Tag | Content |
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EnhancerAtlas ID | HS129-08471 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr12:29769720-29770710 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFAT5 | MA0606.1 | chr12:29770068-29770078 | ATTTTCCATT | + | 6.02 | NFATC1 | MA0624.1 | chr12:29770068-29770078 | ATTTTCCATT | + | 6.02 | NFATC3 | MA0625.1 | chr12:29770068-29770078 | ATTTTCCATT | + | 6.02 | POU4F2 | MA0683.1 | chr12:29770281-29770297 | GTCATTGATTATTCAT | - | 6.15 |
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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 |
GH12I029616 | chr12 | 29769233 | 29771132 |
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Enhancer Sequence | ATCTATCTGC ATAGTGGTGG CTCCAGCTGA GATAAATCCT AAGCACAGGA AGGCTTCTTG 60 GCATCGTTAA ACCATATCAG TGTTTATAGA GATAACATTC TCATGGGTGG GGTGGATGCA 120 ATGGAAATGG AGAAAACCAA GCTCTTCAAG GCACCCTGGG TCGTCTTATA ACTTTATTCT 180 CTATACTCTT AATATTGTTT GAACCAATGA GTGGTCAATT AAATCTCTAA TGTTTTATCT 240 TACTGTTTAC CACTATGTTT TTCCTCTCCA AATGCACTGT CCTATACCTA CATATTCCCT 300 ACATATTTCT TCTGCTTGTT TCAAAAAACT TTGTCAGTTT TTAAGATCAT TTTCCATTTC 360 CATCACACCA CTGGGTATGT GACGGCTCAC TCCAGTTAGT CATGCAATTA GTCATGCCTC 420 TGCCTACAAG AGACACAAAG TACAAGGAGC AGGCAGATGA CGAAGGGAAC CATCAGACAC 480 CTCCACCCCA GTTTACGTGC TTTGTCAAAG CACTCTTGAA AAATTTCCCA TCCTCATCAA 540 TGGTTCTCTT GGAAAAACCT GGTCATTGAT TATTCATTCG TTCAACAGAT ATGTTTCATT 600 GCCATCTAAA AAGATAGTCT CTTTGGGCAC TGTACTTACT TAGAAGCAAA CACTTAAAGA 660 ATTTAGCAAT CAATCACTCC CATCTCTTTT GTATTTTCCA GGTACTAGTC TAGGCTCTTG 720 GGAAAACATC AGTAAGCAAA ACAGACAACA GAGAGAGAGA GAGAGAGAGA GAGAGAGAGA 780 GATAAAAACC CTGCCTTTCC AGAGAGGAAA AGAGAGAAAG AGACCACGAG AAAGTGAGTC 840 AGTGAGGCTG GTAAGGGGTA TCTGTAATAC ACAGATTAAG GTGGACAAGA AATGGAGAGC 900 AATTCTAAAC ACAATGGTAG GCTGCACTGA GAAGGTGGCA ATCAAGCAAG ACTTGGAGGA 960 GATGAACAAT ACTTATTTCA TAGTAGAAAA 990
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