Tag | Content |
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EnhancerAtlas ID | HS055-07698 |
Organism | Homo sapiens |
Tissue/cell | FT33 |
Coordinate | chr7:3311570-3313390 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GFI1 | MA0038.2 | chr7:3312847-3312859 | TGCAGTGATTGA | - | 6.18 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_66968 | chr7:3311889-3313858 | H2171 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH07I003272 | chr7 | 3311982 | 3313270 |
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Enhancer Sequence | TTGCATTTAA GTAGAACCAT CATTAATTAT GTTAAATGAC CTCCACAAGC AGTAAGGATG 60 GAATGGAAGG TGAGGGGACA GAGAATCCCA CCATGATATA CTTTTTCACA AAAGGAATCT 120 TTTTTTTTTT TTTTTTTTGA GATGGTTTCT CACTCTGTCA CCCAGGCTGG AGTGCAGTGG 180 CGCGATCTCG GCTCACTGCA ACCTCTGCCT CCCGAGTTCA AGCAATTCTC CTGCCTTAGC 240 CTCCTGAGTA GCTTGGATTA CAGGTGCACG CCACCATGCC CGGCTAATTT TTTTGTGTAT 300 TTTCAGTAGA GATTGGGTTT CACCATGCTG GCCAGGCTGG TCTCGAACTA CTGACCTCGA 360 GTGATCCACC CGCCTCAGCC TCCCAAAGTG CTGGGATGTC AGGTGTGAGC CACCGTGCCT 420 GGCCGAAATC TTATGAAGAA AATAATTACA AGTAGAACTG TTTGAGGGGA AACAGGTAAG 480 GGGGCTGGAC CCTTGTTTCC TGATCTCTCC AATGACCCTC TGCAGAGGCC CCAAAGGCTC 540 TGCTTCCAGA GACCCCAGGG CTCTATAGAA TTCAGCTATA CTACTCATCA GTTCAGATAT 600 GGTAGATAAT CCTTGCTCTC ACTTATGACC CTCCTGCTAG GTACTTTTCT TATCAGTTTT 660 AATCCTCAGA ACTGCCTTTG GAGTGAGGTG TGATTATCCT AATTTTACAG GTGAGGAGAA 720 TGAAGCTCAG GCAAGGTTTG CAACCAGACC AAGTTCACAA AGTGTAAGTT GGTGGCAGAG 780 CTGGGATTTG AGCCAGGACA GTATGACTCA GAAAATGTAC TGTTTTCCAG ATAAATTGGC 840 TGCTTGCTGT ACATCTCCCA TGTAGAAATT AGATCCATCA GTTTTCCTTT GTACACACAC 900 TGACTCACCC TCTTGGGCCT TGGAAGACTC TAGCACAGCC ATCAAGTATG ATTTCTCTGG 960 GCAGCACCTG CGTGGCAGCT CTTTCTCCCA CTCTCCATTC ATTCCCTGCC CTGTAGGTTA 1020 TTTTTAAGTC CACAGGCTTC TCTCTTTTAT TTCAACTGCC ACCAGCTTGG TCCAGATGGT 1080 GGCTGAGAGC TGACTCATCT GCGCTGTAAT TCCCCAGGCC CCTCTGAGCC ACTCTTATGG 1140 CCAGGGTCAC ATCTGTGAGC TGACATCCTC TCCACTATAG TGGCCTTCTG GGCTGACAGT 1200 TCCCACATTC CTGCCAATCA ACCATCCCAG TTTCATCCAT GAGCTCCTGC AGCTCTCTCA 1260 GGTGGATGCC ATCTGCTTGC AGTGATTGAT CTGCACTTCA TTCTTTCCAA TCTGGCTTAG 1320 AACATCCTGG TATTGACCAC GGTGTGATCT AGTACCTGTC TGTGTAGAGG CTATTCAAAT 1380 AGCCTCTGTA GACCCAGGCT AGAAGTCCAT TCAATCCATT AACTGTTTTC TTTTTATTCT 1440 TTCCTCTGCA GGGAACATCT ATTAGTTACA CCATCCTTTC CAAAAATGGA GTGAGCAACT 1500 GAGTTGGTGG TTTGTGCTCT CCTTGCAGGA TACTGACCTT ATACTGTGAT CAGCAGGTTG 1560 TGTTGCTTAG TGAATGAGAG TATCGGCATT AGAGTCAGGC TGACAAGAGC TGAAGTGCTG 1620 TCTCCATCAC TTCCCACCTG TGAAGCTTGT CTGGCCAGTA CCACTTTGTC TCTCTTTGGG 1680 GAAATGATCT CCTCCACACG CCATCATGGT AGTTGCACTG GAGATCACCA ATCACAGTAC 1740 ACATCCTCCT TGGCCACAGA AATTAGCCCA GGGATGGGTC ACTAGAAGCT TCCCTGAAAT 1800 GTTTCTAACT GGAGCCCATG 1820
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