| Tag | Content |
|---|
EnhancerAtlas ID | HS147-29217 | Organism | Homo sapiens | Tissue/cell | NHEK | Coordinate | chr3:124292620-124293640 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TP53 | MA0106.3 | chr3:124293051-124293069 | AACATGTCAGGGCAAGCC | + | 6.52 | | TP53 | MA0106.3 | chr3:124293051-124293069 | AACATGTCAGGGCAAGCC | - | 6.79 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GTCCATCTGG CTCCGTGATT TCCCAAGAAA TAATGGCTTA ATCCTCTCAT AACTTTCTTT 60
TGACTTTAAC CCAGAGGATT GAGATAATAT TTGATATATT TGAGCTAAAA ATTCAAGTTT 120
TTCCTTGGCT TGTACCTCTG GCACCTCTCC ATGACCTATT CTCTGTCATT AATTCTGTGG 180
TACTTGAAGG TAACATTTGG ACCACATTAT GGAGATGGGC TGACCTGTGT GATGGGGGTT 240
GTGCTGACAC TGTGAGTGTT GGGTGTATAT GAGGGGACCA CTCTTTAATT CAAAGAAGAG 300
CAGGACAGAG AGGAGTTTCG TGGAAACTGC CTCAGGCCTG CTTTGTTCTG GTTGAGATGT 360
CCTGCCTGTG GCTACATCCA TCTAATACTA TTTAGGACAT GAAAGGGCTT AGAATCAAAG 420
CCTCAAATAG GAACATGTCA GGGCAAGCCA CATCCTTCTC TAAATACAAC TCAGTGTCGT 480
GCTGTCTCCA AGTAGAACTG AAGCAGGAAG ACCCAGGTGT CCATGGAAAG AGCTGGTCTC 540
TCTGGGTCCC TCTGCAGAGA TCCTGCATTT TTCCCTTTTG TAGCCAGCCT GCTGTGACTT 600
TGCTTATGTT AAATGCCAAT TTCAACAGCA TGTTTTCATG CCTGCTGGTG CCCACTGTAA 660
ATCTGTGACA TCTACATGAT GATGATGCCC CTTATCATCC AGAGGGGAAG TCAGGGGCAA 720
ACTTGAATAT GCTCTTTGGA GCCAATGAAC CAGCTGATGG AGCTCAGAGC TAAAATGAGA 780
GCCTCAGGAT TTGATCCCAG AGAAGAAAGG CTGCCACTGA CTGCTTTCTG AGAAGAAGCT 840
GGAGATGATA GAGAGGAGGT TACCCCAGCA AACAGAATGT TCCCCCAGAG GAAAGATGGT 900
GCAGTTTTCT TGCTTACAGC TAGCTAAGCT GAACACTTTC CCCCTAGAAG AACACGGGGA 960
CCCAGGAATG ACATGCACTG AATGTGACTT GAGGAAAAGA GAAGGCAAGG CAATGGTCTG 1020
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