Tag | Content |
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EnhancerAtlas ID | HS146-12585 | Organism | Homo sapiens | Tissue/cell | NHDF | Coordinate | chr6:39369370-39370820 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GFI1 | MA0038.2 | chr6:39370163-39370175 | TGCAGTGATTTA | - | 6.92 |
| | 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 |
GH06I039402 | chr6 | 39369791 | 39370816 |
| Enhancer Sequence | CCAACAGTCA TTGATTGAGT CCTCCCGGGG CAGGGGATTT TAATTCCCCA GCACCAGCCT 60 GCCCCACATA TATCTCTTGA GTAGGTGAAA AATGCTCTCG GGGGAGTGGG TAGTGCTAGC 120 AGGTGAAGTC ATGCTAGTGT GCACATGCCT GGCATGTGGA AGGGATGCAG GTGGGGCTCT 180 GACAACATCT ACCCTGTTCC TTATTTCTTG TTTTTCATTA TCCTTGTCTG AAAAATATTA 240 CTACTGCCTG TAGTTAATAT AGTCTCTTAC AAACAAACCT AATTCTTTGG CAACAAAACT 300 AGCAGAGAAA GAGGCAGAGG AAATGAAACA TTCTAGCTAG TCTATTGCCT GATTTCTTAT 360 AGGCCTGGCT GGTATTTTGG GAGTCAGGTT TGTTTTCTGG CCTGGCAAAT AGGAGTAACT 420 GTAGCAGCCC TTGGTTTTCT ATGGACCCTA TTTTAATAGA ATGCAGACTG CTTAGACTTT 480 GGCTCACATT CTGCATGCTG AGGTGAGCTA CTCTTTCCTC ACTTGCTGCC TCAGTTTCCC 540 TTTTTGCAGT GACACCTCAG ATAGGAAGCT CTGACATCAG AAGCTCTTCA ATTCAGCTTC 600 TACTTGGGGC AATGGAAAAG GTACGATGTG TTACTGTGAT GGAAAGCACT GTCAACCAAC 660 CCTGGCAGAG GTGCCAGGGG CATGAGGGAC TCAAGCCGTT TCGAGGACTC ATCCTAGAAC 720 AATGCAAACA ATTGTCCTCA ATCCTGGGTC TATGGGCCTG TTTACTCACT CCGTGCTGTG 780 CCCGGCAGAA ACTTGCAGTG ATTTAGGAAG TCAGGGAGAG ACATTTCTGG CTGTGCGGAA 840 CCTGATGAAA TACTGTTTTG TGGAGACAGA CTAAAAAATA ACCAAACGGT CTTTAAGTGG 900 AACAGAGATC AGAAAATCTC CTGAGGCACA TTTAAGAAAC CCATCAATTT TGCTGGCTTG 960 GCCATAGAAG GGAAAATTGC ACTGCAAATG ATTATCTCTG ATGAAATGTT CCCAAGTCTT 1020 TTACAGGGCA CTTATTTGTA GTGACCTATT ACTCCACCAA CGAGGCCTGA CTGAGAAGCC 1080 CCCACTGGGT GGTTTATAAG GGGAGTCTGC AGAGTAATTG CAGGCTCAAT CCTGAGGGCC 1140 TCCTGTGTCC TATCTTCTCA ACCACCTTAC AGGTATCCTG AGGCTGGGGA CTCTCCTATG 1200 GATTTGTGTG TTTTCCACAG GGCCTCCAAC TTTACAGATG TACATAAATT ACTGAATGAA 1260 TAAACCTGAG ACCAAGGCTT TCTGCCCAAA GTCCTCATCG TAGAAGCCCT CAATTTCCTA 1320 CTTGCCCTGA CCAAACTGAG GAAAAGCTGT GGCAAAAGCT CCTACTGCGT TCAGCCTGAA 1380 ATAATTCACC ACAACCTGTA TCATCAACCC ATACCCAATT ACCTAAAGTG CTCTTTCTAG 1440 AGAAATTAAA 1450
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