| Tag | Content |
|---|
EnhancerAtlas ID | HS073-04308 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr14:100798120-100800120 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Esrra | MA0592.2 | chr14:100800045-100800056 | CTCAAGGTCAT | + | 6.02 | | Esrrg | MA0643.1 | chr14:100800046-100800056 | TCAAGGTCAT | + | 6.02 | | Myod1 | MA0499.1 | chr14:100799265-100799278 | AGCAGCTGTCACT | + | 6.64 | | Myog | MA0500.1 | chr14:100799264-100799275 | CAGCAGCTGTC | - | 6.14 | | Tcf12 | MA0521.1 | chr14:100799264-100799275 | CAGCAGCTGTC | - | 6.02 | | ZNF263 | MA0528.1 | chr14:100798637-100798658 | CCTCCTTCCTGTCCCTGCTTC | - | 6.15 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH14I100332 | chr14 | 100798484 | 100799410 |
|
Enhancer Sequence | TTTGCAGGAA AGGCCTCTGT CCTCACTGTT TTTTTTTTTT TTTTGAGACG GAGTCTCGCT 60
CTGTCGCCCA GGCTGGAGTG CAGTGGCGCG ATCTCGGCTT GGCTCACTGC AAGCTCTGTC 120
TCCTGTGTTC ACGCCATTCT CCTGTCTCAG CCTCCCGAGT AGCTGGGACT ACGGGTGCCC 180
ACCACCACGC CTGGCTAATT TCTTTTTGTA TTTTTAGTAG AGATGGGGTT TTACCGTGTT 240
AGCCAGGATG GTCTCGATCT CCTGACCTCG TGATCTGCCC GCCTCAGCCT GGGATTACAG 300
GTGTAAGCCA CCGCGTCTGG CTGTCCTCAC TGTCTTTACA ACCTCTATGG TAATGACCAG 360
AGAGTCCTGG GCCTCAAGGC CCAGCCAGTG TGACCCTGGG GAGGGCACAT CTGCTGGTGC 420
TGCAGGCGGG CACTGGGGGC CAGAGGCAGG CCTGTTGCTT GCCAAGTGCC GTCCTGGAGC 480
AACGAGCTGT TCCACAGCCA CCCGTGTGCT CAGCCACCCT CCTTCCTGTC CCTGCTTCCC 540
CACCCAGTGC TGTTTTGTGT GCTTCTCAGG CACCATCTCC TTTCAGGCAG GCTCAGCTGG 600
TCTCTCCTCC AGGCTGGGGG CCACGGGACA GAGAGACTGA GCTGGGTTGG CCCCACATCT 660
GTCTGACAAG TGGACATTAC CAGCCAGAGC AGGAGTGCTC TTCCGGCAGA GCCTCTGGCA 720
CCACGGTGGT GCAGGCACCC GGCCTCATGC CTCATCCCCA AACACTCATG GGGCCACTGC 780
AACCTGTCCA TCCTAATCCA GACACGCCCA TGTCTTTCAG GGAACATTTC TCTCAGAAAC 840
CACTGGTTTT TAGCAAAACT GGGGAGGCTT GGGAGACATG TGGCTCCCCT GTGTCCTGAC 900
CAGCAGTGGC CTTGGGCAAG TCACCTGAGT ATTGGACCCA GGGCACCCCT CCTAAGACCC 960
TAAACAGGAG GCATCACTGC TTTTTACAGG GGAGGAGATG GAGGTCCTGG GAGGTTAAGT 1020
GACCTGGCCA GAGTCACACA GCCGGTGAGG GGAGAAGCTG GTTGGTGTTG GCTCACTCCT 1080
CCCTGGGGCC AGGGTCTCAC CAGGGCCCTG CCAATAGATG CTGTGGCTGG GTGGACAATG 1140
ACAGCAGCAG CTGTCACTGA CTCCATTTGT CACCCCTCAT TGCACTTGCG TCACAGGTGC 1200
AGTAGAGCGA CGAGGAGTCA TATTAGTTGC CCAAGGCAAC AGGCTAGTGA GCTATGTGGC 1260
CTCTGTGGGT GGCTCACCCC CACTGGCCAT AGCCAGCCAG GTGAGCAGGG GAGGGCAGGG 1320
GTGGGGCCCA GGCCAGCAGG AGTCGAGACC GGGAGAGGAA GCCTACTTGA GGTCATGGTG 1380
CACCCGGGTA CCTGAGTGGG ACTCGAGCCC AGGCCTCCAG CCTCCAGGGT GGGAACCGTA 1440
GTTCCCTCAT TTGTAAAATG GTCCCTCTGT ATGTGTGTGG AAAGCACCAA GAGTCAGGAC 1500
AGACTCGCTG TATCAGAGTC ACCCTATGGC CTTGGACAAG TCATGTTCTC CTCTCCTAAG 1560
CCTCAGTTTC CCTACTTGCA AAATAAGGAT GGGCCGGTAG AATGAGCCCA GGGCTCCCTT 1620
GCAGCTCGGC CTCTGCCCTG GGCCTCATGT GAATGGGGCC CGACCTGGCT CCCAGCCTGT 1680
GCTCCCCGTC ACTACACAGC ACCACTAAGC ACCCCACGGC CAGCCCCTCC TCTGAAAAGC 1740
GAGGACAACC TCTGCTTGCA TTCTCCATCA GCTGCTGGAA ATGAGAAATG TGGTGTGAGA 1800
GGGAGCCCGC ACCAGGATGC TGCTAAGGGC TCTCCCAGCA CAAGCCCATT CCTGGGAGCT 1860
GTGGCACAAC ACCATGGGGT TCCTGGGACT GTGCGCTTTC ATCCCCAAAT TTTGACTCCA 1920
GCAGACTCAA GGTCATCCAC AGAAGGGTGA GGGGAGGGGT CTCTGCTCCC TCCTCAGACC 1980
TCCCAGACAG AGCACAATGA 2000
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