| Tag | Content |
|---|
EnhancerAtlas ID | HS092-23647 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr2:28940000-28940760 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFAT5 | MA0606.1 | chr2:28940106-28940116 | ATTTTCCATT | + | 6.02 | | NFATC1 | MA0624.1 | chr2:28940106-28940116 | ATTTTCCATT | + | 6.02 | | NFATC3 | MA0625.1 | chr2:28940106-28940116 | ATTTTCCATT | + | 6.02 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_02169 | chr2:28939958-28940678 | Aorta | | SE_41111 | chr2:28938705-28940799 | Left_Ventricle |
|
| | 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 |
| GH02I028713 | chr2 | 28936139 | 28941575 |
|
Enhancer Sequence | AAGCTAGAAG AATGGGGGGA TTGTCCTCTT TTCTATATAT TTTTTTCTTT TTGATGTCCT 60
TTACTTCAAG TTAAGCCTGG TGTTTGCTTT AATCACAGCA GAAAGCATTT TCCATTTCAG 120
GGAAAGGAGA GAACAGGCCA TAAACCCTGT CCCCTGTTTG TTCTCCAACT ACCCATTTTT 180
GTCCTTTGCC CTGCCATGTC TTTTCCCCCT CGTTTGCTTC TCCTTTCTTT GTTGATTTCT 240
CAGTTCTTTT CTGGCCTCAC TCAAAATGGC AGAAATTACG CAACCTAGTA CTTTTTTACA 300
CAAGCTCCTT TAGTGTCAAG GATTCATCAA GTGCCTGCCA TGTGCCGGAA CTGTTCTAGA 360
TGCCGAGAAT ACTACCATGA ATGAAATAGA CAGAAATCCC GGCTGTCATT GGGCTTTGTC 420
TGAGGGCCAT TGGGGAAGGC CTCTCAAAGG AAGTGATAGC TGAGCTGGGA TCTGAGTCAT 480
GAAGAGGAGT GAGCCCAGGG GACAACAGCT GCAAGAGTGT GCCAATGGGA GAGACCAGCC 540
CAGCAAAAAG GAGAAGCATA AGTCTGGTGC ATTCCAGGGA CAGGAAGGAA TGGGGCAGGG 600
TGCCTTTAAG AGAAAAGCAT CAGTTTGGAT GAGGAGGGAT GTAGGGTCGG GAATACAAAA 660
TAAGAGTAAT TATGGCTGGG CACAATAGCT CACACCTGTA ATCCCAGGAC TTTGGGAGGC 720
CAAGGTGGGC GGATCACTTG AGGTCGGGAG TTAGAGACCA 760
|
