| Tag | Content |
|---|
EnhancerAtlas ID | HS092-10424 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr11:111205730-111208050 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF1A | MA0046.2 | chr11:111205849-111205864 | AATCAATCATTAACT | + | 6.84 | | HNF1B | MA0153.2 | chr11:111205850-111205863 | ATCAATCATTAAC | - | 6.64 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_31835 | chr11:111204434-111208027 | Gastric |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I111333 | chr11 | 111204544 | 111208035 |
|
Enhancer Sequence | AAATCCGCAT CTGTGCTCCT CAGCAAAATA CGTTTTATGA CTAGTTAGAC CCTAAAATAA 60
AAGTCTTCTT TAGTCATCTG GGTTTGGGTT GGGAGGTGAT ATTCCTGTGG AACTTAATAA 120
ATCAATCATT AACTTTCTGC CAGTGGGCTA ACTTGTAAGT GGGAAAGTAG GGACTGGGAG 180
TGGGTAGAAG GCTGGATCAT CAGGCTTCCC GGTGTCTGAG GCTGCCGACA AAATCCAAGC 240
CTATCAGCCC AGAGATCAGT GGGGCCAGCC CAGAGGTCAG AGGGAGTCTA AGAGTCCCAG 300
GCCTCTAGCA AAAGACAGGC TTGAAGTGAA GTTACAAAGG GGCAAAGGTT ATCCTCAGCT 360
TCCAGCTGGT GCCTTTGGAC CTTTCAGTGA CATCCAGGAC CTGGGCCTCT TCGCTGTGCT 420
TTCCCTGAGA GCATTCCAGA TCCCTGAATA TTCAAGGGAA AACACAGTGA ATGGGTTTAG 480
GATGGTCAAG ACTCCTGTCC TCCCTTCCTC TAAAGGGGCA GGATTGGAAT AGGAGTTTCT 540
CCCTGGAGAT GCGGCGAGGA GTCCCTATAT CCTAGGCTGC CTTATTAACA GAGAGCTTCG 600
AGATCTTCTT CACAAAGAGG GCTTCTCATG GTAGAGAGCA CTCCAGCTAA GGAGGGGCAA 660
ATGTTCAGAA AGGTGATGAG CTTTGGCCCT TTTAACTCCC TCTGCAGGCA TAAGCCAAGG 720
TTTCTGCTGC ACCTGGCAAA GAAGTGAATC AGATCAGAAG CACAAATGCA CGGAACTGAG 780
TTTTCTGCCT GGACAGTGTC CTAAGACTCT CTGGCAAGAT CTCTGGTTTA ACGACTTCCT 840
GTACTTTCTT CATCATTTCG CCAGACAGCA GATCTCCTGA GGGCATGGGG ATCCCTATGT 900
AAGTGGAAAC CCTGATCACC CCCAGTGGAA TTCCAGAGTT TAGAAAGGTG GCGGCCACAT 960
CTCCCTAGAA CACAGTAGAC AGTTTTCTGT TCAGGGGAGA GCACATTGGC ATCAAATCCC 1020
GCAGGCTTCA TAGAGAAATC CCTAAGAAAG CAGGTTTTCC TCCTCATTGT CATCACAGCC 1080
ACCCATCATG CAAAACATCA GGTCCTAGGC TGAGTGCTTT GCATGCACGT TCCCATTTAA 1140
TCTTCATCAT AATCTCTTAA GGACCCATCT TATAAATGGG GAAACTGGGG CAGACGGGTA 1200
CCAAGCAACT TGTCCTTGGT CACAGATCTA CTAAGTGATA GAACCAGACT TTGAAGCTAG 1260
ATCTGTCTGA CCTCATAGGT CATGCTCACC ATAACCAGTC ACAGACTCCG AGCCAGAACG 1320
CTGAGGTTGC TATAGGAGGG AATAACTTAA TATCTGCTAA ATACTTTCAA CAGTGCTTAA 1380
CACATAGTAA GCCCTATATA AGTGCTTATT AAATAATTAG AGGCTTTGTA GGACAACAGA 1440
AGTTGACTTT GCACACCTGT GTGGCTGGGA TAAACCCTAT GAAAATGAAT ACAATGGGGC 1500
AAGACTGAAG AGCCCCTCAG CCCTTTGTGC CTTACTCCTG ACCTTACTCC TAACCCTATC 1560
TGTTGAGAAG GTGGTGATAG TCACCTCTAG CATAATTCTC ACCCCAACAT AGGAAGTTCT 1620
GTATGGACTT TTGCTGTCTG TCCCCTGGGC TGGAGGATCT GCAAGAGCTC CCAAGAGTGA 1680
TCTGCAAGGG CTCCCAGGAG TGGCCCAGCC AAACCCCTTA GTCTCAGAGG CTAACACAGC 1740
TGGAGCTCAT TTGCATTGGA ATTGCAGGGC ACTGCATCAT CCAGGAGATA AGTCTGCATT 1800
ATGCAAGTTA CTTGTGCCAA TTCTCCAGAA ATTACTGAGC CACAGGGGGA TTGCCTAACT 1860
GCTTAACCCT TTCCATCCAA CTATAGAGCA AAAATAGACA CCACTGGTCA ATGCAAAGAG 1920
TCTTCCCCAG ACGTGACAAC TTGATGAGCA GAGAATGACC ACTCAGGACT GGTGTGACCA 1980
GTGCACACCT CTCCCAGCAG GTTTGTTCTT GCCCCACAGG GTCTAAAACC CAGCCCCTCC 2040
CTATACACAC CTTCTAAAGG GGAGTGAGTT GCCTCCTGGG GATGCTCAAG GTTCACTGGA 2100
AGGGGAAGGA TTTCTTCAAC AGGCTTTGGG AGTTCAGAGT CATTTACTCT GGCCATATTG 2160
GGTTGGCGGG TAGCTCTCAG ATAAAGTGGT ATTTGAACTG GTCATTAGAT GTGAGTCAAT 2220
GAGGAGAAAA AGGGCATGTC AAAAACATAG GAGCAGAAGA TCACAGCTTA TCTTAGGAAC 2280
AGCAGATTGC AGAAGCGTAG ATTATAGCAT TGGACTAGGT 2320
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