| Tag | Content |
|---|
EnhancerAtlas ID | HS076-00829 | Organism | Homo sapiens | Tissue/cell | H1 | Coordinate | chr1:18416860-18417920 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nkx3-2 | MA0122.3 | chr1:18416958-18416971 | ATTAAGTGTTTAA | - | 6.19 |
| | | 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 |
| GH01I018090 | chr1 | 18417082 | 18418986 |
| Enhancer Sequence | CACTACAGCT GCAAACTCCT GGGTTCAAGA GAGCCTTCCA CCTCAGGCTC TTGAGTAGCT 60
GGAACTACAT GCAGCACCCT CCCCCATACC CAGCTTATAT TAAGTGTTTA ATAACTATTC 120
ACTTGTGTAC TAGTCATCAA CTACTGCATA ACACATACCC CAAAATGTAG TCGCATAAAA 180
CAACATTGCT AAAGAATTGA GGGTCAGGAA TCCAGGTGTG GCTTAGCTGG GTCCTCTGGT 240
CAGGGGTGTC CTGCAGTCTG ATCAAGGTAT CAGCCCAGGC TGTGCTTATG TCAGGGCTCG 300
ACTGAGAACA GATCTGCTGC CAAGCTCCCT CCACCCACGG TTGGCAAGAT CAATTCCCCC 360
ACGTGTTGCT GGGCCTTAGC CTGGGAAGCC GTTGTCTTCC CTCCTTTCCT TGCCACCTGG 420
GCCTCTGCAT AGGGAAGCGC ACAACATGGC AGCTTGCGTT ATCAGAGCCA GCGGGGGAGG 480
GGCCTGGAGA GAGTGCAGGC AGGACAAAGC CACAGTCTTT TGTAACCTAA TCCTAGAAGG 540
GACCTCCCAT CACTTTCCCC ATTCTATTCA TTAGAAGGGA GTCAGTCTGT CCAGCAGAGG 600
GGATTGCAAA GACCTGTGAA TACCAGGAAG CCTCATCAGG GCCACGTTGG AAGTTGCCAT 660
TCACACCTAG ACTGGAGGCT GCCTGTGAGA AGGGATGGGG AGAAGGGGCT TTGTCTTTTC 720
CTTCACGGCT CTGTCTCTAG CACCTAGAAA AATGCCTGGC ACGACACAGG AGCTCCACAA 780
ATGTTTGTCC AGTGTATCAG AATGAGGGTA CCTGGGGCAG GGGCTGGATA AAGAGGAGCT 840
TCGTCTCCCC TCTATCCCCC TCTGGGCACC CAGACAGAAT ATTGCAGCCC TGAGCCCAGA 900
ATAATCCCCC TGGGGAGAGC CTTCCCCACT CAGAAAAGCC TCTGGTTGCA TTGCAGTGTT 960
TTGCTACTGA CCTCCCCCTC TGAGGGAAGG CAAATTTCAT CCAGAAGGAG ATGTGTGAAA 1020
ATTGGATTTG CTGCCAGGGT CAAACTTTGC TGTGTTTTAT 1060
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