| Tag | Content |
|---|
EnhancerAtlas ID | HS003-18486 |
Organism | Homo sapiens |
Tissue/cell | A549 |
Coordinate | chr17:2770330-2771800 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFYA | MA0060.3 | chr17:2770493-2770504 | TCTGATTGGTC | - | 6.14 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_31401 | chr17:2770655-2771755 | Gastric | | SE_65245 | chr17:2770305-2772175 | Pancreatic_islets |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I002867 | chr17 | 2770557 | 2771843 |
|
Enhancer Sequence | ATTACAGGTG CCCACTGTCA TGTCTAGCTA ATTTTTGTAT TTGTAGTAGA GACGGGGTTT 60
CACCATGTTG GCCAGGCTGG TCTCGAACTC CTGGTGTCGT GATTCCCCTC ACCTTGGCCT 120
CCCAAAGTGC TGGGATTACA GGTGTGAGCC ACCGTGCCTG GCCTCTGATT GGTCATTTAG 180
CTGATTTAGT CAAGAAACTT TTGGTTTGAA GTGGCAAGCC CCAATTCAAA TTAATGTAAA 240
GAAAAAATGA AGCTTTGGGG TTTAGGTAAC TGGAAGGTTC AAGGGGGACG GATTCAGGCC 300
TGGCTGGATC GAGAGCTCCA GTGGGGTCTT TGGACACTGG TTCTTTCACC CCGTCTCTAG 360
GCTGTGCCTT CCTTTGGGTT GCCTTCGTCC TCAGGTACCT TATCCACGAA GATGGACGAT 420
GGCTGCCCTG GGCTGACCTT CTACCCACTT AGCAATACCA ACAGGAAGAG CAAATCTGTT 480
TCCCAATCAT TTCAGCAGAT GTCCCAGGGA TGGCTCACCC TGGACAGAAA GTGAGTCACA 540
TACGCATCCC TGAACTTTGG CCAGAGGGGT GGGATACACT GATTCATGAA GTCTAGGTCT 600
TACGCCCACC GCTGGTTCCC GGGATGCAGG GACTTGGCTG GGAGTATAGG AGGGATGGGT 660
CACCTAAGGA AACCTGGCAT GTTGCTCTCA GAAGCTCAGG GGATGGAAGC TGGGCAGTAA 720
AAATGCCAAC AGCTGTCCAC TCTGCTGGCC CTAGTGGCTT AGTTGATGCT GATCTTGGCA 780
CGGTCTTGTC AACTTGGCTG GTGGCTGCAG CTGCTGGTAC CCTCCCAGAC GCAAGGAGGC 840
TTCCTTCTGC CTTGGCTGGA TGAGGTGTGC TTTCTTCTTC ACGGATGCAG CTCGCGGGAT 900
CCCCAAGCCT TTGGTAGTAA ACACACTTCC TGGGCTGTCT TTTCTCTGAG TCCATTCTGA 960
ACATCAAAGC ATTCAGCCTG TGACCGCGCT GGACCTGGTC TGAGAGGACA GCCTGGCTTT 1020
GCTCGGGGTT GGCTCTCGGC TCTGGGATTG GATAATGTGT CCCCTTCCTG TTTTGCTTAT 1080
GCTTTGTGGC ACCCAGCTGC CCTCCACCCC AGCAGGTCCG GATTCCTTGA ATACAGATTG 1140
CCCCTCCTTC CAGACGTCTG GCCAGTGGAT GCTTTTGGTT ACGAGGCCCT GGCTGAGAGA 1200
AGGGCTGGCT CTCTGCTATC CATCCCCCTG GTGGAGGGCC AGGCCCAGAG GAAGTCTCAG 1260
AGGTCTTAGA GATAGGCACC TCTAGATGGC AAAAACACGA CTGCAGAAGG GCAGAGGAGC 1320
GGCCTCAGGA AAAACCCAGG GGGATATATG ATCTTGAACG TACATGGTGT CGAAACTGCG 1380
GCCCTTGGCT TTCCCATGTG TGAAATGCGA CTAAGACTAA TGAAAGTCTT TTATGTGTGT 1440
AGGCAAAAAT CTTATTTAGC AATTCCTCTA 1470
|
