Tag | Content |
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EnhancerAtlas ID | HS158-04572 |
Organism | Homo sapiens |
Tissue/cell | Pancreas |
Coordinate | chr1:204694840-204695940 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GLI2 | MA0734.2 | chr1:204695212-204695227 | GGACGTGGGTGGTCA | - | 6.31 | JUN | MA0488.1 | chr1:204695886-204695899 | ATGACATCATTGA | - | 6 | JUND(var.2) | MA0492.1 | chr1:204695885-204695900 | TATGACATCATTGAA | - | 6.19 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I204726 | chr1 | 204695741 | 204695890 |
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Enhancer Sequence | TCCAAAGATG ACTTTCCAAG AGTCTGCTGT TTTACATGCT ACCAAACGGA AGTGGAGATC 60 TAAAATTTCA TGTGCTCACG GAGTGGGCCA CTCCCACAAT GCCATCTCCC CTCCCCTTGT 120 GTGACTGTCT CTGGTGGTCT GCTCCTGAAA GAGTACACAA AGTCAGGATG CAAAGTCCTC 180 TCACTGGAGA ATGAAGACAC CGTTCATTCT GGTGTTTGTT CTGCGGAGCT TCCCAGAGCT 240 GTAGTCAGTC ACCTCACCCC GGTGCCAAAC ACTTGATGTG CTGACTACTC CCGTGCTCTT 300 AATAAGCTTA TAGTCCGGAG AGATGATTGA AGGGCTGGGA GAAGAGGGCT GTGGAGGGAC 360 AGGACCAGCT GAGGACGTGG GTGGTCAGAC TCCTAGATTA ACAAAGCCTA CAGATGCCTG 420 TTGACAGAAG GGAAGGAGAC AGGTTCTCAC TGATAGGAAG ACAGCAGCAA TGCAGGTACG 480 ACTCATGTGT CCATTTCCTG TCATCTGCAG GTGCTTGGTG AGACAGTGTC ACCGTTCTGG 540 GAAGAGCTAG TCTGGGAGAA GGAGTCAGGA TACTAGACCT GTCTGTGAGG CACTGGATGA 600 CTCCAGGTGA GTCATTCACC TTCCCCCCGA CTCCAACCCT CCCAAATCTT GGTGTTCTCA 660 TCTTTATGGA CCTAGGTTCT TTGACACCTC ATTAATCTGA AGGTGGAACC AAAGAATGCA 720 CACCATAGAA ATGGCTACAT CAAAGACTTC ATCCCCAAAT ACATCTCTTC TGGTTCAAAA 780 GCTTCTTGGA ACACAAGCAG ACCTGACCCT CCTCCTCTTC TGCACCCCAT GATGTCCACC 840 CCCTGCCCTC TGTCATTCTT CACTCTCTAC TCTACTTGCC TTCTCTCTCC CTTGTGAATC 900 TCTTGTAAAT GGAAGTCCTG GTCCCAGCAG CGTGCTGGTA AATGTTTAAC AAACAGCTTT 960 GAGACTGGGG GGAATGCCTG ATTTGTAGGG CTTGCCAACT GCCAATTGTA AATACTCCTG 1020 CCATGACTAA TTTCAAGATA CCAAATATGA CATCATTGAA TGCAGAGCCA GGAAAAGAGT 1080 CACAGTAGCA CACTGATGTA 1100
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