| Tag | Content |
|---|
EnhancerAtlas ID | HS043-16240 |
Organism | Homo sapiens |
Tissue/cell | Fetal_heart |
Coordinate | chr16:30941910-30943480 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Six3 | MA0631.1 | chr16:30943247-30943264 | GACAGGGTATCACCATG | + | 6.11 |
|
| | 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 |
| GH16I030930 | chr16 | 30942294 | 30942942 |
|
Enhancer Sequence | TGGCCTGGAC AGGCCTGCGT TCCGTGGCCA GCAGGCTTCC CGCTTGCTGG GTGACCTGCG 60
GTAGGTCTCT GGCCCTCTCT GGGCCTTGCT TTTATATTGG GGATACTTCT CTAGTATGCA 120
CAGATTACAG TGCATCCTTC CGTATTTCCC GTGTGCAGGC TACTTTCCAC TTATGGGCTC 180
ATTTAACCCC CTAGACAACT TTGAGGTAGA GGTTATTTTC CCCTTTTTCA GATGAAGCTG 240
AGGCCCAAGG TCATGTGGAA GAGAAGTGGT GGTAGAACTA GGCATTGGAA CCTAGGCCCT 300
TTGGCTCCAG TGCCTTTCCT CCTAATAGTA GCGACTATAT TGAGTGTCTA GTGTGTGTCA 360
GCCATAGCAC TGAGTGCTGT ACTGCATTGT CACTTCTCAT ACTGCCACTT CCGAAAACAG 420
TCTGACGATT GGTTCCATTC ACTTAGGAGA ACGCCATGTG CTGGGCTGCC CCTGCCCTCG 480
AAAGACAGCC AGGCTTGAAC CTCCTGACTC GGTTCCTGCT TTCCTTCTGC CCTGGAGCCA 540
CCACTAATGC CCTCTGCCCA TCCCCCAGCC CCCCAGCCTC TATTAGAAAT GTCGGTCATC 600
CTCCCGAGCC TCTTGTCTTC CTCTCTGATC TCGCCCCCAA CAAAATTCCT CCTCCTCTCT 660
ATGAAACTCC CACAGCACTC TGTTCCCCTC ATAGAGCAAG CAGAGGCCTT CGGCGTGTTG 720
ACAAGCCTTC ATTCATTTAC TCATTTCATG TTCCCATCAG TTGCTGGGGT GGGAGCAGAT 780
AACTGTGTCT GTTTTATCTT CACGTCCCTA GCACGGGACA AAGGGCGGTA TAAGTGCCCA 840
AGAAATGTTG CAGTAAACGA GGCTATCAGG CTCTTTCCCA GGGACTCGCT GTGGCTGGGA 900
CCAGGCTCCC TGTTGGGCAC TGCACCAAGG TTAGCTGATT TGACCTTCAT AATGGCAGCC 960
CTGTGAGAGA AAAGGGATAC CTGAAGTTAC AGTACAAGTT CATGGCTGAA CTCAAACTCT 1020
AGTCTTCTTT TGGGACCAAG TCTGGGCCAC TGGTGCCTTC TGGTATCTGC AGAGATTGTG 1080
CAGCCAAAAG TACCAGAGTG CAGGCTCTGG AGGCAAATTG CCTGTGACAG AATCTTTTTA 1140
TTTTTATTTT TTTTTAAGAC GGAGCCTCAC TCTGTGGCCC AGGTTAGAGT GCAGTGGCAT 1200
GATCTTGGCT GATTGCAACC TCTGCCTCCC GGGTTCAAGC GATTCCCCTG CCTCGGCCTC 1260
CTGAGTAACT GGGATTATAG GCACCCACCA CCACACCCGG CTAATTTTTT TTTTTTTTTT 1320
TTTGTAATTT TAGTAGAGAC AGGGTATCAC CATGTTGGCC AGGCTGGTCT TGAACTCCTG 1380
ACCTGAAGCG ATCCGCCCGC CTCAGCCTCC CAAAGTGCTG GGATTACAGG CATGAGCTAC 1440
CGGTTATGGT TATAGCTGAA GAGCTATAAA CCATTAGGCC AGTCACTTAA CTTCCTGTGC 1500
CTCGGTTTCT TCATCTGAAA AACCAGATAA TCAACGCTCT TGCATAGTGT TTTCTTGAGC 1560
TAATACACAT 1570
|
