| Tag | Content |
|---|
EnhancerAtlas ID | HS104-28664 | Organism | Homo sapiens | Tissue/cell | HUVEC | Coordinate | chr19:6022110-6023840 | 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: 1 | Chromosome | Start | End |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH19I006022 | chr19 | 6022207 | 6023811 |
| Enhancer Sequence | TCAGATGGGA CCGTGGGCGG GAGGCGCAGG GGTTGTGGGA GGCGCAGGGG TTGTTGAGGG 60
TGGAGGCCAC GCACTGAGCT AAGACACTAA TCCGAGGCAG GCAGGAATTC CAAGGGAAAA 120
CAGCGGCACT TCTGGACAGA GGCCCCTTCT GAGGAGCTGC CGGCTCTAGC AACCCCACTG 180
TGGCCTGCAG GACAGCACGG CCATCGTGCC AGGCTACACA GGTCACCAGC TGAAGGCTAA 240
ATGACCTTTG ACAATGTGTG TTTCTTGATT TCAAAGCAAA AAGTCACATA ACCCAAATAC 300
GACTCTTCCA CACGCAGCTC TCTCCCGCAG GGTGTGCAAG TGATGTGTTT ACTTTAGCAG 360
ACAGCGCCAC CTCATGGTGA CAGAGACTCG GTGAACCTGC TACGGGGTCC CGGTCGGCTG 420
GTAGCCTGAG GGCAGCCCGG TGGCCCCCAG GGGCTGAGGC CGCCTCTTCT GCTCAAGTCG 480
GTGGCCTGCC ACACCCGGTC GGGTGAAGAC ATGTTTCATC CCCAGCCCCG GCTCCGTCCC 540
CTTCCCTCTG GAAGAGCTAA TCCCCATTTT CACGGCGCCA TATCATGCCC TTTTCCAGTT 600
TGGACACTGC TAGGGGGCCT CCTCCTCCCT GGGAGTTTCC ACGCCAGGCT GACCATCAGC 660
TGGCTGGAAG GTTCTTCCAA TGTGCAGACC TCCAGGCCCT GCAGACCCCC TGGGTCCAAG 720
CCCCTAGAGG GGAGGCCTGG GAAGCTCCTG TTGACCGGCT GGGTCTGGAC AATGCTGTCT 780
CGTTTTACCA GGCTCCCAGC ACCTGAATAC ACCTTCCCTC CTGAGACAGC GCAGAGGAGG 840
GAACCAGCTC CGCGGAACAC GTGGCCAGCT CCGCTCAGAG ATGTCTGTGA GGGGTTCCCT 900
AGGTGGGTTT CCCACGTCTT CCACCTTCTG CCCTCAAATG CTAAGCTCCC TGGAGTGACT 960
TTTCCTCCTT TTTTACTCCC TATGTTCGGC ACTGACCTGG CCAGAACCCT GCACACGGTA 1020
GACGGTGGTC TGACGTCACC AGCTGGCAGC AAGGAAGAGG CGCACAGGCC CTGCTGCTGG 1080
GGCGACCTGC CTGGGGCTGT CTGAGAAGGG AGGTCTGGGA GGCCACTGGG AAAATGGGTC 1140
TCCAGGGCCC AGCTGCTCCC ACACACTTGG CTTATCTGCC ACAGGGTCAG GCTGGCAGGG 1200
GAGGTGGCAC TGTGGCTGTG CCCCCGCCTG ACCTGCAGAA GGCCGCTGCC CACCACGACC 1260
TCAGTCTCAG CCACAGGCAG CCCTGGGGAC AATCGTTGCA AGGGCACGTC ACCCCGTCCA 1320
TCAGCAGATC ACGTGCTTTA ACTCCTCTCT TCCTCTCTGG CTCTCACATT TGCCAAAACA 1380
AGATCTAAGT TTATTCTGCC CGTGTGTGTG GTGAACTTTT TAGAAAGATC TTATTTTACT 1440
TCCTTTGCTT CGAGTCACCA AGCCCGGAAT CTTACTGATC ACAGCTCATG ACAGAAGGAA 1500
ACAACTCAAC AGCGAATCAT CAGTGAGTAA AAGAAACGAG AGATTTTACC TTCAGCTCGG 1560
GAATACGAAT CTTCATCGGG GAAGCGACCT GAGAAAGTCT GCCTTTCGGA TGAAGTGTTA 1620
GAAAGCAGGA AGGATCCCAG CAGCCAGAGA CAAGCGGCTC ATGCATTTTC CCATAGACAT 1680
TTTTTCTTTT TTTTTTTTGA GATGGAGTCT CGCTCTGTCT CCCAGGCTGG 1730
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