| Tag | Content |
|---|
EnhancerAtlas ID | HS182-19406 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr6:166671210-166673560 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr6:166671701-166671716 | TCAGGTCAAAGGTCA | + | 6 | | NR2C2 | MA0504.1 | chr6:166671701-166671716 | TCAGGTCAAAGGTCA | + | 6.87 | | Nr2f6 | MA0677.1 | chr6:166671702-166671716 | CAGGTCAAAGGTCA | + | 7.73 | | PRDM1 | MA0508.2 | chr6:166672163-166672173 | GTGAAAGTGA | - | 6.02 | | RARA(var.2) | MA0730.1 | chr6:166671710-166671727 | AGGTCAGTGGAGGGTCA | + | 6.3 | | Rxra | MA0512.2 | chr6:166671702-166671716 | CAGGTCAAAGGTCA | + | 7.58 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr6 | 166671758 | 166671936 | | chr6 | 166672361 | 166672722 | | chr6 | 166672941 | 166673469 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH06I166257 | chr6 | 166671285 | 166674087 |
|
Enhancer Sequence | TGAGTCGGGA GTCCAGCGAC AGACTTGCCG GCTCTCCTGC TGGGGTCTCA CAAGGCGGTC 60
GCCAGGTTAT GTCCAGGGTG GGTTCTCATG CGGAGTCTGA CTGGGGGAGC GTGCATGCCC 120
CTGCTCGCAT GTGTTTGGTA ACACTCAGCT CCTTTCAGTT GTAGGATCTG TGGCAGCTGC 180
TGGCTTCTTC AGAGCCAGTG AGGGAGACAG CGAGTCTCCC CAAAAGACAG TCCTGTGTGA 240
TGTGAGTCAT CCCCAGAGTG ACATCCCATC ACCTTTGCTG TAGCCGTTGG TTAGAAGTCA 300
GTCACCAGTC CTTCTCTGTG ACTCAGGGGA GATGACTACA TAAAAGGCAG TTACACCTGG 360
AGGCACCTGG GAGTCTGCCA CACGCCCCCC TGCCTCCCTC GCATGTGCAA AAGTCATTCA 420
CCTGCTCTAG GTACCTAAGA TTTTCGGAGC TTCATGGCAT CAGCTCAAAG CCTGAAATGT 480
CAACATCTAA ATCAGGTCAA AGGTCAGTGG AGGGTCATGG TGCAATCATT CGGTTCAGGT 540
TCTGGGACAC AATTCCTCTC CATGGATGGG CCCGGGAAGC TAAAGAGATT AGTGACCTGT 600
CCCGTGGTGG AGCAGGCACC AGATGCAGCT GTAGACATTT CAGTTTTCAA GGGGAGGAAA 660
TGGCAGATAA AAGGCATCTT GACTGTGTAG CAATTCCAAA TCCAGAAAAG TAAAGGTTGG 720
GAGTTCTCAG TCAGGTTTCC AGGGCTGGGG AGAATTCTCC TGGCTTCTGG ATTCCCTGTC 780
TGGGCTCTTG GTCCCCGCAT CTACACTGCA CTTGTTTGGA AGGAAAGGTT GCCCATGTTT 840
GCAGCTGAGG AGCTTTTTAG CCTACTTCCA GCCAGCAAAA TCTGGGGAGT CTGGCAGCCT 900
CCTTTCATCC TGTGCTCTCT CTGTTCCTTC CCACCCAGGC TGGCAGTGTT TCTGTGAAAG 960
TGATTTCCTC AAAATCTTTG TCTCTCATGG ATTTCACCTG GGTCTACTCC ATGAGCCGAA 1020
GGCCTCACCT GCCGATGTTT TTGAGGCAAG CCTTTTCTAT CTTTGAGTCC TGCCGAGGTG 1080
ACTCGGAGTC AACGCCCTTC GGCTCCTCAG GGGCTCCCTG GTTCGATCCA TGAGGCTCAG 1140
CCCTGACCTC TCTAAGGCAC CCTTGGTGGG GCAGAATGCT GAGGCTATGA TCTTTCTGAG 1200
GCCTTATCCA AAGGCTGTGC AGACACAGCC CAGCCACCTG GGCTCCTGGG CTTACACTGT 1260
CTTGACAGCA CCATCTCTTG CTATCTGGAG AGGCCGACGC CTCAATTCTG GACGTCTGGA 1320
CCCAAACCGT GAGACATAAA CTTCTGTGGC TGTCCTCTGC CCAGTTTGCG GTCACATGTC 1380
GCAGCCGCCC GAGGTGACTA AGACAGGAAA CTAAAGTGGC TGTTTCTTCC TCCAAGCTTT 1440
CGAAACTTTT TTTTTTTTTT TAATTGAGAC AGAGCCTCGC TCTGTCACCC AGGCTGGAAT 1500
CTAGTGGCAA GATCTTGGCT CATGCAACCT CTGCCTCCCA GGTTCAAGCA ATTCTTCTGC 1560
CTCAGCCTCC CTAGTAACTA AGACTACAGG CGCCCAGCAC CACGCCCGGC TAATTTTTAT 1620
ATTTTCAGTA CAGACAGGAT TTCTCCATGT TGGCCAGGCT GGTCTCAAAA CTCCTGACCT 1680
CAGGTGATCC ACCCGCCTTG GCCTCCCAAA GTGCTGGGAT TACAAGCGTG AGCTCCCGCG 1740
CCCAACCTGA AACTTGGTTC TTTATCAACT TAGGGTCCCG GAGAGCAAAG CACCCGGCCT 1800
CCCATCCGCC CAGTGTCTTG CAGCGTCATC TTCATTTCCA CCAAAAGGTC ACGGATACAT 1860
TGCTGCTTTC GCACCCAGCA CGTTTTAGAC AGTAAGCTTG TTCATGTGTC TTTCGCACCC 1920
AGCACGTTTT AGACAGTATG CTTGTTGATG TGTCTCTGTC CTTAACTCGG TTGAACTTTC 1980
TGAGAAAGTC CCCTCAGCAT TTTAGAACTT GTGATGTTTC AGAATGTGGC CTCTAACCAG 2040
ACCATAGGGC TCAGCTGGCA GCCCTGCTGC CTCCCAGCAG AGGTCACATG AGCTTCTTGT 2100
GCTTCCTTTT TCTCATCTGC ACACTGGAAA CGACAACAAT AGAACCCATC CCACAGCGGG 2160
GTGCTGGCCA GTTGAATTGA TCCCCACAAA GTGCTTACAA CAGTGCCTGC CCCATAGCAA 2220
GTGCTGTATG CACACTGGCT ATTGTGACGT TTGTATCCTA ATACAAATGA AGATTGACCA 2280
TGCTAAGGAT GCGAACATTT GCTGAATGAG CTATAATTTG ATATTCTGTC CTAAACATTC 2340
AATTATATTT 2350
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