Tag | Content |
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EnhancerAtlas ID | HS182-16186 | Organism | Homo sapiens | Tissue/cell | Spleen | Coordinate | chr3:121716660-121718020 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF4G | MA0484.1 | chr3:121717804-121717819 | TGACCTTTGGTCTCC | - | 6.2 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr3 | 121716830 | 121717448 | chr3 | 121717719 | 121718002 |
| | Number: 1 | ID | Chromosome | Start | End |
GH03I121997 | chr3 | 121716249 | 121718446 |
| Enhancer Sequence | CGTTTCCATT TCAAAAATGT CTATCTTTAA GTCCTACAGA GGGCTGTTTA CCACTATTAG 60 GTGAACTATC AAGGGTTACT AAAATTTGGT CTTATTTTCA TTTTTCTCCT CTCTAATCCT 120 TTTTTAACTC TCACTAGAAA GTGGGAGCAG GTTGGGGAGG TGGGATGTGA TCAAAGAAGT 180 TCAAGAATCA CTGACATGTT TCTTGAAGCT TCCTTCTGCA TCTAGAATTT TGATTTGCTG 240 AAATCGAGTC AGGCAGATGT GAGCTCCCTC AGCTTCCTCC CTTACATCTT AATCATCCTC 300 CACATTTTAA TGACTTCCTT TCTGTCTTCA GAGGCCAGGC TGCTTCCCTT TCCCTTCCGC 360 TCCCTTTCTA AGGCCAGTTC TTTCCTTGTA GGGCTGAGGC CACTCCTACC AGCTTCATCA 420 CTCATCAGTG ACCTCACTTC TTAATGCTTC ACTTTACTCA TTTGATATTA ACCTTGGTTC 480 TTTGCTTATA AACATGTTTA GGATTACCTT ATTCTACAAA CACCAACAAT AACTCCTTAC 540 TCCTCTAACC AAAGAGCTTT CTTTAATAAC TCATGCCCTT CCATGCAATT CTTCTTGTCA 600 ACAAACTTCT CAGGACAGTC TACCCCAGTG ACTCACTTTG AAAGTGACCT CATCGGCCCA 660 AGTTCAGGGA TCTTTGTAAT CTACATTTCT TGATTTTACT AGTTTTTTAA AATGAACCTA 720 ATCCCTCAGG AGAAACAACT CTCCCGCAGA ACCTCCATTT ATTAGTTTAC TAATAAGTGG 780 TGCACTTATC ATTTGTGTTA GCTTTGTCCC CAGTCTTGCC TGCTTTTAGT GCCCCACGAA 840 CCTAGGGAGT CTAAGCAGGC ATCTTGGGCG GGTTTTTCTT ATCTCATCCT GCATATTATT 900 ACTCCAGTGA CAGTGATTTC TCCATGGCCT CCTCCCTAAG ATCCCTGAAA GGTAGGGGGC 960 CCCACAGTCC AATGCTGCAT CCTCCACGAC TTTTCCCCTC CTACGGTGTC TTAGCCAATC 1020 CCACAGTGAT CCACCTACAG AGGCTGTGGC AGTCTCTGCT GTAGGAATGC AGACTCTCAC 1080 AAGTCAGATG AACATGGATT CAACTCTGCA AAACCACTGC TACTTCCTAG CTGTGGGGCT 1140 TTTCTGACCT TTGGTCTCCC ATCTTTTAAA AGAGATGACT TCTGCCTTCT AGGGTGGTTG 1200 TGAGGATTCA GTGAGGAAAC GTATGCAAGG GGACTACACA TCAGACATCC AATAAAAGTT 1260 AGTTCTCTTT TCCTGTAAGA CAGCAACCTC AGAGCACAGG CCTGAAACCA GACTCAGGCC 1320 ACCGACTTTC TTCACATTGT AGATCAGGTT TTGTTTCTAT 1360
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