| Tag | Content |
|---|
EnhancerAtlas ID | HS092-16520 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr14:74978070-74980340 |
Target genes | | Number: 23 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myod1 | MA0499.1 | chr14:74979190-74979203 | AGCAGCTGTCACT | + | 6.64 | | Myog | MA0500.1 | chr14:74979189-74979200 | CAGCAGCTGTC | - | 6.14 | | Nr2f6(var.2) | MA0728.1 | chr14:74980289-74980304 | GAGGTCAGGAGTTCA | + | 6.22 | | PRDM1 | MA0508.2 | chr14:74979248-74979258 | GTGAAAGTGA | - | 6.02 | | RARA | MA0729.1 | chr14:74979613-74979631 | CCATGACCTGTTGGCCTT | - | 6.3 | | Tcf12 | MA0521.1 | chr14:74979189-74979200 | CAGCAGCTGTC | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr14 | 74978224 | 74978382 | | chr14 | 74978566 | 74978616 | | chr14 | 74978727 | 74978997 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH14I074509 | chr14 | 74976164 | 74979233 |
|
Enhancer Sequence | CAAAACAGCA GCCCCTCCCT TGGTCATCCC TGGGAACATA GCAAATGGGT AGGTCTGTGA 60
CACAGCAAAT CCTTGTCCCT GCCTTTGGTT GGGGAGAGGG ATGGACAGAG GGAAACTAGG 120
AAAGAATGAG AGCTGCCCTG TGTTCCCAAC TCCACCTCTC ACCCACCGTC TGGGACAAAA 180
GAGGGAGATG GAAGAACTTA AAAATTAGAA AGGGAGACTC CCTGGGTGGG TGCAGTAGGC 240
TATGGTTACC ACCAGCTGTG GGAGGGTCAG AGGCTCCACT TTGTGAGCTG GGCTGTTGGG 300
GATGGGCTTT CATCTCTCCC CTGGCGAATT CCTAATCCTT TATAAGCAGT GACCATTACT 360
GGGATGTGCT TGGCACAGCA GCTAACTGGA TTGCCAGAGG CTCCACAATA GATCATCGGA 420
GGGGCAGTGA AGGCAACTTG GGCTTCCTTG CACCAGGAAA TGAGGACCAT GGAGGAACCC 480
CCAATCTTGG ATATGGCCAA GACCAGCTCT GAGGCAGAGT GCAGACTGTA GGGTAGAGCT 540
GGCAAAGCTT CTCTGCTGGA GAGCTGTCAG ACATTTCTTC CAGCCAAGAA TCATGTAGGG 600
ATCCTGGCAC CCACTCTGGT GAGATCCAGG AAAGTCAGCC AGAAGGGTTA AGCCTGGACA 660
CCAAATGGAC ACCCAGGGGA CGAGAGGACC CAGGAAGGGA GAGTGGCAAC AGGAAGAGGA 720
GGGAGCTAGT TCTCCCCGGA GCCGAGGAGA GGGCTCTTCC CCGACATAAC CTGGCATATC 780
ATGGGCTTCA TCATCAAGGC ACCCAGGGGA CCTGGACTGA GTGAGGGAGG TCCTGTCACA 840
GGGACTGAAC TCTGAGTCAG CACTGCAGGA GGACATTATG CCCCTCTGGC CCGGTATCAA 900
GGCTCTGGCC CACTCTTCAC AACAGGTCCA TTGGCCAAGG AAAGAGGAGG GGTTCTTCTT 960
CCTAAATGGG TAATTGTCAT TCTTCTAGAG GAAGTCCACC AGCTTATGCA TATTTAGAGG 1020
CTCTACTGCC CGAGAGGAGG ACCTACTCAG CACCTATGGA GGAAGTGTGG GAGGCAGGCC 1080
TAGGGTCTGA ACATAGGCTT TCTGCAGAGG GACTAAAGCC AGCAGCTGTC ACTGCTGCTG 1140
GACATGGAGA GGAGAGGACA TGGACCTTAA AGTGGAGGGT GAAAGTGAGT CCTCTCTGAG 1200
GTTGTTTGGC TTCCAGAAGT CAGGACACAT CGAAGCCCTC TGTCCCAGAG GACTGGGACC 1260
CTCTCAAGCC TAAAGCTTCT GCCTGAGGGT CCAGAAGACG GGGACATCGC CACAGGGCAG 1320
GTGGTTTTCA GGTGGGTCTC TGCAAGGAGA GTCCCACAAC TCCCATATAA TCTTGGGGAC 1380
ACTGAGATAA GGCGCATCTC TGGCAAGAGG GTAGCCCCAG CCCCTACTTG AGTTGTGGTG 1440
ACACCAGCCT TAACTATTCT AAGGGCTTCT GTAAAGACAG AGATGGATAA AATGAAGGAT 1500
CTAAGATGAC TAACTTTGGC CACCCAAGAG ACAGAGGCCA GTGCCATGAC CTGTTGGCCT 1560
TGGCCAAGGT ACTTGAAGGA GGATGGGCAA AGCCACTGAG AATGAGCAGC AATCCCTGTT 1620
TCAGGGATGC CAGATGATCT CTTCCAGGAT GAAGAGAACG AGATTGAGGC AAAGCTCCTC 1680
CTAAATCCAT GCCAGGAAAA ATGAAGTCTT TGGACCTTTC CTGCAGGGAT CAGGCAACGT 1740
GGGAAGGAGA TAAGGTTTGC CAGGAGCAAA GGGCCCTGAA GTCTGTCCTG CCCCAAACAT 1800
GCTGGGCACA TCTCTTGGAG GTGGTGTGTG TAGTGTCTTA ATGCTGGGCA TTTAGGATGC 1860
ATGTGGCATT CCAGCTCTCC ACTTTCTGCA CCATGGTAAT CTGGTGCTTC CTAGTCTCTT 1920
GTGGTTGGGT GGAGCCATGA GACTAGTGAG GGCCAACGAA CTGTGAGTGC GTATGATACG 1980
GATAATTTAT GGACCAAACC ATTTAATTTG TGCAACCCTC CAGAGTGCTC TTTTATTCTT 2040
CCACAGAGAC TGGCTATTCC TTTAGCCTAC ATCTCCAATG AGGAAACATG GGGCAGAGCC 2100
CCCAGCTGAC CCTTGATGGA CATGTGGCAC TGATGAGATA GAAACTTGGC TGCTGCTGGG 2160
CATGGTGACT CGCGCCTGTA ATCCCAGCAC TTTGGGAGGC CAAGACAGGC GGATCATCTG 2220
AGGTCAGGAG TTCAAGACTA GCCTAGCCAA AATGGTGAAA CCCCATCTCT 2270
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