| Tag | Content |
|---|
EnhancerAtlas ID | HS088-00623 | Organism | Homo sapiens | Tissue/cell | HeLa-S3 | Coordinate | chr1:16004440-16005820 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NKX2-3 | MA0672.1 | chr1:16005510-16005520 | TTCAAGTGGT | - | 6.02 | | Nr2f6(var.2) | MA0728.1 | chr1:16004479-16004494 | TGAACTCCTGACCTC | - | 6.22 | | RARA | MA0729.1 | chr1:16004476-16004494 | ACTTGAACTCCTGACCTC | - | 6.71 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CTTAGAGACA GGATCTTACT ATGTTGCCCA GGGTGGACTT GAACTCCTGA CCTCAAGCAA 60
TGTTCCTGCC TCAGCCTCCC AAAGTACTGG GATTATAAGT GTGAGCCACT GCACCTGGCC 120
CCAGTGAAGT AGTACTTTTT ATTATACCCA CATATAAGAC TAATTTGGGA CATTGGCAAA 180
CAGTATCTCC CTGCTAATAG TTGTACAGAC TTTGATCATA GTACCTCTAG TACCTCACCC 240
ATTATCTTCC TAGAATGGAA AGGCTCAAAT CAGGTGTATT AGGCCATTCT TTCATTGCTA 300
TAAAGAAATA CCTGAGACTG GGTAATTTAT TTTTATTTTG TTGAGATGGA GTCTTGCTCT 360
GTCACCCAGG CTGGAGTGCA GTGGTGTGAT CTTGGCTCAC TGAAACCTCC ACCTCCTGGG 420
TTCAAGCGAG TCTCCTGCCT CAGCCTCCCA AGTAGCTGGG ACTACAGGCA TGCACCACCA 480
CGCCTGTCTA ATTTTTGTAT TTTTAGTAGA TACAGGGTTT TACCATGTTG GCCATGCTGG 540
TCTCGAATGC CTGACCTCAA GTGATCCACC CGCCTTGGCC TCCCAAAGTG CTAGGATTAC 600
AGGTGTGAGC CACCGTGCTC AGTGAGACTG TGTAATTTAT AATGAAAAGA GGTTTAATTG 660
GCTCGTGATT CTGCAGGCTG CACAAGCATG GGCCAACATT GCTCAGCTTC TGGGGAGGCC 720
TCAGGGAGCT TTTACTCATG GCAGAAGGTG AAGCAGGAGC AGGCTTATCA CATGACAAAA 780
GCAAGAGGAA GTGAGAGAGA GTGGTGGGGA GGTGCCACAT ACTTTTACAT GACTACATCT 840
TGCAAGAATT CACTCACTGT TTTGAGGACA GCACCAAGAG GATGGTGCTC AACCATTCAT 900
GAGAACTCCA CCCCCATGAT CCAGTCACCT CCCATCAGGC CCCACCTCCA ACACTGAGGA 960
TTCCTTTTAT TTATTTATTT ATTTTCTTTT TTTTGAGACA GGTCTTGCTC TGCACCCAGG 1020
CTGGAATGCA GTGGCGCGAT CTCAGCTCAC TGCAACCTCC GCCTCCTGGG TTCAAGTGGT 1080
TCTCCTGCCT CAGCCTCCGG TGTAGCTGGG ATTAAAGCAC GTGCACCACA CCTGGCTAAT 1140
TTTTGTATTG TTAGTAAAGA TGGGGTTTCA CCATGTTGGC CAGGCTGGTC TCGAACTCCT 1200
GACCTCAAGT GATCTGCTTG CCTTGGCCTC CCAAAGTGCT GGGATTATAG GAATGAGCCA 1260
CCGTGCCTGG CCTAAGGATT ACATTTTGAC ATGAGATTTG AAACAAATAT CCAAACTGTA 1320
TCATCAGGTG TAAAGAGAAG CAACCTTACA TCTGTCCTTA GTTCTCTCTT TTTTATTTTT 1380
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