| Tag | Content |
|---|
EnhancerAtlas ID | HS150-02056 | Organism | Homo sapiens | Tissue/cell | NT2-D1 | Coordinate | chr11:1213080-1214070 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2F1 | MA0017.2 | chr11:1213563-1213576 | CCGGTGACCTCTG | - | 6.11 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CCTGTTCCCA CCACCAGCAC AACCTCTGCT CCTACAACCA GCACGACCTC TGGTCCTGGA 60
ACTACTCCCA GCCCCGTTCC CACCACCAGC ACAACCCCTG TTTCAAAGAC CAGCACAAGC 120
CATCTTTCTG TATCCAAGAC AACCCACTCC CAACCAGTCA CCAGTGACTG TCATCCTCTG 180
TGCGCCTGGA CAAAGTGGTT CGACGTGGAC TTCCCATCCC CTGGACCCCA CGGCGGGGAC 240
AAGGAAACCT ACAACAACAT CATCAGGAGT GGGGAAAAAA TCTGCCGCCG ACCTGAGGAG 300
ATCACCAGGC TCCAGTGCCG AGCCGAGAGC CACCCGGAGG TGAACATTGA ACACCTGGGT 360
CAGGTGGTGC AGTGCAGCCG TGAAGAGGGC CTGGTGTGCC GGAACCAGGA CCAGCAGGGA 420
CCCTTCAAGA TGTGCCTCAA CTACGAGGTG CGCGTGCTCT GCTGCGAGAC CCCCAGAGGC 480
TGCCCGGTGA CCTCTGTGAC CCCATATGGG ACTTCTCCTA CCAATGCTCT GTATCCTTCC 540
CTGTCTACTT CCATGGTATC CGCCTCCGTG GCATCCACCT CTGTGGCATC CAGCTCTGTG 600
GCATCCAGCT CTGTGGCTTA CTCCACCCAA ACCTGCTTCT GCAACGTGGC TGACCGGCTC 660
TACCCTGCAG GTTCGTGAGT GTTTCTGGTG CAATTGTTTC TGAGCTCACC CTGGTCAGTT 720
TTTTATCCAG GAACGCCAAG CTGTGATGAT GATAGGAGTC TCTGCTCTTT GTGGCACAGG 780
CTCATTGTCA CAGAGTGGCT GCTGGCATTC TCTGAAATTT TTTCCCATTA CACAGGTGGT 840
AGAAAGTGCC CCTCTGGCTC TGGGAGTTTT TTGCTTCTCC TTTGAGCAGG ACTCCACTAA 900
AGGCTGCCAT GTCCCTTCCT CTTACAGGAT CCACCATATA CCGCCACAGA GACCTCGCTG 960
GCCATTGCTA TTATGCCCTG TGTAGCCAGG 990
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