| Tag | Content |
|---|
EnhancerAtlas ID | HS098-51063 | Organism | Homo sapiens | Tissue/cell | HSMM | Coordinate | chr7:2081860-2083440 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NRF1 | MA0506.1 | chr7:2081865-2081876 | GCGCATGCGCA | + | 6.32 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr7 | 2082891 | 2083148 | | chr7 | 2083256 | 2083318 |
| Enhancer Sequence | CACAAGCGCA TGCGCACACG TACACAGACA CACATACGCA CATGCACACA CACGCGCACA 60
TGGACACAGA CACACGCAGA TGTGCACAGA CACACAGGCA CACGGACACA CGCACAGACA 120
CACACATGGG CACACAGGCA CAAGGGCATG CACACGGCAT TCCTAACTGC CACCACCGAC 180
CTTTTCACAC TCCAGCCACC CCAGAACCCT GGCGTTTAGA ATCTGCAGCT AAAATACACC 240
CAATGATGGT ATCAACGTTC ATTTATTCAT TCAACAAATA CTTGGCGATA TGGTTTGGAT 300
GTCTGCTCCC TCCAAATCTC AGGTTGAAAA ATGTTTCCCA AAGGTGGAGG TGGGGCCTGG 360
TGGGAGGTGT TGGATTATGA GGGCGGATCC CTCACGAATG GCCCAGAGCC ATCCCGAGTG 420
AGGAGTGTTG TTGGAAAGAT TCTGGAACCT CAAGTGTCTC TCTTGCTCCT GCTCTTGCCA 480
TGTGACGTGC CTGCTCCTTG CCTTCTGCCA TGATCAGAAG CTTCCTGGTA CCTCAGCAGA 540
AGCAGATGCC GGCGCTGTGC TTCCTGTACA GTCCGCAGAA TGACCCAGCC TCAGGGATTC 600
CTTTATAGAG ACACAAGAAC GGACTAATAC ACCTGAGGAG CCTTCACGCA CACACATGTC 660
CACGTCCACG TCCACGTCCA CATCCACGTC CACGTCCACA TCAAGGCAGT GCTGCTGAGG 720
GCCAGAGGAC GCTGCCACAG GCCGACCCCG TGAAGCTGAA AGTCACCTTC GCCAAGAAGG 780
ATGGGCTTCT GGAAAACACA GCCCTGCACT TAGAAACTTC AGACCCTACT CTCCACAATC 840
TCTTTATTTA TAAAATTGCT TATGCGAAGA TATTTCCACG CAGAATGCAT TCAATTATGC 900
AGTGTAAGGG GGGGCCTGAA TGGAGAACAT CCAAGTCAGC CACGAAGACA CTTCAGGAAA 960
TACAAGAAAA CGACCCTGCC ACTGACTTTC GAATGTGTCT GCATCCACGC CCCTGTCCCA 1020
TCGGAGGGGC ACAGGGTAAT ACATAGCACT GCGCTCCCCT CCTTCTCCTG TGGTTCCCCT 1080
CCTGACAGCG CAGTGCAGTG CGGCAGACAC CCCTCATCCT CGGTGTCAGG GCAGCATTAG 1140
CATGTAAATA GCTGGCAGAC ACAAGGACGT GAAAGCAAGG AAGAGCTCTT TAATTAACTT 1200
TAATCCTCCA AAAATCCATG CTGCAATCTG TTCTGACAAT CCCACGCTCC TTAGGAGGCC 1260
CTCGGCACGA CCTGGCACAT CCTGTGGGCT GGAGGTGGCC GGAATGGGCG GGCTTGGGAA 1320
CGTGATGCCC GGGTACCGTG CCTACAAGGA CGCTGGGTCA TGACTGTTCT CTGGAGGCTA 1380
CGGGTGCCCT GCAGAGTGGA GGCACGCGGA GGGCCTGGGG GGGCTGGGGA TCCAGACTGG 1440
CTGAGCGCCT GTTTCCCACC ACAAACAGCC CTGCGGAGTG CCAGCCTTTT TCTCGAGAGT 1500
GGGGGCAGCA CCACCCCAGG CCTCCTGCCA GGCCCCAGGG AGCCCTGAGG CAGGGGCCTC 1560
TGCCCATTCT CTCCTCCCAA 1580
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