| Tag | Content |
|---|
EnhancerAtlas ID | HS129-03087 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr1:205244080-205247030 |
SNPs | | Number: 3 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr1:205244602-205244620 | GGAGGGAAGGGAGGAGGA | + | 6.36 | | EWSR1-FLI1 | MA0149.1 | chr1:205244598-205244616 | GGAGGGAGGGAAGGGAGG | + | 6.96 | | Foxd3 | MA0041.1 | chr1:205246485-205246497 | GTTTGTTTGTTT | + | 6.32 | | Foxd3 | MA0041.1 | chr1:205246489-205246501 | GTTTGTTTGTTT | + | 6.32 | | SNAI2 | MA0745.2 | chr1:205244492-205244502 | AACAGGTGCA | + | 6.02 | | YY1 | MA0095.2 | chr1:205245245-205245257 | CAAGATGGCTGC | + | 6.74 | | ZNF263 | MA0528.1 | chr1:205244595-205244616 | TATGGAGGGAGGGAAGGGAGG | + | 6.23 | | ZNF263 | MA0528.1 | chr1:205244599-205244620 | GAGGGAGGGAAGGGAGGAGGA | + | 8.21 |
|
| | Number of super-enhancer constituents: 21 | ID | Coordinate | Tissue/cell |
| SE_03194 | chr1:205244629-205245330 | Brain_Angular_Gyrus | | SE_03963 | chr1:205244152-205246237 | Brain_Anterior_Caudate | | SE_04837 | chr1:205235492-205246343 | Brain_Cingulate_Gyrus | | SE_05801 | chr1:205235705-205246437 | Brain_Hippocampus_Middle | | SE_06736 | chr1:205244582-205246354 | Brain_Hippocampus_Middle_150 | | SE_07799 | chr1:205238382-205246205 | Brain_Inferior_Temporal_Lobe | | SE_11085 | chr1:205242383-205246447 | CD20 | | SE_11085 | chr1:205246688-205250559 | CD20 | | SE_26974 | chr1:205244127-205246130 | Esophagus | | SE_50327 | chr1:205244074-205245184 | Sigmoid_Colon | | SE_52983 | chr1:205244073-205245121 | Small_Intestine | | SE_55645 | chr1:205244180-205244885 | Thymus | | SE_58462 | chr1:205242169-205295027 | Ly1 | | SE_58967 | chr1:205242236-205295022 | Ly3 | | SE_60263 | chr1:205242326-205284722 | Ly4 | | SE_60576 | chr1:205242267-205294889 | DHL6 | | SE_61365 | chr1:205242037-205294994 | HBL1 | | SE_61423 | chr1:205183427-205322469 | Toledo | | SE_62465 | chr1:205242393-205294944 | Tonsil | | SE_65493 | chr1:205242350-205246511 | Pancreatic_islets | | SE_68815 | chr1:205244046-205246099 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 3 | ID | Chromosome | Start | End |
| GH01I205274 | chr1 | 205244116 | 205245425 | | GH01I205276 | chr1 | 205245621 | 205245770 | | GH01I205277 | chr1 | 205246689 | 205250559 |
|
Enhancer Sequence | GGAGGTTGCA GTGAGCCAAG AGTGTGCCAT TGCACTCCAG CCTGGGCGAC AAGAGTGAAA 60
CTCTGTCTCA AATAAAAAAA CAAAAAAAAA GAAGGAAAAA AGGGAGTGCA TTGCCCCCAC 120
TTCAACCTGG CCTCCTTTGC TGGGGACCGT TCTTCAGAAT GCAGGGCCAA CAGGCAGGTC 180
CTTCCCAGAG CATCTGTCAT GCAGGTCCCA GCCCCTCACC TGAGGGTCCG GAGGTCTCAG 240
CCAGGCTGGT ATGCTCCCCT CAGCCTGGGT CCACTACAGA GGGAGTAGCT AAGAATTCAT 300
GTTGAAGTTG GCACGTTACT GCTCCAGCAG CACTGAGCAG GCAGGTGGCA TGTTTACCAT 360
GCCCGTGCAG AGCTGGCACT CCCTGCCAAC CTCATCAAAA CTGTAGGGCT ACAACAGGTG 420
CAGCCCTGGC AAACAGCAAA GCAGGCAGAC AGCACAGGCC AGCAGGAGGT GACTTAACCC 480
CTGCCAGCAC AGGTTACTCT GGAGTGGTTC TGAGCTATGG AGGGAGGGAA GGGAGGAGGA 540
AAGACTTGGG GCCACAGGGT GGGAGAGGAG GGGAGCTGCA GCCTGGGCAC CTGGAGGGAT 600
CTTCATGGCA GGTTCAATTT CCCTTTCAAA GCCAGGGCCC TTAAGTCAAG TCTGGATCCC 660
AATATTAAGG AGCCAGCAGA CCTAGGCTCA AACCCCAGTG CTGCCACTCA CCTTGGACAG 720
GGTTCCAGCT GCTCTCAGCC CAATCTCCTC ATCTTCCAGG AGGAATGGAG ATGACATGGC 780
ACTGGCTCAC AGGCTTGGGT GCAGGAGACT TGACATTCTG CAGGTCAAGA CTTAAGCACA 840
AGGCCTAGAA TATGATGGAT TAACCCGAGA CTGGACTTAT TACTGCTCCT CTTTCCTGAG 900
CCTGTAAGAT ATTAAGATGC AGAAGAACTC TTCAGGGAAG TCTAAGGCCG ACCCCACAGG 960
AACATACAAG GCCAAGGGTG GCTAAGTGAG CCTCAGCCTC TGATTCTGGA AAACCTAATA 1020
GAGGTCCTTA GGGTTCCTCT TCCCTGGGAA CCCAGAGCCT GCTTATTCCC AGCAGCCTCT 1080
CCCCTCGGTC TGGTAGACAA AGCTGGTCCA GTCCCAAGAG GCCAAGCCCC AGCTTGAGAG 1140
AGGACTGGAT TCAGCCTATT TGACCCAAGA TGGCTGCCAA CACCCCAGCT CCACAAGTGT 1200
ATCAGTCTGT GGGTCCCTCC CGCCTCCAGC CCATGGTCCT GGGTGTGGGG TCTAGGAAGG 1260
AGAGCAGGAA TCAAGATGCC TGCTTTTGAG TTGAGACTGT GGAGGTTGTG GGCCTCAGTT 1320
TCCCCAGCTG AAACATGGGG ATAATCATAT CCGTGCTGCC CAACTGTTAG GACACCGGTG 1380
AGGCTCGTAG GTGTCAGCTA TGAGTGCCTG CCCCATGACA CCCCAGGATC TCACTCTAGG 1440
GGAATGACCT GTTAGAATGC TGCCAGCCAT CTGGGGCCCC CAGGGAGGGC TTTGATCTGC 1500
CCAGGGACAG GGCTGGGCAG GGCTTGGGAA AGCAGCCAGC AGTGACCCAT GGGCCTGACG 1560
GCTTGCAGCC AAACTCCAGA TGCAGATGGA AGGAGGAAGC TTGGTCCCCA CTAGGCTGCG 1620
GGGAGGCATG TGGGGAAGGA GGGGAGGCTG AGACTTGTCC CAGCACATTT GGGCCTGCTG 1680
GCAGGTCCTG AGTCACTCAG CCAGAAGAGC AGTCGGGGTG GTGACAGCAG CGATGCCCGC 1740
CAGACACAGG GCCTCCCAGG AGAGCACTCC CGCCTTGGTC CCCCCATACC CCAAGGCTCG 1800
ACTGTCCGGA TGAAGCATCC TGGGCCCAGC GGTGCCACCT CAGCCATGCG CCTGCCTCCA 1860
GGCAGCCATC CACTAAGCTG GCTCTGATTC CAAAAGCCCC AGAGGTGATC CTGAGAGGTC 1920
TGGGTGCCCA GTCTCGGCGC CCTGCCAGCC TCAGCTGAAG GTTCTCTTGT TGCCCTTACT 1980
GTGTTTTTTT GTTTTGTTTT GTTTTTAAGT GAAACAAATT ATTTCAGTTT AATTTTCTCA 2040
GCATGTATCT GGCATTAAGT AGTTGTTATA ATTTTTTTTC CATAGGTTAT TGGGGAACAG 2100
GTGGTGTTTG GTTACATGAG TAAGTTCTTT AGTGGGGATT TGTGAGATTT TGGTGCACCC 2160
ATCACCCAAG CAGTGTGCAC TGTACCCTAT TTGTAGTCTT TTATCCCTCT CTTGTTGCCT 2220
TACTTTGATT TTTTTTTTTT TTTTTTGAGA CAAAGTCTTG CTCTGTCGCC CAAGCTGGAG 2280
GGCAGTGGCA CGATCTTGGC TCACTGCAAC CTCCACCTCC TGGGTTCAAG CTATTCTCCT 2340
GCCTCAGCCT CCTGAGCAGC TGGGACTACA GGTGTGTGCT ACCATGCCCA GCTAATTTGT 2400
TTTTTGTTTG TTTGTTTGTT TTGTTTTTTT GAGACGGAGT TTTGCTCTTG TTGCCCAAGC 2460
TGGAGTGAAA TGGAATGATC TTGGCTCACC GTAACCTCCG CCTCCCAGGT TCAAGTGATT 2520
CTCCTGCCTC AGCCTCCCAA GTAGCTGGGA TTACAGGCAT GCGCCACCAT GCCTGTAATA 2580
CTAATTTGGT ATTTTTAGTA GAAATGGGGT TTCTCCATGT TGGTCAGGTT GGTCTCGAAC 2640
TCCCAACCTC AGGTGATCTG CCCACCTCAG CCTCCCAAAG TGCTGGGATT ACAGGTGTGA 2700
GCCACTGCAC CCAGCCTCAT TTTTGTATTT TTAGTAGAGA CTGGGTTTTA CCATATTGTC 2760
CAGGCTGGTC TCGAACTCGT GACCTCAGGT GATCCACCTG CCTCAGCCTC CCAAAGTGCT 2820
GGGATTACAG GCATGAGCCA CTGCGCCCGG CCACTTTGGT TATTCTTGCT GTGATCTCAG 2880
CTCCCTGAAG ATAAGTCTCA AGTAAACACT TTAGAAAGAT CTGAGTGTTT CTCTGGCTGG 2940
TCTGGGGCTC 2950
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