Tag | Content |
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EnhancerAtlas ID | HS146-04478 | Organism | Homo sapiens | Tissue/cell | NHDF | Coordinate | chr14:35665560-35666980 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GFI1 | MA0038.2 | chr14:35666823-35666835 | TGCAGTGATTTA | - | 6.92 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr14 | 35666202 | 35666508 | chr14 | 35666212 | 35666520 |
| | Number: 1 | ID | Chromosome | Start | End |
GH14I035195 | chr14 | 35664919 | 35667787 |
| Enhancer Sequence | ATGGTAGCAC ACACCTGTAG TCCCACCAAC TCAGGAGGCT GAGGCGGGGG GAGGATCACT 60 TGAGCCCTGG AGATCTAGGC TGCAGTGAGC CGTGATTGCG CTGATGCACT CCATCCTGGG 120 TAACAGAGTG AGACCCTGTC TCAGAAAATA AATATTTTCA TCACATGGGG AAAAGTAAAT 180 CTAATCATGA CTCCTTAGTT TTAAGGAGTT ACTGCTGGGT AGTCAAGGGT GATATAAGTG 240 ACTTGAGGAA ACAAATTTGC ATTAGTGGAT GCCAATCCAG AATTCACTAA AGAACACAAA 300 AGAATGGTTC TTGGGTTTTT TTCTTACTAT TCATTTTTCA TGACATGGCA ACTCAGGGAA 360 GTCATATTGC CCTAGGTCAA ACAGTGCCAG GCTGACTACT TCCTTTTGTC ATGTATCACT 420 TCACCCACTC CTGCCTTGAC ATGTGTTAAG AGTTATGTTT TGTCATGTGA CTGCTGGGAT 480 CGTCTGCATC ACTCAGAATT ATTCTTACCA ACTGCTAATG AAGTTAATGA TCAACTGTCA 540 GGTGGGTTTT TAGTGAAGTG ATCAAGGGCA TAACTAGCAA GATGAATGGA GCCAGGCAAA 600 ATTTCTATAG TGATTTGGCT TCATAGTCCT TTCTTTTCAA ATGTCCCAGA AAGGAACATT 660 CTGCATAGTG TTTGAAACAA GATTTCCCCA ATTGTTGTAG AAGTCAAGTG ATCCAGTGTC 720 TTTGAACAGC ATTAAAAACA CTGTGTTGCC AAGCTCCCAT ATCTTTTCTC TCTCTGGCAA 780 AATCCTAATA GCAAGTTGAT TTCCCATCAC TGATGTGTCA TTGATAATGT CTGTGTGATA 840 ACCATTTAGG GTGTGGTGAG ATTGTCTCGT GAGTCATTAT TGTGTATATC TTGCTTCCAT 900 CACAGTGTTT TAAAACACTC TCATTGAGAG TGTGGTAGGA AGAGGCCACT TATGAAAATA 960 TAATATCCAT TTTAACAAGA AAAGTTTAAA TATTTGTTGT CAGTAAGGTA AACAGCAATT 1020 GCAGAGTGAG TAGTAAATTT ACTTAAACTG TTTATAAAGC TATATAAATT ATTCTTACCT 1080 AATTATTACA GTGGTAACAC TTTAATCATA ATTTTCTGGT AATGTTTATT TTAAAACAGC 1140 ATTTTTTTCC TTTTAAAATT GTTTCTGTTT CACAATTTTC ACTAATATAA AGGCTGATTT 1200 TTATCCCAGT CAAATACGAT TAAGATCAGT TGATTAAGAT CAGTTCAGAT CTTAGATTTC 1260 TTTTGCAGTG ATTTAGACAT GGCTTTTTTT CTAGATAGTA TTAGGAAGGG TATATTGTTC 1320 CTTAGAGTAT TCACTCTGCC AACTCAAGTG GATACTCCTT ATTGGTATAT TATTTCTACC 1380 CCATTTTGTC TTATGAAAGA TGTAAGATGG TTATAATATA 1420
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