Tag | Content |
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EnhancerAtlas ID | HS091-32911 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr22:31957380-31958850 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HOXA13 | MA0650.2 | chr22:31958141-31958152 | GTTTTATTGGG | - | 6.62 | NR2C2 | MA0504.1 | chr22:31958292-31958307 | TGACCTCTGAACTTG | - | 6.1 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr22 | 31958187 | 31958304 | chr22 | 31957728 | 31957832 |
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| Number: 1 | ID | Chromosome | Start | End |
GH22I031561 | chr22 | 31957187 | 31957530 |
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Enhancer Sequence | GAGTCCAGCA GACGTGGGAT TTGGCATCCT CTGTCAGTGT TGTCAAGCCT CTCACCCACA 60 GAGGGCAGTG CTGGGCCTTC CCTGCAGCTC AGGGCCTGAG AGGGGGTGGG GACAGAGGTA 120 ATCTGGAAGG CTGGGCTCTT CCAGAGGGAG GCTGCTGTTA GGAATAAAGT AGAGGCTTGT 180 CCTAGATGAG CCTAGATCAG TGGCTTCCAG AGTGCTTCTG GTAATTGTGG AGCTGGAGAG 240 GGATTTATGA ATTAGTTATA AACATGTTTA GAGAAACAGC AGTATACTCT GATTTCCTCG 300 TTGCTGTTTT CCTACAGCAA ATCAGAAAAT AATTGGGGCA GAAAAGAAAC TTAAGACTGA 360 AAAGAAAACC TGTCTTCCTT TTCTTTATAG TTTTGATTGT CTTAGAGTGT TCTTTTAGGC 420 AAGCCACTAG CTTTTTTTGT CAATCATAAA TGGCTAAGGC CTGTACTAAA ACTTTCTTAT 480 CCTTTGACAT ATTCTCTGAA TTCTTGTCAT GTTTTTGTGT CTGCTGGGTA CTTACAGAGC 540 TGCCAAATAA GTTATAGGAA ATAGAACAGA GAAGAGGAAA AAAAAAATTA GTGCCTGTTT 600 CCAAATGTAG GAATAGTATC TTCTTATTCT AACAACAAAT TGCATAGTCC ATGTGAATAC 660 GTGCAGATCA CATGCAAATA GCATATATAG TCATCTAGAT CAGTGATCAG CAAACTGGCT 720 CACAGGCCAA ATTTGGCCTG CTTTCTGTTT TTGTAAATAA AGTTTTATTG GGATGCTGCT 780 ACACTCATTC ATTTATATAT CATCTGAGGC TGCTTTCAGA TTACAAGAGC AGTGTAGGGT 840 AGTTGTAACA GAGACCTTAT GGTCTACAAA GACTAAACTA TTTGTTTTCT GACCCTTTAA 900 GAAAAAGTTT GCTGACCTCT GAACTTGTAA GGTCTTCTGA GGCAATAGCA AGGAAATAAG 960 AGACACAGTT CTCGCCAATA ATAATAACAG TACCAATAGC AGTAGCAACT GCAGCCTGAG 1020 TGACTGAGTT GGGGCCCTGT CTCAAAAAAA AAAAAAAAAA AGAAGTAGAT TTTATTGTGG 1080 TCTTACTTGT GTTAGGTGCT AGACTAAGTG CTTTACGTGC ATTATCTAAT TTTCATAAAC 1140 CTTTTTTAAA AGTCCCATAT TATTGTTAAG GGAACCAGGA AGGTTAAATA ACTTGAACTA 1200 GGGTCACATG TATAGTGAAG CTTAGAGCCA GGTTTTTTTA TTTTTTTTTG ATTTTTTGAG 1260 ACAGAGTCTC GCTCTGTCAC CCAGGCTGGA GTGGAGTGGC ACAGTCTTGG CTCACTGCAA 1320 GCTCTGCCTC CTGGGTTCAC GCCATCATCC TGCCTCAGCC TCCTGAGTAG CTGGGACTGC 1380 AGGTGCCCGC CACCACGCCC GGCTAATTTT TTGTATCTTT AGTAGAGACG GGGTTTCACC 1440 ATGTTAGCCA GGATGGTCTT GATCTCCTGA 1470
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