| Tag | Content |
|---|
EnhancerAtlas ID | HS050-17794 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr12:130822690-130825140 |
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 | chr12:130822731-130822746 | GATGCGGGGGCGGCG | - | 6.11 | | EGR3 | MA0732.1 | chr12:130823482-130823497 | GGTGCGGGGGCGGAG | - | 6.5 | | Stat4 | MA0518.1 | chr12:130824889-130824903 | CGATTTCCTGGAAG | - | 7.14 | | ZNF740 | MA0753.2 | chr12:130823336-130823349 | GTGGGGGGTGCGG | - | 6.21 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I130339 | chr12 | 130824295 | 130825122 |
|
Enhancer Sequence | GGTGCGGGGC CAGGCTGAGG TGCTAGGTGT GCGGGGGCCG GGATGCGGGG GCGGCGGCTG 60
GGGGTCCGGG ATGTGGAGGT GAGGCTCGAG GTGCGGGGAC CGGGTTGCGG GGGCGAGGTC 120
CCAGGTGCGG GGGATGCAGG AGCCGGGTGC GGGGTCGAGG TCCCAGGTGC GGGAGATGCA 180
GGAGCCGGGT GCGGGGGCGA GGTCCCAGGT GTGGGAGATG CAGGAGCCGG GTGCGGGGGC 240
GAGGTCCCAG GTGCAAGGGA TGCAGGAGCC GGGTGCGGGG GCGAGGTCCC AGGTGCGGGA 300
GATGCAGGAG CCGGGTGCGG GGGCGAGGTC CCAGGTGTGG GAGATGCAGG AGCCGGGTGC 360
GGGGGCGAGG TCCCAGGTGC GGGAGATGCA GAAGCCGGGT GCGGGGGCGA GGTCCCAGGT 420
GTGGGAGATG CAGGAGCCGG GTGCGGGGGC GAGGTCCCAG GTGCGGGGGA TGCAGGAGCC 480
GGGTGCGGGG GCGAGGTCCC AGGTGTGGGA GATGCAGGAG CCGGGTGCGG GGGCGAGGTC 540
CCAGGTGCGG GGGATGCAGG AGCCGGGTGC GGGGGCGAGG TCCCAGGTTT GGGAGATGCA 600
GGAGCCTGGG GTGCAGGGGC CGGGGTGCGG GGGCGATGTA TCAGGTGTGG GGGGTGCGGG 660
GCCGGGGGGA AGCGCTGAGG CCCGACTTGC CGGGGCTGTA GGGCCGGGGT GCGGGGGTGC 720
AGGGGCCGGG GTGCGGGGGC GAGGTCCCAG GTGCAGGGGC CGGGGTGAGA GGCTGAGGCC 780
TGAGTTGCCG GGGGTGCGGG GGCGGAGGTC TCCGCATTGG CGGCCGTGCG TGAGACTGCG 840
GGGACCTGAG AGCTCTGCAG GAGGGCCTTC GGGACCTCCC GCACTACCCA CGCGGCCGCG 900
GGGCGCGATC TCTGCGGAGG GCGAGGGCCC CTTCCCGCGT CCGCCGCCGC TGCGCTGCGC 960
CCCCGGGAGC CTTGGGAGCC GGACGTTGGG AAGAGGACGG AACTCCGGAG GACCCCAAGT 1020
GAGGCGGCGA CCGCGACGGC CGGGCTCTGC GAGGCCCGGG GGTCCTCGCG GGTGCTGGCG 1080
GCCCGGCCCT TGGCACCTGT GGAGGGAAAG GGGCGGCGGG GCGGTGGCGT CCTGGGATGG 1140
ATGCTCTCGC CGTCTTCAGC CCCGGCGGCC TCCAGGGCAA AGCCGGCTGC ACCCCTGCGC 1200
AGCCTGTTCT CTGAGCGCTT TTCTTTTCGT TTTTAAGTTG TGGCCAGAGA GACCCCGCTC 1260
GCATAGAATG TACCGCTCAA CGGTTTTTAG GCGTGTGGCG CGGTGGTGGT TCCCACGTGC 1320
ACGGCGTGGT CCTGAGCTCA GCGCCGGAGG GACGTTAGGT GGAAGCGTCT TTGGCAGAGC 1380
TGGTAGCGAA TCGGAGAGGT GATTTCCAGC GAGTGTGGTT ATTGGAAGCA CACACTTGCT 1440
TTCTGACTTT AAGAATTCAA TATCCAGACT GAGGTGGTTT TGAAACTGGA AGGAGATAAA 1500
GCTGAAAACC AGAGTTGTGC TGGGAAACCT GGACGTAGAG CGCTGAGCCC CCCAGGTATT 1560
TAGTGACCAG CACAGCGCGC CGCCGTGGGT TTCAGGCCCT GGAGATGATG AGAATCAGCT 1620
GGAGGGCTGC TTCCAGTCGG CTTCTAACTC GGGAGGGCTG AGAGCCGCTC CCCACCCCGT 1680
AATTTCTGTT CCCAGCCAGT CCAGATGCTG CCCGTCAGGG ACCAGGCTTT GAGAACTGAC 1740
GTGCTGCTTT AGGAATATTT CCTGCTGGAG ATGAGAGTTC AGCTTGTCAC TGTTTTTTAA 1800
TCACTGTTTC ACACCGTTGT TTGTAAGGTG TCAAGCGACG GACTGGGTGC AAAGGCATCA 1860
ATTGTGATTC GCAGCCTAGT TGGAGAAGCT ATGGAGTGCA GAGATGTGGG GAGGGAGAAA 1920
ACAGGTTACC ATGTAGTAGG GTGACCGTGG TCACGCCGGG GAAACGGCTT TCGGAGAAGG 1980
GAGCAAGGGA TGGCCTGCGA GCTGGTCCTT AAGCGGTTCA CTGGATTCTT GTGGTTTCAG 2040
AGGAGGGTGA GGCTTTGTTA GCAGAGGGTG TGCCACGGTG TAGGGTGAGT CACGGAATTG 2100
ATAGTGATAG GAAGCAAGTT GTGTTTGCTG GAGTCTCAAG CGGATGCTTT CAGATTGATT 2160
TGTAGATCAG CAGTCCCCAG TCTTTTTGGC ACCAGGGACC GATTTCCTGG AAGACAATTT 2220
TTCCACGGAC CGGTGAGGGA TGGTTTCGGG ATGAAACGGT TCCACCTCGG ATTATCAGGC 2280
ATTAGATTCT CATAAGGAGC AGGCAGCCCA GACCCTTGGC ACGCCGACTT CACAGTAGGG 2340
TTCTCACTCC TAGGAGAATC TAATGCCTCC ACTGATCTAA CAGGAGGTGA GCTCAGGCTG 2400
TCCTGCTCAC TCACTGCGGC TCACTTCCTG CTGTGTGGCC TGGTTCCGGT 2450
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