| Tag | Content |
|---|
EnhancerAtlas ID | HS101-36206 | Organism | Homo sapiens | Tissue/cell | HT29 | Coordinate | chr5:168416390-168417360 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFAT5 | MA0606.1 | chr5:168416635-168416645 | AATGGAAAAT | - | 6.02 | | NFATC1 | MA0624.1 | chr5:168416635-168416645 | AATGGAAAAT | - | 6.02 | | NFATC3 | MA0625.1 | chr5:168416635-168416645 | AATGGAAAAT | - | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CACAGCCACC TGAAATGAAT TTGCTGAAAA CACAGCAGGA GACTTGCAGC AAACTTTCAG 60
GTGGGATTTG CCACACTTGT CTCGCTCTTT GGGGTAAGGA GGAGAGCCCG AGCAGAGGGA 120
GAATGTGAGG TGACAAGTTC CAGCTAACAT CTCTGCATCT AATGTAATTC TGAAAGTTCT 180
AAAGCGCGAA CTAGTTGTAT CCTAAAAGAG TGAGGCAAAT CTGAGTGGTA ACCAACATCC 240
ACCAGAATGG AAAATGCAGG CACAAACTAG TGCAAAGCAG GGCAAAGACC CAGGAAAGTA 300
ATTGGTAGTC ACTGTTCCCA TAGCCACCCT AAAACGAGAA GATCAGAGAG AATGAACAAG 360
AAACGTAGAA AATCAGCTCA GAGATCTGGA TTTTCACCCC AATGATGCCA GAAACCAGGA 420
TGGGACCTGA ACAAGTTATT CACCCATCTG AAGTTTCATT TCCGTTTTCT GCAAAGTGAA 480
GGGGCCAGGT TGAATGTCCC CTGAGGTCCC TTTTATCTCT AACAGTTCTG TGAATAAATA 540
TGTAGTTGGC ACATTATAGT CAAGAGGTTA AGCTGAGTAA ACAAGAAAGT CCAGGTTCAG 600
CCATCAAAGT TCCACGGCCG CCTATCCTGC TATTCATGTG GGTTCAGGAC AGGGCCCTCT 660
TCTCAGGCCA AGCTGGCAGA TTCCTAGTTC CATTCCCCTG AAGATGTGAG AGAGGATGGG 720
ATTGTCTAAT GAACTCACTA CAGTCCAACT GAGGCAAGAT TTCTACATCA GGGTCCATCA 780
GGATGTCCAT CTTGCACCCT TGGCAATTGC AGCCTTGCAA AGCATAGCCA CGAGCCACCT 840
TCTCTTCCCA CAATCTCTCC TCTCTTCCCT GCATCCCCAG TCAACAAAGG AGAGAGTCAC 900
AGAGAAGGGT GAGGGTGGGA CAGGGTAAGA AACTCCAGCC CCAGCTCTAA AACCTTTACA 960
GAAAGCCTTT 970
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