| Tag | Content |
|---|
EnhancerAtlas ID | HS043-21690 |
Organism | Homo sapiens |
Tissue/cell | Fetal_heart |
Coordinate | chr2:12964130-12965560 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr2:12964732-12964750 | AGAAGGAGGGAAGAAAGG | + | 6.75 |
|
| | 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 |
| GH02I012824 | chr2 | 12964201 | 12965530 |
|
Enhancer Sequence | ACTTCTCTGG GTGCTCTCAG AATTCTTATT TATGCAATGA AATAACCTCT ATGGGTCCTT 60
TCCAGGATCA TGATGTGAAG GAAAAGGTGG AATATTGGGC TGCATTTGTG GTGCTCTGCC 120
AGTGCAGGTG AGGAGTGTGT GAGCATCCTA GGAGTGCATC CAGGTAGTTA GGAGGGAGAG 180
GACAACACAT AGTCTCCTAG GTGCAGGCGG CGGGGGAAGT CCGGTGGACA CCTGTGAAGC 240
TAAGTTCCAG GACCTTCTGG GGGCTGTGGA GAGGAAGGGG ACCTTCTCCA GAGGGGCCGT 300
GTTGATTGAC TCATTCTTCT CTGACTCCTC AGAAGCCAGT TCATTGCAGT AGAGGGGCTG 360
TCCTGCAAGT CATATGCTTC TCCTCCTTGC CTTAACTACA GGAATTCCAA GATGTTTACA 420
CAAACTTCAA GGAGTGAACC AAGTTATTAA AAGAGTAGCA ATTAGGGTGG CCCATCCCAG 480
CAATTTAGTT TCCTGTCTAA GGAAGCATGA AGGGGGAGGG GTTTCCAGGG AGGGGAGAGG 540
GAGGGAGCAT TCTTGTCTCC TGATTGGACC GCCCCAGGAT TTCCATTTCT GAACACAGAC 600
ACAGAAGGAG GGAAGAAAGG TTGCCAGATG CCAGCTCCCA GCTCCCTGGA GGAGTTACTC 660
GCCGCCACAG ATGCTCCAGC AGCTGGTTGG GCCCCTCCTC AAAGTGTCTC TCCTGCTTCC 720
TTCTTTTGGG GGATTCTGGC TCAGCTTTGA AAGCCTTTTG GCATCTTTTG CCTGCCTCCA 780
AAAATTAAGC TGTGTTGGAA GCTGCCTGAT AAATCACTCT TTGCACCGTG GCTGCCATGG 840
GGCTTGCAGA GAGTGGCTGC CTAGTGATTT ACCGCGGCTG TCTGAGAGGG CTTTTCCAAG 900
CAGCCAGCGT AGACCAGGGA GTCATCTCTG GCAAAAGGAG CATTTTGTCT AGCTCAAATG 960
GACACTACAG AGAGGAAGTG GGATTGCTTT GTTCAAAACT TGTTGGTCAT CCATTCCTCA 1020
AGCCAGCCGG AATCTCCAAG TTCATTTCTT CCATGCAACT TGAGCTCAAG AAAAGAGGTC 1080
CAGAAAAGTG GTTTTTCATG ACAGGCCTGC TGGAGCCTTT CCTAGGGGAA GGAGAACTTT 1140
CTGGTTCTGA ACTGCAGTTA CACAATGCTG GGCAGGCCCT CTGATTTGTG GTCATAGTTT 1200
CCCAGAACCC CAAGGGACCC ATCCAGGAAA ACGCCCATGT CCCCTCGCCT GCGTTGTCAT 1260
CTGCTCCCTC CCAAGGGGAT TTTGTTTCCT TGATTGTGTT CCATAGTGGC TGTTGGAAGT 1320
CAGGTGCCCT GGACGCAGCT TGGACAGGAA CCATGTGGTG TGAGGACCTG AGCCTTGTGC 1380
ATACGTGGCT TTTGCTTCTG GTTCTGGCTT GACAGTGTGA CGAGTTAATT 1430
|
