| Tag | Content |
|---|
EnhancerAtlas ID | HS118-16873 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr6:166671300-166673810 |
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 | CGGAGTCTGA CTGGGGGAGC GTGCATGCCC CTGCTCGCAT GTGTTTGGTA ACACTCAGCT 60
CCTTTCAGTT GTAGGATCTG TGGCAGCTGC TGGCTTCTTC AGAGCCAGTG AGGGAGACAG 120
CGAGTCTCCC CAAAAGACAG TCCTGTGTGA TGTGAGTCAT CCCCAGAGTG ACATCCCATC 180
ACCTTTGCTG TAGCCGTTGG TTAGAAGTCA GTCACCAGTC CTTCTCTGTG ACTCAGGGGA 240
GATGACTACA TAAAAGGCAG TTACACCTGG AGGCACCTGG GAGTCTGCCA CACGCCCCCC 300
TGCCTCCCTC GCATGTGCAA AAGTCATTCA CCTGCTCTAG GTACCTAAGA TTTTCGGAGC 360
TTCATGGCAT CAGCTCAAAG CCTGAAATGT CAACATCTAA ATCAGGTCAA AGGTCAGTGG 420
AGGGTCATGG TGCAATCATT CGGTTCAGGT TCTGGGACAC AATTCCTCTC CATGGATGGG 480
CCCGGGAAGC TAAAGAGATT AGTGACCTGT CCCGTGGTGG AGCAGGCACC AGATGCAGCT 540
GTAGACATTT CAGTTTTCAA GGGGAGGAAA TGGCAGATAA AAGGCATCTT GACTGTGTAG 600
CAATTCCAAA TCCAGAAAAG TAAAGGTTGG GAGTTCTCAG TCAGGTTTCC AGGGCTGGGG 660
AGAATTCTCC TGGCTTCTGG ATTCCCTGTC TGGGCTCTTG GTCCCCGCAT CTACACTGCA 720
CTTGTTTGGA AGGAAAGGTT GCCCATGTTT GCAGCTGAGG AGCTTTTTAG CCTACTTCCA 780
GCCAGCAAAA TCTGGGGAGT CTGGCAGCCT CCTTTCATCC TGTGCTCTCT CTGTTCCTTC 840
CCACCCAGGC TGGCAGTGTT TCTGTGAAAG TGATTTCCTC AAAATCTTTG TCTCTCATGG 900
ATTTCACCTG GGTCTACTCC ATGAGCCGAA GGCCTCACCT GCCGATGTTT TTGAGGCAAG 960
CCTTTTCTAT CTTTGAGTCC TGCCGAGGTG ACTCGGAGTC AACGCCCTTC GGCTCCTCAG 1020
GGGCTCCCTG GTTCGATCCA TGAGGCTCAG CCCTGACCTC TCTAAGGCAC CCTTGGTGGG 1080
GCAGAATGCT GAGGCTATGA TCTTTCTGAG GCCTTATCCA AAGGCTGTGC AGACACAGCC 1140
CAGCCACCTG GGCTCCTGGG CTTACACTGT CTTGACAGCA CCATCTCTTG CTATCTGGAG 1200
AGGCCGACGC CTCAATTCTG GACGTCTGGA CCCAAACCGT GAGACATAAA CTTCTGTGGC 1260
TGTCCTCTGC CCAGTTTGCG GTCACATGTC GCAGCCGCCC GAGGTGACTA AGACAGGAAA 1320
CTAAAGTGGC TGTTTCTTCC TCCAAGCTTT CGAAACTTTT TTTTTTTTTT TAATTGAGAC 1380
AGAGCCTCGC TCTGTCACCC AGGCTGGAAT CTAGTGGCAA GATCTTGGCT CATGCAACCT 1440
CTGCCTCCCA GGTTCAAGCA ATTCTTCTGC CTCAGCCTCC CTAGTAACTA AGACTACAGG 1500
CGCCCAGCAC CACGCCCGGC TAATTTTTAT ATTTTCAGTA CAGACAGGAT TTCTCCATGT 1560
TGGCCAGGCT GGTCTCAAAA CTCCTGACCT CAGGTGATCC ACCCGCCTTG GCCTCCCAAA 1620
GTGCTGGGAT TACAAGCGTG AGCTCCCGCG CCCAACCTGA AACTTGGTTC TTTATCAACT 1680
TAGGGTCCCG GAGAGCAAAG CACCCGGCCT CCCATCCGCC CAGTGTCTTG CAGCGTCATC 1740
TTCATTTCCA CCAAAAGGTC ACGGATACAT TGCTGCTTTC GCACCCAGCA CGTTTTAGAC 1800
AGTAAGCTTG TTCATGTGTC TTTCGCACCC AGCACGTTTT AGACAGTATG CTTGTTGATG 1860
TGTCTCTGTC CTTAACTCGG TTGAACTTTC TGAGAAAGTC CCCTCAGCAT TTTAGAACTT 1920
GTGATGTTTC AGAATGTGGC CTCTAACCAG ACCATAGGGC TCAGCTGGCA GCCCTGCTGC 1980
CTCCCAGCAG AGGTCACATG AGCTTCTTGT GCTTCCTTTT TCTCATCTGC ACACTGGAAA 2040
CGACAACAAT AGAACCCATC CCACAGCGGG GTGCTGGCCA GTTGAATTGA TCCCCACAAA 2100
GTGCTTACAA CAGTGCCTGC CCCATAGCAA GTGCTGTATG CACACTGGCT ATTGTGACGT 2160
TTGTATCCTA ATACAAATGA AGATTGACCA TGCTAAGGAT GCGAACATTT GCTGAATGAG 2220
CTATAATTTG ATATTCTGTC CTAAACATTC AATTATATTT GCTTTTCTTA AAAAAAAAGA 2280
AAGGTGTGAT TGTGTGTGTG TGTGTTTACT ATAAGCCACA TCAAATTCTT TCAAGCAATA 2340
GGTATAAATG AAATAAGCAG CAGCAATTTA TAAGGTCCCT TTCTACTCTA GAAATCTAAA 2400
AGTAAAACTT CAGCAAACCT AAAGTTTAGG GCAATGAGAC AGGCTGGATG GTCGGGTTGC 2460
CTGGTACCAA GGTCTGAATG TGCCCCTCAG AATTCATGAA TTAGAAACTT 2510
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