Tag | Content |
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EnhancerAtlas ID | HS129-05693 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr10:124082460-124084760 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EBF1 | MA0154.3 | chr10:124083822-124083836 | ATTCCCAAGGGACC | + | 7.17 |
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| Number: 2 | ID | Chromosome | Start | End |
GH10I122324 | chr10 | 124082861 | 124083010 | GH10I122323 | chr10 | 124083032 | 124084720 |
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Enhancer Sequence | AAGCATGGCT CCCGCACTGG CCATTTGCAG CAAGGGCTGT GTCTTACTCC CTTTACCCTC 60 CCAGTCCTCA ATCTTTCATT AAAGAACAGC TTCTAGCTGT TGACTAAGTA CTGAATGAAT 120 GGTGCTTTGA ATGTTCTTTA ATGGTGGTTT TAACCTCTGA AATATTTCAC TTTAACTCTG 180 AAAATTACTC TAAATTGCAT GTCAGGTACA CAGTGTAAGA AGGAATATAG TGACTTTCTG 240 GCCAGTTGTT TAGTGTTAAA TGGAAACAAG TGTCATGTTT ACAGAGTGAT AGCTTGAAGT 300 GCACAAAGCA TGGGCTGGTT TCAGTCCTGC TGGGTATGGA TTTGATCTTG ATTTGCAACT 360 TTCTCCCTCC AGCCTTAGGC ATTACGGTGT GTGTGCTACA TTTCAAGTGG AACAGTCTTC 420 TCAGGGCCTA GGGATGACTC TCCAGTTGCT TTGTGTATGC TCAGGCTCAG CAGGAGATTG 480 ACAAGTAGCT TCTTGTTGCT TCTTATGTGT CCTTTTATGG TATGTGGGAC AGGGCTGGAT 540 CTGAATGACT GCTAGAAGGG TGGAGAATTC AGTCCTCAAT CAGGTGAAAT TGGTCAGTAT 600 TATTAGAAGC AGAAAATGTC TTCCCACCTT CAAAAACCCT TCTGCAGGAG GATAGTGTAG 660 AACTCTTCTT GTGATTATAC TAATTGAAAT GAGTGGCAGT TTGGGAGCTA CAGGACAGCA 720 AAATGCATTC AGTTCATGTC AGTTTGTAAA TTACTCACTT TACTAAATCA AAGAAGGTCG 780 ATGCTGGAAA GTGCCTTAGA GATCATCTGG TCTCACCCTT TCATTTTGCA GTTGAATAAG 840 CTAAGGCCCA GGGATAATGA GGAGGTTACT TAGGCTCCTT TTGCAAATTG ATGGTGGTCC 900 TGGGGTTGAC CTTGGTCTTC TAGGTCTTCT GACACTCTTA GCTCTTAGGA TCAAGGGCAA 960 ATCATAACAG ACATGTAATT CTAATCCTTA GCTGATTTAT AATCACTAAA TAGGTATCTC 1020 TCAGACACTG AAGGGTAGAT TCTGGCAATG AGCTTCCACC TCACCAGAGG GAAGTAATTT 1080 GAATGTAGCC AATGAAGCCA ATTCCCATAT GATCCCAACT TCTAGATTCC CCTGATTCTC 1140 CAGCTGAGTC TCTTCTTTCC TGTGCCCTAC CCAAATCTGA CCCAGCCTTT ACAGAGCTTG 1200 ACAAAGCCGG TTCCAGAAAG CCTTCTCTGA TCTCACTTGT GCACTGGATG AATTCCTCCT 1260 CTTAGCTCCT CTTTGCGGAG AGAAAAAGAG CATGTGCTGG CTGCATGGGT GTGCACTGGT 1320 GAACCCAACA GCACCTTCCC CCACCCATTC CCCCCACATA CTATTCCCAA GGGACCGCAG 1380 GGGGAAACTT TTAAGGAGAG CTTCCCTGCC ATGCCCTGTA CCATGGGTGC CCTGAGCCCA 1440 CTGATTTCTT GAGGGCAATG TGCTATGATG CTGTGTCCCC AGGGTGGGCG AGGCCATGTG 1500 CCTCTTGTGA TTCATGAATG GCATTTGCAG ATGTAGCCAG AGTTAGCATG AAACTGGGCA 1560 ACCCTGGTGT GTCAACACTG ATCTCTTTAC CAGCACATTA ATTTTGAAAT ATCCCATGAG 1620 TCATGGACAT TAGGGCCATT AAATTGTTCT CTTTTAGAAT AGCTCAACAA AGCCTTGTGC 1680 AGGGAGGTTG GTATATTCTG GGTCAAGAGG ATTTCTCATT ATCTGACGTT CATGCTTCTT 1740 GCCTTGTTGT GTCTTCTCTT GCTCTGAGAG GTGATGACTC TGCTCCCCTT TAACTTGGAT 1800 CTCTGGAACC TGAGTCTCTC TTGTTCTCAA GGTCCCTAAA TATTATGCTT AGTTCTTACT 1860 AACTTTCCAC TTCCGCCATG TTGCTTCTTG GCTTCCCAGG CATATTGAGA AGCACCAAAA 1920 CATACCTTCA ACAATAAGCA TGGAGAAGTG GAAGGAGCAC AAGAGTCTGG GTGTAGGAGT 1980 TTCTTAAAAA GGGCAGCTGT GGTTATGATT AGACAGGATT TCCCTTTGTG CTAGGGTCAG 2040 GACCATCTTG ACAGACAGAA GGACATTGAA CTTGGTCTCA GTGAAAAGCT GATAGGTCAT 2100 GGTGACAGCA GACAGGACCA CATGGGCATG GAGATAGTGG CATAGACTGG CCTGTATGTG 2160 CAGCAAGTGT GTGTGAGCAT GTGCACCAGG GCTGGCCCTA CTGGCCTAGA AGATAAGTTG 2220 TGGGTGAATG GAGGGATGGG ATGATGGAAA TGAGGCTGGA AAGTTGGCAG GGACCAGGTC 2280 ATTCATCCAA TTAATTCACC 2300
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