| Tag | Content |
|---|
EnhancerAtlas ID | HS110-01078 |
Organism | Homo sapiens |
Tissue/cell | KATO3 |
Coordinate | chr12:130823450-130825570 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EGR1 | MA0162.3 | chr12:130823482-130823496 | GGTGCGGGGGCGGA | - | 6.01 | | EGR3 | MA0732.1 | chr12:130823482-130823497 | GGTGCGGGGGCGGAG | - | 6.5 | | RREB1 | MA0073.1 | chr12:130825162-130825182 | TTGGTGGTGGTGGTTGGGGG | - | 7.96 | | Stat4 | MA0518.1 | chr12:130824889-130824903 | CGATTTCCTGGAAG | - | 7.14 | | ZNF263 | MA0528.1 | chr12:130825177-130825198 | GGGGGAGGGGGGGTGGGGGGA | + | 7.28 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I130339 | chr12 | 130824295 | 130825122 |
|
Enhancer Sequence | CGGGGTGAGA GGCTGAGGCC TGAGTTGCCG GGGGTGCGGG GGCGGAGGTC TCCGCATTGG 60
CGGCCGTGCG TGAGACTGCG GGGACCTGAG AGCTCTGCAG GAGGGCCTTC GGGACCTCCC 120
GCACTACCCA CGCGGCCGCG GGGCGCGATC TCTGCGGAGG GCGAGGGCCC CTTCCCGCGT 180
CCGCCGCCGC TGCGCTGCGC CCCCGGGAGC CTTGGGAGCC GGACGTTGGG AAGAGGACGG 240
AACTCCGGAG GACCCCAAGT GAGGCGGCGA CCGCGACGGC CGGGCTCTGC GAGGCCCGGG 300
GGTCCTCGCG GGTGCTGGCG GCCCGGCCCT TGGCACCTGT GGAGGGAAAG GGGCGGCGGG 360
GCGGTGGCGT CCTGGGATGG ATGCTCTCGC CGTCTTCAGC CCCGGCGGCC TCCAGGGCAA 420
AGCCGGCTGC ACCCCTGCGC AGCCTGTTCT CTGAGCGCTT TTCTTTTCGT TTTTAAGTTG 480
TGGCCAGAGA GACCCCGCTC GCATAGAATG TACCGCTCAA CGGTTTTTAG GCGTGTGGCG 540
CGGTGGTGGT TCCCACGTGC ACGGCGTGGT CCTGAGCTCA GCGCCGGAGG GACGTTAGGT 600
GGAAGCGTCT TTGGCAGAGC TGGTAGCGAA TCGGAGAGGT GATTTCCAGC GAGTGTGGTT 660
ATTGGAAGCA CACACTTGCT TTCTGACTTT AAGAATTCAA TATCCAGACT GAGGTGGTTT 720
TGAAACTGGA AGGAGATAAA GCTGAAAACC AGAGTTGTGC TGGGAAACCT GGACGTAGAG 780
CGCTGAGCCC CCCAGGTATT TAGTGACCAG CACAGCGCGC CGCCGTGGGT TTCAGGCCCT 840
GGAGATGATG AGAATCAGCT GGAGGGCTGC TTCCAGTCGG CTTCTAACTC GGGAGGGCTG 900
AGAGCCGCTC CCCACCCCGT AATTTCTGTT CCCAGCCAGT CCAGATGCTG CCCGTCAGGG 960
ACCAGGCTTT GAGAACTGAC GTGCTGCTTT AGGAATATTT CCTGCTGGAG ATGAGAGTTC 1020
AGCTTGTCAC TGTTTTTTAA TCACTGTTTC ACACCGTTGT TTGTAAGGTG TCAAGCGACG 1080
GACTGGGTGC AAAGGCATCA ATTGTGATTC GCAGCCTAGT TGGAGAAGCT ATGGAGTGCA 1140
GAGATGTGGG GAGGGAGAAA ACAGGTTACC ATGTAGTAGG GTGACCGTGG TCACGCCGGG 1200
GAAACGGCTT TCGGAGAAGG GAGCAAGGGA TGGCCTGCGA GCTGGTCCTT AAGCGGTTCA 1260
CTGGATTCTT GTGGTTTCAG AGGAGGGTGA GGCTTTGTTA GCAGAGGGTG TGCCACGGTG 1320
TAGGGTGAGT CACGGAATTG ATAGTGATAG GAAGCAAGTT GTGTTTGCTG GAGTCTCAAG 1380
CGGATGCTTT CAGATTGATT TGTAGATCAG CAGTCCCCAG TCTTTTTGGC ACCAGGGACC 1440
GATTTCCTGG AAGACAATTT TTCCACGGAC CGGTGAGGGA TGGTTTCGGG ATGAAACGGT 1500
TCCACCTCGG ATTATCAGGC ATTAGATTCT CATAAGGAGC AGGCAGCCCA GACCCTTGGC 1560
ACGCCGACTT CACAGTAGGG TTCTCACTCC TAGGAGAATC TAATGCCTCC ACTGATCTAA 1620
CAGGAGGTGA GCTCAGGCTG TCCTGCTCAC TCACTGCGGC TCACTTCCTG CTGTGTGGCC 1680
TGGTTCCGGT ACAGGTCCAT GGGGCGTGGG GGTTGGTGGT GGTGGTTGGG GGAGGGGGGG 1740
TGGGGGGAGG GGGGTTGGTG GTGGTGGTGG TGGTGCTGCT GCTGCTGCTG GGGACGCTGC 1800
CTGTAGATTA TCAGTAAGAG ACTTTCATGC GCCAGTATGC CCCGTGTGTA AGCCGAGCAT 1860
GCATACGTAA TCATTGTCAT GATGCGCACA TTATAAAATA AATACAAAGC AGTTTAAAAT 1920
GAGATTTAAA ATTAGTTGTA ATATGCTGGC ACCTCAGCGG ATTATCCTGT GTAAACTCCT 1980
TTGGAAATTG CTGATTTAGA GTCATATTGT AAGGGGTCTT ATACAATGAA TATTTGCTTT 2040
AATCCTGTAA AATACAATAG GAAGTCGGAG GTTTTTAAAA TTGAAAAATG GCATTAGATT 2100
TATCTTTCTG TGAAGATCAT 2120
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