Tag | Content |
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EnhancerAtlas ID | HS092-38880 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr9:130685360-130686640 |
Target genes | Number: 33 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFYA | MA0060.3 | chr9:130685564-130685575 | GGCCAATCAGA | + | 6.02 | Nr2f6(var.2) | MA0728.1 | chr9:130686552-130686567 | GAGGTCAGGAGTTCA | + | 6.22 | Zfx | MA0146.2 | chr9:130686528-130686542 | GAGGCCGAGGCGGG | - | 6.01 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_44595 | chr9:130685039-130686650 | NHDF-Ad |
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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 |
GH09I127923 | chr9 | 130685320 | 130686810 |
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Enhancer Sequence | ACCCCAGTTT GCAGATGGTG TGTCTATGGT TTTGCCTCAA AATGTCTTCC ATACCAGAAG 60 GTACCTTTGG CAGGGCGCCC AGTCCCAGCA GAAGCAGGTT CAATTCCCTA ACTTTGTCCT 120 CAGGCGTCAT TGAAGGGCTT TAATCCTGTC CTGTCTGGGT CTCGGGGTAA ATAGACCAAT 180 GAGAAAAAAG CCCTGCCCGG CGCTGGCCAA TCAGAGCTCA GTGGTCTGAG AGTCTGAACA 240 GAATGCTGGT ACCCTGTGGG CTACCTGGAT GATGGGGAGA TGTGGGATGG GGGCGTTCTC 300 AGTAGGGGCT GGGAACTGGG TTGGGGTGGG GCTGGGACAG CCAACATGAA AATATTTCAA 360 TGTCACAACA ATTCCATGCA AACCAGGACT CACTGACTGA ATGACAGCGG TGGCCTAAGT 420 ACCAGCTAGG GGGAGAGGGC AAGGGAAAAG CTGACCTCAC TTGGATGGGC AGGTGTGGGA 480 GGCTCCGTGC CCCATGGCAG GCTTGCCACC ATCCGGTCAG GACGTGTCCA GCCCAGCCAA 540 AGGCCAGTGA CTCCAAATTC TACCCAAGTC TCACCCATAC CAAGTTCTTC CTCTGAGGGG 600 TAGGAACGAG GCAGGGGACA GGAGGGGTGG CGGCTGGACC TCCTCTTTCA CTCCCCTTGT 660 CCACCCACTG GATCAATGGA GTGCCTGTCT TAGCTCCTAT GTAATTCTGT TCGACCACAG 720 GGGTGGGCCT GAGGGAACTG AAATGGAAGT AGCTGGCCAA GTACTAACAT GAGTCCTCAG 780 AAGTCATTCT GCAACCTTGT GTCTGCTTCC CGAGCCTCAG TTCTCACATT TCTCAAATGG 840 GGATGAGTCT ACCCTCCCAG GGAGGCTCCC AGTCAGCATG AAGGAATGAC AGTTACCACT 900 ACTGAGATGA AGACAGGAAG ACGGTGCCAA TGATGATGAC GTCAGCGTCC TGGAAGTGGA 960 ATGACCAGCT AAAAAGGGCA AGGACCCTTT CTAAAGCAAA AATTAGGCTG GGCGCGGTGG 1020 CTCACGCCTG TAATCCCAAC ACTTTGGGAG GCAGAGACAG ACAAATCTCT TGGTCAGGAG 1080 TTCAAGACCA GCCTGGTCAA CATGGCGAAA CCCCATCTCC ACTAAAAATA CGAAAATTGG 1140 CCGGATGCTG GGCCTCCCAG CACTTTGGGA GGCCGAGGCG GGTGGATCAC TTGAGGTCAG 1200 GAGTTCAAGA CCAGCGTGGC CAACTTGATG AAACCCCGTC TCTAATAAAA ATACAAAAAT 1260 TAGCCGGGCA TGCTGGTGTG 1280
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