| Tag | Content |
|---|
EnhancerAtlas ID | HS108-08186 | Organism | Homo sapiens | Tissue/cell | K562 | Coordinate | chr11:75895020-75897360 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr11:75895127-75895142 | GAGGTCCAAAGGACA | + | 6.29 |
| | | 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 |
| GH11I076184 | chr11 | 75895101 | 75898882 |
| Enhancer Sequence | TCACACAGCA GGTGCACAAT AAATGGTAGC AGTTATATCA TGTGGCCACC CTTTCTGAGA 60
GCCATTCTGG GTCCTTGGTC TGGTTTCCCC ATTTACTTGT CCTGACAGAG GTCCAAAGGA 120
CACTCCCAAA TCCAACATTT TGGAGGTATG TTTTATACCC AGCCCTGTTG TGCTGCCCCC 180
CAGATCCCAG GGCCCATTGG TGCATATGGC TGGTCCCAGC CCATGAAAAG GCCCCAGACA 240
GGTGGGGAAG ACAGATGATA TGACACAACA TAGGCCTCCA CAACACCTTG GTTCCATGAA 300
ACATTGCAGG GAGCACAGAG GCTGTGGAAA CCCAGAGGAG GCCCCTGACC CAGGCTGAGG 360
GTAGTTGGGG AGGGCTTCCT GGAGGAGGGA GCCATTTACC TGGCTTTTGC AGAAGAGGGC 420
ATTGGCTGGC AGCTTGAGAA GGAGGGTGAT GGCTGCTTTA AATGTTCAGA GGGTTGTGGG 480
GTGCCTGAAG AGGGGGAGAT CCCTTCCACC TAGGGCACTG GGGAAGGTTT TGTGGAGAGG 540
GCTGTGAGGG TTGTGTGGGA TTCCAGCAGG GAAAACAGCA CTCTTGGCGA GGGAGAACAG 600
CAGATGCCCA GAGGGCAGGC AGGCTGAGCA GCTGGGAGTT GCAGGAAATG CTGTTGGAAG 660
AATCGCCTGG GGGACAGGCC TTGTGTTCCA GGCTAGGGAC TGGGGATTGG TTTTGTGGGC 720
TAGGAGGTTG CTGAGAGCTA TGAAGCAGGG AAGCCCTGGG CCTGGAGAGC GCACATTCCA 780
GGGGCTCCTT CCAGGGAGGC TGGGGGTTTT CAACAGAGGG GCTGGCAGGG GCCCCACCCG 840
GGAAGGCTCC ACCTCCCCCC GTTCCCAGCC CCTTATCAGC TCTGTGACCA CAGGAAGGCC 900
CTTCCCATCT CTGAATTTCC TCATCTGCAA AACACACCAG AAGACTTATC TTGAGGTTCC 960
TTGCAGCTGG TGACGCTGTG GCTCTGGCTG TCCGCACTGC AAGCTTTCAG GCAGGGCCTC 1020
GAGGATGGCC ACAGAAGGCC CCCTTCTTCC CACTCAGGAT GGGTCCAGCC CCTGAGGGGT 1080
CATCCATGCC ATCCCACCCC CAAGGATGTG GCTTCACTTC TCCAAATCCT GTGCAAGGCC 1140
CCGCTCTGCC CCAGCCCCTC CAGGTGGTGT CTCAGTCCTC AGCCGGCTCG GGGAGGGAAG 1200
AGCACTGGTA CTAAGTCCGA GTCTCTCTGG TGCATGCAGA GATTTGGATT ATAACATCCT 1260
CTTACACCCC AGCCACAGCA AGATCCAGGT GATGAACCAC TGCTTCTGTT TCGGGGCCAC 1320
CTGCCCTGGC CAGGCACTGG GGATACCCCA CTTACTCATC TCTTGGTTAC TGGTGCTGCC 1380
TCCATGAGGG AGGTGACACG GAAGCTCAGA GGGACAGTGA TGTGCCTGCG GTGATCCTGT 1440
TCCCCTTGGC ACCCTGTCTT CACTTGGCAA CAGCCAGGAC CGCCGACCTC CCTCCTGCCT 1500
CCCTGGCTGT TCCTTCTGTC TCCTGTGTCT TCTCTGAGCT TCATCTCCCC AGCCTCCAAG 1560
GCAGGAGTGC CCCAGGCCTT GGTCCTCTTT ACTCTTCTAT CCCACACACT CCCTTAGCGA 1620
TGACACCCAA ATGTGGATCT CCAGCCCTGG CCGCTCCCCA GCACTCCAGA CCCGGATATC 1680
TGCCCGGCCA CTCAGTATTT CCACTAGGAG CGTAAACTGT ATCACAATCC CCACGGGCCC 1740
AAATCTGAAC CCCAGGCCTC TCCCCACCCC CATGTCGGCA TTCGGCCCCT TCAGCCTTCC 1800
CAGTGCTCCA GCCAAAACCC CGGCAGTCAT TCTTGGGCCT CCTTCCCCTT ACACCCCACA 1860
TGCAAAAAGA GAACAAATCC TGTTGGCTCC CCCTTCAAAA CAGAACCAGA ATCCAACCAC 1920
TTCTCAACAC GTCCAATGCT GCCAGCCTCC AGGCACGAGG CCTTTCCCAA CCTTCAGCCT 1980
TCCTCCCCAC CACTCCCATT TTACAAATGG GGAAACTGCA GCTGGCAGAG AGCCCTCCCC 2040
AGGGTCACGC AGAAAACCCA CCAGGGCTAG CTAGAGCCTG GATCTGCACC ACCTCCCCGA 2100
AGTCTGCATC CCAGCTGCCC AGGGAGTGTT TTCCCTTGAA GCCAGCTTAG CAGGCAGGCC 2160
TGACAACACG GCCAGGCTTT GAGCTGCGCC TGCGTGTGTG TCCCTGAGGA AAAAAGATGC 2220
TGCCAGCTGG GTTTATGTTT CAAGACGTCT GTCCTCGCCC TTGACCAAGA GCTCTTACAG 2280
GGAGATCAGG GCCAGGGCCT GGTGTGGGGG GAGCGCGGGG GGAGAAGGGA CATCAATCGG 2340
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