Tag | Content |
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EnhancerAtlas ID | HS007-04910 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr14:34891810-34893700 |
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) |
MEF2C | MA0497.1 | chr14:34891943-34891958 | TTCTATTTTTGTTAT | - | 6.07 | Nkx3-2 | MA0122.3 | chr14:34893591-34893604 | TTAAACACTTAAA | + | 6.37 |
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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 |
GH14I034423 | chr14 | 34892801 | 34892950 |
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Enhancer Sequence | TAGTTCTCAA CAATAAGTAA TTATTACAAT ATTAATATGA TTTTAACAAA GTGTAATAGG 60 TACCATCCAA TTTTTCTGAA ATTTACTTTA CAATAAGCTC ATATTATTTT AAAATTAAGA 120 AAAATAAAGC TATTTCTATT TTTGTTATGG AATGACAGCA AATAATAAAT TAGGTACTAG 180 ATACCAAAAA CAAGATACGT AATTTTCTTT TTGAGACAGA GTCTGGCTGT GTTGCCCAGG 240 CTGGAGTGCA GTGGCATGAT CTCAGCTCAC TGCAGCCTCT GCTTCATGGG CTGAAACCAT 300 CCTCCCACCT CAGAGTGGTT AATTTTGGTG GTTATTTTGT TTGTTTTTTT GGTAGAGATG 360 AGTTTTCATC ATTTTGCTCA GGTTGGTCTC GAACACCTGG GCTCAATCCA TCTGCTCGCT 420 TCAGCCTCCC AAAGTTCTGT AGCTAGAGCA CTAGAATTTT CTTGTATGCT CCAAACCCCA 480 CAGTGTAGCA CAAAGAGGAC ATCTACACAT GCAATGGGTT TCATTGCAGG AGAGGACCCC 540 AAGCTTAAAG AACCCTAATC TTTTTATACT AAACAATAAG TATGCCTGCC ATTTGTTTCA 600 GAGGTAGACA TTATATCTGT CTTCTAAGTC TCTAAGCAAA CCTGCTCCTT CTGCTGGAAG 660 GGGACACTAT CTGTCTTCCA AGGCTGTTTC CTATACAAGC TTCTTTGAGG AGATAGTATG 720 GAACAAAGAC AATCAGTGCC ACTGTTCACA AGACATGCAG ACATGCAAAA GACTCAGAGA 780 GAATTTCTTC CCAACAATAG CCATAAGACT GTATAGTTTC CATACAGTGG TGGCTCCTGG 840 AAATTTTTCC CATATTATGC CACTCCATCA GCCACTCTAA ATAATTTAAC AGAGGCTGGG 900 ACCAAATCCA TTTGTCTCAC ACAGCACTTA ATTAAGGCTC TTATCAACAG CACTTTGTAC 960 AGCAAGATGA GGCCATCCGG CAGTATTAAC CCCAGCCATG GCTCCCGGGG TCCTGGTCCC 1020 AATCAGCTTA ACAAATCCCA TACACCATCA TGGTTTACTT AGAAAGCCAA ATGGCTTTCT 1080 CTTTGTTTCT ATATTGACCT TTTCACTTGG CCTAAGGCAT TAATCCTGGC ACAGCAAGAT 1140 AGAGCAGAGA TTGCACAGAC TTCACCTGAG AAGAAAGTCT GGGGCAATTA TTTCATTCAT 1200 AACAACCATG GCTAGTGAGC TGAGGCTGAC CTGCTTTTCC TTTCAGGGTC CAGGCATGTC 1260 ACTGAAAACT TCAGCGAAAT TTTTACCACT TCACTTTTCT AATTGGATGA CTACTGTTAT 1320 AGGGATAACT GCCAGCAAAG TATACATAAA TAACGAATCT GTTTGATTCT TTTTTTTTCT 1380 TTTTTTTTGA GACCGAGTCT CACTCTGTCA CCCAGGCTGA AGTTCAGTGG AACCATCTCC 1440 GCACAATGCA ACCTACACCT CCCAGGTTCA AGTAATTCTC CTGCCTCAGC CTCCCGAGTA 1500 GTTGGGATTA CAGGCGCACG CCACCATGGC CAGCTGGTTT TTGTATTTTT AGTAGAGATG 1560 GGGTTTCACC ATGTTGGCCA GTCTGGTCTC AAACTCCTGA CCTCAAGTGA TCTGCCCACC 1620 TCGGCCTCCC AAAGTGCTGA GATTACAGGC ATGAGCCACC ACGCCCAGCC TAAGAATCTG 1680 TTGTCTTACT GCAGAGATCT CTCCATTACC TAAGAAAAGT CTCATTTTGG AGAGATCTCT 1740 GTGGTCATCT GAGGGCCACA TGATCTGTCA GTGATGCTTC CTTAAACACT TAAAGGGATC 1800 TTATGATTAC CCCTAAGGTG TTTTTAGGGG AGACAAAATA ACTCCTGGAT TCCACACAGG 1860 AAATAAAGAC CTGAGGGCAC ACAGAGTGCC 1890
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