| Tag | Content |
|---|
EnhancerAtlas ID | HS127-28964 |
Organism | Homo sapiens |
Tissue/cell | Macrophage |
Coordinate | chr7:75298990-75301280 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2C | MA0497.1 | chr7:75300926-75300941 | TTCTATTTTTAATTT | - | 6.12 | | Nr2f6(var.2) | MA0728.1 | chr7:75299337-75299352 | TGAACTCCTGACCTC | - | 6.22 |
|
| | 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 |
| GH07I075670 | chr7 | 75299819 | 75301402 |
|
Enhancer Sequence | TTTACCTATT CTGAACATTT CATATAATGG GGTTATAATA AAATAAGTGG CCATTTCTGT 60
CTGGCTTCTT CACTTAGCAT AATGTTTTCA ATGTTTAAGC ATGTTGTAGC ATGAATCAGC 120
ACTTCATTCC TTTATTTATT TATTTACGAG ACAGAGTCTT GCTCTGTCAC CCAGGCTGGA 180
GTGCAATGGC ACGATCTCGG CTCACTGCAA CCTCCATCTC CTGGGTTCAA GTGAGTCTCC 240
TGCCTCAGCC TCCTGGTAGC TAGGACTACA GGTGCTCACC ATGATGCCCA GCTAATTTTT 300
GTATGTTTAG TAGAGACGGG GTTTCGTCAT GTTGGCCAGG CTAGTCTTGA ACTCCTGACC 360
TCAGGTGATC CACCTGCCTC AGCCTCCCAA AGTGCTGGGA TTACAGGCAT GAGCCACCAT 420
GCCCGGCCTT AAAATTTTTT TATTGTGATA AAATATACAT AAAATTTATT ATCTTCACTA 480
TTTTTCTTTT TTTGAGACAG GGTCTCACTC TGTTGCCTAG GCTGGGGGCC TGTGGTGGTA 540
CAATCACAGT TCACTGCAGC TCCAAACTCC TGGGCTCAAG CCATCCTTCC ACCTCAGCCT 600
CCCGGGTAGC TGGGACTACA GGCGCACACC ACCATGCCTG GCTAATTTTA TTTTTTGTAT 660
TTTTTCTAGG GATGGGGTTT CACCATGTTG CCCCGGCTGG TCTCAAACTC CTGAGCTCAT 720
GCTATATCTG CCTGCCTCAG CCTCATAAAG TGCTGGGATT ACAGGAGTGG GCCACTGTGC 780
TCATGAGGCT CATTATCACT GTTTTTAAGT GTACCATTCA GTGGTACTAA ATATATCCAT 840
AATTTGTGCA ACCATCACGG CCGTTCATCT TTGTAAAACT GAAACGGTCC CCATTAAACA 900
TAATTCCCCA TTCTCCCCTC TCCCCAGCCC CTAGCAAACA GCAGTCTAAT TTTTTGAGAC 960
AGGGTCTTGT TCTGTCAGTC AGACTGGATG GAGTGCTGTG GCACAAACAC AGCTCACTGC 1020
GGCTTTGACC TCCTGGGCTC AAGCAATCTT CCCACCTCAG CCTCCAAAGT AGCTGGGACT 1080
ACAGGCATGC TCACTGTACT CAGCTAATTA AAACTTTTTT TTTTTTTTTG GTAGAGATAG 1140
GGTCTTGCTA TGTATCCCAG GCTGGTCTCA AACTCTTCGG CTTAAGCGAT CCTCCTACCT 1200
CTGCCTCCCA AAGTGCTGAG ATTACAGGCG TGAGCCACCG CGCCCGGTCT CACCAGTCTA 1260
CTTTCTATCT CTACGATTGT GACTAAGTAC CTCATATAAC GGGAGTCATG CTGTATTTAT 1320
CATACAGTAT TTGTCTTTGT TGTGACTAGC TTATTGCACT TAGCATAATG TCCTCAAGGT 1380
TCACCCATGT TGTAGTATGT GTCAGAATTT CCTTCCTTTT TATTGTTTAT GTTATTTTTA 1440
GATGGAGTTT CGCTCTTGTT GCCCAGGCTG GAGGGCAATG GAGCAATCTC GGTTCACTGC 1500
AACCTCCCCC TCCCGGGTTC GAGTGATTCT CCTGCCTCAG CCTCCTGAGT AGCTGGTATT 1560
ACAGGCACCC GCCACCATGC CTAGCTAATT TTTGTATTTT TAGTAGAGAC GGGGTATCAC 1620
CATGTTGGCT AGGCTGGTCT CAAACTCCTG ACCTCAAGTG ATCTGCCTGC CTTGGCCTCC 1680
CAAAGTGCTG GGATTACAGA TGTGAACCAC CGCACTCGGC TAGAATTTCC TTCCCTTTTA 1740
AGGCTGAATA ACATTCCATC ATATAACACA TTTTGCTTAT TCATTCAGCT GGTGATGAAC 1800
ACTTGGCTTG CTTCCATGTT TTGGCTATTG TGAATAATGC TGCTATGAAC GTGGATGTAC 1860
AAATATCTCT TCAAGGCTCT GCTTTCAGTT CTTTTGGGTA TAAACCCACA AGTGGAATTG 1920
CTGGATCATA TGGTGATTCT ATTTTTAATT TTTTGAGGAG CTGCCATACT GTTTTTCACA 1980
GCATCGTACC ATTTTATATT CCCTCCAATC ATGCACAAGG ATTCCAATTT CTCCACAACC 2040
TGGCTAGCAA TTTTTATTTC ATGTTTTCCT TTTTTTTAAT TTTTGAGATG GAGTCTCGCT 2100
CTACCAGGCT GGAGTGTAGT GGTGTGATCT CAGCTCACTG CAACCTCCGC CTCCCAGGTT 2160
CAAGTGATTC TCCTGCCTCA GCCTCCCAAG CAGCTGGGAT TACAGCTACG CGTCACCATG 2220
CCTGGCTAAT TTTTGAGTTT TCAGTAGAGA TAGATTTTCA CCGTGTTGGT CAGGCTGGTC 2280
TTGAACTCCT 2290
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