| Tag | Content |
|---|
EnhancerAtlas ID | HS043-03190 |
Organism | Homo sapiens |
Tissue/cell | Fetal_heart |
Coordinate | chr1:180145170-180146700 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| STAT1 | MA0137.3 | chr1:180145743-180145754 | TTTCCAGGAAA | + | 6.62 | | Stat4 | MA0518.1 | chr1:180145743-180145757 | TTTCCAGGAAAATG | + | 6 |
|
| | 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 |
| GH01I180177 | chr1 | 180146549 | 180147504 |
|
Enhancer Sequence | ACTTTGGGCT GGGGCAGGCT TAGTGCATTG TGGGCCAGGA TCCCAGGCCT GGGAGTGAGA 60
GGGTGGTGGG AACAGCAGGG CGGGGACCCC AGTTTATTTT CCTTGCTGCC TTTGCCTGTG 120
GGGCTCACAC ACCAGTCTGC TGGAGCTACT CCAGAACCAA GTGGCAGCTG ATGGCTGGTG 180
GTGGGCTTCC TATCGCACAG GTCCTGCTGA AGAGCCCTGT TTTTCTGGGG CTGACTGATG 240
GTGCAAGGGT CCATCCCACC AGGTGGGAAG GAAAAGATGG ATGGGGCTTC TCCAGGTTGT 300
ACCTGCTGCT GTTTCTTGCT ACCTTCCCTC AAAATGTTTG CGGGACGCAG CAGGATTTCA 360
CATGCTCTAT CCCCGGGAAG GCCACTGAGA GTCAGAATGG CATGAGGAGG AAAAAGGAGA 420
TCAAATATTT TGAGGGAAAT TGGGGGGAGG TGGAGAGAAG GTGGTCATGC CTGGGGCATG 480
GGGGTGGCCC CTGGCTCTCT GTATGGCAGA GCATCAGGTG CAGTGGCCGG TGCTCTGTAT 540
CTGTCAGCCA GGCAAGCTTC CCAGCTTGCC TCTTTTCCAG GAAAATGAAG ACAGTAAGGT 600
GCATGGTCTT GCCCATACTT TCCCAAAGAA GAGACAGCTA GATTAAAAAC ACTAGGCCCC 660
CCACTTCTGG ATCAGAACTC AAGATAGGAT AATGCCCACC TCGGAGGACT CTTGCCAAGA 720
AGGAACAAAT CCATGTACCA GCAGGAGCTG CTAGAGGGAG CCCAGCCTTG TACACAGTGG 780
AGGCCCCAGG TGCTAAGAAG GCCTCACAAG GCCGCTGTTG GTGCGCAGAG GCTCTCTTAA 840
AAGTTTGTGT GCAGGTGCTC TCAGAGACAT GGCCCTGCTG AGAGATTGTG TTTCCAAGTG 900
TCAGTTGGGG TTGAATCCAA CTCACAATGA CTCCTTTGTC ATCTTTCCCA ATTTTCCATC 960
CTCCAGAGGG CCTCCAGGGG ACCCTGGATA CAGCATAGTC TTTATGTGGT TTGGGGTTCC 1020
ACAGCCAGAC CCTGTCTCTC CAGAAAACAC CCATGTCAGC CTGTGCCCTG GTCCTTGCTG 1080
CTTCTATTTC TCAATGACTG TGTTTCCATC TCCCTCCTTA CACACACACG TACATCCTCA 1140
TGGCACATTT TCAGCCCTGG GGTATCTCAA AAGCAACAGC TCAAGCAATC CTGCCAAGGT 1200
CTCTCAAAGT GATCCTTTTT TTTTTTTTTT TTTGGAAGAC AGAATCTCGC TCTGTTGCCC 1260
AGGCTGGGAG TGCAGCGGCA CGATCTTGGC TCACTGCAAC CTCCACCTCC TGGGTTCAAG 1320
CAATTCTGCC GCCTCAGCCT CCCGAGTAGC TGGGACTACA GGCGCCTGCC ACCAAGCCTG 1380
GCTAATTTTT TGTATTTTTA GTAGAGATGG GGTTTCACCA TGTTGCCCAG GGTGGTCTCA 1440
AACACCTCAG CTCAGGCAAT CGGCCTGCCT TGGCCTCCCA AAGTACTGGG ATTACAGGCA 1500
TAAGCCACTG CACCCAGCCC AAAGCAATCC 1530
|
