Tag | Content |
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EnhancerAtlas ID | HS095-04340 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr10:102995370-102997620 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
PLAG1 | MA0163.1 | chr10:102996383-102996397 | CCCCCTCGGGCCCC | - | 6.65 | RREB1 | MA0073.1 | chr10:102995494-102995514 | TGTGTGTGTGTGTTGGGGGG | - | 6.69 | ZNF263 | MA0528.1 | chr10:102997196-102997217 | TCTTCCTCCTCCGTCTCCTTT | - | 6.46 | ZNF263 | MA0528.1 | chr10:102997193-102997214 | TCTTCTTCCTCCTCCGTCTCC | - | 6.4 | ZNF263 | MA0528.1 | chr10:102997184-102997205 | CCCCCATCTTCTTCTTCCTCC | - | 7.44 | ZNF263 | MA0528.1 | chr10:102997187-102997208 | CCATCTTCTTCTTCCTCCTCC | - | 7.91 | ZNF740 | MA0753.2 | chr10:102995509-102995522 | GGGGGGGGGGCGC | - | 6.1 |
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| Number: 2 | ID | Chromosome | Start | End |
GH10I101236 | chr10 | 102996521 | 102996570 | GH10I101237 | chr10 | 102997381 | 102997510 |
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Enhancer Sequence | AGAGAGGAAG AATGGACAGA AGATGGGAGG TGATGGGCAG GCAGGAGTGG CAGGAAACAG 60 ACACCCACAC GCCACTCCAG TAGCCCAGGG GTCTGTGAAG AGGATAAAGG AACCTAAGTG 120 AGCATGTGTG TGTGTGTTGG GGGGGGGGGC GCGGTGTGGG GGGAGAGTCT GGTTCTGTTC 180 CTGATGGAGG TGGCATTTGA GTTGAACTTT GTAAAACCAG GAGCATGTAA ATAGGTGCAG 240 GAGCAGGGAC CATCCTGGAG GCAAAGGGAA CAGCCGAGCA CAAGCCCGAA GATGCCACCC 300 TAAGAGAGGT TCCAGAGTTC CCTATAGCTC CTCCCTCTGT TGTCCTGGCG GTGAGCTACT 360 GGGTAAGGGT GAAACCCTTA GTCTCTTGTT TATCGGCAGC AGGTCTGCAG CCTAGAGCCA 420 GGGGCTGCTG GACTCCTGGG ATGGCTATTT ACTTATTTAT GGGGTGGGGT GAGGGGTGGG 480 GATGGGATGA GAGAGGCTGC TTTCCTGGGC CTACAATTGG AGTTCCCTTC TCCTTGCCAT 540 CCCCAGAAAC TCCAAGAGCT GACCCTCTGT CTTACTAACT CAAACGGCCC AGAAACATCA 600 AAGTCTGACC AAAAACCGTT AATGGTAGTC AGCTCCCTCC CTTTCACAGA GGTCTCACTA 660 CTGTCGGGGG GCGCCGGGCG CAGGCCGGGC ATGGGGCCTG AGCTTAGGCC AGGTGGAAAG 720 GTGGAAGGAC CTAGTGGGGA CAGACGAAGA GACCGAGGAG CCGCCCGCCC GGCTAAATGG 780 ACACAGGAAA GGCCTGAGTC AGGCTTCTCA TAATAAATAA ACTGCACGTG AATAATTCAG 840 CAGTCGCGCG GGGGCCGGTT GCATCAGCGC CGCCGCCGCC GCGCGGCGCC CAATTCCCCG 900 CGGAGGGGAG TAGCCAATTA AGGCACTTGA AAAGGGAGTC GGGTGGAAGA TCCCCCGCCC 960 ACCAGTATCC TGGATTTACC CAGGTCGAGT TCAGAGAGCC TCCCCGGTCC CAACCCCCTC 1020 GGGCCCCATG GGTCAGGGGG CCGCCTGCTG GGAAGTGCTA CCTCAGCTAA GCCGCTCAGG 1080 TGTCCCGAGA CTCCGGGCAA GGGAAGACAG GCGGCGAGAC GGAGCCAGAA TAAGGGATGC 1140 GGACGTCTGA CCTGTGGAAA ACCCAGCATC TGCAGTGCCC AGCCGCACAG GGAACGTGGG 1200 CGGCGTGGTT CCAAGCACAG TGAAGACGCC AGGCTCGGAT CTGTGCTCAG AGCCGGGATC 1260 CCTCCGGGCT GCTTCGTCCT GGCCAGGACT TTCCTTGCCC TGAAGTGAGG CGCCAGGGAA 1320 GCTGCAGGGC CCTCCGCCCT CTCTGAACTC CCACGTACTT GGGCCTCTCC CAGCCTTTCT 1380 TGGACCTGTG GAAGCAATTC CTGCAGGACC AGACTCCCCT GTCTCCCCGC GGCCCCCTAG 1440 GTACACTCCG TAACTTCCGA AACCTTATTT CGTTTGAGCG AAACCCGGCC CCTTTGGCTC 1500 TTCCCACTTC CCACAAGTCC CTGGGTTCCC GATCCTGAGG GATTGCATTC ATCCCATCTC 1560 ACACCCACCA ACGCTCAATC CCTCCAGTTC CTCCCCAGCC CCTTCACTTC CATTAATTAG 1620 GTCGACTCCC TTCCTTCGCC GCTCCCTCCT GTCCCCACTC AGCCTCCCTA CACCTATGCG 1680 GCGAGCCTCG GGCCAAGACC TCCGCCCTGG CTCCGCCAGT CCTGCGGGGG CCGGCATGCA 1740 CCAGACCTCA AAAGGGATCT TCACGGGAAT TCCGCATAGC CAGATCCCAA GCCTCCAGGG 1800 AGGCCACCAG CCCTCCCCCA TCTTCTTCTT CCTCCTCCGT CTCCTTTCCT CTTCCCTCCG 1860 CCTCTACGTA TTTCTTTCTA TTCGTTTCTT TTCGTTTGGT GAGGTGCCAC CCGCCACAGC 1920 CCTGTCCCCT AGGGAGAGGC CTGGACTAAC TTTGCCGTCC TCGTGGCCTT AGCCCGGACT 1980 GTGAGTCTCG AGCGGCTTCC GAGAGGCAGC TCGGGTGTCT TCGCAGAGAC AGATGAGGTG 2040 GGCTGGCGAT TCCCTAGCCT CAGATGGCTC TGCCACCAGC CAGCTCTGTG ATCCTGGGTA 2100 AGTCTTTCAA CCTCTCTGAG TCTTGACGTT GGTAAAAGGC AGGAGATTTA GAGAAGGTGT 2160 TGGGAGACTA AATCTTTTCA TTCGTTTGAG AAAGGGAGTC GCCTGTGTTG GGACCTAAGG 2220 AGGAAGTGAG GTTCTTGAGA ATTCTAGATC 2250
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