Tag | Content |
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EnhancerAtlas ID | HS076-39006 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr3:9862430-9863500 |
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) |
Nr2f6(var.2) | MA0728.1 | chr3:9863470-9863485 | GAGGTCAGGAGTTCA | + | 6.22 |
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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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Enhancer Sequence | TCCCCTGCAG CTGGGACTTT GGGCTGTGGG CAGGTGCTTA GGGATAGACC CTTTCTGTCT 60 CGTGCAGCCC CTACCCCTTC CCCAAGCCTC CCGCTCGTTT ACCCCGCTGT TCTGCTCAGG 120 AACCCTCGAG GACTCCCACT GCCTCCGTGA TAGGGTCTGG GCCACTTTTC TTGGTTCTTG 180 GCATAGCATA GTCACTAAGA GCATGGACTG TGCCACCAAA TGGACAGCAC ATTACCCAAA 240 GTGTGTGTTG TGTGGATGTT AATTCTACAG GAAGTAAATA GATTTTATGA AAAAAGGGCT 300 TTTGTGGTCC ATCACATTTG GAAAACACTG GATTAAGCAG TTAAAGAGGC TTCCCTGGGG 360 CAGTACTCTT CAGAACCTGT GGGTGGTGTA AGCCTATAGA GAGAGTGCGC TGCTTATCCT 420 GTACTTAAGT GAGCCCAGTG CCCTGCCTCC CACCAAGCAT CCTGAGGGGC AGTGTTTTCT 480 GAACACACTT TGGAAGAAGG TTCTTAGGTG GGGAAAGGGA GGATCAAGGT GAGCCTGGTG 540 CTGCTTTAGG GAGATTCCAT TCGGGAGAAG CATGCAGGAG CAACTGGAGG GAGAACAGCC 600 CTGAAGGCAG AACACACAGT AAGCATTTCT TGAGCAACTC CGATGTGCCA AGCATTGTGC 660 CAGGTTCTGA AATGAAGCGT AGCCCCTGTT CTCAACTGGG ACACAGCTCA AGGTTTGAGA 720 CCTGCAGGAA GCCAGGTGGG AGTGCTAGGA ATCTCAGCTG GGGTGGTGGT AATGGGAAGA 780 AATGGATAGA TTTAATTACT CAGTAGGGGA AACCGAAGAA CTAATGAATG ACATGAGCAG 840 CAGATCCACA TCATTAGCAC GTAATTCACT GCATCTTTTC TAAATGCCAG GACATAACTC 900 AGGTGGCCCG GTACTTTCTC TTTAGCTACT GGAAAATGTA AAGCTGCCCA TTTTAAATTA 960 AGAATTATCA AGGTGGCCAA GCGTGGTGGC TCACGCCTGT AATCCCAGCA CTTTGGGAGG 1020 CTGAGGCGGG CAGATCACTT GAGGTCAGGA GTTCAAGACC AGCCTGGCCA 1070
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