Tag | Content |
---|
EnhancerAtlas ID | HS176-21927 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr2:160494190-160495330 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFE2L1 | MA0089.2 | chr2:160494571-160494586 | AGGTGACTCAGCACA | + | 6.38 | Nfe2l2 | MA0150.2 | chr2:160494569-160494584 | CCAGGTGACTCAGCA | + | 6.02 |
|
| 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 |
GH02I159637 | chr2 | 160493785 | 160496052 |
|
Enhancer Sequence | CTCAAGTAGC TGGGACTACA GGCGCACACC ACCATGCCCG AGTAATTTTT TTTGTATTTT 60 TCTGTAGAGA CAGGGTTTCA CCATGTTGAC TACACTGGTC TCGAACTTGT GAGCTCAAGC 120 AATCCATCTA CCTCAGCCTC CCAAATTGTT AGGATTATAT GTGTGAGCCA CCACACCTGG 180 CTGTAAATTT CTAAAGTTTT TGACTCCAAT CCTTGGCTCC CAGACAGCAT CTCTGGATAT 240 GCCGGGGACC TGGAGGAACT CGCCACCCTG AAGGAAAGGT CCTTGGGCAA GGCCCATTGC 300 TGTGCTGGCT TCAGGTCTGA CCCACTGCAG TAACAGTAGT GGTGGCTAGA AGGGTGCTTG 360 CATCACCATA CCCCCAGTTC CAGGTGACTC AGCACACAGA GAGAGAGAGA CTCCGTTTGT 420 CTGGAAGAAA GTAAGAAAAA AGAACAAAAG TCTCTGCGTG GTAATCAAGA GAATTCTGGC 480 TCTTATCCAT GACCACCAAG GAGATACCTT AGGCATGAGT CCACAAAAAA CACAGCATTA 540 TTGGGCTTGG GGCCCAAGTC CCTTTGAATA CCTAGAAAGA CTTCTCAAGA ACGACAGGCA 600 CAAACAAGCC CAGACGGTGG AGACTATAAT AAATACCTAA CTCTTCAATG TCCAGACACT 660 GATGAACATC TATAAGCATC AGCATCATCC AGGAAAACAT GACCTCACCA AATGAACTAA 720 GTAAGACACC AGGGAACAAT CCTGGAGAAA AAGAGATATA TGACCTTTCA GACAAAGAAT 780 TCAGAATAGC TGTTGTGAGG AAGCTTCAAA GAATTCAAGA TAACACAGAT AAGTCATTCA 840 GAATTCTATC AGGTAAGTTT AACAGAGAGA TTGAAATAAT TTAAAAGAAT CAAGCAGAAA 900 TTCTAGAGTT GAAAATGCAA TTGACATGCT GAAGAATGCA TCAGAGTTTT TTAATAGCAG 960 ACTTGATTAA GCAGAAAAAA AACAGTGAGC TTGAAGACAA GCTATTTAAA AATACAAAGT 1020 CAGAGGAGAC AAAAGAAAAA AAATAAAAAT ACAATGAGGC ATGCCTACAA GATCTAGAAA 1080 ATAGCGTCAA AAGGGCAAAT CTAAGAGTTA CTGGCCTTAA AGAGGAGGTA GAGAAAGAGA 1140
|