Tag | Content |
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EnhancerAtlas ID | HS048-30628 | Organism | Homo sapiens | Tissue/cell | Fetal_small_intestine | Coordinate | chr5:167797540-167798420 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6 | MA0677.1 | chr5:167798089-167798103 | TGACCTTAGACCCT | - | 6.18 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GTAGAATATG TATTTTAGGC AGAGGCAGTG ATGGGAAGAA ACCAAAGTGA CTGTCTGGAG 60 GGGCCACCCA GGCTGAATCT CATATACCCA GATTCCCAGC TTCCCATACT CTGGTTTAAA 120 TACTTGACAA ATTGTTTGTG ATAGTTTTCT AGCACTGACA AGCCTTTGTT AGTTTAGTTG 180 AGTGATTTGT TTATTTGATT TAGCCATTGA GACTTGGTGA TTACTACCAC TTTGATCCCC 240 ACAAGATGGG GACATAGAGA GCGGTTATTG CTAAAAGATC AGTTTGGCCT GGATTGTCTA 300 AGGAAGCGCC ATTGTGGGTG CAAGCATTTG GGAATCAGCT CAAGAGGAAA ATAAATACTG 360 CTCATTGGCC AAACTCACAG GGATGGAACA TCTGCTATTC TTGATGTTGC GGCAAGCCAG 420 CCTTCCAAAG GGCAAGTGAG CATGACAGGC GTGAGACAGA GCCAGGATAA GGATTAGAGG 480 TGGGGTGGCT GAGTGCGTTG CAGGTGAAGA AGCCAAGGAG GGCTGGAGTC CAACTCAAGA 540 AGCAAGACTT GACCTTAGAC CCTTTGCCTG CAAACCCTCA ATCAGAGTTG CAGAAACAGA 600 GGCCCAAAGA AGGAAGTTGA CTTGCTCCAG TCACTTCTGA AGGAGTGGCA AAGTTGGGAC 660 CAGAACACAG ATTCCCTGCC TCCCACACAG GGTGATCTTA TCCTGCTGCT GCAGCTATGT 720 GTTCACCTTC CCGGGAACAA AGGGGACAAC AGAGCTGGTG CTGCTGTGGT GTAAAACTTT 780 TGGATCTGTT GAGCCAGCCC AGAAAAGCAG GAGGCACAGG GAAGCAGCAG GTTGCAGGCA 840 TTTGGGGACT GTAGGCTGAT GGAGTCTGTT TCTCCTCTCC 880
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