| Tag | Content |
|---|
EnhancerAtlas ID | HS034-02530 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr1:205286110-205289270 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr1:205286137-205286155 | CCTGCCTGCCTCCCATCC | - | 6.35 | | Gata1 | MA0035.3 | chr1:205287197-205287208 | ACAGATAAGGA | - | 6.14 | | RREB1 | MA0073.1 | chr1:205288229-205288249 | AGGGGTGGGGTGGGGTGGGG | - | 6.98 | | TCF7L2 | MA0523.1 | chr1:205287932-205287946 | TTCCTTTGATGTCC | - | 6.93 | | ZEB1 | MA0103.3 | chr1:205287969-205287980 | CCCACCTGCCC | + | 6.14 | | ZNF263 | MA0528.1 | chr1:205286701-205286722 | GCCCCCTCCTTGCCATCCTCC | - | 6.29 |
|
| | Number of super-enhancer constituents: 22 | ID | Coordinate | Tissue/cell |
| SE_05801 | chr1:205285083-205291843 | Brain_Hippocampus_Middle | | SE_11085 | chr1:205269398-205291943 | CD20 | | SE_26974 | chr1:205285172-205289484 | Esophagus | | SE_29391 | chr1:205282226-205291639 | Fetal_Intestine_Large | | SE_32765 | chr1:205287465-205288278 | H1 | | SE_41963 | chr1:205285226-205289265 | LNCaP | | SE_46173 | chr1:205285018-205286568 | Osteoblasts | | SE_46173 | chr1:205286604-205287822 | Osteoblasts | | SE_46173 | chr1:205288162-205289498 | Osteoblasts | | SE_47803 | chr1:205285806-205288843 | Pancreas | | SE_50327 | chr1:205282155-205289483 | Sigmoid_Colon | | SE_52983 | chr1:205282180-205289461 | Small_Intestine | | SE_54130 | chr1:205285111-205289470 | Spleen | | SE_56879 | chr1:205285957-205287901 | VACO_400 | | SE_56879 | chr1:205287922-205289091 | VACO_400 | | SE_58462 | chr1:205242169-205295027 | Ly1 | | SE_58967 | chr1:205242236-205295022 | Ly3 | | 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 | chr1:205285421-205291844 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | AGCTTCCATC TCAGCCATAG AGATTTCCCT GCCTGCCTCC CATCCCTGGA GAAGGGAATG 60
CCCCATATCT TGCCCTAGGC CAGGCTGTGT AGTATCACCA GCCACCCCAT CCCACTTACA 120
GATATACAAA TATGCCCACT CCTCTGCCAA CACCCTGGAG AGGTAGGTGC TGTGGCTCAA 180
TTGGTAAACA CTGCCTCCCT CCCAGGGACT CAGATCAGGA ACGATCTGGA TTCAGGAGAG 240
GATGGTAGAA AGGTCTTAGA AAAAGAAGAT CCAGAGATGC TGGTTCCAGG TGGAGGGAGA 300
GAAGGTGCAA GCTGGGCATC TCTGGTCATA GTTATCACCC AGAGCTGGAG CCAAGATCCT 360
TGATTTCTCT CTGGCCTTTT GTGGAGCAGC TGCTGTCTGG GAGGCAGGGC AAGGAGCTAG 420
GGGATGACCC ATTTAGATAA CGGAGGAGAG GTTGGGCTGG GTTGGCCCAG GCTGGGCAGA 480
GTGGGGGTGG GCCTAGGGGT GGCTCGCCAT CCCACCACAC CAGCCAGAGA GCTAGGCAGG 540
GATCAGGAAT GGGCTCCAAG GGGAGCCTGA GCCACCTCCC TATACTGTGC TGCCCCCTCC 600
TTGCCATCCT CCAGCCCCCT CTACCGGGTT GCTGGGCAAG GAGCTTCCCT GCCCAGCCTT 660
CTTGTGTGGT TTGGCTGGGG CTCAAGGACA AGAGTGGCCT GCAGCCTCCC TCCCTGCCGC 720
TTAGCAGGCA GGTGCAGAGG GAGCTGGGAG GGCAGTGTCC TGCCAAGCAA GCCCTTGGCA 780
GCCAGCCAGG CAGGAGTCCT TCTCTGGAGC TGGGGCCGAA GGAGAGACGA GGACTTTGAA 840
CAAAGCAGCA ACCAAAGTGG TTTGGCTTAG GGAAGCCAAG CACAATCCAT ACTCTTTCTC 900
AGGGTAGGAC AGACCTCCAG GACGCAGGGA TTCCCCAGGA AAGGGAAGGG CAGGACTTCA 960
TCAAAGCCAG CCTTGCTGGG ATAATAACAC TGTGTGTGTC AGACACTGTG CTAAGCACTT 1020
TACATATGCT ATCTTACTTA ATCCTAAGAG AATCCCACGA GGTAGGAATA ATTATCACCC 1080
CTACTTTACA GATAAGGAAA CTGAGGTACA GAGAGGTTGC ACAGCTGGTA AGCAATGGAG 1140
CCACGATTTG AATGCTTGCA ACCTTGACTG TCAGCTAGGC AGCATCCCCA ACAAGGTTTG 1200
AAACCCAGGA ATATAGTGTA GTTCACCCAC CCAGAATCCT TCAACACAGT CACTGTATGT 1260
GAGGGTGGGG GTTGGTTCCC AGTGACTCTT CCCACCTGAA GCACTGCCTG TAGTGCTGGG 1320
AAAGACAGCG GGAGCTAACT GTTGGAATAA CAAAGCACAC TGAGGCAAGC CTGGGCTCAT 1380
CTCAAGACCA ACTCCCAGTC TAGGACTCAG TACTTGGTCA TCCAGGAGCC CATATTGCAG 1440
GCATGCCACT CACCAGCTAC AGGATAAGTC ACTTCCCCTC TTCGGGCCTC AGCTACTCTA 1500
TCTGTCAATG AAGGACTCGG ACCACCTCAG TCATTTCCAA ACATTTTGAA ATCCTGCACT 1560
GCACTCCAAA ACATAAAAAA GACAGAAGCA CTCTTGCTCC AGAGCACCAT ACACTTGGAC 1620
TCACGGCCCT AATGGTTCCC CTTGGAGGTA AGACTTCCAT GCAGATCATC CAAAGGCTTT 1680
GGTGGACTCC ACCATTTCAG AGACCCCAGC ATGTGTTTTT CTCTTTAGGG GAAGGGGTGG 1740
CCAGGGGAGC TGGGTGAGTC CCAGGAGGAA ATGTCATTTG GATACCAGGA ATGTATTGAA 1800
GAGCCAGAGC AAATATTTGT TTTTCCTTTG ATGTCCTCCT AGAGCAGCCA TTAGTTCCGC 1860
CCACCTGCCC TTCCCTCAGC CAATCCCATC TGGCCCTGAT AATCCCATCT AGGCAGGTTG 1920
GGAGCGGGAA GTGTGCTAGA AAGGTGGAGA GAAAATTGGG ATGGAAGTCA CCCAGCTGGC 1980
TTTCCTCTGA ATCTAGCTCC CACCAACAAT CTCAATTCAT TCTAGGGGAG GTCTTGGGCA 2040
AGCTCCCACA CCCCTCTCCC GCACTGAAGT ATCCTGAGGC ACTAGGTCTC TCTCGATTCA 2100
CGAAGGACAG TCAAGAGGCA GGGGTGGGGT GGGGTGGGGA AGAGGCAATG CTCCAGAATT 2160
GAGAAACCAT TAGCACAGCA GGCAGCTGCT CTCCAAGAAG GAAGGAGACC CTGAGCAAGT 2220
TCCCAGCTGC AGAACTGGGT GGTCTATGGA TCAGGGAGGT TCACAGCAGG TCCCATGCCT 2280
ACTGATCTTG GCTTCCTACA TAGAGCAAGA GGCATGAGGC CAGGGAGTAT CTTCTGATGT 2340
AATAAGAGCT GGAATCCCTG CCTAAATCCA CTTAAGTTTG AAAACTGAAA GCTAGTTTAT 2400
CTCATTCTGG AATCAAATGA GATCTCTCTC TTACTCTCTC TCTCTCATGC ACATCCACAC 2460
ACACACCCCA CAGTGACCTG GGTCAAGAGC CTGATGGGAA CTCTGAACTT CAATCTCAGT 2520
TTCTCAGTCT CTGGGCCACC CCAGTCCCCA CGACCCAGTG TCTCCACCCC CAAGAGGCAC 2580
GAAGCACAAG CCACCAGCAG CTATTTTCCA GCTAAGCCCC TGACAAAGCC TGGGTCCAAC 2640
AGCCTCAAGC CTGGAGCCTC ACCGGGCCCT CACACTTTGC AGAAAGAGAA AGAAAAGGCA 2700
AGCCAGGAAG TACATGATTG CCCAATAGCT GTAACCTGGC AGCAGGCAAC TGGGGACTGT 2760
GCCAGGCGAT AGCAGGAAAA ACATACTCGG TCCTATTGAT GGGGCCATAA TCTACCCCTT 2820
TCTCCAACAT CCACTCTCCT TCACCAATGA AATGACTTCT TGAATTTCAA ACCAGCTACT 2880
GGCTGCAAAA GCAAACACAA TCTGGGGAAG TAACTGCTGA TGTAGCCAAT AGGGCAAACC 2940
ATACACACAC ACACACACAC ACACACACAC CCCCTCACAA CCAGCACCCA ACTGGATTTG 3000
GCAAAACATA ATAATGCCTA AACCACCTGC TCTAAAAGGC TTGTTAAAAT ATACATTATA 3060
TGGCCCTATC CTAGACCTTC AGAATAAATT ACTCTGGGTG TGGAACCAGA GAATGTAAGT 3120
ATTTTAAACA AACATCCCAG GTGATCCTTA CGTACTTTAA 3160
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