| Tag | Content |
|---|
EnhancerAtlas ID | HS050-49999 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr3:194084710-194086960 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr3:194086108-194086128 | TGTTGGTTGGTGGGTTGGGA | - | 6.56 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_63431 | chr3:194084376-194118088 | NCI-H69 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH03I194364 | chr3 | 194084977 | 194086825 |
|
Enhancer Sequence | AGGTCAAGCG GGTGCAGAAG TTATAGAGTA GCAGATTTCA GTTCACACTG AAAATGGGCA 60
ACCTCACAGA GGGAGTAAGC TCACTGTCAC TGGAAGCAAT CAAGCAGAGG CTAAAGCAAT 120
CACTTGGCAA GCAAGCTGTA GAGAAGACTC CCATGCCTGG TAGGGTATTG GACTGGAAGA 180
CAACTGGTGT CCTGTCCATT CCTAAGACCT TAGGATTCTA AGGCTGAGTT TCAGGGCATG 240
AGAAAACAAT CTGTCCACCA AGACAACGGT GCCTGTACTC TTAGGGGTCT GCGTGGACAG 300
TGTGGGTATT TGCCCATCTC TTTGGTGTAA GTGTACGTGA GATATTTACT GCCTGGGCTG 360
ACGTGCAAAA GGTGGAGCTT GAATTGCTCC TGGAGACAAG CTGGCTGGCA CTTATATTTA 420
ATGTACACTC ATATACCCAG CATGCTTCAA AACGGTGTCA CAGCCCAAGT GTCAGAGACT 480
AAATTAAGTG CATGTCACCT GGCCAGCCCA GGGCAATCTT GAGTTTCCCC ATCTATGAAG 540
GACAGTGTAG GATGAGGCAC CCTCTGAGGA CCCATCTTTA TGTGGCTTTC TAGGAGTCTG 600
CACTCCCCAG CTGGGGAGGG GCATCAAGCC AGCCCAGGAA GGGCTTGTGC CAGGGAAGGT 660
GCCCCTTGAC CTGAGAGGAC TGCACAGATA ATTCCCTATG GGAACAGGGC CACCACTGTC 720
TAAAATGGGC CACACTCAGC ATGACAAATA TTGCAAGAAT TTGCAGATTT TCCTCTGTAT 780
AAATCCTCAC ATCTGCAAAG CCCATCCCAG CACCACATGC AGCAGTTTCC TGTTTTCCAG 840
CACTTTCCAC TGCTGTGGCT GGCGGCCAGG GCTCCACAGG GCCTCCAAAG TGCTCCCCTG 900
AAACCCGGCT GCAAAGCCCG CAGGGGAGGG AGGGGCCACA GAACCAGGAC TGACAGCTGG 960
GCCCTTGGAT TCTCAGCATG TGATGCCAGC TCCTGCAGTG GCCACAGCCT CTAGGAGCCC 1020
AGCACCTGGA GGCCTAATAG CCCACGCTGC CTGGTGCTGC TTGGCAGCTC TGACAGATGG 1080
CAGTTAAAGG GCCACAAAGC TGCCCTAATT ATAACTTCTC CCCCAGGCAG CCGAGAGCGT 1140
CGTCAATCAC TTCAGTGACT CAGTCCAGCC CCTGTCCAGC TCCTGGGAAG GGGGAATAGC 1200
CTGGTGTCTA TCACTGGCCC ATGAAGTCAG CAAGCCGAGC AGACAAACCG AAGGACAGCC 1260
TGACAGCTCT CCTGGGCGCT CTGATGCATT CCCTCCCCGT GAGCAGAAGT GCACGAACCA 1320
GGGCTCTCGG CTTTGGGTCT CAGCAGAAGC ACCGTGACTC ACGAGCAAAC GCGTAATTAG 1380
CCTCGAAGCC CTGGGCTTTG TTGGTTGGTG GGTTGGGACG TTTTTGGTTT AATACCATCG 1440
TTCACATTCC CTGAACACGA GGTTTCCTGG AAGGAGACTC CTCCTTATTT TAATGACACA 1500
GAGCATAACT TTTGGAGGGA GGCTGGAAGA CCAGCGTTCT ACTCTGGTTG ACACTAAGTT 1560
GAAGTGTGAG CTTAGGGAAA TTCTCCAGGC CTCAGTTTCC CCTTCAGTAA AGACGTCCAA 1620
GGGCCCTTGG AGCTCTGCTA TCTTCTGATG TGAGGCAGGA AGGAAATTTG GCCTGAAGCC 1680
CCTCATTCTC CTCATCTTCT CTTCCCCAGA GGACCTGCTG GACCTCCAGC AGGGCCGCCC 1740
GGCCCGGCTC CAGCTTCATG CTGAGGCCTG AGGAACTCAT GCCCATCTTT TCAGGCCCAC 1800
CTGCCTCCAA GTTTCCCAGC CAGGGCAATC CCACTTAGTA ATCAGCATGT CCGCACACAG 1860
CCAATAGCCG TTCCATGGAA CCCAGGGACT GGGAGGGGCC TCTGGGAGCT TCTGGTCCTG 1920
CCCACTCCCA GTGCACCTGG GGAAACTGAG ACCCAGAGAG GGGCTGTCTC TCCCTGGCTT 1980
CTCCCTTCTC CCCACAGAGG GCTGCCCAGT CATGGCCTTG TCTGCAGAGA GATGTCACCC 2040
AACAAGCCTG AGGGCTCCCG AGGAAGATGT CAGGCTTGGA GCAGCCAGGG TCTGTCCCCA 2100
CTGCCCACAG CTGGTGCTGA CCTCAATCAC GCGCTCATGG GGGCTCAGGC CAGTGGGTCT 2160
GCCTGAGAGG CTTGGCCTGA AGCTCGGGCC TCCGTGCCTC CAGACCTCCC CATCTCACCA 2220
AACATCCCCT CTCCTGGGGC AGCACATAAA 2250
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