| Tag | Content |
|---|
EnhancerAtlas ID | HS130-02111 |
Organism | Homo sapiens |
Tissue/cell | MDA-MB-231 |
Coordinate | chr1:159818080-159820270 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NEUROG2 | MA0669.1 | chr1:159819773-159819783 | AACATATGTC | + | 6.02 | | Sox3 | MA0514.1 | chr1:159819480-159819490 | AAAACAAAGG | - | 6.02 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_27216 | chr1:159818257-159820698 | Esophagus | | SE_34829 | chr1:159819258-159820570 | HeLa | | SE_56622 | chr1:159817508-159821445 | u87 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I159848 | chr1 | 159818381 | 159820253 |
|
Enhancer Sequence | CCCCACCTTG TCTGCAAGTT CCCATGTCCT CCACACACCC CTCTACTGCA CATTCTTCCC 60
AACCTAACTG CAAAGAACTG AATGGAATCA GTTTTGTTTC CATACACCAG GAATAAATAA 120
AATGGTTACT CCAGATGGGC TGAATGAACG TTGAGTTAAC TCCAGAATGT TAACTGTTAA 180
CTCCAGAGCA GGGGTTTCCC AGGTTCCCAC CAAATCAGGG AAACGAGCCA TGAGGAGACT 240
CCCTGGGCAG CTTAGTGGAC AGGGCTACAG ATTCAGTCCC CTGCCTCCAG GCAGGCCCCA 300
ACCTAAACCC ATAGGAGTGA AGTAGTTTTT GTAACTCTGG AAGGATCATG ATTGGGTAAT 360
TCCCAAAACT TCCTTGTTCC CAGAGAGGCA AAATAATAAT AATTATTATT ATTAACCCCT 420
CCCCAGAGTC ACCGCAGTCT GACTGGGCCT TGAGTAGCTG AAATGTAATT GAGCAGCATA 480
CATGGTAATA GTTACTCAAA GAGGAGCACA CAGGCCGGGT GCGGTGCCTC ACACCTGTAA 540
TCCCAGCACT TTGGCGGGCA GATCACAAGG TCAGGAGATC GAGACCACCC TGCTAACATG 600
GTGAAACCCT GTCTCTACTA AAAATACTAA AAATTAGCTG GGCGTGGTGG CGGGCGCCTG 660
TAGTCCCAGC TACTCGGAAG GCTGAGGCAG GAGAATGGCG TGAACCCAGA AGGCGGAGCT 720
TGCAGTGAGC CGAGATTGCG CCACTGCACT CCAGCCTGGG CGACAGAGCG AGACTCCGTC 780
TCAAAAAAAA GAAAACAAAA GAGGAGCACA CAGAAGAAAA TTCCGTGGGA CTCCATATGA 840
CTCATGGTCT TGGGAATTAG GGGCTTAAGA GAAGATGACT AGAGGATGAC TTCCTAGAGC 900
CTGGGGAGAG AGTCAGAGAA GGAACTGAAA CAATGAGGAC TCACAGGCAT CTCTTGAATA 960
GATTTCCCAT GGCTAGATGC CCTGGGAGAC AAATGTAGGC AAATTCTGTG GATGCCAACG 1020
CAGGTTTCTG ACGGCTATCA AAAGAGTAAC CTGGAACCAA GGGGATACAA ATTCTCTCAA 1080
TAATTCTTCA GTGACCTGAG GAACCAGAAT TCAGCTCCAG CAAGGCGGGG GAGAGATGGA 1140
AAAGGCGGAA CTAGGAAGTA GGATGAAGAC AATTTATGTA GTATTTAATA GAAGTAGCAT 1200
AACTTTGTGC TGTTTGCATC TCTCTAGAAA AATAGAGAAA AATCAAGATG TACTTGAGAT 1260
TTCCATTCTT GAGGCAACAC TTGTGTGCCC AGCGTTCTGC TTGCCTGGGG TGACATGGTC 1320
CACCTAACTT TCCCAAGCCA GTTGTTAAAT GCAGCCATTA TTAAAAAGTA AATTACATAC 1380
ATTTATAATT AAATGATATT AAAACAAAGG TGATAAGTAC TCAAAACTCA CCACTTCCTG 1440
ATGACTTTAC TACAGTTCAC TATTACCTAA GCTCTTAAAG TTATTTACTT CCTCCATTGT 1500
ATCTGTATCA TGGAAATACT ATACAATCAT GTGCTACTAA ACATTTCTCC CAATTCCATG 1560
CCAGTCACAT CATGTTGGTA GCTTGAATTC AGCCATAGTG GAAGCATTGA CATCATGGAA 1620
ATCAGCAAAG GCTACAAATC AGGGCTTCCC AGTCCCTACC CCACCCTACA CCCTACTCCC 1680
AAAGCCACTG TTGAACATAT GTCACCACAA GTGCTCTCCT CCAGCACTGA ACAAGGTTTC 1740
ATGCAGGAGA AATGAACAAA AAACACCAAG GCATCCCTGA AGCAAAATTG TTCAAACAGA 1800
AACTTCCTTC CCTCGTTCTC CTGGGGTGGT AAGTACAGTG ACGACTGTGA TCTCAGCATT 1860
GGATTTAGGA AATCTCTACC TTCCCTGTTG ACTCACCCTA ACAGGAAGCT GTTCTCAGAG 1920
TCTCTATAAA ATCTCTCTTG CTGCTCTTTA GTGAGCCTTT CTTGCCAGAG CCTCACTGGT 1980
CCCACCCCCC AAATAGAGGC CAAGTCTGAT CATGGCTCCC TTGTTCCTGG AATAGGGAAG 2040
ATTATATCAT TCAACAACCT GCACAGCCAA CTGGCTGCCT CTGTCCCTCA GCACCTTTCA 2100
GGAAGCTAAG CTGGAGGCTC CTCAGACAGG GAGCACCCTC CCCAAGTCAT CCTATACCAT 2160
CCCCTGCCTT AGGGGATATT TTGCCTTAGG 2190
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