| Tag | Content |
|---|
EnhancerAtlas ID | HS050-12444 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr11:64163020-64164510 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nfe2l2 | MA0150.2 | chr11:64163779-64163794 | TGCAGAGTCACCGTG | - | 6.03 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH11I064394 | chr11 | 64162073 | 64164406 |
| Enhancer Sequence | TAGGCGTGAG CCACTATGCC CGGCCACAGT CTATGTTTCT AACCTGGACT GACTTTTCCA 60
AAGAGCCAGT TCCTGGCACA TATGAGATGT TCCTAGCACA CTCCACACCC ACAAAGTATA 120
AACATCAGAC AGACAAAAGC AGCACCTCCA TCATCACAGC AGCAAACCCA GCAACGCATG 180
GTCCAGAGTC CAGTCCAGAG CCCACTGCGG TGGGCAGCCA GAGGCCTAGA GGAGCTGGCT 240
TAGCTGGAGC AAAGATGCAG GCACAACGCA CCGGCGACAA GAGGAATGAT GTTGCACTTC 300
ACCAGGAGAC GAGAGTCCAC GACCCAGGAA TTGAAACTCC ACTGGTGGAA ATTGCCCAAT 360
GAGAGGCAAA CTGTGTCCCC TGCCGTCCGT ATCCACCCAG GCTCACAGCT TCCTCTGAGA 420
GCAGCGGGGG GACAGTTGTC TTCTTGGGTC ACTTAACATT TGCAGTGAAG TCATTCCTGG 480
AGCCCTTACC TAGGGCTCCC CGCCCCTCCC CCACCTTGTG CTCATCCTGC TTATTCAAAG 540
GCTCTTAATT TTGATGAGTT TCCCACTCCT CCGGCAGGCC CTTCTCAGAG CTGCATGCTT 600
GATTCTCTGC AGTTCCGGTG GTGTCCTGCT TTGCCCTCTA AGCTTCTCCT TCCTCAGCGA 660
GATCTGCAGG AGGCTTACAG CTCTGGGCCG TGAAGTCTCA GCAGCTGCTC AGGAATTCCC 720
GGGGCCCTCC AAGGGGCCTC AGACCCGAGG TGTCTCCGCT GCAGAGTCAC CGTGGAATAT 780
TCCTGATCCA AAGCAGCTGC CAATGCCTCA GACGCCTGTG CCCCCAGAGG GCCAGGGGCA 840
GCTGTGTGTC TTTTCCCAGG GGCTTTTGAA TTTCCTAGGA CTTATTTTTA GAGCTGCAAC 900
AGAAGCCCTC CTTTCTGCCA CTCCGTCTCT GCAGCAGTGG GTCAGGCTTC CGGTGTTTAT 960
TTCCATCCAT GATTCCTCCC CAACTGAGGT TCCCAACCGC AGCAGCTCAT TGGAATCGCG 1020
AGTCTACCGA TGCTCAGACC CCACTCCAGG GATCCTGATG AATTGATCTG GGGTGAGAGC 1080
AGGGGAGGGG CCTGCATCAG CATCTTAAAA TTCCTCAGTG GTTGTAGCAG CCAGATGGAA 1140
AACCGAGGCT TTTCCAGGGG TGCAGCTAGG TTGTTTTTCT TTTTCTTTTT CTTGGAGTCA 1200
GGGTCTTACT CTGTTGCCCA GGATGGAGTT CAGTGATGCA GTCTCCGCCT TACTGCAACG 1260
TGGACCTCCC TGGGCTCAGG TGATCCTCCC ACCTCAGCCT CCCAAGTAGC TGAGACCACA 1320
AGCGTGCACC ACCATGCCTG CCTAATGTTT GTATTTTTTG TAGAGGAGGG GTTTCACCAT 1380
GTTGCCCAGC CTGGTCTTGA ACTGTGATTC TCCTCCCTTG GCCTCCCAAA ATGCTGGGAT 1440
TACAGATATG AGCCACCATG CCCAGCCCCA GCTAAGTTTT TTAAACATAA 1490
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