| Tag | Content |
|---|
EnhancerAtlas ID | HS128-11568 |
Organism | Homo sapiens |
Tissue/cell | MCF-7 |
Coordinate | chr2:20430730-20433030 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chr2:20431539-20431550 | CCACACCCTCC | + | 6.32 | | Klf1 | MA0493.1 | chr2:20431537-20431548 | AGCCACACCCT | + | 6.02 | | POU2F2 | MA0507.1 | chr2:20432857-20432870 | ATATGCAAATTCA | - | 6.67 | | ZNF263 | MA0528.1 | chr2:20431270-20431291 | GAAGGATGAAGGAGAGGAACA | + | 6.43 | | ZNF263 | MA0528.1 | chr2:20432100-20432121 | AGGGGAGGGGCGGGGGGGGGG | + | 6.75 | | ZNF263 | MA0528.1 | chr2:20431267-20431288 | GGAGAAGGATGAAGGAGAGGA | + | 6.89 |
|
| | Number of super-enhancer constituents: 20 | ID | Coordinate | Tissue/cell |
| SE_02914 | chr2:20430841-20431728 | Bladder | | SE_02914 | chr2:20432323-20432755 | Bladder | | SE_23108 | chr2:20430728-20433031 | Colon_Crypt_1 | | SE_23761 | chr2:20430771-20431844 | Colon_Crypt_2 | | SE_23761 | chr2:20431878-20432712 | Colon_Crypt_2 | | SE_24805 | chr2:20430733-20432995 | Colon_Crypt_3 | | SE_26530 | chr2:20430669-20434103 | Esophagus | | SE_31478 | chr2:20430789-20432802 | Gastric | | SE_33954 | chr2:20430757-20433179 | HCC1954 | | SE_35878 | chr2:20430227-20437683 | HMEC | | SE_42432 | chr2:20430732-20431952 | Lung | | SE_42432 | chr2:20431959-20433013 | Lung | | SE_50296 | chr2:20430643-20431888 | Sigmoid_Colon | | SE_52465 | chr2:20430618-20432815 | Small_Intestine | | SE_56896 | chr2:20430348-20431529 | VACO_400 | | SE_56896 | chr2:20431583-20433112 | VACO_400 | | SE_57761 | chr2:20430451-20431506 | VACO_503 | | SE_57761 | chr2:20431527-20433114 | VACO_503 | | SE_58069 | chr2:20430905-20431840 | VACO_9m | | SE_64257 | chr2:20430356-20433549 | NHEK |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr2 | 20430848 | 20432571 | | chr2 | 20431248 | 20431615 | | chr2 | 20432677 | 20432919 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I020230 | chr2 | 20430368 | 20437558 |
|
Enhancer Sequence | AATTCCCAAT AATCGCCCCT ATCTCAAAAT TCTTAATCAC ATCTGCACAT CTGCAAAGAC 60
CCACCACCAC CACCTTGTAT TGGTTGTTGT TCTATAAGTT AACATTCACA GGCTCCAGGG 120
GCTGGGATAT AGATATCTTT TAAGGGTAAT TATTCAGCCT ACCGCAGGCA GATAGAGCAG 180
GGAAAGGACA TTCCAAACAG GAAACCCAGC AAAGAGCAGG CAAAGAAGCA AGACAGAGCT 240
TCAGGATGTT CAGGAACTGG AAGGAGTCTG AGGTGGGCTG GACTGGCCGG GGCACAGGAC 300
CTCTGGCAAG GGCTGGATCA GAGGGAGAGA GCCTGAGCAG TGTGTGCCAG TAACGGGCCG 360
TGCCTAGGCT GGAGGAGCCA GTGGTTTGCA TTTTGAAAAG ATCCTCTGGC CACTGTGCGA 420
AGGGCAGGCT GCAGGGAGGG AGACTGTGGG CTGGGACACC CTATGCAGGG GCCGTGAAGG 480
TACAATGTGG GGAGCCAGGA TTGAATAATA TGGAGGAGGT GGGATGCGAT GAGGCTTGGA 540
GAAGGATGAA GGAGAGGAAC AGTGCAATGT GGAAAATCCT TGGTGAGGGT CCATTTCCAC 600
CTGGTTTACG TAAACAGCTA GCGTCAGAGG GGCCGAATCA GTGTGTAAAG TGGCTGCCTA 660
GGCTGGGGCA GCACTGGGTG CTGAAGTCCT TTGGTAGATC ACCCCGGGGC TCGTGACTCA 720
GTTCTAGGCT GCCTCAAGGA TGAGCCTTTG TTGCCTTTGT TGGAAGCTTG GACAGGAAGC 780
TCTCCAGCAG GGAGGAGTGC CAACACCAGC CACACCCTCC CAGGTGCAGC TAGGCCCAGT 840
CACCCTGAGC AATTTCCTGG AGTGAGGCCA CTCGCCACTG GCTCACACTA GCCCCTGCCC 900
TGCAGGGCAT CATCAAGGAT CTGGAGTCTG AGCAGCACCA GGCTCTCTGT GACTCAGCCC 960
CTGTGGGGAA GGGGAGCCCG TGCTGGTGCT CTTCGGGCTG GAGCAGGGAA GTAGCTCCCC 1020
CTGTCCCACC TCACCTGCTT TGCTAGGGAC AGACTTTTTT TTTTTTTTTT TTTTGAGACA 1080
GAGTCTTGCT CTGTCACCCA GACTGGAGTG CAGTGGCACA ATCTCGGCTC ACTGCAACCT 1140
CCACTGCCCG GGTTCAAGTG ATTCTCCTGC CTCAGCCTCC TGGGTAACTG GTATTACGGG 1200
TGCCTGCCAC CACACACGGA TAATTTTTGT ATTTTTAGTA GAGATGGGGT TTCACCATGT 1260
TGGCCAGGCT GCTCTTGGAC TCCTGAGCTC AGGTCATCCA CCCGCCTTGG CTGCCCAGGG 1320
ACAGACTCTA CAAAGCCCTG CTAATTGCTG CATGCAATAT GCTGTTTGTG AGGGGAGGGG 1380
CGGGGGGGGG GGAGCTGGGA GGAGTTGTTG TTGTTTTGAT TTTTTTTGAG ACAAGGTCTC 1440
ACTCTGTCAC CCATGCTGGG GTAGTGCAGT GACGTACATA ATCACAGCTC ACTGCAACCT 1500
CTGCCTCCTG GGCTCAGGTG ATCTTCCCCA CCCAGCCTCC ACAGGCACAT ACCACCATGC 1560
CTGGCTAATT TGTGTATTTT TTGTAGAGAT GGGGTTTTGC CATGTTGCCC AGCCGGTTCT 1620
TCTACACATT CTTTGAGCTA CTTTAGCTGT GTGACTTCAG GCAAGCAGTA ACCTCTTTGC 1680
TCTTTAATTT GTTCCTCTGT GAATTGGAGA AATACTAGTA CCTACCTCAA AGAGTCAAAA 1740
GCATTGAATG AGCTAAGCCC TCCATAGGGC CTGGCACACA CGTGTAAGTG CCCCCTGCAT 1800
GCTAGTGATG CCGTGGATAC CCACAGTGGG ATTCACTGGG AGAGGCAGAT AGACTCATTT 1860
TAGGCAAGTT CCTAAGCATT CTGACATAAT ACATATAAAA CACTTAGCAC TTTACCTGGC 1920
ACAAGGTAGG ACCCTAGAAA TCATAGAGAA GTTGGAGATT CTAAAGCCCG CAGGGGAGAA 1980
TCTGGGCTGG GCTCTGAAGA GATTCCTGAG CTCACCGCAG CCAGGATGTA TAAGTCATAG 2040
TGTTATGTCA GCGCTCATAC CTGTGTGTAG CACATGTGCA CGCACCTTCA CGCACACAGG 2100
TGTGCCTCAC CTCCAGCCCC AGGATGCATA TGCAAATTCA TGTAACAGAT GAGTAACTGA 2160
GTTCACTCAA CAGGTGAGAA AGTGACTTTG CATTCCCTAG GAATGGGACA GAGGTTGCAA 2220
AGGGACAGCC CCTAGGGCTG CATTTGGCCT GTAGAAGTGT TTTGCCTTTA AACTATTTTA 2280
TTTTGTTTTC TTTTTTTTGT 2300
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