| Tag | Content |
|---|
EnhancerAtlas ID | HS150-00308 |
Organism | Homo sapiens |
Tissue/cell | NT2-D1 |
Coordinate | chr1:44349940-44351640 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NKX2-3 | MA0672.1 | chr1:44350045-44350055 | TTCAAGTGGT | - | 6.02 | | SREBF1 | MA0595.1 | chr1:44351378-44351388 | ATCACCCCAC | + | 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 |
| GH01I043884 | chr1 | 44349837 | 44351801 |
|
Enhancer Sequence | TGAGCTACCT CTCTCAGGAC ATATGATGCC CACCTGCTCT TAAACTTACC ATCCTTTCTC 60
CTTCGACTCC TGCTCTCCCA TAGGACCCAT CTCCCATGGA ATTCATTCAA GTGGTCAGCA 120
AGGGGAACGC AGCAAGACAC ATATTTGACA GGGCATTTAG AAAGTGTTCG CATTACTTGC 180
TTAGACATAC ACCAGGCTCT TCCTGTGCAT GGCCCTTTAT GGTGGGGCTG CAGCAGCTAG 240
ATCCCAAGCA AGACCATGTA GACTCTAGAA CACCTATCTC CCTACGTTAT GTCTATCCCA 300
CCACTACTCA GAGAAGGTTC TAGGAAGGTG GATCTGTGGG ATTTGGCTTC ATCCTGTTGG 360
ATGACAGTCT CACCTTGTGG GAGCCAAGGC CTGTGGTTGA ATATAACGGA CTGATGTGCT 420
GTGGTCCCTG GTCTAAGAAC TCATTGCTGG GCTCTGCCTT CCCTTTGTCT CATGGGCTGC 480
TTGCACTCGT CACAGTCATT GGGAGAAGTG GCTAAAAGGC TGGCCACCCA ACCAACCAGG 540
CACAGATGTC AAGCTGAAGC CATCTGTTAC CCTAATCCAG CAAACCCATA TCTGGAAGCA 600
CCTCTTTCAG TTGGGTTGGT AGGAACTAGG AGAAGACCCT ACCCTAGATC TGCTGGTGCC 660
CACACATAAC TACTCCCTCA CCTCACTCCT TAATAAGACC AGTCAGCTTT CTTGCCAGTC 720
TGTGGATACA GGCTTAATAT TCCAAGCCTT AGAACATGGT TTAGGTTGAT GAGCCAGTGT 780
TGAGGACATT CACCTTATAC GCTGCACCTT AGCCACATTT TTGAGCATTA AGTGAGCTGG 840
AAGATCTCTT AGGAGGGCCC CAGGTTGCCC TTCCTGGCTG GTTAGCCTGA CCCTTATGCT 900
TAATCATAGT CCTCTTTCAG TCTACAGGTC TGCGAGCAGG GCAGCCTCCT GGCTCCTGAG 960
GTTCCATCTA TGCTGTGAGA GACACAGGGG TCAGATCCAC ACTCAGCATG TACTCTCCCA 1020
GGGCCCAAAA CCCCCAAACT ACTAGGCTGT AGGATCTAAG GAGAAAGGAT AGGCAAGTTC 1080
CAGTGCAACT TCCGTCTCCT CCTTCCCCGG GTCCTTCTCA CGCACTCACA CACACCCTGC 1140
TGAAACCTGA TCCTGAGGCT GCCTCGCGTG CCGGGGTGCT GGCGGGGCTG GCGGGCTGGG 1200
GCCTGTCTTT TGGAGCCTGC CCCACCCTCC CCTGCTACCC CCTAGGCCAG GGCAAGCAGG 1260
TCAGGCGTCC CACACCCCCG CTAGTCTGAC CAGTCATTCT ATACCTTAAG GGCCACCTCC 1320
ACCCTGGCCA GGCCCCCAAA CTGGCACACT GGTCTGGACG GAAGCCCCTG GATTCTGTTC 1380
CAGGCATAGC CTGAGGTTAG GCCACCTGCA TAATTAACAC ACACACACCA TCTTTACCAT 1440
CACCCCACCC CGACATTTCC TGTTGTTTAT AGGCCCCAGC CCATTTTCCA AGGCCTCTGC 1500
AGGTGTCAAG CCACCTCACA GGGGATGAAC AAAGTGCAGT GGGAACACTG GAGGAAGAAT 1560
GCAAGCCTCC CTCGGGGAGT CAGGGGAGAC TGTCCTGAGG AAGTAGTCTT TCAGCTTGAT 1620
AAGAATGAAA CAGAGCAGAG GATGCCAGAG GCTGGGAAGG GAGAAATAGG GAGAGACTTG 1680
TCAAATTATA CAAAATCACA 1700
|
