| Tag | Content |
|---|
EnhancerAtlas ID | HS175-04607 | Organism | Homo sapiens | Tissue/cell | SK-N-MC | Coordinate | chr11:64162990-64164460 | 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 | CCACCTTGGC TTCCCAAAGT GCTGGGATTA TAGGCGTGAG CCACTATGCC CGGCCACAGT 60
CTATGTTTCT AACCTGGACT GACTTTTCCA AAGAGCCAGT TCCTGGCACA TATGAGATGT 120
TCCTAGCACA CTCCACACCC ACAAAGTATA AACATCAGAC AGACAAAAGC AGCACCTCCA 180
TCATCACAGC AGCAAACCCA GCAACGCATG GTCCAGAGTC CAGTCCAGAG CCCACTGCGG 240
TGGGCAGCCA GAGGCCTAGA GGAGCTGGCT TAGCTGGAGC AAAGATGCAG GCACAACGCA 300
CCGGCGACAA GAGGAATGAT GTTGCACTTC ACCAGGAGAC GAGAGTCCAC GACCCAGGAA 360
TTGAAACTCC ACTGGTGGAA ATTGCCCAAT GAGAGGCAAA CTGTGTCCCC TGCCGTCCGT 420
ATCCACCCAG GCTCACAGCT TCCTCTGAGA GCAGCGGGGG GACAGTTGTC TTCTTGGGTC 480
ACTTAACATT TGCAGTGAAG TCATTCCTGG AGCCCTTACC TAGGGCTCCC CGCCCCTCCC 540
CCACCTTGTG CTCATCCTGC TTATTCAAAG GCTCTTAATT TTGATGAGTT TCCCACTCCT 600
CCGGCAGGCC CTTCTCAGAG CTGCATGCTT GATTCTCTGC AGTTCCGGTG GTGTCCTGCT 660
TTGCCCTCTA AGCTTCTCCT TCCTCAGCGA GATCTGCAGG AGGCTTACAG CTCTGGGCCG 720
TGAAGTCTCA GCAGCTGCTC AGGAATTCCC GGGGCCCTCC AAGGGGCCTC AGACCCGAGG 780
TGTCTCCGCT GCAGAGTCAC CGTGGAATAT TCCTGATCCA AAGCAGCTGC CAATGCCTCA 840
GACGCCTGTG CCCCCAGAGG GCCAGGGGCA GCTGTGTGTC TTTTCCCAGG GGCTTTTGAA 900
TTTCCTAGGA CTTATTTTTA GAGCTGCAAC AGAAGCCCTC CTTTCTGCCA CTCCGTCTCT 960
GCAGCAGTGG GTCAGGCTTC CGGTGTTTAT TTCCATCCAT GATTCCTCCC CAACTGAGGT 1020
TCCCAACCGC AGCAGCTCAT TGGAATCGCG AGTCTACCGA TGCTCAGACC CCACTCCAGG 1080
GATCCTGATG AATTGATCTG GGGTGAGAGC AGGGGAGGGG CCTGCATCAG CATCTTAAAA 1140
TTCCTCAGTG GTTGTAGCAG CCAGATGGAA AACCGAGGCT TTTCCAGGGG TGCAGCTAGG 1200
TTGTTTTTCT TTTTCTTTTT CTTGGAGTCA GGGTCTTACT CTGTTGCCCA GGATGGAGTT 1260
CAGTGATGCA GTCTCCGCCT TACTGCAACG TGGACCTCCC TGGGCTCAGG TGATCCTCCC 1320
ACCTCAGCCT CCCAAGTAGC TGAGACCACA AGCGTGCACC ACCATGCCTG CCTAATGTTT 1380
GTATTTTTTG TAGAGGAGGG GTTTCACCAT GTTGCCCAGC CTGGTCTTGA ACTGTGATTC 1440
TCCTCCCTTG GCCTCCCAAA ATGCTGGGAT 1470
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