| Tag | Content |
|---|
EnhancerAtlas ID | HS129-07550 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr11:109994540-109996860 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CDX2 | MA0465.1 | chr11:109995273-109995284 | AAGCAATAAAA | + | 6.32 | | Nr2f6(var.2) | MA0728.1 | chr11:109996261-109996276 | TGAACTCCTGACCTC | - | 6.22 | | SOX10 | MA0442.2 | chr11:109995497-109995508 | AAAACAAAGCA | + | 6.02 | | SPI1 | MA0080.4 | chr11:109995935-109995949 | TACTTCCTCTTTTA | - | 7.06 | | SPIC | MA0687.1 | chr11:109995935-109995949 | TACTTCCTCTTTTA | - | 7.73 | | SREBF1 | MA0595.1 | chr11:109996424-109996434 | ATCACCCCAC | + | 6.02 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I110124 | chr11 | 109995389 | 110000458 |
|
Enhancer Sequence | AACAGACAAA GGAGCCAAGC ACATGGAGAT CAAAATAGCA GCCCTTTCCA TCCATAGAAC 60
TATTGGAGAG AAGGTGATTT AAGAGAACAG CATAAAGAGC TTAGTAACAC TGAACCCCAG 120
AATTAGATTT AACCATCCAG TCCCAGGCCA TGCTGGAGGG CAAAGCACCC AAGTGTTTTC 180
TGCCTGTGGG CAGATCTCAA AGAGAAATGT GCAGTTGAAA AGGACTGGTC CTTACAGACT 240
TACCCATCAA AGTGATCCTC AAGTGGGGAG GCAGAAGCTG CAGTGGAACT TCCGCAGTTG 300
CAGCTCTAGT TGGGAAGAGA ATCCAGAGGA GACTGCGGGA AAAGACCCGT CATCACTGGG 360
AGTCTTGAGC TTCTTTGAAT GTTGGAAGCA GCCCCAGTGG CAGTATCAGG GCTACAAGAA 420
CTTTGCCAAT GGCCGAGGGC TCTGATAAAC CCACCCTGTC ACAGGGAGAA ATAAAGACTA 480
GCAGAGCAGC ATTTTTGTTC TTGTGAATGC CTGCATTCAA ATTTGCAGGG GTCTATTTTT 540
TTTTTATTGG TCGATTTTTC ACTTGAAGAT CTTCTAGAGA TCAGCACACT GCTGCATGCC 600
ATATTGGTTG TACTATGTAG ATTATGGGAG AATGAATGGT TCTGCTCTCA AGAAGCCTAC 660
ATCCTGGTTC ATAAATAAAT GCTAAATTGT ACTGTACACA CTATTCATGT TACAGAAGTT 720
TGAAGGAATT GGAAAGCAAT AAAAACCGAA CTAGTCCAAG AAGGCTTTAT GGAAAAAATA 780
AGTCTTGAGC TGGGCTTAGA ACAATAGATA AGAACTGGAT AGGTGAGGCT GTAGTGCAAG 840
ACAACACTTA AGGCAAAGAG ACATCTGTGC CCTCACTTTT GCTGTCCCTT CACCTTAAGT 900
GGGAAATTAG ATTACAGGGC CAGAGGAGGC CCCGTTTGTA GATGGAGCCT CGAAAACAAA 960
ACAAAGCAGA GGACCAGAGA CTTGTGATTT GCAGCTGAGA TTTTTTTTTT TTTTTAAGCA 1020
GAAGAGTGAT GTCATTGAAA ATTACTTTGG CAGGGAGGTA CCTAAGGGAT ATTCAAGGAA 1080
GGAGATAAAT TAAGATAATC TAAGCCTGGG GGAATAAATG CTTAGCCTAA GGGATGCTCA 1140
TGGCCATGGG AATGAGAAAA TTGGGAAGAG AAAAATAATC AAGAATTGAT TAACTGGATC 1200
TTCAGTATGT ATTAAATGAA TGAAACAATT GAGAAATAGA CAAAGGTGTC TATGAGGTTT 1260
TAAGAATGCA CTGTTGCAAC AATGATAGCT ACTCTTAAGG AAAATGGGGA ATGAGATACA 1320
CTGTTGCTCA TAGATGTGAA AACGGAAGCC AAGCAATACA TAAGTTCTTC AAGACTGATA 1380
AGTTTATTCC ATTTCTACTT CCTCTTTTAA GTCATTTGGA TGGATTTTAT GGGAACCATA 1440
TAGGATCTCT CACTAGTGTG TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG 1500
TGTGTGGTTT TTTTTGTTTG TTTTGAGATG GAGTCTCGCT CTGTCATACA GGCTGGAGTG 1560
CAGTGGTGTG ATCTTGGCTC CCTGCAACCT CCACCTCCAG GTTCAAGGGA TTCTCCTGCC 1620
TCAGCCTCCC GAATAACTGG AATTACAGAC ACATGCCACC ATGCTAATTT TTTTGTATTT 1680
TTAGCAGAGA CGGGGTTTCA CCATGTTGGC CAGGCTGATG TTGAACTCCT GACCTCAAGT 1740
GATCTGCCCG CCTTGGCCTC CCGAAGTGCT GGGATTACAG GCGTGAGCCA CCATGGCCAG 1800
CCTCTCTAAT GTGTTTAATG TCCTTCTGTA CTGGGTGTCT GATGTTCTGT CCACCTAGCA 1860
TTTTCCTGCT CTGCTTCTGT TACTATCACC CCACCTAAGG AATGCCCCGC CACCATCTCC 1920
TTACGGCCTG ACAGGGCAGC CCATCATGGC CCCACATACA TCTGGCCACA GTACTAGGGC 1980
AAACAGGTGA GTAACATGAC TTCAGCTGTG CTCATCAGAT TCTCTGTCTC AGGAATTTGA 2040
ACCTTGAATG GAGAACACAA GGTCAGAGAA CATAGTGCTG AATCATCAGA GAGATAGTCT 2100
AGAAGCTCTG CAAATGAAAC CCGGGGTTTA GTCCTCATCT CTGACCTGAA GGCTTGAATG 2160
TTGAGATCTC TTTCTGACCC TGAGAGCTCC TTCGTGTTCT TCCAGTAAAT GTCCCAAGCC 2220
CTTTCTCAAA AGTCCTGTTT TTCTTGCTGA TGAATAGTAA ATTGATATGC ATCTATTATT 2280
TTTATTTACC TATTGGTAGT TGCTTAGTAT TTTTAGGAGC 2320
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