Tag | Content |
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EnhancerAtlas ID | HS148-00687 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr1:85411500-85412170 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFE2L1 | MA0089.2 | chr1:85411785-85411800 | AAATGACTCAGCATT | + | 7.42 | Nfe2l2 | MA0150.2 | chr1:85411783-85411798 | GTAAATGACTCAGCA | + | 6.1 | POU4F2 | MA0683.1 | chr1:85412101-85412117 | TTCATTTAATATTCAA | - | 6.3 | ZNF143 | MA0088.2 | chr1:85412035-85412051 | TTCCCATAATGCCTAG | + | 6.46 |
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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 |
GH01I084944 | chr1 | 85410221 | 85412524 |
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Enhancer Sequence | TTCACTGCAG CCTCTGCCTC TCAGGTTCAA GCAATTCTCC TGCCTCAGCC TCCCAAGTAG 60 CTGGGATTAC AGGTGCATGT GCCACCATGC CCGGCTAATT TTTGTGTTTT TAGTAGAGAC 120 GCGGTTTTGT CATGTTGACC AGGCTGATCT TGAACTCCTG ACATCAAGTG ATCCACCCGC 180 GTAGGCCTCC CAAAGTGCTG GGATTACAGG TGTGAGCCAC TGTGCTCAGC AGTAGCCCAT 240 TTTAAACATG TGGATTAAGA GATGTTTTTT GAGCAATGAC TGAGTAAATG ACTCAGCATT 300 TGCAGCGGTT GCTGTCTGGG CTCTGAAGGC CCTGATCCTT CCCCACTGTC CAAGGCTCAG 360 ATCAAAGCAT ACCTTCTCCA AGAATCATTT CTTTTCCTAC TCTGCCCCAC TCAAACTTAT 420 TACCTTTGCT TTTTTTCTCC TCATACTTTT TGTATGTATA CCCTTATTTC TCTCCATAAC 480 ACATCACAGA TTTTATAAGC ACGTCAGTCT CTCTCACTAA GGCATTTTCT TCCTTTTCCC 540 ATAATGCCTA GCAATTAATA TGTGCCAACT CTTGTGTTCA GTGCTTTGCT TTATATACTA 600 ATTCATTTAA TATTCAATAT CCTGGAAGGT AAGTTTAGGC TGAGTATGCC CTATCCAGAA 660 TGATTTGGGA 670
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