| Tag | Content |
|---|
EnhancerAtlas ID | HS105-20616 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr12:115199500-115201890 |
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 | chr12:115201332-115201353 | TTTTACTTTTTTTTTTTTTTT | + | 6.16 | | Nr2f6(var.2) | MA0728.1 | chr12:115201563-115201578 | TGAACTCCTGACCTC | - | 6.22 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I114761 | chr12 | 115199493 | 115201286 |
|
Enhancer Sequence | GCTGGGATTA CAGGCATCCG CCCCCATGCC TGGCTAATTT TTGTATTTTA GTAGAGACAG 60
GGTTTCACCA CGTTAGCCAG GCTGTTCTCG AACTCCTGGG CTCAGGTGAT CCACCTGCCT 120
CGGCCTCCCA AAGTGCTCCC AAAGGCGTGA GCCACTGTAG CTGGTCCCCA TTTATTTTCA 180
AGAAGGAATG AGAGTGGCTC ATTGATTGAA TCAACACATA TTTCATGTGG GGCTGGGATT 240
ACGGATGGTG GCTCACATTT GTAATCCCAG CACTTTGGGA GGCTGAGGAG GATGAATTCC 300
TTGGCCCCAG GAGTTCAAGA CCAGCCTGGG CAACATAGTG AGACCCCAAT TCTACAAAAA 360
CTTTAAAAAA TTAGCCAGGC GTGGCGTCAC AGGCCTGTGG TCCTAGCCAC TAGGGAGGCT 420
GAGGTGGGAG GATTGCTTGA GCCTGGGAGG TCAAGACTGC AGTGAGCCAT GATCGTGCCA 480
CTCCACTCCA GCCTGGGTAA CAGAGCAAGA CTCTGTCAAA AAAAAAAAAA AAAAAATTCA 540
TTTGGAGGAT GCTTCTATAA GCCCACTGCA GTGCTAGGTC AGTAGTTCTC AACTAGGGGT 600
GATGTCCCCA GGTGACATTG TGCAATATCT AGAGACAATT TTGGTTGACA CAACTTGGGG 660
TGCATCTAGT TTGTAGAGGT CAAAGATACT GTTAAATATA TTGCAATGCA CAGGCCGGCT 720
CCTATAACAA AGAATTACCC AGTTGGAAAT ATCAAGAGTG CTGAGGTGGA GAAACCCTGA 780
GTTTAGGCCC AAGTGTTATA CGACAAGGCC CAAGCGTTAT ACGACAAGAC AGAACAAGAC 840
AGACGTGGTC ATTGCGCTGG CTGGGTTTCC TTGAACTTGG CCGGCTTAAC TATTTCTTTA 900
AATAGCTGGA TGTGGAGAGA GGCCCCTTTA AGGACAGTGT TGGTGTTTCT TTTCTCCTCT 960
AGCGTGTGTC TCTGGGGCCT GCTGTGTGGC CGGGTGTTGG CTGGTGAGTA TGTATGTGCG 1020
TGCGTGTGTG TGTGCGTGCG TGTGTGTGTG TGCGCGTGCG TGTGTGCGTG CGTGTGTATG 1080
TGTGTGTTCA GAGCTGTGGG GGGTGTCTGT TTGGACTTGT GCGGTTGTCT GTTTATGTCT 1140
GTGTACATCG GTGTGGCTCT GTAAGAACTT TTCTGTCATT TCCTTCCCCT GCTTGCCAGA 1200
GAGGCAGATG TGGCTTGCAA CGTCCTTCTA AGGTCAAATT CATCACCAGA CGAGATTAAG 1260
AAACCATTAG GGAAAGACCC TCCTTTGCTC CCTTCCATCT TCCCATCCAA TCCCAATACC 1320
CTTCCACCCT CCCTGCCCCC ACCTCGGGGA TAAAACTAGA GGTCAGTAAA CTTGCCTCTG 1380
AGCTGAAGCT TTGAACTTGA AGTTCAGGCT AACTCCACTG TGCCTGCCTA GGCATCCAGG 1440
AAGTATTAAA AATGGTGTTT CAGAGGAATC AAAGCACAGC CAGGACAATG ATGGATCCAA 1500
ACTGGAATTT TTTATCTCTG CATTATTAAA ATTTGGGGCT GGGTAATTTG TGTGTGGCGG 1560
GGGGCGGCGG GGAGGGAGGC TGTCCTGGGC CTTGTAAGAT GTTGTGCAGC ATTTTTGGTC 1620
TGCATCCACT AGATGCACCC CCAGTTGTGA CAACCAAAAA TGTCTCCAGA CGTTGTCTAA 1680
CATCCCCTGA CGCACACAAT GAATCCCAGT TGAAAAGTCA TCGATCTACA AATACATAGA 1740
GCAATGTGGT GAATCTCACG TGCTTAATTT TTTTTTTTCA GTATTGATGA GATACTTTTG 1800
GTAATAACGA GATACTACTG AATCAGCCCA TTTTTTACTT TTTTTTTTTT TTTTTTTTTT 1860
TTGAGGCAGT CTAGCTCTGT CACCCAGGCT GGAGTACAGT GGGGCAATCT CGACTCACAG 1920
CAACCTCTGC CTCCCGGGTT CAAGCAATTC TTCTACCTCA GCCTCCCAAG TAGCTGGGAT 1980
TACAGGTGCC TGCCACCATA CCCGGCTAAT TTTTTTATAT TTTTAGTCGA GATGGGGTTT 2040
CACCATGTTG GCTGGGCTGG TCTTGAACTC CTGACCTCAG GTGATCCACC CACCTCAGCC 2100
TCCCAAAGTG CTGGGATTAC AGGTGTGAGC CACCATGCCG GGCCTCACAC ACTTAATTTT 2160
GAAGGAAAGA AGCCAGCTAC TCAAGTGTGA TGTTGTGTGG TTCTGTTGAT GAAAAGCACA 2220
AAAATATGCA GAGCTAATCG ATTCTGTTAG ATGTCAGGAG AGTGGTTGCT TTATCCTAGT 2280
GCATATTGAC TGGAAGGAGA CACTGTGGGG ACTTCTGGGG ATGTCTGTTT CTTTTTAATC 2340
TGAATGCTAG GTATGCATAT GTTATGTGTG TAGTTTTCTG TGTATGTTGC 2390
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