| Tag | Content |
|---|
EnhancerAtlas ID | HS108-07489 | Organism | Homo sapiens | Tissue/cell | K562 | Coordinate | chr11:57279900-57281430 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TFAP2C | MA0524.2 | chr11:57280831-57280843 | TGCCCCAAGGCA | + | 6.62 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr11 | 57280129 | 57280600 | | chr11 | 57280424 | 57281029 |
| Enhancer Sequence | CTAAAAATAC AAAAATTAGC CAGACGTGCT CGCGTGAACC CAGGGGGAGA AGGTTGCAGT 60
GAGCGAAGAT CATGCCAATG CACTCCAGCC TGGGTGACAG AGTGAGACTC TGTCTCAAAA 120
AAAAAAAAAA AAGTTACATA GGGGACAGTG GCAGGTGTCA AGGGCAGGCA GGGTCTCTCC 180
TATCTCCAGG ATAAACTCAT AGGGGACTTA GATGCCATGT GGGTCCCTAA TAGCCCTCCA 240
CTTGGTTCTT GCAGCCACTC TTATGTGTAT CATTTCATGT CAGGCCTCTT CTTCCCAACC 300
CACCCAGCCA TCCCAGCCTG GCTGCCAACC CCACCTCCTC CAGCCCCTGT CACCCCATAA 360
TTGGGGCCAG GAGGCATGGG AGAGTCGCCA TCTCTCGGTG CCATCTGTTG CATCTTTACA 420
GATAACCATG GCTGGATGCG GCAGATCCTG GGGTGGAGCA GCCGCTGTTC AGAGCAGTGA 480
TCAAGACCTC CCCATCTCCA CCCCTCAAGG AATCGGTTTT CTTCCATAGC CACATCAGGT 540
GCTGTGCAGG AAGGAGTTGA AACGAGAAGC CAGGAGCAAC GAGAAGGACA CTAACATTTA 600
TTAAGCACTG CAGACTCTCA CAGCACTCCC ACGGAATCGA TATTATTATC CCCATTCTGA 660
AGACCAGGCA ACTGAAGCTC AATGTTTAAG GAACTCACCG AAGTCACCAA CTGATAAAAG 720
TGATGGAAGC TGGGATTCAA ATCCAAGCTA AACTTCCTTC CAAGCTTACT CCACAACACA 780
GAGGTTGGGG AAAGGGGATA AAAAGAGAGG GGAGCCCAAT TCCATTTCCA CCCAGCTCCT 840
GAGGCGGAGC TTGTCAGCAC AGCTCTCTCC TTCCCAGAAT AGGAAGATAC CCATCAGAGG 900
CAAGTCCTAG ACACCAGCAG TGGTAACTCC CTGCCCCAAG GCAGCTGCAG ACAGCCTATG 960
GCTGTAGTTA CTGCTCCCAA AGAGTGTTAG AATTCCCACT CCCAGCTTCG GGGCCACTCA 1020
CACAAGGTGA TTGAAGTGGA AACCAGAGAC TCTCCACAAT GCCCTCCTAG AGTAAATGAG 1080
GCTATGTAAC TTTGTCCAAA TGAGTAATTT GAAAACCTGG GGGCTCCCAG CTCCTGAAAA 1140
GGGAAGGATG TGGGGCCCTT TATATTCATA CTCCACTTTG TGCAGCTCTC CCTTGTCTTA 1200
TGATAGCCCT ATTAAGAAAT TCCTCTCCCA GCACGTCTCC TTCAAAGAGC TCTAGACCTG 1260
AGGCTGTCAG AGGCTTAGGA CTCTGCCTAT TAGTCCCAGG GTCTGGATGA CCAGCAGGAC 1320
ACCTGGCATT CAGTGACCAC TGGATTAGAT AAATGAAACA GTGGGCAGAG TGCCACCCAA 1380
TCTCCCCCTG AAGTTTGAAG AGGTCGAGAA GTGAGGCTGT CCAACTGCTG ACCCTGCTTT 1440
CTGTCCACCT GGCCACCTAA CCTTTTCTGG CTTCCACCTG CCCCTTTGCC ATCCCTCCCC 1500
CCAGCCCACC CAGCCCATTT TCAGGCATAC 1530
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