| Tag | Content |
|---|
EnhancerAtlas ID | HS187-22203 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr6:166671320-166673600 |
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 | GTGCATGCCC CTGCTCGCAT GTGTTTGGTA ACACTCAGCT CCTTTCAGTT GTAGGATCTG 60
TGGCAGCTGC TGGCTTCTTC AGAGCCAGTG AGGGAGACAG CGAGTCTCCC CAAAAGACAG 120
TCCTGTGTGA TGTGAGTCAT CCCCAGAGTG ACATCCCATC ACCTTTGCTG TAGCCGTTGG 180
TTAGAAGTCA GTCACCAGTC CTTCTCTGTG ACTCAGGGGA GATGACTACA TAAAAGGCAG 240
TTACACCTGG AGGCACCTGG GAGTCTGCCA CACGCCCCCC TGCCTCCCTC GCATGTGCAA 300
AAGTCATTCA CCTGCTCTAG GTACCTAAGA TTTTCGGAGC TTCATGGCAT CAGCTCAAAG 360
CCTGAAATGT CAACATCTAA ATCAGGTCAA AGGTCAGTGG AGGGTCATGG TGCAATCATT 420
CGGTTCAGGT TCTGGGACAC AATTCCTCTC CATGGATGGG CCCGGGAAGC TAAAGAGATT 480
AGTGACCTGT CCCGTGGTGG AGCAGGCACC AGATGCAGCT GTAGACATTT CAGTTTTCAA 540
GGGGAGGAAA TGGCAGATAA AAGGCATCTT GACTGTGTAG CAATTCCAAA TCCAGAAAAG 600
TAAAGGTTGG GAGTTCTCAG TCAGGTTTCC AGGGCTGGGG AGAATTCTCC TGGCTTCTGG 660
ATTCCCTGTC TGGGCTCTTG GTCCCCGCAT CTACACTGCA CTTGTTTGGA AGGAAAGGTT 720
GCCCATGTTT GCAGCTGAGG AGCTTTTTAG CCTACTTCCA GCCAGCAAAA TCTGGGGAGT 780
CTGGCAGCCT CCTTTCATCC TGTGCTCTCT CTGTTCCTTC CCACCCAGGC TGGCAGTGTT 840
TCTGTGAAAG TGATTTCCTC AAAATCTTTG TCTCTCATGG ATTTCACCTG GGTCTACTCC 900
ATGAGCCGAA GGCCTCACCT GCCGATGTTT TTGAGGCAAG CCTTTTCTAT CTTTGAGTCC 960
TGCCGAGGTG ACTCGGAGTC AACGCCCTTC GGCTCCTCAG GGGCTCCCTG GTTCGATCCA 1020
TGAGGCTCAG CCCTGACCTC TCTAAGGCAC CCTTGGTGGG GCAGAATGCT GAGGCTATGA 1080
TCTTTCTGAG GCCTTATCCA AAGGCTGTGC AGACACAGCC CAGCCACCTG GGCTCCTGGG 1140
CTTACACTGT CTTGACAGCA CCATCTCTTG CTATCTGGAG AGGCCGACGC CTCAATTCTG 1200
GACGTCTGGA CCCAAACCGT GAGACATAAA CTTCTGTGGC TGTCCTCTGC CCAGTTTGCG 1260
GTCACATGTC GCAGCCGCCC GAGGTGACTA AGACAGGAAA CTAAAGTGGC TGTTTCTTCC 1320
TCCAAGCTTT CGAAACTTTT TTTTTTTTTT TAATTGAGAC AGAGCCTCGC TCTGTCACCC 1380
AGGCTGGAAT CTAGTGGCAA GATCTTGGCT CATGCAACCT CTGCCTCCCA GGTTCAAGCA 1440
ATTCTTCTGC CTCAGCCTCC CTAGTAACTA AGACTACAGG CGCCCAGCAC CACGCCCGGC 1500
TAATTTTTAT ATTTTCAGTA CAGACAGGAT TTCTCCATGT TGGCCAGGCT GGTCTCAAAA 1560
CTCCTGACCT CAGGTGATCC ACCCGCCTTG GCCTCCCAAA GTGCTGGGAT TACAAGCGTG 1620
AGCTCCCGCG CCCAACCTGA AACTTGGTTC TTTATCAACT TAGGGTCCCG GAGAGCAAAG 1680
CACCCGGCCT CCCATCCGCC CAGTGTCTTG CAGCGTCATC TTCATTTCCA CCAAAAGGTC 1740
ACGGATACAT TGCTGCTTTC GCACCCAGCA CGTTTTAGAC AGTAAGCTTG TTCATGTGTC 1800
TTTCGCACCC AGCACGTTTT AGACAGTATG CTTGTTGATG TGTCTCTGTC CTTAACTCGG 1860
TTGAACTTTC TGAGAAAGTC CCCTCAGCAT TTTAGAACTT GTGATGTTTC AGAATGTGGC 1920
CTCTAACCAG ACCATAGGGC TCAGCTGGCA GCCCTGCTGC CTCCCAGCAG AGGTCACATG 1980
AGCTTCTTGT GCTTCCTTTT TCTCATCTGC ACACTGGAAA CGACAACAAT AGAACCCATC 2040
CCACAGCGGG GTGCTGGCCA GTTGAATTGA TCCCCACAAA GTGCTTACAA CAGTGCCTGC 2100
CCCATAGCAA GTGCTGTATG CACACTGGCT ATTGTGACGT TTGTATCCTA ATACAAATGA 2160
AGATTGACCA TGCTAAGGAT GCGAACATTT GCTGAATGAG CTATAATTTG ATATTCTGTC 2220
CTAAACATTC AATTATATTT GCTTTTCTTA AAAAAAAAGA AAGGTGTGAT TGTGTGTGTG 2280
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