| Tag | Content |
|---|
EnhancerAtlas ID | HS051-08652 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr14:100814070-100816310 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myog | MA0500.1 | chr14:100815005-100815016 | CAGCAGCTGTC | - | 6.14 | | Tcf12 | MA0521.1 | chr14:100815005-100815016 | CAGCAGCTGTC | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr14 | 100814974 | 100815646 | | chr14 | 100814752 | 100814808 | | chr14 | 100815648 | 100816095 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH14I100348 | chr14 | 100814511 | 100816303 |
|
Enhancer Sequence | GCCTGGCTAA TTTTTGTATT TTTAGTAGAG ATGGGGTTTC ACCATGTTGT CCAGGCTGGT 60
CTCAAACTCC TGACCTCAGG TGATCCACCT GCCTTGGCCT CCCAAAGTGC TGGGATTACA 120
GGTGTGAGCC ACCGCGCCCA GCCAAGTGGC TTCTTATATT GCATCTTTGT ATTACTATAT 180
TCAGTAGCTT TTTCTCTAGG CCCTACCATG TGTTAGACAC TACGAGGGAA AAGGGGGAAG 240
GCTGGTGTCT TTTAAGTGTT TGCACCATGT GGCAGGAGCT GTGCTAGATG CTGCGTATGT 300
GTCAATACTC CTAAAATCCC CTTCAAAGTA GTAGCATTGC CTCCACCTTA CAGTTAGACT 360
AGGCTCAAAG AAGTTCAGGG TCATAGTCAC AGGCCCAGTG AGTACAGGGG CTGGGATCCC 420
AACACAGATT CACCTGGCCC CAAAGCCTAT GCTTTTCTCA CCACATCTTA TCCTTTAGAA 480
GAGTTTAGAC TTTTGGGGCA GGGTGGAGAA CTACTGAATG TCTTTGTGCA GGTGGGGTGG 540
GGTGTCAGGA GTGCAGGAAC ACTGGCCGTT TGTGCTGGGC GAAGCACAAT GCTGGGAGGC 600
CTGTAACGGT CAAGGTCAGT GCCAAGGCCT GTCCAGGTTG AGCAGAGGCA GCACGTGAGG 660
GATGGACTGT GTCTTTCGCC TAGCAGCCGG CTGAGTTTCA GGCCCTGGGG GGCACTGGAG 720
AGGGCGGGCG CAGTACTGTG AAGGGGCATG CCAGGAGAAC CCAGCATCTG TGTCACCCAC 780
TCAGCACAAT GGAAACAACA GAGAGCAAGA GCACAGCCAA CAGCAGCACT GCCTGGAAAG 840
ATGCGGCCTT TGTCCTCCTG CCAAGCAAGC CAAGAACACC GCAGGCAGGG AGGGTCCCTC 900
CTGGGCACCG CAGCAGGACT CACAGCCAGT AAGGACAGCA GCTGTCTGTC ACCTGGGGAG 960
ATGGGCTGCA GCAAAGACTC CATGCGCCCT TGGGATTGAG GCACCTGGGA CACCCTAACC 1020
CCTACAAGGA GGGAAAGTCT CCAGTACCCC CAAACTGTGG CAGGACTGTA GCTTCACGGC 1080
GTCTGACTGG TATTTCTGAG TTAGAGCACG CTGCCCTTTC TTAGAAGACT GGTCATTACT 1140
TGCTGCAAGC TGCTGCCACT GTGCTGGCTG CAGGGTGAAT GCAGGTGCTG CACCGTGAGC 1200
ACGTGTGATC CTCCCCTCAA GGGACGGCTG TCCCCCTGCA CAGCTGGGAC GGACCCATCA 1260
CGCAAAGCAG CCATGCCAGT GCCGGCACAT GGAGGCTTCT CACTGGCTGC AGTGAACACA 1320
CCTAACTGTA TATCACATGT GGCTGAACCA CCAGTTACCC CAGGGAGGGC ACCTGCTTTT 1380
CACTCTCAGA CAGGGTTTAA AGTGGGAAGA GATTTTAGAT TACAACATTT ACTGAGCACT 1440
CCCCAGGTGC CAGGCGTGGC TTGAAGCACT TTATATGCAG TGCAGGCACT ATCATCTCCT 1500
GACCACAGTC TTCTCTACCC CTGCCCTTTG TCCCTATTAT CACCATAGAA CTTATTATCA 1560
CCTGATTGAT CACCTGTTAG CTGATTCTCC CCATTAGAAG AGAGGCTTTA CACAGCTGCT 1620
GAGATAATGG TTTTGCTCCC TGCTGTACCC CCACCATGAG TCTGGCATAT AGCAGATGTC 1680
CAATAAATAT TTGTAGAACA AAGGAGCAGA GTGAAGAAAG CAGGCAGAGA GGAGCTCCTC 1740
CCATGCCCGG GCCACACAGT GGAAGGCTCC TCCCATGCCC AGGCCACACA GCGGACGGCC 1800
GTCAAGCAGA GCACTTGCAA CCTCTGCTAT GCTGCCCCCC ACTAGCACCC AGCTCCCTTC 1860
CTCACAGGAA CATGGAAGCT CAGAGATTTA AGGACTTGCC CAAGGGAACA AGACCAGGCA 1920
GGGGCAGAGC TGGGTCTGGA ACACAAGTTT TCAGACTCCC AGCTCAGTGC CTTTGCATCC 1980
CTCAGGGCCC TGGGCAGGAA GGCCGTTCTG GGGCCATGTG CAATGTGCAG GGGGAACTGC 2040
ACTGGCCTCC TCCCTCATGG AGGCCTCACC ACCTCCCTCC CACTCAAAGA GGGCGATGGC 2100
TGGCTTTGTT GAATTTCCAG CTCCTAAACA CCAGGAAGGA GCTTTATTAA GCCAAAGATA 2160
TAGATTTTGA GTTAAATTCA AGAAAGAAAA GTAAAATGCT CAAATGTTTA GAAGAAACTC 2220
TTAAAGTAAA ATGTTTGAAT 2240
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