Tag | Content |
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EnhancerAtlas ID | HS092-35440 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr7:75682920-75684140 |
Target genes | Number: 10 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr7:75683063-75683081 | CCTGCCTGCCTGCCTGCC | - | 6.1 | GLI2 | MA0734.2 | chr7:75682995-75683010 | TGACCACACACGGTG | + | 6.19 | PRDM1 | MA0508.2 | chr7:75683227-75683237 | TCACTTTCAC | + | 6.02 | TFAP2A | MA0003.3 | chr7:75683585-75683596 | TGCCTGAGGCT | - | 6.32 |
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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 |
GH07I076053 | chr7 | 75682437 | 75684775 |
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Enhancer Sequence | CTGATAACCA AAGCCTGTTA TTAGCTGGCC TCAGCTACTG TAGAAGACTG TGCAGTGATG 60 CTGTCAGGCC CCAGATGACC ACACACGGTG CCGAGAGTTC CCGTGTCTGC CACTTTGTTT 120 GCCTCTTCCC TCACTGGTAG CTGCCTGCCT GCCTGCCTGC CAGGGATCGG CTGTGCTTCT 180 CATTTGTGAG TTTAGATCAG AAACAAGCTC CCTGGGTATG GCTGTAATTT TGGTCAGACC 240 TTGAGTGAGA CCTAGAGGGG AAGAGTGCCT TCGAATAACG GGAGTGATTG CTGGATGCGG 300 GGCCGGGTCA CTTTCACCCC ATCACTTTCC TAACTGTTCC AAGCTGAAAT GCCCAGGGCC 360 AGCTGCTACT TTGCTGCCTG TTCTTCTGAT TAGCCTGGTA TGAAACAGTG ATTCTCAAAC 420 TGTTTGGTAT CAAAATCATC TGGGGAAAAT GGCAAAAATG CCAAGGCCTA AGCCCCATCC 480 CGCTTCCAGG AGCCTAGTCC TGAGTGGGCT TCATTAGCTC AGCAGGTGGC TCTGATGCAC 540 ACCTAGGCTG GAGAACCAGT GTGAGATACT GGAGCCCGAG ATGACAGATC TGACTCACCA 600 GGAGGGTTGG AGTCTTTCGC AACGTACGTA ACCCCTTCCA CCTCTTGTTA GGCAGCTCCT 660 TGTCCTGCCT GAGGCTCCAG CCACAAGTTT GCTGCCTGGA TGAATCTTCT CTGATTCCCC 720 ACCCCTGCAG GGAGTTGATT GCCGCAACCC CATCTGCCCT CTTGCACAAG GGGCTTCTGT 780 GACAGTGTTC TCCCTGCTCC TAATGCATCT CATTACCTGT CTCCTACAGA GCCAGCAGGG 840 ATCTTCCTGC AACCTCAGTT ACCGGGAGGG CCTGTTGCTA GGCACTCAGT GTGTGTTTAT 900 AGTTTATAAA GCTGCAGGTT GAAGGGAAGG CTGCTGTTAC CAGTCCAGCT GCCTGATGGA 960 GTCCAGCTTG TTCTTCATCT TTCAGGAGGG TTTTGAAGTA CCCTGAGTAT CACAGACTCT 1020 ACAGACATAA ATTCTCCCCA TTTGAAAGTG GACCTTTGGA ATGAAGGTCC TGAATTCTTC 1080 CAGAATGAGA CTGTTACAAA TACAATGATT GTATCTTGCT TTGGCAACTG CAGTAAAAAG 1140 AGGCCCAGTG CAACATTATA GGATACCATG TGAATCCTTT TCATGCTCAT TTCCTCCTAA 1200 GAGTCCTTTC TCTGTGCCTC 1220
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