| Tag | Content |
|---|
EnhancerAtlas ID | HS092-16546 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr14:75382560-75384790 |
Target genes | | Number: 28 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SREBF2 | MA0596.1 | chr14:75383958-75383968 | ATCACCCCAT | - | 6.02 | | ZNF263 | MA0528.1 | chr14:75382576-75382597 | CCTTCTTTTTCTTCCTCCACC | - | 7.21 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 4 | Chromosome | Start | End |
| chr14 | 75382795 | 75383052 | | chr14 | 75383599 | 75384144 | | chr14 | 75382630 | 75382732 | | chr14 | 75384322 | 75384775 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH14I074915 | chr14 | 75382142 | 75385230 |
|
Enhancer Sequence | GAAGTGACTT GGATGACCTT CTTTTTCTTC CTCCACCCTG TCTCAGAGCC TGGCTCCTGC 60
ACGAGGCTCA GCAAATACCC GGTGATGTCT CCCTGGCCCC CAGGCTCTGA GGCCAGGCCC 120
TCGGGTATTC TGGCTGCTTG CCAAGTCCCG ACCCACCCAC CTCACTGCTC CCTGCCACCA 180
TCTCTTCAGC CCTTAGTTAT CCTAACAGCC GGACACGTTA GGGGTCACTC AAGCATCATC 240
CCGAGCAAGC CCTTTGCTTC CTCCCTGGGC CTGAGGGTTG CTGCTGGCTG GCACTGCCCA 300
CTTGCCCAGA TCTGTCTGGG CACAGCTGTG GAATGGAACA AGGGTGACAG TATATCCAAG 360
TCTGGCTGCA GGGACCCAGG CCCAGGGGCA GTAACACCTT TCCTAATTTG AGGAAAGTGA 420
TGCTCCTGGC TTGGGCATGA CACAGGGAAA GGAAGTAGGA TCTCAGGAGG GAGGTGAAGT 480
CCTTAAGTTG AGTACCCAAG ACAGGATAAA AAAGAAAAAA AAGAAGGGTA GTCCTGAAAT 540
AGAATGCGGC GGGCCACTGG CTCACGCCTG TAATCCCAAG TGCTTTGGGA GGCCTAAACG 600
GAGGTGGAGG ATCACCTGAG GCAAGGAGTT CGAGACCAGC CTGGGCAACA CAGCGAGATC 660
TCTCTACAAA AAATAGAAGA CAATAGCAGG GCTTGAGACT GTGGTCCCAG CTACTCAGGA 720
GGCTGAGGTG CGAGGATTGC TTGAGCCTGG TAGGTCGAGG CTGCAGTGAG CCGAGATCAC 780
GCCACTGCAC TCCAGCCTGA GCTACAGAGC GAGACCCTGT GTCAAGAAAA AAAAAAAATG 840
GTTGGGCTTG GCTTTAATTT GTGCTTTCCA TCTGCAGGGG CCTCGAAACA CTGGATTCCT 900
AAACCACTTT CCTGAGGCTA AACAAGTTTG GGGAATTCTG TGTCACAGTG TACATCTGCA 960
CCTAAACACT CTAAGAACTC CGATCATTAA GAAACAAAGC CATATAACTT CAACTCGCTG 1020
TTTTCCTATC ATACTCAGCT CAGAACCCCT CTCACCACAA CACCTATGGT TCAGCGGGAT 1080
CGTACCGGGA GGCACGGTGT CAGTCACCTC CCGGCCAGTC CCTGGGAACG GCTGTGCTCA 1140
GCCAAGGTTG GGTCGTGGCC ACTGACACTC AAGCAGTGGG GAGGGGACCG TGGCAGATGG 1200
AAGCTGGCAG GGCCTGCGCT GACAGTCTGG GACCTGCCCC AGGGACCCAG GAGAAGCAGC 1260
TGGAGTAAGG CCCGGGAGCA GAAGCCTGCG TGCCTCCCAG CTCACTCCTG TCACTTGTAT 1320
TTAGAGCCAT CAAGCACGTA CTCAGTGTCA CAGCATGTGC CAGGTCTTTC CCCAAAATTG 1380
TTTTGTTTTA CCTCCCAGAT CACCCCATTG GGGGAGAATT CTCATCTCAC TTTCCAGAGG 1440
AAGAAACCAC AGCTCAGAGA GCAGGGGGCT TGCCCGTGGC CACCCGGGGT GGTGCCCAGC 1500
GCGGGGCCTT CCCTCAGGCA GCATGTCATC CTCTTGCCTG TGGGAAGTAC AGGACTGTCT 1560
CCTTTTCTCT GTGGGCCCCC AGATCTACCA AAATCACCCA GTGAGTATGT TAAATAACAG 1620
ATTCTTGGGC ATCTGTATTT TTAGGAAGCT CTCCATTTAG CCAGCTTGGT AAAGAACTTC 1680
TTGGGTGACT ATTCCAGGGT TCAGGGGAAG AGGGGAACCT CATACTGGCT GGACTCTGAT 1740
TTGACCTCAT TGTCTGTCCT TCTAATCAGA AGCACTCTAA CAATGAGTGC CCCGAGTAAG 1800
GGTTGGGACG TCGCCTCCTA TCTTCTTGTC TGCCCTGAAT AAGGCAAAGC ATGCGAGATA 1860
GCATTGGGAC AGGGTAAAGT TACAGTTAGG TCAGGAGAGG AAAAAAAGGG CAGACTTGCC 1920
AAGGCCCTGG GCAAGGACGG GCCAGAACGG GCCCTCTCTG GACAGGTTTC TGGAGTTGAG 1980
CACGTCCCAG CCGCAGGAAG TCCCCAGCTG TGCTCGGTAG AGCGTCTTGG CTGCAGCCCT 2040
GGGGTTCAGG GTGAGTGTGG TGGGGGTGCT GTGGGAAGCG GGAAGTGGGA GTGAGCAGGG 2100
CCTCGAGGAC TGGCAGGGTG CCCTGGGCAT AGCTCCTCGC TCCTCCTGCA GTTTCTGTCC 2160
CAACTCTCCC AAGGAGCAGG TTTTCTGGAT CTGAGCTGCA GGGCTGTGGA AAGGGCCTGT 2220
CTGCCTCTTC 2230
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