| Tag | Content |
|---|
EnhancerAtlas ID | HS055-03203 |
Organism | Homo sapiens |
Tissue/cell | FT33 |
Coordinate | chr16:75766670-75768730 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr16:75767761-75767782 | GCTTCCTTTCCTTTTCACTTT | + | 6.02 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH16I075732 | chr16 | 75766748 | 75768421 |
|
Enhancer Sequence | AAAAATACCT TTACCATTTC TTTTTTTCTT GTGTGTTCAC CTCTTACTTA AGCTCCTTAG 60
GGATGCAATG ATAACCTTTA CCTTCTCTCC ACCAGGCACT TCCTGCATGG CAAGTTTATC 120
TTACTAAATG TTTGCTTAGA AATTCTAATG ACCAAATGTT GAACCAAACC AGGCACCCTC 180
TGGAACTCCT CCCGACCAGG AGAATGCATA GAGACAATGG TCAGTTTACA ACCTAGTTCT 240
GGCCAGATGG TGCCAGGCAG ACCATCCCCT AGCTAAGAAT AGAAGCCAGT CACATAGACC 300
CTGCACCTCC TCGTGCCCCT CCCCTGCATG CCATTCATGA CATGCCCCCC TTTAAAGCCC 360
CTGCTTTTTG CCCCAAAAGA TGAAGTGGTT TCCTTAAGGG AGGAGCCTGT ACTGTTTCCC 420
CTCAGCTAAG CTCTGGAATA GAAGTCACTT TCTTTTACCA CCTCATGCTT GTTATCTAAA 480
TTTACAAGAA GCTGAACCTG CATTCAGTTA CAATTTTGGT GGCCCATACA GGGACTGTTG 540
TGTGTTCCAG GGGCCTGAGC TTGCTGGTCT GGTTTCTACT GGAGAGGGCA TATGGCTGCC 600
TGTGAACACC AGCTGCTTAT GGCTAGCTGA CCCCATGGCT GGAACATTAG GAATTTCTCT 660
GAAGCTGCCA AGATGCTTTT GTTTTTGGGA AACTGTCTTT CACTTCCTGG CATGATGCCT 720
GCGGCTTTCA AAGCTTCGTT GGTACAAAGA AAATGAACTC TGAAGAAGGC AAACTTTGGA 780
ACTGGGTGAG CAAGTTGGAG TGTACCTGAC CACCCCCTGC CTCTTTTGGA GTGTTGCTGT 840
GGCTCTGTTC TATTTAGATT TGGCTGCCAG AAACAACATT TGAGCTTTTT CTGCATTTGT 900
GTTTGTATGT GAATCACCCT TGAGGCATGG CTTGGTTTGG ACTCGGTCAT CTGGAAGAGC 960
TATTTGGAAC TGAGGCAGGA GATTTAGGAC TAAACCCAGC CTCTTAACTG GGGATCTGTT 1020
TGGAAGCACT CCATTTGTTC ATGCCTTTGT GTATACTCCA TTTGTATGAC CTTTGTGTAT 1080
AGGCCCTAAT TGCTTCCTTT CCTTTTCACT TTATCTTCCT GATTATCTCA GAGAGCCACC 1140
TACAGCCTTA ATCTTCTTGG CCAAAGGCAC CCTTAGCTCT GTTTACCTTG ACCAGTGATT 1200
TACGGAGGTG GGAGGGATTC ATCCCACACC GTGCAGGTCT AGGATACTGT GGCTCTTCCT 1260
GATGGGAGAT AAATGGGAGT GGTGAAGGTA CCGCCCACAC ACCACTTAGT GGCTTTAAGG 1320
CTCATAAATC TCCTTTTCTT TCTTTCTCTT CTTTTCCCTT CCTTTAAAGC CTGGCTCCTT 1380
TGCTGAGGCC TGCCAGGAAC TTCATACTCT CATCCTCTTT GGGATTCCAG CTAGTTACAT 1440
ATTATGACCC ATTTTTAATG CATGTTTTAA ACGGATGGGC AAATTATAGC AAGAAAAATT 1500
CAGAGCTCAA ATGGTTAGCC CGTAACTAAC TGCAGAGTTA AACAGAGTCT TCTAAAGCTC 1560
TCTATCTTCC TCTCTTTTCT TTACTGTCTG CTTTGAATCT GCTGTTACTG AGTTGCTGGT 1620
GCTGAGATAA GACTCATTAT TTGTGCTCTA AATGGAATGT AAACATTGGA AATTTGTTTG 1680
AAACGGAAAG AAAAATAAAA GAATAAAAGA GACTTTAAAA AAAACAAACT GCCATAGAGA 1740
CTGCTTTACT CAAATTTTGT TTTATTTATT TATTTATTTT TTGAGACAGG GTATCACTTC 1800
ATTGCCCGGG CTAGAGTGCA GTGGCATGGC CATAGCTCAC TCCAGCCTCC ATCTCCTGGG 1860
CTCAAGCAGT CCTTCTGCCT CAACCTTCCA AGTAGCTAGG ACTACAGATG TGTGCCACCA 1920
TGCTCAGATA GTTTTAAAAA ATTGTTCGTA GAGATGGGGT TCTTGCTACG TTGCTCAGGC 1980
CAGTCTTGAA CTCCTATCTC AAGTAATCCT CCTGCCTTGG CCTTACCCAA ATTTTGGTTC 2040
ACAGTTTTCT TTTTTCTTTT 2060
|
