| Tag | Content |
|---|
EnhancerAtlas ID | HS092-16270 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr14:65501300-65502270 |
Target genes | | Number: 12 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2C2 | MA0504.1 | chr14:65501910-65501925 | TGACCCCTGACCCCT | - | 7.2 | | RELA | MA0107.1 | chr14:65501484-65501494 | GGGAATTTCC | + | 6.02 | | ZNF263 | MA0528.1 | chr14:65502206-65502227 | TCTTTCCTCTTCTCTTCCTTC | - | 6.45 |
|
| | 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 |
| GH14I065035 | chr14 | 65501881 | 65502030 |
|
Enhancer Sequence | ATGCTCAATG GTAAGGCAGC TATAGTTGAG AGCTGGAGAG TAGGCACTGC CTGTGTTTGG 60
TTCTCTTTTA TATTTTGTGT TTCTCAGCTG AGATTTTCCA TCTTTTTATT CTTTATGAGT 120
GCATTTTTCT TCATTTTGCT GTGGTAAGTA TGGAATTATA ATGTCTGCTT TAAATTGCTT 180
GTCTGGGAAT TTCCACATCT GTGTGTCCTG GAGTTGGCAT GTCAGCTCCA TGAGTCTTCC 240
TGTGCTGAGT GATGTTGTGT TGTGTCCTAG ACATTGTGAT ATGATGGTGG AGGTGTCATA 300
CAACAGAACG GTATGGATTC TGTTGGTTTG CCCCAAAAGG GGTTGATGTT TTCAGTTTAG 360
CAGGCAGTCA ACTTGGTCAG ACTCAAGCTA CAAACTGTCA CTCATGCAGC AGCTCAGAGC 420
TCAGTTCTTG CTTAGAAGTT GCTTTGTTTC CCCAGCACGT ATGTGGAAAC TTGAACTGAG 480
TTTAAATGCA GAATTTGGGA TTTTTCTTCT TTGACTTTCC TGTTTCTGGA TTCGTCCTCA 540
GTTTCTGGCA GCCTGCATCT TCCTGCCAGA AGGATGGTTG GCTTCCCATT AGAGTGTTGG 600
CTGCCCGCCC TGACCCCTGA CCCCTGGCCT GCTGCTGCCG CCCTGGGCTA TGGCTGCCAT 660
CCTGAGGGCA AACCAGAGAG AAAAAGTTGT GGGGGAAGGG AGGGACTAAC TGCATGCTGT 720
TCTCTGTTCC AAGTTTCAAA CTCCACCAAA ATCTGCCTGC CCTTTTTCAG TCAGCTGAAC 780
CCTCAGGAAG CTGTTTTTTT GTATTTTGTT CAGTGTACAG CTGTCATTTG CAGGGGGGTT 840
GACTGGTTAG GCACAGACTA GATACGGAAC TCAGACAGCC TGGGTTTGAA TCCCAGTTTT 900
GCCCTTTCTT TCCTCTTCTC TTCCTTCTTT CTTCCTCTGT CTTTCAATTC TCTCTTTCTT 960
TTTTTGAGAC 970
|
