| Tag | Content |
|---|
EnhancerAtlas ID | HS091-28169 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr2:174075000-174076380 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxa2 | MA0047.2 | chr2:174075144-174075156 | TGTTTACTTTGT | + | 6.18 | | MEF2A | MA0052.3 | chr2:174075396-174075408 | ACTATAAATAGC | + | 6.11 | | MEF2B | MA0660.1 | chr2:174075396-174075408 | ACTATAAATAGC | + | 6.74 | | NFIC | MA0161.2 | chr2:174075875-174075886 | TACTTGGCACA | + | 6.32 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_45738 | chr2:174073986-174076388 | Osteoblasts | | SE_47134 | chr2:174073113-174076005 | Panc1 | | SE_55735 | chr2:174074926-174076257 | u87 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I173209 | chr2 | 174074473 | 174076433 |
|
Enhancer Sequence | AACCTGGAGG CAGAGGTTGC AGTGAGCCGA GATCATGCCA TTGCACTCCA GCCTGAGCAA 60
CAAGAGTGAA AAACTCCATC TCAAAAAAAA AAAAATTGAA ATCCTGTCTT CTGAGACAAA 120
AGATGGTTAC CAGACATTTC TCTGTGTTTA CTTTGTTAGG AAGCTTTGTC CTCTGTTGTG 180
TAAGAAACAA GAATACTGTT TACCTTGAAA TTCGCTGAGC ACTGTGTCTG CTAGTGAAGG 240
GGGATAGGGA GACATCAAAA ATACTCTTAA AAGAAAACTT GATATCATAA ATCCTATTAA 300
AGCTTGTTAA ATAAATTTAG TAATGAGAAA ATTGTATTGC ATGAGTGGAA GAGTAAACCC 360
AGGATGAAAC ATTTGAGCCA GGTCACATGA TGCATGACTA TAAATAGCAT GTTTGGAAGC 420
TGACATTATT CCCCCCCTGA CTCAGCGGAG ATTTAGGTAA CTTCATCTCT GCTCCCGATA 480
GCCGTGGGCA GTAACATGAC GCCTTACGCC ATCTGCTGAT GCCAAATGAA TACTGCATGC 540
ACTTTGAAAA TTACTGCGTT GTTTACTCCT GTTACTAGAT ACTTCTTTGG GCTTTCTGTT 600
TGTTGTTTTA CAATAACCTT ATTTATTTTT ATTCCTTTGA AATATCTTAT CTAGGGCTAG 660
TGAGGTAAAT GAATTTTTAT TTAGGGATAC AAAAATTATA CAGTGAGCTC AAGTCTAGGT 720
ATAAGGGACT TTTTTCTGGG CTGAGATAAT TAACAAAACA GAACATTTAA GTAATATTTG 780
TTTTTTGCAG TAAGAGATCA GTATACATGT CATCAGATCA TTCTCCTTTA AAATCCATAT 840
ATGAGTTCCC ATTACTCTTA AGACAAAGAC CAGAATACTT GGCACAGTGG CTCATGCCTG 900
TAATCCCAGC ACTTCAGGAG GCCAAGGCTG GTGGATTACT TGAGCCCAGG AGTTCAAGCC 960
CAGCCTGGTG ACAGAGCAAG AATCATTCTC AAGAAATGAA AAGGACCAGA ATACTTAAGA 1020
AGACTCACCA GACCCTCATT ACTGTGGCCT CACCAGTGTC AGCTTAAGAA GATCATTCTC 1080
CCCTTAATTT CTGGCTTTCA GTCCCTCAAC AGATGCGTAT TTCTCCCCTT TTCAGGATCT 1140
TTACAAGCAG TTTCCTCTCT TTGAAGCTTA TCCCATTTCA GCTGTGTACC ACGCCTGCCG 1200
TCACACCCCA CCTTAACTCC TGTTCATCAT TCACATGGCA GTTGAATAAC ACGTCTGCAG 1260
GGAAACACTT CCTGACCCCA GGCCAGATCA GGTTCCACTT TATGTGCTCT GAGAGCATCT 1320
CCTTCATAGG CTTTGCTGCT ATTGGAATTA AGAAGTAATT CGGGCCAGGC ACAGTGGCTC 1380
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