| Tag | Content |
|---|
EnhancerAtlas ID | HS118-02947 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr10:119173320-119174570 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Crx | MA0467.1 | chr10:119173708-119173719 | AAGAGGATTAG | + | 6.62 | | mix-a | MA0621.1 | chr10:119173419-119173430 | AATTAATTAGT | + | 6.62 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH10I117414 | chr10 | 119173581 | 119173650 |
|
Enhancer Sequence | TTGGAGGTTG CAGTGAGCAG AGATCGTGCC ACCGCACTCC AGCCTGGCGA CAGAGTGAGA 60
CTCCGTCTCA AAAACAAAAT ACAAACAAAA AAAAATTTGA ATTAATTAGT ATCATTTGAA 120
AAGCAGGAGG TTGGATATAA ACATCTAGAT TTTTCATTTC TCATGGAAAT TTGGAGATTT 180
GGCCACATCA TGTATCTTTC CTCATTTATC TCCTGTCTGG GCTCTGGAAA CTTGCCAGGC 240
TTTGACTCTT GGATGACTGT ATGGGGCACA GTTCCTGCTC CTTCCTTGCC CTGGAATCTT 300
TCTCAATCAA TGTTTGTTTT AAAGAATCAC AAAGCTGGAA CGTCCCTACA GGTTCTCTGG 360
GTTCAAACCC TCATTTGTCA GTGGAGGAAA GAGGATTAGG GAGGAGGAGG TGACTTACCC 420
TATGTCATGT GGATCACCAG TGATGTGGGT GGGAAAAGAG CCCAGGTCTT CTTCCTCCTG 480
GTTTAGTGCC CCTGTTCAGC CCTTGGGGAC AAGTGGCCAT CATCCTCCTC CTAAAAATTG 540
AGACCTTCTT AAGAGATGTG TTTGATTCAC CTCAAAGGTC ATCAGCCCTT ACTTTTCTTT 600
CCTGTCTCAG CCAAGGCAAA TGTTTACCTT GCAAAAGTGG AATTAGATCC AGAGTGGTTC 660
CTCTTGGCTT ACATGGTATT TAAATGTCTC TGTCTTTGTC CTCTGTGACT TTTCCTCATG 720
GCCTTGCTGT GGTTGCAGCT GTTTTAAGAG ATGCCTGCAC AAAGTCATTC ACCTAAGTGG 780
GAGTTCAAAA AGGACACTTA TTTTCAATGT TGGCTGGTTA CTTTTTTAAA GCCTTTTACC 840
GCAAGGTAGA GGAAAAACAG CTTGGGGTGC ATTTTTTGTC AAGCATGGTC ACAGATAATA 900
CCAGTATTAA CAGTTTGACA TATGTGTAAT CCCCTGACTG TCCCAGAGAA AAGGTGCGGG 960
GTAGCAGCCA TGAGCCATTT GCAGAGGGGG ATGCCACACT GCACTGGGCA CTGGGCCAGG 1020
ATTAGCCGAT ATTTTCAATT GTTTTAATTT TTTAAAATTT ATTTTGCATT AGAAAATAGC 1080
CAAGCATAGG CTGGGCGCGA TGGCTCACGC CTGTAATCCC AGCACTTTGG GAGGCCAGGG 1140
CGGGTGGATT ACCTGAGGTC AGGAGTTCGA GACTAGCTTG ACCAACATAA AGAAACTCCT 1200
TTTCTACTAA AAATACAAAA TTAGCCAGGC ATGACGGCAC ATGCCTGTAA 1250
|
