| Tag | Content |
|---|
EnhancerAtlas ID | HS050-17272 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr12:115888580-115891220 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| INSM1 | MA0155.1 | chr12:115890854-115890866 | TGCCTGGGGGCA | + | 6.04 | | Sox6 | MA0515.1 | chr12:115889467-115889477 | AAAACAATGG | - | 6.02 | | ZNF263 | MA0528.1 | chr12:115890054-115890075 | CCCTTCCTCTCCCTCTCCCTC | - | 6.3 | | ZNF263 | MA0528.1 | chr12:115890022-115890043 | TCCCCTCCCCTCCCCTCCCCT | - | 6.91 | | ZNF263 | MA0528.1 | chr12:115890027-115890048 | TCCCCTCCCCTCCCCTCCCCT | - | 6.91 | | ZNF263 | MA0528.1 | chr12:115890032-115890053 | TCCCCTCCCCTCCCCTCCCCT | - | 6.91 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I115451 | chr12 | 115889005 | 115891497 |
|
Enhancer Sequence | GCAAAGATCG GCCATCAGAG CAGTCCCAAA CCAGGCAGGA GAGGCTGGGC TCTAGCACCT 60
CTGCCATGCC CAATCATTGG TTGGCGGCAG CTGGGAGAGC GGGTCCTGGC TGTGCATGCT 120
TGGGTGGATC TTAAGTTGGG TCATCTGGAG GCTCTCAGCT TGCAGGACTT CACACACGGA 180
GGTCTGAAAA ATCCCAGCTC CAGGGCTGCA GCACCCAGAT AATCCCCACA ACGCCCCTAG 240
GCACCACTGC TGCTATTGCC AAGCTGCGCC TTAGGGGAAG TGACATGACC TGGTCCAAAG 300
CTACAGAGCT CTTAGAGATG GAACCAGATA TCAATACCAA ATCAGGCGTG TAGCCACCCT 360
GCCCTTGGAT CCTCGGCAAC CCTCGGGGAA AGACAGGTTA TTAGAGTCTT GGGTTGATGG 420
CCCAAGGCCC ATTTTTCTGA GAAGGAATAT GGGACCCTGA GCCAGGAGTT GACTTGGCCA 480
TTCCCGAGGG AGGCCAGCAG GCACACCCAG GACTCCTGGC CTCCTGCAGC CGAGAGGAAG 540
GAGACTCCGA GGCACCGATC CTTGGGGTTA GCAGGAGGTG GATGTCCACC AGCTCCTTTG 600
TCAACCCTTC CCCAGCCCCA CTAATGATGA TAACACCAGC CTGGTCCTAC AGAACAGCTT 660
CTATGTGTTG GGGACTGTTG AACCACTTAT ATCTTTGCCT GTCTTTAACC TCCCGGCATC 720
CCTGTGACGC AGACACCTTT ATTCTTCCCG TTTCCCAGGG GAGAAGATAG AGATGCAGAG 780
AGGCAAGACA CTAGCCCAAG GCCACAGTTA GAAAAAGGCA AAGTTCAGAT GCAAAGCCAG 840
GTAGGCCCTG CTATTCAAGG CTCTGCTAAC TTCAGCCAAG CAAGTAAAAA ACAATGGATG 900
TCCTGTGAAC AGTGGCATCT TTGGAAAACG TCGCTGTTTT TATTAATCTC TCTCAAGATA 960
GATGTTGCTC AAACACAGCA GCGTCGTGAC AGTGCCAATA GCCAGCAGTC TCCTGTCCGC 1020
GTGGGTTGCG AGCCCCGGGC GTGGACGGAG TTGGGAGCGG AGGGCGGCAG GTGCCAGCGG 1080
GGCCCGCCTC TCCCTGCAGG CGGCCCCGGC AAGTTCACGG CCGGCCCGGG GCGAGGGGCG 1140
AGCGGCGCGC GGCCGTGCGG CTCATTCTAC CGCCCTGCGT GCGAAGGGGA GGCCGCGCCC 1200
CCGCGCCCCT CGCTCGCGCC GTGCCTGCCG CCGCCACCCG CCCGGCCGCC GGGCCGGCCA 1260
CTGAGCGGCC GCTGCAGACT CGGCGGCGCC GGCGCACCTG CAATCAGGCC CCGCGCCGCG 1320
CCGCCTCCTC GAGCCCAAGG CCGCCGCGCG CCGCGCTCGC CGCTGATAAG AGGCGGCGGG 1380
GGAGGGGCGC AGGATGCTGG CGTTGCGGAA GGGCGGGGGA TGGGTGGGCA GCTGGAGCGG 1440
GCTCCCCTCC CCTCCCCTCC CCTCCCCTCC CCTGCCCTTC CTCTCCCTCT CCCTCTGCGA 1500
TGTCTCTCCC GAAAGTGTGT GACTTGCCCA TGTCTGTCTC TTGTCTGCGC CTCTCCCCTA 1560
AATTCCCTCC CTCCCCAGCC CTCGCCGCGA GCGTGTGTGC GCGCGTGTTC GTGTGTGTGT 1620
GCGTGTGCAT GTGTGTCTGT GTCTCCAGTT GCTCCCTGTC TCCTGTACCT GTCTCTGTGC 1680
ACTTCCTGAC CTTTCTGTCT CCTACTCCCC ACCTCTCTGA TTCTCTCCAC CTCCTGCTGA 1740
TTCTGTCGCT CTCTTCTCTC TTAGCATCCC CTCTTAGTTT CTCCCTCTCT CCCTGTTCTA 1800
TTTCTCTCTT CCTCACCTAA CTTGGAGCCA GTCCCTCCCC TCTCCCTGTG TCTGTCTTCT 1860
CTCCCTCTCT CCATCTTTCT GACTCTGACC TGCCTCTCCC CTTCTCTCTC CCTTCCCTGT 1920
CTCTCCGAGT CCTTGCCTGT CCTCCTCTCT CTGCATCTTT TCTTTCTGCG TCCCCAACTC 1980
CCTCTCACTT CTCCGTTCTT TCACTCATTT GTCTGTATCT TCCCTTTTCT TTTCTCGCCC 2040
TGGGCTCCTC CCCATAACTC TGCGTGTCCC CTGCCCATCT CAGCATCCTG TGGCACTTTC 2100
TGCATGGCCG GCCCGCCTGC AGGGACAAGG CCTTCAGAGC CAGCGGTTGC AGGAATAGCT 2160
GGACCCCACA AGGGGCTAGG CTCAGCAGGT GTCCTGACTT CAGGGGGCAG GACTGTGCTC 2220
ACCTGTGCCT TTCATGTAAG GCTCTGGCGC ACTTCACAAA CAGTCATTAA GGCCTGCCTG 2280
GGGGCAGGTC AGGGAATATC ACAGCCTGGG CTGTTTGGTT ATCTTCATTA TTAATACACA 2340
CTCCCCTGCC TTAAATGAGT TTAGTGCAGG GGACAGAATC CCGACTGACG CCTGGAGAGA 2400
TTAAGGTTTC CGAGGGTTGC ACAGGCCAAA GATGACAAAC TGATACAGCA GGGATGTGAG 2460
TTTCTGCTGC TTCCTTCCTG CAGTGCAAGC CTCTGCCAGG AGCTTATAAA CCACCCTTTC 2520
TGAGACGGCT CTGGGGGTCA AGAGATGGGG CTAGATTTAT CTGAATGGGT CCTGGCCTGG 2580
TGGTCTGCTT TGCACCAAAC ATGCAAGCAG GGATCTCAGT GGAACCAGCC CCTTTTGCAC 2640
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