CCACTCATCA TTCTCTATTT CTCTTGTGTG 60 TTTTTCTTGA TTTCTAGTGG CAGCAGGATT TCAGCCAATG ACCCCGGCCG GGTCCCACTC 120 CCTACACTGA TGATGGACTT CACTGTGAAC AGCATACTTG TAGGGGTGGG GGATGGTGGT 180 GTAACGAGTA ATTCCCTCTC ATAAGGAGGC CAGAGACCCA CTGACAAACA TGAAGCTCTG 240 GTTCAGATCC ATTGAGACAA AAAAAATAAA AATAAAAATA ACCCGGACCG CTTGAGTGAA 300 TAGTCAGGAA CTATACAAGA TTTGTGTTTT TGAAAAATTC TCCACGTCAG TGTACAGTGG 360 AATGAGGAAA TGCCATTGTG GGGGGAGGGT AAGGAGACAT AGATGCCTTT CTGTAAAATT 420 AATTAACAAA TTAGTGGTTG ACGTAACATT CTCTCCGTTG ATTCTCTTGT CTCCGGGACG 480 AAGCGCACAC TCTGCCGCTG ACTGCGCCTT TTGACTCATC AGTATCACTC ACATCATCTG 540 TTGCCTCCTG TCTAGCTTTT TTTTTAGTCT CAGATGAAAC AACTTGTGCC TCTTCTTTCA 600 GCTTGGTTTC CTTGTTTGTT GATGCAATGG GAACCAACCA TCTGCCTAAT CATTTAAAGA 660 AAATTTTTTA ATCAGGCTTT TTGGGTGATT TAATCCAAAA CTCACACTTT TCCCCCATTT 720 TCAAAAAAAA TGAATCTTAC TCGTGAGGAC AAAACATCAA ACCACAGTTC GCTCCAAATT 780 GTTCTCGATG TTATATTTTT AACAGAATCC CAGGCATACA TAATATTAAA AATTACATCC 840 CTGATGCTAT TGTGAGATTA AAAGTCTGGC ATGGTGCCTG GATAATGGAT CATATGATTA 900 TATTGCTTAC AAAACCTCTT CTGCAATATT TCAGTTTCTA AGTAACACCC TCAACCATGG 960 ACTAAATCAA TGGGGAAATA CTAACAGCCA GAAAAGAAAT AATGGAACCC ACCCTAAGAA 1020 AGCATCAACA GGATAGCTTT ATTTTTATTG CGTGAGCTTT TGATTCTGTG GCGCAACCAC 1080 CAATTAGAAA AACAAATTGT CTGTGCTTTC ACTTGTCCTC AGTAAGCGGC AGGTGAAGGG 1140 GCCATCTTTG CAAGCACTAA AATGATTCTT TCAAACACCT GAGGTTTCAT TTTTTGGCTT 1200 CCTGCATTTT TTTAAAGACT AATCAACATC TGTAAGAATA GAGTTTTGCC AACTTGCCCA 1260 TTTCGTTTGC ATTGCAAGAC TTCAGAACTT TCATCAAAAT TCTTTCCATC CACTTTCTAA 1320 TGACAAAACT GTTCTATGCA TCAAGGGCCT TGCATTCTGA TCCACTTTGA GGCTGTTAAA 1380 GGATAAACAA ATTTATTGTT TTCCTTCCCC ACATTATAAA GAGCAGTTTT GACATTATAT 1440 GCTATTATTT CTGATTTATA AATGATAAAA TTATTCACAG TTGCATGACA TCCAATCAGG 1500 GAAGAATAAT GATCACATTT GGAGAAAAAA AGCTTAAATT GTAATTGGGT AAAGAGTGAC 1560 CTTGGGCTCC TCGTGCCCTC TACCTAGTAA TTGGAGCCCT GCTTGCTGTG TCTGATGCAT 1620 TCTCCGTTCA GCCTCATGGC TTCCTGGTCA AAGGGCCCCT CGGCTTCCTC AGGATGGTCA 1680 TGAGGGCTGC CTCACCCACA CACCCAGGGC TTTCCGGCTG ATAACCTCGG TCTATCAGTT 1740 AGGCTTGTTC AGCTTGCATG TGTCCTCTGT GCAGAACCAA TGCAGAGCGA GCACTTGGAC 1800 CTGTGGCAGG TGAAGCTAGG CATTTATTAA CTCAGGCTTC CTGTAAACAC AGGGCACAGG 1860 AGCCGTCACA ATGAGAACAT GAAAATGAGA GTTATATGGG AATGAGTGCC TCAAGAGCCA 1920 TCCCGTGACT GGTGCTTTAA AAAAGAGAGA AAGTTGTGAG CAGCGAAACC CAGGAGAGAG 1980 AAGCAGCATG GGGGCTCACA CCAGGTCGTA GCCCTGCACA CCTGCTGCCA CTCTCACAGC 2040 AGTGCTGGCC TCCTCATCCA GCATCTCTCC TCCACCTGCT CCTCCACTCC AGCCTGGAGG 2100 TCTCTGCTCT GGTCCTGCTT GCCCATGAGA GGGAAACTCA CACTGTGGCC CTTTTGCTAC 2160 TTAGAAGTGC AGCCATTTGT TGGATGGTAA CCCTGTACTC AGTGCTGGGA TGACATGTCA 2220 CTTACTTTGT CCAATACAAG TCTCAGTACC ATCTCATGAG GAAAGAACAT GATTAATCCA 2280 CCTTCACAGA AGTGGATAAG GAGGCTCAGG GGTCCTGCAG CATTTTCGTG GTCACATGGC 2340 TGCTAAGCAG CAGAACCAGG AATACCAAGT CTGTCTGATA CCAGAGCTGG ATTCCAACCG 2400 ATTCCCTAGA CATCCTCCCC CCAGGCCAAA TCCATTGAAC ATCAGCTGCA CTCAGAGACG 2460 GCACCAACCA AGCACTTCCT GTGTATCTTT GAACTTAAAT GAAATCTAAG TACTCTGCAG 2520 CCTTGTTCTG TCTCAAAAGC CCAATAATCT CCATTTCTCC ACAATTCTCA GCAATTAGCT 2580 AACATAATTC 2590
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