| Tag | Content |
|---|
EnhancerAtlas ID | HS157-13143 |
Organism | Homo sapiens |
Tissue/cell | PANC-1 |
Coordinate | chr7:76639130-76640600 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFE2L1 | MA0089.2 | chr7:76639672-76639687 | AGATGACTCAGCAGG | + | 6.66 | | TCF7L2 | MA0523.1 | chr7:76639689-76639703 | AAACATCAAAGGAA | + | 8.12 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_26739 | chr7:76638557-76640122 | Esophagus | | SE_68923 | chr7:76639200-76640242 | H9 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH07I077009 | chr7 | 76639119 | 76640130 |
|
Enhancer Sequence | CAAAACCCCG TGTCTACTAA AAATACAAAA AATAGCCAGA TGCGGTGGCT CGTGCCTGTA 60
GTCCCAGCTA CTCGGGAGGC TGAGGCAGGA GAATCGCTTG AATCTGGGAG GCAGAAGTTG 120
TAGTGAGCCG AGATCACACC ACTGCACTCC AGCCTGGGCA ACACAGCGAG ACTCCATCTG 180
AAGATAAAAA AAAAAAAAAA AGAAGAACCC AAGGGAGGGG GCACTGCCCA GCACAGGCAC 240
AGTCCCATCA GGCCCTGGGG AGCCATGCCA GGGCGTTCTG CCCAGCACAG TCACACCTAA 300
AAGGGTCCTC AGCCGAACCC CATCCCCTTG AATACCAGCT CATGACGGCT TTGAGCAGAA 360
CATGTCACGG GAACGGCATT GTGTAGAACT TTTTATTAAA TGGCATTTAA AATATTCCCC 420
AGGACTGTGT AGCTGGGGAA ACACCACAAA ATCCATTGGC CCGGAACATA ATGGCTCAAT 480
GGTACGAAAC AAATGCATTG TTAAAAAGGA AAAACAGCAA CTGTTGCGGG GTAATGACTT 540
GCAGATGACT CAGCAGGCCA AACATCAAAG GAATTCGGAT GGCAGCAGGT GGGCACAGGC 600
AGCCAGGAAG CACCCCTCCC TCGCTCTCAC TTCCAGCGAT CGCTTTACCT CCCTGGAGTG 660
TCTAAGCCAC CCATTTCTCT CCATCATCCC TGCAATCCCC AAGCAAGAAC CACCTTGGTC 720
TCCCGCTGGG ATGTCCGTGG TTCCTCTCTA GCTGAACTCT CCATGTCCAC TCCTGCCCGT 780
CGCCCATTCC CCTCTCAGTA TCCAGAGGGA CCAGGTTCTT TGTTCTTTTT TTTTTTTTTT 840
TTTTAAGATA GAGTCTCACT CTGTTGCCTA GGCTGGAGTG CAGTGGTGTG ATCTCGGCTC 900
ACTGCAACCT GCAGCTTCAG GTTCAAACGA TTCTCCTGCC TCAGCCTCCC AGGTAGCTGA 960
GACTATAAAC GTGCGCCACC GTGCCTGGCT AATTTTTTTG TATTTTTAGT AGACGGGGTT 1020
TCACCATGTT GACCAGGCTG GTCTCAAACT CCTGACCTCA GGTGATCCAC CCACCTCGGC 1080
CTCCCAAAGT GCTGGGATTA CAGGTGTGAG CCACTGCACC CAGCCAGGAC CAGGTTCTAA 1140
ACCTGATCAC ATCACACCTC TGCTCCCAAC ATTCAGGAAC TTCACACTGC AAGAACAGAA 1200
TCTAGGTTCA GACAGGTGTG GCGGCTCACA TCTGCAATCC CAGCACTTTG GGAGGCCAAG 1260
GCAGGCGGAT CACTTGAGGC CAGGAGTTCG AGACCAGCCT GGCCAGCATG GTGAAATGCC 1320
ATCTCTACTA AAAATACAAA AATTAGCCAG GCATGGTGAT GGGCGCCTGT AATTTCAGCT 1380
ACTTGGGAGG CTGAGGCAGG AGAATTGCTT GAACCTGGGA GGCGGAGGTT GCAGTGAGCT 1440
GAGATCACAC CACTGCACTC CAGCCTGGAC 1470
|
