| Tag | Content |
|---|
EnhancerAtlas ID | HS050-25045 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr16:11484020-11486480 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gfi1b | MA0483.1 | chr16:11484885-11484896 | AAATCACAGCT | + | 6.14 | | Myog | MA0500.1 | chr16:11485665-11485676 | GACAGCTGCAG | + | 6.62 | | Nfe2l2 | MA0150.2 | chr16:11485307-11485322 | AAAAATGACACAGCA | + | 6.07 | | Sox3 | MA0514.1 | chr16:11485331-11485341 | AAAACAAAGG | - | 6.02 | | Tcf12 | MA0521.1 | chr16:11485665-11485676 | GACAGCTGCAG | + | 6.14 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr16 | 11484397 | 11484654 | | chr16 | 11485233 | 11485698 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH16I011391 | chr16 | 11484891 | 11485075 | | GH16I011392 | chr16 | 11485441 | 11485670 |
|
Enhancer Sequence | GAACGTGGCC TCAGCCCAAG ACAGCATCTG TTGGGCGGCC TGGAGAGGGA GGGGACAGTG 60
AGAGCTGGCT CAGTCATCCT CACCTGCCAA CTACGCCCCA TCCTTGCTCA CTCACCAGCT 120
CCAGGGCTCC TTTCATGGCC CCCAGGGCCG CCCTGATGGG CCTTGGACCC CCTTTGCCTG 180
GCATCCCGGG CACCCAGGCC TGCAGCCGCC GCATGGCCTC CTCTGCTCGC TCCCGCCACA 240
CCTCCTCCAG GGGCCGCAGT GTCACCTCCA GGTAGGCATC CTTCAGTGTG GCCAGGGGCC 300
CTGCAACAGG CAGCCACCAC CCACCATGAG ACCTCAGGGC AGGTCAGAGA ACCAGCCCTG 360
CCCAGACACG CCAGGCCTCG AGGAGATAGG GCCTGTTCCT GGGATTAAGA TGTGGGGAGC 420
TGGGGGAACT GGAACAGAGC AGTGGCACTG GAGATTGCAG GGGAGTTGTC ACAGCAGGCC 480
TGAGCCGTCT CTGCAAGGCC TGCTTATAAG GTTGTCTGGG AACTTGGATT GGGGGAGGGT 540
TCCCACCAGT CCTAGAATTG ATATGAGGCT CCCTGCATCT GAACTGTTTG TACAAACGTG 600
GTTTATGCCG GACCCCTGCT TGCTTCCTAG GAGTCTGACA GTGTGGTCCG TGCCAAGCAG 660
CACCTGCCAG TGTGGCAGCC CCCAATAAAA ACCCTGGGTG CTGAGTCTCC CAGGAGCTGC 720
TCTGGTGACA GCTGGGACAG CTAAATGCAT CCTGTGTGAA AGCGCTGGGA CTGGGAGAGT 780
ACCCTGGGCA CTGGCCCTGG TTCTCCCTAG ACTCCGCCCC AGCCCCCTTC CCTGTGCTGA 840
CACTCCTGCA TCCCCTCACT ATAATAAATC ACAGCTGTGA ATAGCGCTGG GCGGAGTCCT 900
GGCGCATTCC TCCTGATTCA CTGCCCTGGG GGTGGTCACA GGAACACTCT GGCACAGCAG 960
GGAGGATCGG GAGGTAACAT TCAACAGCCA GTCAGAGGGA TGCCCACCCT GGCGCTGGGC 1020
AGGGCCTTGG GGGCTCTGTG CTGTGCTGGG CATTAGCCCT GGATGGCGGA GAGGCCAGAG 1080
GTTCCCAGTC CTGCCACGAG GCTGGTTGGG GCAGCAGGTG TGAGCCTTTA ATGACCACCT 1140
GGCCACATTG AGCTCATCGT GGAACCAGAA AGAGATGCTG TGGCAGTGAG CTTCACAGAA 1200
ACAAGGCTGT ATACTCAAAA GAAAGCAGGC GGGAGACTGA AAAAACCTAG GCAGCAGGCA 1260
TAAGGGAGAT GAGCTTGGAG ACTCTGTAAA AATGACACAG CAGACCCAGA AAAAACAAAG 1320
GCTGTAGATC TATAACAAAT AAGGCAGGGG GCTAAACACA GCTGGGCTAC AGGCCCATGG 1380
GAAGCGAGGC CACATTTCTG ATTGAAACAG TGCCACAGGC CAATGTGAGC GCTTAGGGCC 1440
CCGGTGGAGA GGGGGGACAT TGATTTCCGC ACAGGATTGA GCCCTCCCCC TCCCACACTT 1500
ACATTCCAGC TCCTCCCGCA GCTGCTCCAG CCCCACCTGC AGCCACTCCA GGTAAAGAGG 1560
CAGGTGCTGG GTCAGTGCCT GGCTCCGGGC CCACAAAGTG GCTACTGCCC AACCACTCGC 1620
CTGCATGGCC TCCCGCCCCG CCTGGGACAG CTGCAGAAGG AGGCCTGCCA CGCCGTCCAG 1680
GGTGCCTGCC GGCTGCACCT GGACAGGGAA ACCGAGGCAG AATCAGGGTG AGGTCCAGGG 1740
CAGAGAGAGC CCCAGACCCT CCTGCCTGGT GAGTGGGGGC TACAAGCCAG GTCAGAGGGG 1800
GACCTCTCCA ACCTGAGCCC CCACCCTCCC CTGCTGTGAT ACCCACCAAT TGCTGGAACC 1860
TTCTCACAGA GGCACCCAAG CCTTGAACCT TCTCTTCCAG CCGGGCTTGC ACCTGGGAGC 1920
CAACTGCTGC AATCCTGGAC TGTGAGGACA GAGGAAGAGG CTGGGGCCTC GCAGGAATGA 1980
AGTAGACACA AGGTTCTCGG TGCCAGCAGC AGGTGTGGGC CTCACAATGG GGTTGTCTGC 2040
CCTGGTTTCT GGGCACAGCT GGACCCCAAG GGCTCGGGGC TCCTGGCACG GGGGCCTCTG 2100
CCCAGTGGGA GAACGGTAAC CCCTTCCCTG TGTCCCAGCC CAGGCCCTCT CACCTCCACA 2160
TGGCCCAGCA GGCCCCCCTG GCAGCCGCGC GCGGCCAGCA GGAGACTCTG GTTGGCAGCC 2220
TGCAGGGTCA GGCGTCCCAG CGGCTGGGAG GGCTGCCTGC CATCCCGGAA CAGGACCTCC 2280
GCCTCGGCTG TCCGCCCATG GGCACATGCC CGCAGCACCA CACTCTCCTC TCTGCCCCCT 2340
GGAGCCAGAA AGGGACCTGC TGGTGCCCCC ACCATGTCTC TGGCTGCCCA CTCCCCCTCC 2400
ACCGCTTTCC GTAGCTCCCC ACTGCCCCAG GCCAAGCCTC AAGGCCCTAG GATTTGAGAA 2460
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