| Tag | Content |
|---|
EnhancerAtlas ID | HS098-10242 | Organism | Homo sapiens | Tissue/cell | HSMM | Coordinate | chr11:64163220-64164410 | 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 | CCCACTGCGG TGGGCAGCCA GAGGCCTAGA GGAGCTGGCT TAGCTGGAGC AAAGATGCAG 60
GCACAACGCA CCGGCGACAA GAGGAATGAT GTTGCACTTC ACCAGGAGAC GAGAGTCCAC 120
GACCCAGGAA TTGAAACTCC ACTGGTGGAA ATTGCCCAAT GAGAGGCAAA CTGTGTCCCC 180
TGCCGTCCGT ATCCACCCAG GCTCACAGCT TCCTCTGAGA GCAGCGGGGG GACAGTTGTC 240
TTCTTGGGTC ACTTAACATT TGCAGTGAAG TCATTCCTGG AGCCCTTACC TAGGGCTCCC 300
CGCCCCTCCC CCACCTTGTG CTCATCCTGC TTATTCAAAG GCTCTTAATT TTGATGAGTT 360
TCCCACTCCT CCGGCAGGCC CTTCTCAGAG CTGCATGCTT GATTCTCTGC AGTTCCGGTG 420
GTGTCCTGCT TTGCCCTCTA AGCTTCTCCT TCCTCAGCGA GATCTGCAGG AGGCTTACAG 480
CTCTGGGCCG TGAAGTCTCA GCAGCTGCTC AGGAATTCCC GGGGCCCTCC AAGGGGCCTC 540
AGACCCGAGG TGTCTCCGCT GCAGAGTCAC CGTGGAATAT TCCTGATCCA AAGCAGCTGC 600
CAATGCCTCA GACGCCTGTG CCCCCAGAGG GCCAGGGGCA GCTGTGTGTC TTTTCCCAGG 660
GGCTTTTGAA TTTCCTAGGA CTTATTTTTA GAGCTGCAAC AGAAGCCCTC CTTTCTGCCA 720
CTCCGTCTCT GCAGCAGTGG GTCAGGCTTC CGGTGTTTAT TTCCATCCAT GATTCCTCCC 780
CAACTGAGGT TCCCAACCGC AGCAGCTCAT TGGAATCGCG AGTCTACCGA TGCTCAGACC 840
CCACTCCAGG GATCCTGATG AATTGATCTG GGGTGAGAGC AGGGGAGGGG CCTGCATCAG 900
CATCTTAAAA TTCCTCAGTG GTTGTAGCAG CCAGATGGAA AACCGAGGCT TTTCCAGGGG 960
TGCAGCTAGG TTGTTTTTCT TTTTCTTTTT CTTGGAGTCA GGGTCTTACT CTGTTGCCCA 1020
GGATGGAGTT CAGTGATGCA GTCTCCGCCT TACTGCAACG TGGACCTCCC TGGGCTCAGG 1080
TGATCCTCCC ACCTCAGCCT CCCAAGTAGC TGAGACCACA AGCGTGCACC ACCATGCCTG 1140
CCTAATGTTT GTATTTTTTG TAGAGGAGGG GTTTCACCAT GTTGCCCAGC 1190
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