| Tag | Content |
|---|
EnhancerAtlas ID | HS104-30390 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr19:55484520-55485860 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR1 | MA0112.3 | chr19:55484811-55484828 | CGGCTCACTGTGACCTC | - | 6.01 | | Foxd3 | MA0041.1 | chr19:55484565-55484577 | AAACAAACAAAC | - | 6.32 | | Gata4 | MA0482.1 | chr19:55485748-55485759 | AGGAGATAAGA | - | 6.14 | | Nkx2-5(var.2) | MA0503.1 | chr19:55485382-55485393 | CTTGAGTGCCT | - | 6.14 |
|
| | 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 |
| GH19I054973 | chr19 | 55484969 | 55485568 |
|
Enhancer Sequence | TGCGCTCCAG CCTGGGTGAC AGCAAGACTC CATCTCAAAA AAAAAAAACA AACAAACATG 60
GTATTAATTA CACAATGGAA TACTCCTCAA CCTTAAGGAA CTCCTATCTT TTTATTTAAA 120
AATTGCCAGT TTTATTTCAG CTAGAGATCA CTTTTTAGCA TAATGTTTCC TGTCTTTAAC 180
AATGGGTGAG GGTTTTTTTT TTTTTTTTTT TGGTTTGGTT TGGATTTTGG TTTTGCTTTT 240
GAGTCGAAGT TTCACTCTTG TCTCCCAGGC TAGAGTGCAA TGGCGCGATC TCGGCTCACT 300
GTGACCTCCT CCTCCCAGGT TTAAGTGATT CTCCTGCCTC AGCCTCCAGA GTAGCTGGGA 360
TTACAGGCGC CTACCACCAT GCCCGCTAAT TTTTGTATTT TAGTAGAGAC AGGGTTTTAC 420
CATGTTGACC AGACTGGTCT CGAACTCCCG ACCTCAGGTG ATCTGCCCAC CTCAGCCTCC 480
CAGAGTGCTG GGATTACAGG TGTGAGCAAC CATGCCCGGC CAAGGGTTTT TAACTTTAGC 540
TGACCTCCGG AGGTTACAAG TTTGAAAACG GCAGGAGGAA ACCCAGAGAG TTGTAAACTT 600
ACGAAGGTCT GGGCTCTGAA AAAGATACAA ATTTTCTTTC CATGCCAATA GCGCTCACAC 660
AGACATGGTG AATGTTCCTG AAACCCGCCG GACTTTCTGT AAGAAGTGTG GCAAGCACCA 720
CCCCCACAAA GTGACACAAG GCAAGGATTC TTGGTATGCC CAGGGGAAGT AGTGTTATGA 780
CAGGAAGCAG AGTGGCTATG GTGGGCAGAC TAAGCCGATT TTCCGGAAAA AGGCTAAAAC 840
TACAAAGAAG ATTGTGCTAA GGCTTGAGTG CCTTGAGCCC AACTGCAGAT CTAAGAATGC 900
TGGCTATTAA AAGATACAAG CAGCCAAGCG CGGTGGCTCA CGCCTGTAAT CCCAACACTT 960
TGGGAGGCCG AGGTGGGCGG ATCACAAGGT CAGGAGTCTG AGACCAGCCT GGCCAAAATG 1020
GTGAAACCCC ATCTCTACTA AAAATACAAA ACTTAGCTGG GCATGGTGGT GTATGCCTAT 1080
AGTCCCAGCT ACTCAGGAAG CTGAGGCAGG AGAATCGCTT GAACCTGGGA GGCAGAGGTT 1140
GCAGTGAGCC AAGATTGTGC CACTCCAGCC TGGGCAACAG AGTGACACTC TGTCTCAAAA 1200
AAAAAAGATG CAAGCATTTT GAACTGGAAG GAGATAAGAG AAAGGAACAA GTGATCCAGT 1260
TCTAAGTGTC ATCTTTTCTT TTATGAAGGC AATAAAATCT TGAGCTTATG GTAAAATGCA 1320
AAATTTTCCC CCCTTCTCCT 1340
|
