| Tag | Content |
|---|
EnhancerAtlas ID | HS091-18645 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr17:1646370-1648280 |
Target genes | | Number: 22 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF9 | MA0653.1 | chr17:1647765-1647780 | AACGAGAGCGAAACT | + | 6.17 | | STAT3 | MA0144.2 | chr17:1647107-1647118 | CTTCCCAGAAG | - | 6.14 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH17I001742 | chr17 | 1645364 | 1646687 | | GH17I001744 | chr17 | 1647859 | 1648338 |
|
Enhancer Sequence | GTCGGAGTCG GGGCCCTGGC CAAGGGCTCT TGTGTGGGAT GGGGGTGGGG CCGGGGGGAC 60
CAAAGGATCC TCCAGAAGGG TTGGCCCCAA GATGGGGGTG GGCTGGAGGT AGCTGAGACC 120
TGCTCTGACT TATCCTCCTG AGACCAACAC CTGCCCTTCC CAGAGCCAGC CTGGAGCAGA 180
GGCCTGTGAT GCTCCTAAGT GCAGAGGTGG CTCTGGCCAG AGTCATTCAC TGGGCTCTGC 240
TGCTGGGTCA AAAGGCAGCT CTCTGGCTGC CTTGCCACCC ATGGTGAGAC CTCAGGGCCT 300
CACAGGTATG TCCAGCCTTG TGGGCAAGAC CTGACCAGCC TGAGAAAGAC GGGTTGGGGC 360
CAGGCGTGGT GGCTCATGCC TGTCATCCCA GCACTTTGGG AGGCTGAGGC AGGTGGATCA 420
CCTGAGGTCA GGAGTTCGAG ACCAGCCTGA CCAACATGGA GAAACCCTGT CTCTACTAAA 480
AATACAAAAT TAGCCAGGCA TGGTGGCACA TGCCTGTAAT CCCAGCTACT CGGGAGGCTG 540
AGGCAGGAGA ATCGCTTTAA CCCAGGAGGT GGAGGTTGCA GTGAGCCGAG ATCGTGCCAT 600
TGCACTCCAG CCTGCATGAT AAGAATGAAA CTCCATCTCA AAAAAAAAAA AAAAAAAAAA 660
AAAGACAGGC TAAATGGATG CAGCAGGCTG GGTAGGAGCT CTGTGTTGGA GCTCTGCGGT 720
GGAGGCTTCA GGGCAGGCTT CCCAGAAGAG GTGGCCTTGA GCCAAGCTGA CCCCAGCCAT 780
CGGGGGAGTG CCAAGCATTG TACTCAGGGT TTACAAAGAT GGTCTTATTT ATTTTTTTGA 840
GACAGAGTCT TGCTCTGTCG CCCAGGCTGG AGTGCAGTGG CGTGATCTCG GCTCACTGCA 900
ACCTCCGCCT CCCGGGTTCA AGCAGTTCTC TGCCTCAGCC TCCCGAGTAG CTGGGATTAC 960
AGGGGCCCAC CACCACGCCT GGCTAATTTT GTATTTTCAG TAGAGATGGG GTTTTACCAT 1020
GTTGGCCAGG CTGGTCTTGA ACTCCCGACC TCAGGTGATC CACCTGCCCC TGGCCTCCCA 1080
AAGTGCTGGG ATTACAGGCT TGAGCCACCG TGCCTGGCCA CAAAGATGGT CTTTTGCCGG 1140
GTGCAGTGGC TCATGCCTGT AATCCCAGTA CTTTGGGAGG CCGAGGCAGG AGGATCACCT 1200
GAGGTCGGGA GTTTAAGACC AGCCTGACTA ACACAGAGAA ACCCCGTTTC TACTAAGAAA 1260
TACAGAATTA GCCAGGCGTG GTGGTGCATG CCTGTAATCC CAGCTATTCG GGAGGCTGAA 1320
GCAGGAGAAT CGCTTGAACC TGGGAGGTGG AGGTTGCGGT GAGCCGAGAT CCTGCCACTG 1380
CACTCCAGCC TGGTCAACGA GAGCGAAACT CCGTCTCAAA AAATAAACAA CAAAAAATCC 1440
CAAAAAGACG GTCTTATTTT GGTCCTCACC ATGCATGTGA GAAGAGTGAG GGACTTGTGC 1500
CACCGTTTTA CAAGGTAAGG CCAAGCCTGG TGGAGTTACG GGAAATGCCG AGGTCCTTTG 1560
GCAAGAGGTA GCCTGGATTC AGACACAGAT CTGATTCACA GCGCAGGGCC TTGTAGAATG 1620
AGAACGTTTT TGATTTGGTA TCTCCCTCCT ATTCACCAAA ACACCCTCAG TGCATGAAAT 1680
GCATGAAATA TGAAACACCA GAAACTAAAA AGGGGGAGAA GCCAGGGCGG ATGTCCCAGC 1740
TGCAGGAGTG GGAGCCGCTG CTCGTGTGTT TGGGGTCTGT TCTGATTCTG GAGCCTGCTT 1800
CTTCCCCTTG GCAATCATGA CCCAGGACTT GGCGTTATCT GTGATCGCGT GGGTAGGATT 1860
CCCTGGCGGG CGTGGGGATG TGAGATGGGA ACAGAGCTTT CTGTCCCTGC 1910
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