| Tag | Content |
|---|
EnhancerAtlas ID | HS146-07673 | Organism | Homo sapiens | Tissue/cell | NHDF | Coordinate | chr19:41156040-41157180 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr19:41156056-41156071 | TGAACTCCTGACCTC | - | 6.22 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr19 | 41156262 | 41156415 | | chr19 | 41156655 | 41157088 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH19I040650 | chr19 | 41155999 | 41157401 |
| Enhancer Sequence | TTGGCCAGGC TGGTCTTGAA CTCCTGACCT CAAGTGATCT GCCTGCCTTG GCCTCCCAAA 60
GTGCTGGGAT TACAAGCGTG AGCCCCCGTG CCCGGCCAGA CCCCATTTCT CCCATTTCTT 120
TTTATCTCTC TGCTTTATCT TTTCCAGTGG AAGCTCCCAA GATGACTACC TCCAGCCTCT 180
GGCCACAGGG AACCTTCTTC ATATCCCACA AGCAAAGGAG AGCACCTTTG GCTCAGGTTT 240
CCTGCCAAAG TAATGAGGCT AACTCTGATT GGGCCAACAG AGGGCACGTG TTCATGCAAG 300
AGCCAATCAC TGTGATCGGA GGGACAGAAG GAAAAACCAT AATGGCCAGA TTGGCTGAGC 360
CAAGTCACAT GTTCCTCAAA TAGTAAGGTG AGTGGCTCAC ACTAGGGCTG CAGGAGCCAC 420
ACCTGGGTTC AATTTCCATT CCAAACAAAT TTCTGTCTTC TCTGCCCTGT TTCCCGTCAG 480
TAACATAGAG ATAATGAAGG CACTCATATG GTAGAGTTCC CGTGAGGATT AAATGAGTTA 540
GTTAATGCAA AGCACTGAGA ATGGTGCCCA TATACAGAAA GCGTTCAAAT GTTAGCTTCT 600
GTTATCGTCA TTACATGGCC ATTCTCACCT CTTAAGGCTG CTTTTCTTTG CAAGCTCCTT 660
ATGCTCCACA CATTTCCCTC TTTCTAGTTA CTATTGCTTG GTAACAAATC ACTCCAAAAT 720
ATGGTGGCCC AAAACAACAA CAGTCATCCT ATTATTTTTC ACTGTGTCTG TGGTCAGAGT 780
TTTGGGAAGG ACCCAACTGG GCAGTTCTGA CTTGGAATTT CATATGGTTG CAGTCACTTG 840
GCAGCTGAAA CTGGAACAGG GAAGCAGCTG GGGGTGGATG GATCTCTCTC TCTCTCTCTT 900
TCTCTTACTC TCTCCCCACT CCATGTTGTC TCAGGGCTTC TCAATGTGGT CTCTCCACGC 960
GAACTGGTTT GGGCTCCCTC ACATCATGAC AGCCTCTGGG CAGTTGGACT TACATGGCAG 1020
CTTCGGCATC CAGTACAAGT GTTTTATGAA AGTAGCAGCC GCGACTGGGT GCGGTTGCTC 1080
ACGCCTGTAA TCCCAACACT TTGGGAGCTT GAGGCAGGTG GATCACCTGA GGTCGGGAGT 1140
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