| Tag | Content |
|---|
EnhancerAtlas ID | HS052-18256 | Organism | Homo sapiens | Tissue/cell | Fibroblast_foreskin | Coordinate | chr19:6022010-6023800 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GSC | MA0648.1 | chr19:6022665-6022675 | GCTAATCCCC | + | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr19 | 6022070 | 6022416 | | chr19 | 6023211 | 6023679 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH19I006022 | chr19 | 6022207 | 6023811 |
| Enhancer Sequence | TGAGGTTGAA GAGCATCTGG GGGTGGGCAT GAGAGGAGCA AGGAGGCGAG GACGCAGTGG 60
GGTTGGGGGC CGAGCGCCTG GAAGATTGGC TGCCCCTGCC TCAGATGGGA CCGTGGGCGG 120
GAGGCGCAGG GGTTGTGGGA GGCGCAGGGG TTGTTGAGGG TGGAGGCCAC GCACTGAGCT 180
AAGACACTAA TCCGAGGCAG GCAGGAATTC CAAGGGAAAA CAGCGGCACT TCTGGACAGA 240
GGCCCCTTCT GAGGAGCTGC CGGCTCTAGC AACCCCACTG TGGCCTGCAG GACAGCACGG 300
CCATCGTGCC AGGCTACACA GGTCACCAGC TGAAGGCTAA ATGACCTTTG ACAATGTGTG 360
TTTCTTGATT TCAAAGCAAA AAGTCACATA ACCCAAATAC GACTCTTCCA CACGCAGCTC 420
TCTCCCGCAG GGTGTGCAAG TGATGTGTTT ACTTTAGCAG ACAGCGCCAC CTCATGGTGA 480
CAGAGACTCG GTGAACCTGC TACGGGGTCC CGGTCGGCTG GTAGCCTGAG GGCAGCCCGG 540
TGGCCCCCAG GGGCTGAGGC CGCCTCTTCT GCTCAAGTCG GTGGCCTGCC ACACCCGGTC 600
GGGTGAAGAC ATGTTTCATC CCCAGCCCCG GCTCCGTCCC CTTCCCTCTG GAAGAGCTAA 660
TCCCCATTTT CACGGCGCCA TATCATGCCC TTTTCCAGTT TGGACACTGC TAGGGGGCCT 720
CCTCCTCCCT GGGAGTTTCC ACGCCAGGCT GACCATCAGC TGGCTGGAAG GTTCTTCCAA 780
TGTGCAGACC TCCAGGCCCT GCAGACCCCC TGGGTCCAAG CCCCTAGAGG GGAGGCCTGG 840
GAAGCTCCTG TTGACCGGCT GGGTCTGGAC AATGCTGTCT CGTTTTACCA GGCTCCCAGC 900
ACCTGAATAC ACCTTCCCTC CTGAGACAGC GCAGAGGAGG GAACCAGCTC CGCGGAACAC 960
GTGGCCAGCT CCGCTCAGAG ATGTCTGTGA GGGGTTCCCT AGGTGGGTTT CCCACGTCTT 1020
CCACCTTCTG CCCTCAAATG CTAAGCTCCC TGGAGTGACT TTTCCTCCTT TTTTACTCCC 1080
TATGTTCGGC ACTGACCTGG CCAGAACCCT GCACACGGTA GACGGTGGTC TGACGTCACC 1140
AGCTGGCAGC AAGGAAGAGG CGCACAGGCC CTGCTGCTGG GGCGACCTGC CTGGGGCTGT 1200
CTGAGAAGGG AGGTCTGGGA GGCCACTGGG AAAATGGGTC TCCAGGGCCC AGCTGCTCCC 1260
ACACACTTGG CTTATCTGCC ACAGGGTCAG GCTGGCAGGG GAGGTGGCAC TGTGGCTGTG 1320
CCCCCGCCTG ACCTGCAGAA GGCCGCTGCC CACCACGACC TCAGTCTCAG CCACAGGCAG 1380
CCCTGGGGAC AATCGTTGCA AGGGCACGTC ACCCCGTCCA TCAGCAGATC ACGTGCTTTA 1440
ACTCCTCTCT TCCTCTCTGG CTCTCACATT TGCCAAAACA AGATCTAAGT TTATTCTGCC 1500
CGTGTGTGTG GTGAACTTTT TAGAAAGATC TTATTTTACT TCCTTTGCTT CGAGTCACCA 1560
AGCCCGGAAT CTTACTGATC ACAGCTCATG ACAGAAGGAA ACAACTCAAC AGCGAATCAT 1620
CAGTGAGTAA AAGAAACGAG AGATTTTACC TTCAGCTCGG GAATACGAAT CTTCATCGGG 1680
GAAGCGACCT GAGAAAGTCT GCCTTTCGGA TGAAGTGTTA GAAAGCAGGA AGGATCCCAG 1740
CAGCCAGAGA CAAGCGGCTC ATGCATTTTC CCATAGACAT TTTTTCTTTT 1790
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