| Tag | Content |
|---|
EnhancerAtlas ID | HS105-41166 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr19:55484430-55485860 |
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 | CTCCTGTAGT CCCAGCTACT TGGGAGGCTG AGGCAGGAGG ATTGCTTGAA CCAGAGAGTC 60
AGAGGTTGCA GTGAGCCAAG ATCGTGCCAC TGCGCTCCAG CCTGGGTGAC AGCAAGACTC 120
CATCTCAAAA AAAAAAAACA AACAAACATG GTATTAATTA CACAATGGAA TACTCCTCAA 180
CCTTAAGGAA CTCCTATCTT TTTATTTAAA AATTGCCAGT TTTATTTCAG CTAGAGATCA 240
CTTTTTAGCA TAATGTTTCC TGTCTTTAAC AATGGGTGAG GGTTTTTTTT TTTTTTTTTT 300
TGGTTTGGTT TGGATTTTGG TTTTGCTTTT GAGTCGAAGT TTCACTCTTG TCTCCCAGGC 360
TAGAGTGCAA TGGCGCGATC TCGGCTCACT GTGACCTCCT CCTCCCAGGT TTAAGTGATT 420
CTCCTGCCTC AGCCTCCAGA GTAGCTGGGA TTACAGGCGC CTACCACCAT GCCCGCTAAT 480
TTTTGTATTT TAGTAGAGAC AGGGTTTTAC CATGTTGACC AGACTGGTCT CGAACTCCCG 540
ACCTCAGGTG ATCTGCCCAC CTCAGCCTCC CAGAGTGCTG GGATTACAGG TGTGAGCAAC 600
CATGCCCGGC CAAGGGTTTT TAACTTTAGC TGACCTCCGG AGGTTACAAG TTTGAAAACG 660
GCAGGAGGAA ACCCAGAGAG TTGTAAACTT ACGAAGGTCT GGGCTCTGAA AAAGATACAA 720
ATTTTCTTTC CATGCCAATA GCGCTCACAC AGACATGGTG AATGTTCCTG AAACCCGCCG 780
GACTTTCTGT AAGAAGTGTG GCAAGCACCA CCCCCACAAA GTGACACAAG GCAAGGATTC 840
TTGGTATGCC CAGGGGAAGT AGTGTTATGA CAGGAAGCAG AGTGGCTATG GTGGGCAGAC 900
TAAGCCGATT TTCCGGAAAA AGGCTAAAAC TACAAAGAAG ATTGTGCTAA GGCTTGAGTG 960
CCTTGAGCCC AACTGCAGAT CTAAGAATGC TGGCTATTAA AAGATACAAG CAGCCAAGCG 1020
CGGTGGCTCA CGCCTGTAAT CCCAACACTT TGGGAGGCCG AGGTGGGCGG ATCACAAGGT 1080
CAGGAGTCTG AGACCAGCCT GGCCAAAATG GTGAAACCCC ATCTCTACTA AAAATACAAA 1140
ACTTAGCTGG GCATGGTGGT GTATGCCTAT AGTCCCAGCT ACTCAGGAAG CTGAGGCAGG 1200
AGAATCGCTT GAACCTGGGA GGCAGAGGTT GCAGTGAGCC AAGATTGTGC CACTCCAGCC 1260
TGGGCAACAG AGTGACACTC TGTCTCAAAA AAAAAAGATG CAAGCATTTT GAACTGGAAG 1320
GAGATAAGAG AAAGGAACAA GTGATCCAGT TCTAAGTGTC ATCTTTTCTT TTATGAAGGC 1380
AATAAAATCT TGAGCTTATG GTAAAATGCA AAATTTTCCC CCCTTCTCCT 1430
|
