| Tag | Content |
|---|
EnhancerAtlas ID | HS128-00911 |
Organism | Homo sapiens |
Tissue/cell | MCF-7 |
Coordinate | chr1:109370490-109373180 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr1:109370909-109370928 | TGGCCACCAGGTGGCGTCA | + | 7.66 | | FOSL2 | MA0478.1 | chr1:109372116-109372127 | GGATGACTCAG | + | 6.32 | | Foxd3 | MA0041.1 | chr1:109370709-109370721 | AAACAAACAAAC | - | 6.32 | | Foxd3 | MA0041.1 | chr1:109370713-109370725 | AAACAAACAAAC | - | 6.32 | | Foxd3 | MA0041.1 | chr1:109370717-109370729 | AAACAAACAAAC | - | 6.32 | | Foxd3 | MA0041.1 | chr1:109370721-109370733 | AAACAAACAAAC | - | 6.32 | | Foxd3 | MA0041.1 | chr1:109370725-109370737 | AAACAAACAAAC | - | 6.32 | | Foxd3 | MA0041.1 | chr1:109370729-109370741 | AAACAAACAAAC | - | 6.32 | | JUNB | MA0490.1 | chr1:109372116-109372127 | GGATGACTCAG | + | 6.14 | | Nkx2-5(var.2) | MA0503.1 | chr1:109372001-109372012 | CTTGAGTGCTT | - | 6.02 | | Nr5a2 | MA0505.1 | chr1:109370665-109370680 | GAGTTCAAGGTCAGC | + | 8.73 | | SOX10 | MA0442.2 | chr1:109372564-109372575 | AAAACAAAGGA | + | 6.32 | | Sox3 | MA0514.1 | chr1:109372564-109372574 | AAAACAAAGG | - | 6.02 | | TCF3 | MA0522.2 | chr1:109372398-109372408 | AACACCTGCT | + | 6.02 | | ZNF143 | MA0088.2 | chr1:109372298-109372314 | TTCCCACAATGGAATG | + | 6.01 |
|
| | Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
| SE_30391 | chr1:109370337-109374495 | Fetal_Muscle | | SE_36681 | chr1:109370360-109373490 | HMEC | | SE_37339 | chr1:109370071-109375258 | HSMMtube | | SE_44724 | chr1:109370379-109375021 | NHDF-Ad | | SE_44981 | chr1:109370319-109374859 | NHLF | | SE_46396 | chr1:109370357-109374983 | Osteoblasts | | SE_52099 | chr1:109370333-109374370 | Skeletal_Muscle_Myoblast | | SE_63886 | chr1:109370319-109374573 | HSMM | | SE_65077 | chr1:109370440-109375164 | NHEK |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 109371058 | 109371477 | | chr1 | 109370643 | 109372061 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I108827 | chr1 | 109370415 | 109375263 |
|
Enhancer Sequence | CCGAGGTTAA TATCTAATCA TCACATACAC ATTCACAAAA CACATTTGAA GTATGGAATT 60
ATAAAATTTG GAGTTTTCCT CATGCATCAA AATCCATTCC AGGCTGGGTA TGGTGGCTCA 120
TGCCTGTAAT CCCAGCACTT TGGGAGGCCA AGGAGGGTGG ATGGCTTGAG ACTAGGAGTT 180
CAAGGTCAGC CAGGGCAACA TGGCAAAACC TCATCTCAAA AACAAACAAA CAAACAAACA 240
AACAAACAAA CAGTTCCTAC CAGGGGAAGA AACTATGCTA TACGTCAGTA ATGGGTCACG 300
TAGCTTTGGT CCTGGAAGTA CAAGCTGATT ACATCCAACA ACTCCAGCAA AGTGGGCTTT 360
GCCGGGTGTC TGTGGGACTA AAGGCTGAGG GAGCACGTGA AGGTGATTTT AGTTGCACAT 420
GGCCACCAGG TGGCGTCAGA AAGAAGCAAC TGCAATGGAC ATTGTTCAGG AGCCTTCCTG 480
TGGCCCACCT GCAGCTTCCT CCCTCCTCCT CAGAAATCCC AACTCCTCCA AAGGAATTCG 540
AATTAATAAC AGTTCTGAAC AAAGCTCTTG CTAAGCTCCT GGGATACAGT CATAGCCCCC 600
AGGGAAAGTT GTTCATTCTT AGTATGGAAG GCACTGTGCC CGAGATATCC TGGCATAAAT 660
GAGGCAGATT GCCCAGGGCT AGGGTTTGAG CCCAAGGCAT TGCTGGGCAA ACACATGCTC 720
GCCGCGCTGT GCCCTGGCCT GCTGTTGGCG GAGAAGGGAT GGGGCTGCGG GTTTGTGGGG 780
CTGGGGCTGA GAAGCCAGGC TCTTTCCCTC CTCTTGGAAA AACATGCTGT CCTCTTGAGT 840
CACATATTTT CTCACACCTC ATTTTCTGTC TCCACCCTTC TCCTCTGGGG CATTTGAACA 900
TCTGCTCTCC AAAGTGGGAA ACTTGGATCT CACTCAAGTG CATGCAGTCC AACACAGGAC 960
TTTTTCTGCT TTTAAACTCC TTTGTGTACT CAAATCTTCT GGCCAAACAT AATTCCTCTG 1020
GAGAAGACAG TTTTTCAACA AGACAAAGCA GCTAAAGTAC ACACTTAAAT CCAAAGTTTT 1080
GCATCAGAAA TAACATAAAG GGATAAGCAT ATTTTACATT TTATACATAT GTAATTTATC 1140
CACTTATATA TAAACAATTT ACAAATATCC TGAAAACAGT ATGTACCTCA GCAAGCTTCA 1200
TAAAGGACAA GTCCCATCAG AGAGAGATTT AATCTTCTAA CAGAAAGAAT ATATAGTCCT 1260
CCCTTCAATC AATAATTCCT CAGGGATTAT GTAAGTTACA AGATTTTAAT TCATAAGTCA 1320
TGTGTATCTT CTCATCACTC CCCAGCAGTG GATTCACTGT GAGATTTGAT TTTACACTTG 1380
GTTGTGCTTG TCTTTCCAGC TTGTCTATCA TAAAAAAGTA TTATTTAGTC TGGAACATTG 1440
GTCCCTGTCT TGGTACTTAA TGTACTTCTG TAGGGTCTAG ACTAGGAATT TAGAAGAGAG 1500
AAATTTAGTA CCTTGAGTGC TTAATAAAAA TGGTTCTTTA ATGTCAAAAT ACTTTCATTA 1560
TACTTAGTAA AACCTTTAAA AATCCAAAAT TAGACTTTAA TTCAATAAAT AAAAATAGTA 1620
GGCCTGGGAT GACTCAGTGA GTAAGCTTCA TGAGTGCCCC TTGGATTAAA GGGCAGCTCA 1680
AAGCTGATGA CTGACATGGT GGTTTAATGA CCCACACACA ATGACACATG ACCATTTTTA 1740
GCACGAGCTT CATGCAGTTT CTTTTTTCAG GGGTGGACAC TCATTAGAAC TCTTAAGGCA 1800
GGTGCCCATT CCCACAATGG AATGCTTTCT AACAGGAAGC CTCAGTCTTT CAGACCCTGT 1860
CATCTGCTTC TATTAGAATC CATTACGTAC ATATAACAGT GGTTGCTAAA CACCTGCTGC 1920
CTCCCTGACT CTTGACCTTC CAAAGGTCAA TGAGCCGAGC TTTGGCCGGA GTCCACAGTG 1980
AGCTTAGAGG TAACATCTCT CGCTACCTGA AAGAAGCTTC AAATAAATGA TACTGAATCG 2040
ACACAGATTA ATAGTTGCAC CAATGGGTGT TTCAAAAACA AAGGATTTCT CCTGAGGATT 2100
TTACATGATT TACAGCTTGT TAGCTCTGGA AGATTTCGTC CTTAGGAATG GGAAGAAATC 2160
AGCCCTGAGA AGAGGGATGA GGCTTGTTCC TGGGACTGGG GGGCTCAGGT GAAACCCAAC 2220
AGAGAAGACT TTTGCTCATC ATAAGGAGAG AGTAGGGATG GTGGGAGCTG TTTGTTATAC 2280
AGGATAAGAA TCCCCCATGT GGGCAATGAT CAAAAGCCTA CAGGACCACC CTCCGTGGGC 2340
TGTAACCATG ATTCTTAACC AAGGGGGCTT ATCGGAATCA CCTGGGGAGA TTTAAAAGCA 2400
ATATTCCTAC CAGAGCCCCA CCGCTGGCGA TGCTGAGACA GTAGGTGGGA TGGAGGCATG 2460
TGCATGATTG TAAAATCTCC CATGGTGATT TTGATGGTCT CCCCAGTTGA GGACCACTGC 2520
TAGAGGATCT GTAGGGTGCG AGGGAGGCTG GGCTCTGTGC CCAGGCCTGA GATCTGTGAC 2580
TCTATAACTC AGCCAGTGGC CTCAGTTAGT TGCCGCCCAC TCTCACTGGA GTTACTATGC 2640
CAGGACTGAC TCCAATCCAC CCTGGGAATG TAGCCACAAG AAGCCCTCAC 2690
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