| Tag | Content |
|---|
EnhancerAtlas ID | HS045-05079 | Organism | Homo sapiens | Tissue/cell | Fetal_lung | Coordinate | chr1:204671930-204673770 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| INSM1 | MA0155.1 | chr1:204673478-204673490 | CGCCCCCTGGCA | - | 6.74 | | TFAP4 | MA0691.1 | chr1:204672505-204672515 | AACAGCTGAT | + | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TGACTCATAC ACCATTCCCC ACAAGGGAAC AGCACCGTGC CATCAAGTGC TGATCTGGCC 60
ATCAGGTACT GACAGTGTGG TGGGGACCAT GGGGGCTGTG GGTGAGCAGG GGGAGGGCTG 120
GGCTGTCCCC TGAATGGGAT AGAGCCCCAG AGTGACCATC GCTACCTTCC TTCTGCCAGA 180
CATCATCATT GGCCCTTCTC CCCTTGGCAC CAGGGAGAAG CTGGTGAGGT AGCCGCATGG 240
ACTCAAGAGC AGTTTCCAGG TATGCCTGGC TAGAAGGCAG CAAGGTTTGG ACCTGTGCCC 300
CTTTCTCTGG AGGGATCCTG GGAGCTTCCC AACTGGCTGT CCCATGCAAT TGGCTTTGGT 360
TTCCCCACTA GCTTCCTTAA ATATGTCTCC CACCCTCTCA GGGCCCCAAG GGAATCACTT 420
TGGAAGATCT GTCACCAGAG GACCTCGGCT CTCCAGCCTT GGAGACAGAG GACCTGACAC 480
AGCAGACAGG CTGGGAGGGC CAAGGTGGAG GGGAGACATT GTTCCTCTGG CTACTTTATT 540
TCTTTGGTTT GTGGCTGTTT GACAACAGCA GTAAAAACAG CTGATAAATT AGGTGCCTGG 600
CTGTAAACTG CAGCACCAGC CATGGTGCAG GGAGCAGAAG TGCTCCCCGC CCTCCAGCTC 660
CCTGCACACT CTTCAGACCC ATCAGGGCCT CATCCTCTCC AGCACCCCCA GGTCTCAGTC 720
CTGAGGCTCG GACACAGACA GGGGCAGGGG TAGGAGGGCC CGTGTCTCCC TACTCCCAAG 780
TGCTTTCTCT GATCACAGAA GGACCGGAGA GCCGCTGTTG GCTCCTCAGA GGCTCTTCAA 840
ACAGAGAGAT GTTTATATCT TTTCAGGGCG ATCCAAATTA CAAGCAGGGA ACTGGAGCCT 900
AGGGAAAGTA AACCAAGGGA TACCAGATAG AGATTTTTTT TAAAAGCTTG GTTTAAATCA 960
ACTTCCAGAA GACCTCAAAT GAGGCCAGTG GGGCGGAGGA AGTGCCAGAA GAAGAAGGCC 1020
GGCAGGTCTG GCTCTCCAGA GTCCAGCGTG ACCCAATGCC CAGTTCCTTT CTGCCCCGGG 1080
CTCAGTTTCC CTCTGTGTAC CGTGGCCTCT TCTCTCCCAG CTTGTTCAGG AGGCCAGTTA 1140
ATCTAATGGA GAAGGAGCCC TGCAGAACTG AGGATGGAGT CCTGGTGCAG CTTTGAGGAG 1200
CTGCCAGGGC AGGCCAGATC TTCTGGCAGC CATCGACTGC ATCGGTGGCC ACAGGAGGAG 1260
GCTGGCCTGA GGCCTATATG GAGGCACTTG TTCTACCCCT TGGCAGAGAC AGTCTGTCTG 1320
GTCTCCTGTC ACTTCACCTT TCTGCTCCAG GCCCCGCAGG TGCCTCGGAC CCTGGGTCAG 1380
AGCCCATGGG GTCTAAGGCA TCCATTCGAT AGTGCTCCAT GCCAGACTAT GCAAGAGGCC 1440
TTGAGGCATA GGTACCAGCT AGAGCTTGCC CTTAGAGTTC AGTTCCTGAA CACAGAACAC 1500
AGCTGCTTTG ACTCAGCACC CCCGGTTCTG TTTCTCCACT CATCCGTCCG CCCCCTGGCA 1560
CGGCTGTATA AAGCTTCTAC AGCTGGGTTA TTACTCTGCG TTTGTTTGTG TGTTTTCTTT 1620
GACGGTGTTA AGTCATTTTG CATGTGCATC CTGCCCACAT GAGGACAGCT TGGAGAGCAG 1680
GAACTGAAAC TGCTCCCTCT TATAGATCTG GGATTCTGCT CTGGGAGCAG GCCTGGTCAC 1740
AAGGATGCCA ATAGGCAGGG AGAGGACACC CGGAGTGCAC AGGGAGAGGG CACCCAGGCC 1800
GTGTGTGTGT GTGTGCATGC ATGCAAATAA ATTGACATTG 1840
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