Tag | Content |
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EnhancerAtlas ID | HS098-11984 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr11:132501820-132503860 |
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 | TCCAGGACAT CTGTGAGACC CTAAGGACCT ATTCACAGAA GGCCACTGAA TTATAAGTTT 60 TGTCCAGGTT TTCAGCTGGG TAACGAAACA CGTAGCTGGA AATGAAAATG TGGCAGCCAT 120 GCTGATCAGG GCTGGGCTGT TAAAATGGTT TCTGCCTGAA AGAGTCCCTC CTGTAAACAT 180 CCCTAGGATA GGGAATGCAG ATCCAGCTTA AAAAAAAAAA AAAAGAAAGA ATGAGAACAT 240 GATTGTGCCA CATGGAGATT TGGGCAGGAT CTTGTTAGGC CCCTGAGGGT GCCTCAGGCA 300 TCTTTATTCA AACACATTTT TTTTTTTTTT TTTTTTTTTT GGAGGGAGCA AGGAGGAGAT 360 CACACAGTTG TGGAACTGTC GTCAAAGCAA GCAGCTGACA TTTAAATAAT ATTATGATTT 420 AAAAGGTTCC TTTGCATTCG TTCCTTAACT CATTACACCT TCACAACTCT GTGACACGAG 480 AAGAGGAGGT GACACTATTT CCATGTGAAA AATGAGAACA CTGATATTCA GAAAGATGAA 540 CTGATTTTTG TAAGGTCAGA TATCTTTTAA GTAATGGAGC AGGGACTTCA AGTGATGTCT 600 GTCTCTCTCC AGTGGCTCTA TGATTCTCAG GATATCATCC TATCTCCACG CAACACAATG 660 TCGCCGCAGA GGAGTCGCTT CCTGAGTGGT TCCATGATAG CCAGCCCGGT ATATCTACTC 720 CTTTTGGTCT TTTTCTGCTT CCCTATCTTC AGCAAGGCGA GGTAATCACT CTCTCTTTGG 780 TATGTGAGAT ATGTATCTAT TCTGTCATAT CCGCCTTTCA GTTGTCACAT AGCCAAACTA 840 TGCAAATGTG GCCATCTCCA CATCTCTGCG TTCAGCACGG CTGCTGCTCC ACTCTGGACT 900 CCTTCCAACT GTTCAGATGG GCAGGGAGGA GTTTCATCAT CAGAGATGAT AAAGAAACAT 960 GACTATTCAG CCTTTCTCGT ACATCTACCG AATACCTAAC TAATGATGTT CTCACCATAT 1020 TGAAAAAAAA AAAAAAAACC ATCCAGGATG ACGAATTTAT TCCCTGAGTG CCTCATGACA 1080 AGTGAGTCAG CTCTCAGCAA CCAGAATTAC AAGTGGACTG AGCTGGGTGA CGGTGGAGCA 1140 TGAGGAAGTG CAGTCTGTCC TGCCTATAAA GGTGGTCCTA GGCTAATCGA AAATCTGCAC 1200 CAACAACACA GCAAAGTGTC TTCTGCTGCC AGTAACAGAG CACCCAACTG TTGGTGTTTG 1260 AGGGGGACAA TCGGTAGCTC TCTCTCTTTT TTTCTGAGAC AGAGTCTCGC TCTGTCGCCC 1320 AAGCTGGAGT TCAGTGGTGT GATCTCGGCT CACTGCAACC TCTACCTCCT GGGTTCAAGT 1380 GATTCTCCTG CCTCAGCCTC CCGAGTAGCT GGGACTACAG GTGCTGGTAG CTCTCTTTTC 1440 CCTGCCTAAG TTCAGAACAA CTTGAGAGAC AAACAGGGAG AAAATAGATG GAAATAAAAA 1500 TAGCCCTTCA TTTCTGATAG AAATTAAAAG CCGGGAATGT GGTTTATATC TTTACGTAAG 1560 CAAATGGGCA TCCCAATCCT GAGCCTCAGG ATTCGACCCC ACTCCCCCAG TCACAGGAAG 1620 TGCGAGGAGG CCCCAGGCCC TGGGTCTGAG CCTGGCCTCT TACGCTGCAT GACACAGGAC 1680 ATCTGTTGGA AGGTCAGTTT CTAAGACAAA ATAAAGAGCT GATACCTCCT GATTTATCCT 1740 TCCACAAACC TGATCAGATT GAGCCATCTC TTCTCCCTGG TGGTAAGGGG TGTGTATGGG 1800 TGTGGGGTGG GGACAGCAGG AGGGAAAGTA AGGGAGGGTG CCAGGAAAGG CACAGAGTGT 1860 TACTTGGTAG AGTTTCTTTT GGGTAAAAGA GGCATCAATA ATGTTTCCTT CCAACACCAA 1920 CTAAAAAGGG TTTCAACAAG AAAGACGTTT ATTACCTCAT GTAAGAAATC GGGGGTGGGA 1980 GGCTGGGGGT GGAAGTCAGG GCTACAGTGA GAGCCTCAAG GCCCAGGTTC TTCCTGTCTT 2040
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