Tag | Content |
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EnhancerAtlas ID | HS018-01190 | Organism | Homo sapiens | Tissue/cell | CD19+ | Coordinate | chr1:120800240-120802010 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF4G | MA0484.1 | chr1:120801025-120801040 | AAAGTGCAAAGGTCA | + | 6.78 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AGCACCATAC TGCTTCGGAA GAAGAAGTCT TTATCTTAAT GAATTGATCT CATCAATTTA 60 GCTGTACATT TGATCCCAAG ACCCTTTGTG GACCTGATAA CCCTGGGGAG GCCCTTAAGT 120 GAAGCTGTCC CTAGGGTGGC CCACTTCATC ACAGAGACCA GCAGACAGGA AAGGGCCATT 180 GGGGAGATTC TTATTTTATT ATGTAAGTCA GAGGAAGCCA CGTTTAGCTC CTCTGCTCTA 240 CTGCAGCATC CCTATTTGTA CCTGGTATAA CCAGCAGAGG TAGAAAAGGA AGTCTGTCTG 300 CATAAATGAA AACAAGGGCT AGCCACTCCC GTCTGATGGT AGGTGGTCCT CCACTAGTAC 360 CTAACTATGA ACACCCACAG TTAAGTTTCT TTCTCTTCTT CTCTCTCAAA CCCATTTCTT 420 TTGTTTTTTA GGGGTTTTTT TGTTAGCTTG TTTTTGAGAC AGGGTCTTGC TCTTTCACCC 480 AGGCCAGAGT GTAGAGGCAT GATTACAGCA CCGTAGCCTC GACCTTCCGG GCTTAGGTGA 540 TCCTCCTGCC TCAGCCTCCC AAGTACCTGC GACCACAGTT GGGCGCCACC AAGTCCAGCT 600 AATTTTTAAA TTATCTGTAG AGATGGGGTC TCCTTATGTT GCCCAGGCTG CTCTCGATCT 660 CCTGGGTTCA AGCAATCCAC CCACCTCAGC CTCCCAAAGT GGTGGGATTA CAGGTGTGAG 720 CCACAGCGCC AACCCAAACC CATTTCAATT TACTTCCAAG GAATGGAAGA AGTAACATAA 780 ATGGCAAAGT GCAAAGGTCA GGTTCAGCAG CCCTATGGGA AAAGCATAGG CTTTAGAGGC 840 AGACTTTGGG ATCCTGGATC CCAGTTCCTA GGACCTGTGT GACCATGAGC ACATATCTTA 900 ATTTCTGAGC CTTAGTTTCC TCACTTCTGA AAAGAGGACA ATAATATCCA CCTCACTAAG 960 GTGGTATGGG ATAGTTGCTA TGTTTGTTTT GTTTTTGTTT TTAAGCCTCT AAGGCCAGAG 1020 GTTTTGTGAG TGCTGGATGA CTTCATTTCT AGCTCAGGCA AGCAGAAACT GGATATGAAA 1080 CTGAAGAAGA GTGACATCCA CATATGGCCT AGGTGTGAAC AAATTCTGTT TGCTTGCATG 1140 CTTGCATGGC TAGGACGCTA GCATTTCAAG GAGCCAGCTC CATGAGTTTA CAGCCAAACT 1200 GGAGAACCAT TCTATAGTGA TGAGTACAGC ACATTTACAC AGACATGCTC AAAAGCACTG 1260 CAAAATTCTC TCCCTAGTCT AGAATTCCTG AGTTGGCCAA CTCTACACAG TTCAGAATAA 1320 AACCCAAAGA CTGCCAAGAC CAGTCAATGT TTTTTTTTTT TTTTTTTTTT TTGAGACGTT 1380 GTCTCACTCT GTTGCCCAGG CTAGAGTGCA ATGGTGCGAT CTCAGCTCAT TGCAACCTCT 1440 GCCTCCCGGG TTCAAGCAGC TCTCCTGCCT CAGCCTCCTG AGTAGCTGGG ATTACAGGCG 1500 CCCACCACCA TGCCCAGCTA ATTTTTTTGT ATTTTTAGTA GAGACGAGGT TTCACTATGT 1560 TAGTCAGGCT GGTCTCGAAC TCCTGATCTC GTGATCCGCC CGCCTTGGCC TCCCAAAGTG 1620 CTGGGATTAC AGGCGTGAGC CACCGTGCCT GGCCCAATGT CTTTCTTTTT AAGGAACATA 1680 AAGTAATCCA AAAAAGACCC AGAGATTTCA TTCTAATATG AAATCAGTCT TGCTAATAAA 1740 GTTACTGCCT CTATCAAAAT CTATAATCTT 1770
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