| Tag | Content |
|---|
EnhancerAtlas ID | HS050-24596 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr15:102067640-102070200 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MSC | MA0665.1 | chr15:102068653-102068663 | AACAGCTGTT | + | 6.02 | | MSC | MA0665.1 | chr15:102068653-102068663 | AACAGCTGTT | - | 6.02 | | MYF6 | MA0667.1 | chr15:102068653-102068663 | AACAGCTGTT | + | 6.02 | | MYF6 | MA0667.1 | chr15:102068653-102068663 | AACAGCTGTT | - | 6.02 | | Nr5a2 | MA0505.1 | chr15:102067700-102067715 | GCTGGCCTTGAACTC | - | 8.25 | | Zfx | MA0146.2 | chr15:102070128-102070142 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH15I101527 | chr15 | 102067697 | 102069556 |
|
Enhancer Sequence | CACCATGCCC AGCTAATTTT TGTATTTTTA GTAGAGACAG GGTTTTGCCA TGTTGCCCAG 60
GCTGGCCTTG AACTCCTGAG CACAAGCGAT CCGCCCACCT CAGCCTCACA AAGTGCTGGG 120
ATTACAGGCA TGAGCCACCG TGCCCAGCCA AAGTTGTGGT TTTAAGCAGG ATGTTCCAAA 180
GTCCAGTGGT TATGACCAAA CGCCACACAG AGACAGAAGC CTCCCGCACA GCCCCAACTC 240
CCAGCAGCCA TGGTGTTCCA GGTCCTCCAA AGTCAGCTTC TCCTCCAGGA GGCCACTGAG 300
CTCCCCAGCT GCGGGGCTGA GGCCACACAG CCCTGTGCGG TTCATCTGCC ATCCGGGCCC 360
TTCTTCCTCT TCTGAGCTTC ACAGTTAGCC CAGGGAAGAA AACAGGCGTG TCTTCCACAA 420
ACCCTGAAGG GAATGGGAAG TGCCAACAGT GAGAAGGACT TAGATGTAAA GGATTTACAC 480
ACGGTCACGG CATTTCCACA ACCCTCTGGG CACCTGAGTA CACGTGTGCA GACACACCCC 540
CAGATGGGGG CGAGGGGTGG GGTGCCCCAG CTATTCACAC CTAACCATGA GCGTGTGAGG 600
CAGCAACACT TAAAGGCCAC TTGCTTTCCG CAGCATCTCG ATGGAGCAGG AGCCTGCCTG 660
GGGCATCTCC AGGCAGCTTG GCTGAGCACC CAGGACTGAG TGCAACCCTC AGCGTTTACA 720
TTTTTTAGTA CTATTCACTA AGAGAGAGAG AGACAGAGAG ACAGTGATAG AGACAGGGAA 780
GGACAGAGAC AAAGAGAGCA ATGGGTGAAG AAAGAGCAAG CAAGCAGGGA TGTCGGACAT 840
TTCACACAAC GCAGTCACCA GGGAGGCAAG AACACTTACA GAACAGTTTG AGCCAAAGAG 900
TCACTCAGGG ACAGGAACAG CAATTTCTTA AATATTTAAA GCAGACACCC TGTGAGCGGC 960
TGTGGAGGCG GCTCTTTGTT AATATTTAAC ACGAGCTGGG CAGTTGCCGG GAAAACAGCT 1020
GTTTACAGGA GAGATTAACC AATATTCATC ATTGCTCAAA GCTGTGGGGA GGCTTCAGGG 1080
GACAGGCAGC TGCCGGTATT TCTAGAATAC AGCAGCTCAA GGCCACAGGG CTGGGGAGGC 1140
TCACGGTGTC CCCAGGGTGC ATGAAAACTG TAAACAGGCA GTTCGGGGTC ACCTACCCTG 1200
CTCCAGAATC ACGGTTTGCA GGAAACCCAG CCCTGCAGCT GGGCCTGGGT GGTGGCTGCT 1260
GGCCGGCCAG CCAGCACCTC GCTGGACAGC TGCGTCCCAC AGTCCCAGGC TGGGCTGTCC 1320
TTCAGGCCCA TCCACAGTCC CAGGCAGACT CCTCGTGCAC TCCCTGCATG AAGTCGGGGG 1380
CAGGTGCTCG AAAGTAGAGG GGTTCCCACT GATGGAAAGT GTCACCAGCC TGCCTGCGAA 1440
TCCCCCAGCT CACACTTGGG CTTGCAGGGA CACCAGCCAG GCCGTCTTGC AGAGAAGACA 1500
AGCTGCCTAT TTTCAGGGGC TATGAGTCTT GTTCATGACA GTTTTCTCCT CTATGTGCCA 1560
AACATTCAAG AGCCTGGCCA TTTTCACACA GCCCCATAGC CTGGGTGAAT CAGGCCTCAC 1620
TCCCCTGTAC TTCCTTCCAA ACATTCTATC ACTCCCAACA CCCTCCACCC AGGCCTCATG 1680
GAACTACACA CAGATCACGC TTGGGCCCAA CTGGATGCGG AATCCCAGCT CAGGACCAAG 1740
GAATGCTGCT GCTGTCTCCA CAATGCCCTA GACCTGCAAC CCTGGGCGCT TCCTGGCATA 1800
CCACTGCCCA CTCTGCCCAC ACCACAGCTG ACTGACTCCT AATGGCTCTT CAAACAGTTG 1860
TTTGCACACC TGACCATTTA TTATAAAGGA AGAAGCGCCG AACAGCACGT GCTGCTCTGA 1920
GGAATCTGTA CAAGAATTGG GGCTCTGCGT ATTAATCTTT GCTAAAATGA ATTTAGTTTG 1980
GGTATTTAGG TTTCACAGCA TAAATATATT TTTCTCTACT CTGAGACCAA TTGGCACAGG 2040
CTGTCTAAGG CATTAGAAGA ACAGTCCTTA ATCTTTCTGT GTTCACAGCA TAGTTCTGAA 2100
TACCAGAAAT CTAGAGGAAT GCTTGAAGAG GTTTTTAAAA AATTAAACAA CATTAAAGGA 2160
GTCAGCAATG ATTTCCATCT CAGCAAAACA GGGGCCCTCA GGGTCCAGAA ACATCCATGG 2220
CCATTGAGCA GTCACTTGGT CATTCTTGTG GATGCTTTTT TTGAGATGGA GTCTTGCTCT 2280
GCCACCCAGG CTGGAGTGCA GTGGCGTGAT CTCGGCTCAC TGCAACCCCT GCCTCCCAGG 2340
TTCAAGTGAG TCTCCCGCTT CAGCCTCCCA AGTAGCTGGG ATTACAGGCA TTAGCCACCA 2400
CGCCTGGTTA ATTTTTGTAT GTTTAGTGGA GATGGGGTTT CACTATGTTG GCGAGGCTGG 2460
TCACGAACTC CTGACCTCAA GTGATCCACC CGCCTCGGCC TCCCGAAGTG CTGGGATTAC 2520
GGGCGTGAGC CACCACGCCT GGCCTTCTGG ATGCTTTTTA 2560
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