Tag | Content |
---|
EnhancerAtlas ID | HS147-05566 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr10:17429610-17431140 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GRHL1 | MA0647.1 | chr10:17430381-17430393 | TAAACCGGTTTA | + | 6.22 | GRHL1 | MA0647.1 | chr10:17430381-17430393 | TAAACCGGTTTA | - | 6.22 | Sox3 | MA0514.1 | chr10:17429854-17429864 | AAAACAAAGG | - | 6.02 | TFCP2 | MA0145.3 | chr10:17430382-17430392 | AAACCGGTTT | + | 6.02 | TFCP2 | MA0145.3 | chr10:17430382-17430392 | AAACCGGTTT | - | 6.02 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH10I017386 | chr10 | 17428311 | 17431022 |
|
Enhancer Sequence | AGCTAACATA CAGGACTGGA CTGCTGTCAC ATCGATTAAC CCAAATCAGA GATCTTAGCC 60 AGTATCAAGC TTTCCTAATA ATTTCAAAGA TCTGCAGAGA AATGAGGGGA AATGGGGCTA 120 GAGGTGAAGT GAAAAAGTTA AGAGATTTCT GCTGAACTCT AGGAGAGAGA TTGCAACTCC 180 TTTTACTTGT CAGGATAGAA TAGACTATGA TATGATAACA ACGCCAAGCT CTCAATTGCT 240 TTACAAAACA AAGGTTTGTT TCTTGCCCAT GAAATGCCCA CTGTATATCT GGAGGGCCGT 300 CTAGGACAGC TGTGCTGTGT GTGGTTTAAG GCTTTCAATG GTTCATTTTC TGTGTCGACC 360 TGACTGGGCT CAGGCATGCC CAGATAGCTG GTAAAACATA ATTTCTGGTT ATGTCAACAG 420 ACTCAGACAA AGCAGAGACA GGCTTGGGAC ATCAAGGGTG GACACCCCAG TCCTGTCTTC 480 CCACACTGCA CATGGCCCAG GATCGTAGGT GAGGTTTCTA GGTGAGGTCA GTGGGCTTCC 540 TCACACAGCA GGAAACTTTA AATTGTTAAA CGGTTTCTCT TTTAGACCCA GGGAGTTCCA 600 CAGCCTTTGA GCCATTCTCC AGGCAGTCCT GCCTCCTGGA TCCTGGATTC CATTAACTTT 660 AAGCAGGACC TCAGCCAGAG ATCAGCCTGC TAGGGACACT CAATGGATGT GTCTCTTCCT 720 CTAAGCAAAT ATCGTTAGTC TATTTACCCA GAGGCTCAGT GGAGAAACAG TTAAACCGGT 780 TTACCTACCT TGGTTTCTTT ATCCCCAGAT CAAACTCCAA CACCCCCAGG GAAGGGAAGG 840 AATGGATTAG AGGCAGCTGT ATAAACACTA TTTCTAACAT TAAAAGAAGC AGTGTGTGTG 900 TGAGAGAGAG AGAAAGAGAA TTATTATTAG GAAGAGAAAG TGAAAAACAT GAAGGCAGGA 960 AGACCGCTCA CTGGGTCTTC CTTGTATAGG ATTGGCATGT GGAAATCAGC AATACCTCTT 1020 ACTGAAACCA TCTTTGAAAA TTATAACTGA GGAAATTATG ACATGAAAGA AATCAGACCT 1080 AACTGACTAC ATCTTGCTTC TAATCTTTAA GCTGTCCTTG TTTATTCCTG GGTGTAGGCC 1140 GAGCTAACTT TGAGAAGGAA TTCAGTTCGT GGTTTGAGTC TGAAACAAAA TTGATAATAG 1200 CGCTTTCCTG AAAGGACCCC CTTCTGCCAG GGGACCAGTC TGCCTTTGCA GGACTAACAA 1260 ATTAGCTACA AGATTAGAAA TTACAGTTTA GGGGTCATGC AGACTCTGGC TCCAAGAGTC 1320 TGAACCTCCC CATGTTGCTC CTGGGGATAC CATCACTATT GTAAAACCTA AGATCAGTAC 1380 TTGAGATATT TTTCAGACCC TAGACTGGAT GGATCAGCTG ACACCCCCCA GACTCATAAT 1440 CTGGCTCAGC CAGTTCTGCC ATCCCACCCA GGAACAGAAG ATGGCAAGAA AAACTCATTT 1500 CAACTCCCTG ATTCGCTCCA GCCTGACCAT 1530
|