Tag | Content |
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EnhancerAtlas ID | HS091-08153 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr11:70057280-70059600 |
Target genes | |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
BCL6B | MA0731.1 | chr11:70058567-70058584 | TGAGTTCCTTGCAAGCA | - | 6 | IRF1 | MA0050.2 | chr11:70058634-70058655 | TTCAGCTTTCACTTTTGGTTG | + | 6.32 | ZNF263 | MA0528.1 | chr11:70058260-70058281 | CACCCCCTCCCACCCTCCCCC | - | 6.14 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr11 | 70058304 | 70059000 | chr11 | 70058385 | 70058983 |
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| Number: 2 | ID | Chromosome | Start | End |
GH11I070212 | chr11 | 70058144 | 70059155 | GH11I070214 | chr11 | 70059461 | 70059635 |
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Enhancer Sequence | CAGAAGAATT GCTTGAACCT GGGATGGGGA GGTTGCAGTG AGCTGAGAAC ACGCCACTGC 60 ACTCCAGCCT GGGCAACAGA ACAAAACTCT TTCTCAAAAT AAAATTTAAA AAAAATAAAA 120 TAAATTAGCT GGCCACAGTG GTATATTCCT GTAGTTCCAG CTACTTGGGA GGCAGGAGGA 180 TCACTAGAGC CCAGGAGTTC AGGGCTATAG TGAGCCATCG TTGCGCCACT GCACTCCAGC 240 CTGGGCAGCA GAGCAAGACC CTGTCTCAAA AAACAGAGGA AAGAAAAGAA AGGAAAAAAT 300 AGTAATCATA CCTGACGTTA AATATGTTAT TAATCTGAAT TCTACGAGTT TTGTAGGCTT 360 CTCTCTCCCC AATTTGCAAT TTTATTGGCG ATTTATAGTT TCCAAGGGCT AGACACATGG 420 GCTTCTATTC CACATCTGGC TATATATTTG TGCCTATTGA TGTTTCATTA TTGAAATGAA 480 AACCTGGTCA TCATGGGAGT CTGGGCAATG TTTTACTACT TCCAAATCAG TTTCTGGCTG 540 GAGAACCCCA GCTACAATGT CCCCATGTCC CTCAGGATGA AATCTTTTTT TTTTTTGAGG 600 TGGAGTCTCG CTCAGTCGCC CAGGCTGGAG TGCAGTGGCG TGATCTCAGC TCACTACAAG 660 CTCCGCCTCC CGGGTTCACA GCATTCTCCT GCCTCAGCCT CCCGAGTAGC TGGGACTACA 720 GGCATCCGCC ACCACACCCG GCTAATTTTT TGTATTTTTA GTAGAGACGG GTTTTCACCA 780 TGTTAGCCAG GATGGTCTCG ATCTCCTGAC CTCATGATCC ACCCACCTCG GCCTCCCAAA 840 GTGCTGGGAT TACAGGAGTG AGCCACCGCG CCTGCCCAGG ATGAAATCTT AATCCATGCA 900 TCATCATGCA TGGGACGGGG TACACAACTG TGCAGAGCCC AGCCCAGTGC CATGTTCCCT 960 CCACAGCAAG ACTGTCACCT CACCCCCTCC CACCCTCCCC CGCAGCCCTT GCCCCTGCTG 1020 TTTCCTCTCC CTGCAGCCTT CCTCACTATC CACCCCAAGC CCCCCAGCTC AGAAGACATC 1080 CTTCTGATGC AGGCTTGCCC ATGCACCCAC TCACAGTGGG ATCCCTGCAG CCCCCACTCC 1140 TGCCCGGGTC CTGCTTCCTC TAGCGCGACT CCCTGAGGGC TGCTTCCAGC ACTTTCCAGC 1200 GGCTTCTGAG TGAAGGCTTA TTTTGTGTTT GCTGAGTGAA TGAGTAAACA GCAGCGATCA 1260 AAGGCCCACT AGCGTCTCTC AGGGGCCTGA GTTCCTTGCA AGCAGGAAAG CAAAAGATGC 1320 CTCCGCCCCA GGGTTTCAGA TTCCTGGATT CCCCTTCAGC TTTCACTTTT GGTTGGGCTT 1380 CCCAGCCCAG TCAGTCGGAC TGTGAAAGCA CCTGCCCCGC AGTAGGCACG GGCAGGGCAA 1440 GAGGGCATCT TCTCAGGGGA GCCAGGTATG CCCCTTGGTC TGCCACCCAT GCATCATATG 1500 CCCCTGTTCC CTGAGCCTCT GCTCCCCGCC CCTGGTCCAC ATACCCCCGC CCCGGTGCCC 1560 TTCACTCTGA CCAGGCCCAG TGAGCTCCAG CCAGGAACCC CAGGGAGGAG TCCCCACCAC 1620 CTGAGTCACT GCAGGCCATC CCAGGGGTCC TACTCGCCAG GAAGGGTTGA CGCCCACGTA 1680 CACATACACC TCTGGGCTCC TGGCACTCTG AGCTGTATGT TTCATTCTGG TTCATTCACC 1740 ATTCATTCAT TTACTCGGTA GATTCTTAGC AAAGGGCTAC CAGCTCAGAC CGGGAGTGGC 1800 CAGCTCTTCT CCCTCACCAA TGCTCCCTCT CCCAGCAATG TTGTAAGGTT CAATGAGATG 1860 TGGTGTGGCG AGGTCTGGGG GTGACAGCCC AGGATAAACG TCACTAAATG TCATCATTGT 1920 TACTATTCTT AAGGAACTGC CTGTTTTAAA ACAAGCAGCC TTAAAATTAA AGTGTAGGTA 1980 TGGGGCCAGG CACAGTGGCT TACACCTGTA ATCCCAGTAC TTTGAGATGC CAAGGTCGGC 2040 ATTTCACCTG AGGTCAGGAA TTCAAGACCA GCCTGACCAA CATGGTGAAA CCCTATCTCT 2100 ACTAAAAATA CAAAAAATGA GCCAAGTGTG GTGGCGGGTA CCTGTAATCC CAGCTACTTG 2160 GGAGGCTGAG GCAGGAGAAT CACTTGAACT TGGGAGGCAG AGGTTGCAGT GAGGCAAGAT 2220 TATACCACTG CACTCCAGCC AGGGCAATAG AACGAGACTC GGTCTCAAAA AAAAAAAAGG 2280 CCAGGCACAG TGGCTCACAC CTGTAATCTC AACACTTTGG 2320
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