Tag | Content |
---|
EnhancerAtlas ID | HS076-12394 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr11:134271470-134273550 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr11:134272534-134272545 | AGTGACTCATG | + | 6.14 | Gfi1b | MA0483.1 | chr11:134271557-134271568 | AAATCTCAGCA | + | 6.32 | Klf1 | MA0493.1 | chr11:134271847-134271858 | AGGGTGTGGCC | - | 6.32 | STAT3 | MA0144.2 | chr11:134272198-134272209 | CTTCCCAGAAA | - | 6.02 | ZNF263 | MA0528.1 | chr11:134271475-134271496 | GAAGAAGGGAGGGGGGAAGGG | + | 7.01 | ZNF263 | MA0528.1 | chr11:134271471-134271492 | GGAGGAAGAAGGGAGGGGGGA | + | 8.28 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 5 | Chromosome | Start | End |
chr11 | 134271615 | 134271671 | chr11 | 134271722 | 134271892 | chr11 | 134272017 | 134272173 | chr11 | 134272303 | 134272557 | chr11 | 134272280 | 134272582 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH11I134402 | chr11 | 134271968 | 134272616 |
|
Enhancer Sequence | GGGAGGAAGA AGGGAGGGGG GAAGGGTTGA AAAACTACCT ACTGGTTACC ATGCTCAGTA 60 CCTGGGTAAG AGGATCAGTT ATGCCTCAAA TCTCAGCATC ACATAATATA CCCGGGTAAC 120 AAACCTGCAC ATGTACCACT GAATCTAAAA TAAATGCTGA ATTTATAAAA AATTTAAAAA 180 AAAGTAAAAC TCAGCTGAAT CCAAGTGCCT GGGAGAGGAA GGGCAGAGGA AGGAGGCACC 240 TTGGCCCCTT CCTCATGGCT CAGTGGCGAC CAGCCTTCGG GCAGCCTTTC CAGCACATTC 300 TTCTCTCCCC AGCACGAGGC GGTGCTGTGG CTTGAGCTCA ATGGAAACTG GGCACACCAG 360 CATGCAGTTG TGACAAAAGG GTGTGGCCTG GGGCGGGGGG GGGCGGGCAG CCTGACCACT 420 GTCGGGAGGC GGGGCCCCTG GAACCTGGCG CTGTGGCCCT GGCTCCCTCT GTTCCTGCTT 480 GGAGGACGTG CCCCTGCACA GGTGGACCAG GCGACAAGGC ACTTTCTCAT GCCTTTTCCT 540 GCTGTAGCCT CGGTGCAGCC ACCTGAGATG AGGTGGGCAC CCATCCTGTC ACCCTGCTTC 600 TTCAGGTGGG GAGACTGAGG TTTGGAACTG ACACACTGAG CTAGAGTCAA GTCGCGGGTA 660 TGCCCCAGTG TGCGGTTGCT GCTTCCCTCC CGTCACCCTG CCCAGTCTGG TCCTGTGTCT 720 CTGCCCAGCT TCCCAGAAAG GCACTCAGGA AGGACCGGTG ATTTCAGAGA TTCCCCATCC 780 CTCTTCTCTT CTCCTGCCTC CAGAGCTGTC AGAGAACTGA CTTGTCCATG GGGCTCTAGG 840 GCCAGCGAGC CCTGGGCACT GTCACTCCCT GCCCCGTCTC CCCAGGATGC AGGCTCAGGC 900 TCCTGGAGAA CTTTCCTTTC ACCACCTCCT ACTTCCAGGG CTCCCCCACC TCCCTCTGTT 960 ACACCTGCCC TGCCCCTAAG GTCCCTCCCT CCTCTGGGGT GTCAGCTAAC CCCCCTGCCT 1020 GAAGAAGAAA CAATTAACAT AAAATGTTGA ACTGGGTCAG GCACAGTGAC TCATGCCTGT 1080 AACCCCAGCA CATTGGGAGG CTGAGGTGGG TGGATCACTT GAGGTCAGGA GTTGGAGACC 1140 AGCCTGGCCA ACATGGGGAA ACCCTGTCTC TACTGAAAAT ACAAAAATTA GCCAGGTGTT 1200 GTGGCAGGTG CCTATAATCC CAGCTACTGG GGAGGCTGAG GCAGGAGAAT AACTTGAGCC 1260 CGGGAGGTGG AGTTTGCAGT GAGCTGAGAT TGCGTCACTG CACTCCAGCC TGGGCAACAG 1320 AGCGAGACTC TGTTTCAAAA AAAAAAAAAA AAGTCGAAGG GGCTTGGGTA GGGGACTTGC 1380 CCCCTGAGCA CATGTGTGAA CCAGAGTGGG CAGTGTGTGC CCTACACAGC AGAGGAGGTG 1440 TGGGTGCGAT GATCCCGCGG TCCTCAGTCT CAGTGCCCCT GACAGTGGAG TGTGCTGATA 1500 CTATCTCTGG GTTTCCCAGG CTACCTATCA CACAGTGAGC ACCAGGGCGG CTACGGATCC 1560 ACGGTCCACC ACCGACATGT AGCCCAAGGC ACAGGCTCAA GACAGGCCTC CACATACCTG 1620 GGGGAGGGGA TCTCCAGGCT CTCCTGGGCT CCCATCCCCA GGTAGACTCT AGGAGTACCC 1680 GGCCGATTTC TTTCTCGGGG TCCCGGGAAG GCAGCAGGGA TGAGAGCAGG AGGCTGGCAT 1740 CCCTTCACAC CGGTACGTTT GCCTGGGACA TGCTTCCCTC CCTCATAGTC CCTCCACTTG 1800 CTGAGTTGCT TGGCCCCCAG GACCAGGCCA GGTACACTCA GCCCAGGGGC TTCACACTCA 1860 GGGCTGGGCA CCACAGGGTG CCTGGGCAGC CCTGGATGCA GGAAGGGAGC CCCAGAGGCC 1920 AGACCAGATG CCAGGTAGAA TGGGGTGCCT CCTTCTTGAT GCTCCCATGA CACTGTGACA 1980 TAGCTTCCCT CTGGGCAGAA GTATTTGCTG GGTGGCCCCT CTGCTCAGAC ATCTCCTGAG 2040 TGGGAAGGGC AAGTGGGGAG AATTGCCATT TATTGAGCTT 2080
|