Tag | Content |
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EnhancerAtlas ID | HS095-06466 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr11:132501800-132503930 |
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) |
RREB1 | MA0073.1 | chr11:132503612-132503632 | TGTATGGGTGTGGGGTGGGG | - | 6.18 | TFAP2A | MA0003.3 | chr11:132502109-132502120 | TGCCTCAGGCA | + | 6.02 |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I132631 | chr11 | 132501679 | 132504056 |
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Enhancer Sequence | TGTGTGAATG TGTGTTAACA TCCAGGACAT CTGTGAGACC CTAAGGACCT ATTCACAGAA 60 GGCCACTGAA TTATAAGTTT TGTCCAGGTT TTCAGCTGGG TAACGAAACA CGTAGCTGGA 120 AATGAAAATG TGGCAGCCAT GCTGATCAGG GCTGGGCTGT TAAAATGGTT TCTGCCTGAA 180 AGAGTCCCTC CTGTAAACAT CCCTAGGATA GGGAATGCAG ATCCAGCTTA AAAAAAAAAA 240 AAAAGAAAGA ATGAGAACAT GATTGTGCCA CATGGAGATT TGGGCAGGAT CTTGTTAGGC 300 CCCTGAGGGT GCCTCAGGCA TCTTTATTCA AACACATTTT TTTTTTTTTT TTTTTTTTTT 360 GGAGGGAGCA AGGAGGAGAT CACACAGTTG TGGAACTGTC GTCAAAGCAA GCAGCTGACA 420 TTTAAATAAT ATTATGATTT AAAAGGTTCC TTTGCATTCG TTCCTTAACT CATTACACCT 480 TCACAACTCT GTGACACGAG AAGAGGAGGT GACACTATTT CCATGTGAAA AATGAGAACA 540 CTGATATTCA GAAAGATGAA CTGATTTTTG TAAGGTCAGA TATCTTTTAA GTAATGGAGC 600 AGGGACTTCA AGTGATGTCT GTCTCTCTCC AGTGGCTCTA TGATTCTCAG GATATCATCC 660 TATCTCCACG CAACACAATG TCGCCGCAGA GGAGTCGCTT CCTGAGTGGT TCCATGATAG 720 CCAGCCCGGT ATATCTACTC CTTTTGGTCT TTTTCTGCTT CCCTATCTTC AGCAAGGCGA 780 GGTAATCACT CTCTCTTTGG TATGTGAGAT ATGTATCTAT TCTGTCATAT CCGCCTTTCA 840 GTTGTCACAT AGCCAAACTA TGCAAATGTG GCCATCTCCA CATCTCTGCG TTCAGCACGG 900 CTGCTGCTCC ACTCTGGACT CCTTCCAACT GTTCAGATGG GCAGGGAGGA GTTTCATCAT 960 CAGAGATGAT AAAGAAACAT GACTATTCAG CCTTTCTCGT ACATCTACCG AATACCTAAC 1020 TAATGATGTT CTCACCATAT TGAAAAAAAA AAAAAAAACC ATCCAGGATG ACGAATTTAT 1080 TCCCTGAGTG CCTCATGACA AGTGAGTCAG CTCTCAGCAA CCAGAATTAC AAGTGGACTG 1140 AGCTGGGTGA CGGTGGAGCA TGAGGAAGTG CAGTCTGTCC TGCCTATAAA GGTGGTCCTA 1200 GGCTAATCGA AAATCTGCAC CAACAACACA GCAAAGTGTC TTCTGCTGCC AGTAACAGAG 1260 CACCCAACTG TTGGTGTTTG AGGGGGACAA TCGGTAGCTC TCTCTCTTTT TTTCTGAGAC 1320 AGAGTCTCGC TCTGTCGCCC AAGCTGGAGT TCAGTGGTGT GATCTCGGCT CACTGCAACC 1380 TCTACCTCCT GGGTTCAAGT GATTCTCCTG CCTCAGCCTC CCGAGTAGCT GGGACTACAG 1440 GTGCTGGTAG CTCTCTTTTC CCTGCCTAAG TTCAGAACAA CTTGAGAGAC AAACAGGGAG 1500 AAAATAGATG GAAATAAAAA TAGCCCTTCA TTTCTGATAG AAATTAAAAG CCGGGAATGT 1560 GGTTTATATC TTTACGTAAG CAAATGGGCA TCCCAATCCT GAGCCTCAGG ATTCGACCCC 1620 ACTCCCCCAG TCACAGGAAG TGCGAGGAGG CCCCAGGCCC TGGGTCTGAG CCTGGCCTCT 1680 TACGCTGCAT GACACAGGAC ATCTGTTGGA AGGTCAGTTT CTAAGACAAA ATAAAGAGCT 1740 GATACCTCCT GATTTATCCT TCCACAAACC TGATCAGATT GAGCCATCTC TTCTCCCTGG 1800 TGGTAAGGGG TGTGTATGGG TGTGGGGTGG GGACAGCAGG AGGGAAAGTA AGGGAGGGTG 1860 CCAGGAAAGG CACAGAGTGT TACTTGGTAG AGTTTCTTTT GGGTAAAAGA GGCATCAATA 1920 ATGTTTCCTT CCAACACCAA CTAAAAAGGG TTTCAACAAG AAAGACGTTT ATTACCTCAT 1980 GTAAGAAATC GGGGGTGGGA GGCTGGGGGT GGAAGTCAGG GCTACAGTGA GAGCCTCAAG 2040 GCCCAGGTTC TTCCTGTCTT TCTTCTCCAG TGTGTGGCTT GGACCATCAC AGTCAAAAGA 2100 TGGGGGTAGC AGTTGCAGGC AAGCATACAG 2130
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