| Tag | Content |
|---|
EnhancerAtlas ID | HS091-39538 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr5:156753280-156754980 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR2 | MA0258.2 | chr5:156753820-156753835 | AGGCCTCGGTGACCT | - | 6.45 | | MYC | MA0147.3 | chr5:156753654-156753666 | GAGCACGTGGCC | - | 6.92 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH05I157327 | chr5 | 156754694 | 156756008 |
|
Enhancer Sequence | TGATGTGCTT CTCTTTTTGC TCCTTTAATC TTGTTCCAAA TTCCGGACTT TTCCAGTCTT 60
TTGCTATTAG CATGAAGTAG GAGTATCAGT GACTTGTTCT GGAGAGGAAT CTCTGTAACC 120
ATGGCCATCA GAAGGCCTGT GTAACCTCTG AGGGCAGAAG TACAAACTGA GACACCCAGC 180
TCAGGGCCTG CTGCCTTTCT CTTCCCACCC ACAAACTCTG TGCTGCACCA TGAAGGGCTT 240
CATGTGCATG TGTATAAATA CCCAAGCTCT GCCTGCCAAC TCTGCTCAAA AACAGTGGCC 300
CTTGGCTAGA CCTAAACCCT AGGGTCACAC ACACCCATAG TGGAGTCCAC CCTCAGAGGG 360
GAAGCCAGGG AAGAGAGCAC GTGGCCCTGG AAGAGGCTTG AGCCGCCTGT AGAAGGCTTC 420
TCAGAACTGG TTCTAGAAGG GGAGAATGGG GCCTGAGTGC ACACGCCCAC CTTGACCTTA 480
TGGATTCTTT GCCTGGAGGG AGGTCCGCTG ATGACCCTTG AAGCTCAAAG TGCAGGTCAG 540
AGGCCTCGGT GACCTGGGTC TGAGGAAAGC ACTAAACACA GCGCTGGGGT TTTGTGTTCT 600
GCATACCACG TAGGGTGTGA GATGAAAGAT CTGAAAGCTT TTTGAATCAT TAACCTTATG 660
GAGCCAAGAG TCTGGTGAAA AAAGGACCAA AGGTTAATCA CATAAATATT AAACATGAAA 720
GACTTAAAAT ATTAAATCTG ACAGTAAATA GGATCTGTTT CCTTTGACTC TTACCTAGCT 780
ACTGCCTTTG CCCCATCTCA TGGTCATGTC CTGCTCTTGC CATTTCTGAA ATATTTGGTT 840
TGATTCTTCA TGTCTGTGTG AATTATCTTC CCACCTGAGC ATCACAGTCT ATCACTGATG 900
ATGAGACCCT GAAATGGCAA GACTTTATTC ATTAAAAACC AAAGTTATGT AAGCAAAGTT 960
TGAAGGAAGG CGCTTTTAAA TGTGACTATC AACTTCATAA ACAAATTTGT GGCCACATGT 1020
GGTGGCTCAT GCCTGTAATC CTAGCACTTT GGGAGGCCAA GGTGGGTGGA TCACCTGAGG 1080
TCAGAAGTTC GAGACCAACC TGGCCAACAT GGTGAAACCC CGTCTCTACT AAAAATACAA 1140
AAATTAGCCA GGCATGGTGG TGGGTGCCTG TAATCCCAGC TACTTGGGAG GCTGAAGGAT 1200
GAGAATCACT TGAACCCGGG AGGCGGAGGT TGCAGTGAGC CGAGATCACA CCACTGCACT 1260
CCAGCCTAGG TGACAGAGCA AGACTCTGTC TCAAAAAAAA AAAAAATTGC AAATCAAAGA 1320
AAAATACAAT GAAAATAACA TCCATCTGAA GAGATGGATG GGGAGGCTGC CGAGTTAGCG 1380
GACGAATTTG AGCACTGATG GGTTCTGACA GTCTGTCTGT TGCATCCCTC CAGGCAGGCG 1440
GCCTCGAAAC AGCTGAGGAG AGGGGCCGTG GGGAGATTGG GTCCTTTTTG AACTTTGACT 1500
TGTCTGTTCA CTGACTGAGG ACCCTGAGAG CAAGGGACCA AATCTCCCAA ACTTAGCCAC 1560
AGAATATTTT TCCCCTTCAA AGCGTCTTTC CCCAGAATGC ACTCTGGGCA ATCCTGCCTG 1620
ACTGCTGTCT TTCAGTTGGC TCAGTTTCTG TCATAAAGCT GAACGGGCAC CAGTGATGTT 1680
TCCTGCTTCC TCTCCACCAG 1700
|
