Tag | Content |
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EnhancerAtlas ID | HS129-05444 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr10:104986670-104987740 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr10:104986842-104986853 | GGTGACTCATG | + | 6.62 | JUND | MA0491.1 | chr10:104986842-104986853 | GGTGACTCATG | + | 6.02 | Nr2f6(var.2) | MA0728.1 | chr10:104986897-104986912 | GAGGTCAGAAGTTCA | + | 6.38 | RARA | MA0729.1 | chr10:104986897-104986915 | GAGGTCAGAAGTTCAAGA | + | 6.88 |
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| Number: 1 | ID | Chromosome | Start | End |
GH10I103226 | chr10 | 104986411 | 104993435 |
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Enhancer Sequence | CGGGATGCAG AGGTTACAGT GAGCCAAGAT CGTGCCATGG CACTCCAGTC TGGGTGACAG 60 AGTGAAACTC CATCTCAAAA AAAAAAAAAA GATTATTACA TAAACTTAGT TGGTAAAGCA 120 GTAGGGTTTG AGAGGATTGA CTCCAATTTT GAAAGAAGCT TGGGCTGGGC GCGGTGACTC 180 ATGCCTGTAA TCCAGCACTT TGGGAGGCCA AGGCAGGTAG ATAACCTGAG GTCAGAAGTT 240 CAAGAACAGA CTGGTCAACA TGGTGAAACC CTGTCTCTAC TAAATATACA AAAATTAGCT 300 GGATGTAGTG GTGGGTGCCT GTAATCCCAG CTACTCATGA GGCTGAGGCA GGAAAATTGC 360 TTGAACCCGG GAGGCAGAGG TTGCAGTGAG CCGAGATCGA GCCATTGCAC TCCAGCCTGG 420 GCAACAAGAG CGAAACCACT GGTCTGATAA GTCAGCAGCC ATCAACATCG AGCAAGACCC 480 TCCACCAGCA AAAAGATTAA AGGCTCAGAT GATTGTTAGC ACTATTTAGC AACAAAGTAT 540 TTTTAAATTA AGGTATAGTT TTAAAAGACA TAATGCTATT ACACAATTAA ACTATTGCAC 600 ACTTAATAGA CTACAATAAC ATAGCTTTTA TATGGACTAA GAAACAAAAA TCATGTGACT 660 CACTTTATTG CTTTATTATG ATTGTCTGGA ATGGAATCCA CGATATCTCT GAGGTATACC 720 TATAGTTGCA AACCTCAAAA CAAAGTTAGC ACATCCAGGG TTTCCCAGAT GCATTTGAAC 780 ATGAAATTGT TTTTTTCCAT AACACATTCT ATGAGACTAA TATCTTCCCT AGAAAAAGCT 840 GGTCTGGAGC AATGGTCTTC AGACTGTTCC TCAAAGCTCT AGGGTCCCAG ATAGTGGCTC 900 AGTGTTACAT GAGGGATGAG AATAAGGCCA ACTGGATCCC TAGTTCTTCC ACACAACACC 960 TCCACTTTAA TCTGTTTTAT GAAGGGGTTC CACCTAAGGA TATATGTGTA TGTATATATG 1020 TACATATACA TACATGTTAC ATATCTTACC TATTTTCTAT GTATACTATT 1070
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