| Tag | Content |
|---|
EnhancerAtlas ID | HS131-00912 | Organism | Homo sapiens | Tissue/cell | ME-1 | Coordinate | chr1:247802230-247803540 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF16 | MA0741.1 | chr1:247802768-247802779 | GGGGGCGGGGC | - | 6.02 | | KLF4 | MA0039.3 | chr1:247802327-247802338 | CCACACCCTCT | + | 6.02 | | KLF4 | MA0039.3 | chr1:247802268-247802279 | GGAGGGTGTGG | - | 6.32 | | KLF5 | MA0599.1 | chr1:247802769-247802779 | GGGGCGGGGC | - | 6.02 | | ZNF263 | MA0528.1 | chr1:247802733-247802754 | GGAGGCGGAGTGGGAGGAGCG | + | 6.09 | | ZNF263 | MA0528.1 | chr1:247802393-247802414 | AGTGGAGGAGGGAGAGGGGCA | + | 6.27 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AGATCGGTGA CTTGCTCCAC CCCACAATAA CCCCGGGAGG AGGGTGTGGT CAGTCCAGCT 60
GTACAGGTGA GAAAGTGAGC TGGGAGCTGT GACTTATCCA CACCCTCTCA GCAGCAGTTG 120
TGACAGCTGG GGTCACACAG TTGATTCACT GCCATAGGGG AAAAGTGGAG GAGGGAGAGG 180
GGCAGAGAGC GAAGAACAAC TCAGGAAAAT GAAGGAAAAG CAGAGGCAGA GAGCGAAGAA 240
CAACTCAGGA AAATGAAGGA AAAGCAGAGG AGAAATTAAC TGACTGGAAA AATGACAATA 300
GTTGGAAGAC AGACGAAAAA GGGACGAGTG CATCAGAGTG TATTTTGGCA CTTATTACTC 360
TATCTCCTTT TTATACTACT TCGCTTTTTC AACTTAATAG TTAAGGCACG TCGGTCTAGT 420
CTTCCCCGAA GGGAGCTTGC CAGGCTCTGC GACAGGCTTG GAAGTTGGAG CCCGGGCCCT 480
GGGTTCTCTC AGCTTCCAGC TCAGGAGGCG GAGTGGGAGG AGCGGGCCTG GCGGCCGTGG 540
GGGCGGGGCT GCTCCACTAA CGGTTACTGG TCGCTGCTGC CGCCGCGCTC CTCCCCCGGC 600
TGCGGCAGAG GCGCGCGCCT GCGTCCTGAG GATCCCGCCC TTGGGCCGCC GGGAACCTCG 660
CAGAGCGGCG GGGTGGCCCT GGCGAGGCGC GGTTGTTGGG GGTTCGCTCG AGCCTCACGA 720
CGCCCGCGAC TGGGGACTCG GAACCTGGGC CAGGCTGGGA CGAGGCCGCG CGGGAGGGCG 780
CGCTGGGCGG ACGCTGGGGC CGCGGAGCCC AACCGCCCTT GTCCTGGACG CCCCTTGGCG 840
GTCCGCACTG GCGGGTGCCC TCTCCCGAGG GGAACTGAGG CGGGGCGCCT GCCACCATTC 900
GTGATTTTCC GTGACTCACC CTCTCAACAG TGTCCCGTCA GCCCCCGCTT TCTGGAATTA 960
AGATGATTTT CCATGGGCAT TATAGTCAGA GGAGGTTTTC TGTGAGACAT CTGGGAAAGG 1020
TGACTCAATG ATCACTCATA TTGTTCTATG ATGTTATACA TTTAACCGGA ATACTGGTGA 1080
ACAGCTTTTA TATCTTGGAA TTTTTTCCCA TTTTTGAATC AGAAATTTAG GACCAAGAAT 1140
CTTCTGTCAC AGAACCTATT ACTTTGAGGA GTGAACTTAT ATTAACGGTG CTAAACCGTA 1200
CATGAACGAC TTGGTAGATG AAAACTTTGG AAAATAGGAA CATTTCATGT CATCACATGT 1260
ATCCTCCAGC ATTGGGGAAA ATTCAACAGT TGCCTTAAGG CGGGAGTTTA 1310
|
| |
|
|
|
