| Tag | Content |
|---|
EnhancerAtlas ID | HS073-01363 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr1:226314240-226316610 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Hnf4a | MA0114.3 | chr1:226315652-226315668 | CGGGTCAAAGTCCTCT | + | 6.49 | | STAT3 | MA0144.2 | chr1:226315755-226315766 | CTTCCCAGAAG | - | 6.14 |
|
| | Number of super-enhancer constituents: 25 | ID | Coordinate | Tissue/cell |
| SE_10465 | chr1:226314329-226317263 | CD19_Primary | | SE_11118 | chr1:226314228-226323738 | CD20 | | SE_23364 | chr1:226314431-226316913 | Colon_Crypt_1 | | SE_23849 | chr1:226314482-226315331 | Colon_Crypt_2 | | SE_23849 | chr1:226315334-226316161 | Colon_Crypt_2 | | SE_23849 | chr1:226316204-226316855 | Colon_Crypt_2 | | SE_24831 | chr1:226314416-226316628 | Colon_Crypt_3 | | SE_26794 | chr1:226314386-226317368 | Esophagus | | SE_31597 | chr1:226314394-226317203 | Gastric | | SE_41844 | chr1:226314696-226315324 | LNCaP | | SE_41844 | chr1:226315457-226316066 | LNCaP | | SE_41844 | chr1:226316166-226316615 | LNCaP | | SE_43265 | chr1:226314581-226317218 | Lung | | SE_43763 | chr1:226314330-226317236 | MM1S | | SE_47729 | chr1:226314790-226315311 | Pancreas | | SE_47729 | chr1:226315339-226316040 | Pancreas | | SE_47729 | chr1:226316205-226316603 | Pancreas | | SE_50502 | chr1:226314371-226317219 | Sigmoid_Colon | | SE_52861 | chr1:226314391-226316889 | Small_Intestine | | SE_56941 | chr1:226314700-226316129 | VACO_400 | | SE_56941 | chr1:226316193-226316621 | VACO_400 | | SE_62016 | chr1:226296810-226321627 | Toledo | | SE_63137 | chr1:226295246-226322063 | Tonsil | | SE_65669 | chr1:226312586-226317084 | Pancreatic_islets | | SE_67238 | chr1:226314330-226317236 | MM1S |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 6 | Chromosome | Start | End |
| chr1 | 226314917 | 226315002 | | chr1 | 226315055 | 226316024 | | chr1 | 226316027 | 226316129 | | chr1 | 226314646 | 226315237 | | chr1 | 226315631 | 226315825 | | chr1 | 226315308 | 226315548 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I226126 | chr1 | 226314498 | 226317175 |
|
Enhancer Sequence | GGACTTTGGG AGGCCAAGGC GGGTGGGTCA CGAGGTCACG AGATCGAGAC CATCCTGGCT 60
AACACAGTGA AACCCCGTCT CTACTAAAAA TACAAAAAAT TAGCTGGGCG TGGTGGCGGG 120
CACCTGTAGT CCCAGCTGCT CGGGAGGCTG AGGCAGAAGA ATGGCATGAA CCTGGGAGGT 180
GGAGGTTGCA GTGAGCTGAG ATCGCGCCAC TGCACTCCAG CCTGGGCGAC AGAGCAAGAA 240
TCCGTCTAAA AAAAAAAGAG AGAGTCCCAG TGCTAAAACT GAGAGTCCTG GGCAAACTGG 300
AACAATTGAT CACACAATAA AGTGGGGGTT CTTGGGCTGG GTATGGAGGC TCATGCTTAT 360
AATCTCAGTG CTTTGGGAGG CCAAGGTGGA AGGATTGCTT GAGCCCAGGG CTTCAAGACC 420
AGCCTGGACA ACATAGCAAG ACCCTATCTC TACAAAAGAA AAAACAAGCA CACACTTGTA 480
GTCCCAGCTA CTTGGGAGGC TGAGGCAGGA GGACTGCTTA AGGCCAGGAG GTGGAGGTTG 540
CAATGGGCTA TGATGGCACC TCTGCACTCC AGCCTCAGTG ACAGAGCAAA ACCTCATTTT 600
GAAAACACAC ACATGAGGGG CGCTGGGAAT AGCCGCTCAT GTCGGCTGAC GGAGCGGTGT 660
GGGGCCGCAT GCGAAGCTGC CTCCGCGCCT TCCCCGAGCG GCTGGCCGCC TGCGGGGCCG 720
AGTAAGGACT TCTGCGCGCG GGAGTTCGAG GCCCTGCGGA GCTGCTTCGC CGCCGCGGCC 780
AAGAAGACGC TGGAGGGAGG CTGTTAGGAG GGACTCTGAG CTTCACACCT GTCTGCTGCC 840
GTGGTTGCAG AGCCCTAGTC CTGATGGCCC CCGGTGGCAT ACATTGAATG CCTAGGGCAG 900
AAAGGAAGTG GGAATGGCGA AGATGTGACG TGCCTCGGTG TTAGATACTG TTTCTTCTTA 960
ACAAGTTGAG GCGTGGGTAG AGCAGGAACT GGTTTTCCAG CATTGTGTCC GTAAACCTGA 1020
GTCAGAATAA GATGTAACAG AAGCCAGATA AAGACTCTGT CAAATCCTGC AAAAAAAAAA 1080
AAAAGAAAAA AAAGAAAACA CACACACACA CACATGCACA CAATGCATAA AGTGTTTCTG 1140
AAACTTTGGT GTGCATGAGA GACACCTGGG GACTTACAAA AACACAGATG GCTGGCCCCA 1200
CCCTAGAGTT TCTAATTTAG TAGGTCCAGG GTGGGGTCCG GTAATTTGCA TTTCTAACAA 1260
GTTTCCTGAT ACTGCTGCTG TTGCTCTTGG TTGGGGCCCA AACTTCCAGA ACAACTGGTC 1320
TGAATGAAGG GCTGGGTCCG GGACCTGCAA GTCCCACTGT GCTGCTTGCC CCGGTACCTC 1380
CTCCTAAGTC TGGCCCAGCA GGAAACGGAG CGCGGGTCAA AGTCCTCTCA CAGTCAACCA 1440
GGAGAAACCT GTGTCTTCCT GGCAGGGTGG CTGGGTGCTA TGGAAACAAG GCTCAGCCCA 1500
GAAGTGCCCA GCCTCCTTCC CAGAAGCAAC TTCAGCCTCT AGGGGAGGAG TGAAGTGAAC 1560
AAACAAACGG AAGGGCAGAG CTCAGTTCCT GGATGGAAGC GGCACCTGCA TGGAAGCGCC 1620
CTCAGCAACC TCAGGGCCCA GACTTCCGGG AAAGTCTCAC AGGGCCCCTG GCTTGAGTTT 1680
TGGAGCTGGA AGGGAACTTT GCAATCTTGG TTCAACTTTT TGTTTTATTT TCTGAGATGA 1740
ATCCTCGCTC TGTTGCCCAG GGTGGGGTGC AGTGGCGCAA TCTCGGCTCA CTGCAACCTC 1800
CGCCTCCCGG GTTCCAGCGA TGCTCCTGCC TCAGCCTCCT GAGTAGCTGG GATCACAGGT 1860
GCCTGCCACC ACGGTTGGCT AAATTTTGTA TTTTTAGTAG AGATGGGGGT TTCACCATGT 1920
TGGCCAGGCT GGTCTCGAAC TCCTTACCTC AGGTGATCCG CCCACCTCTG CCTTCCAAAG 1980
TGCTGGGATT ACAGGCATGA GCCACCGTGC CCGGCCCAGT ACATCTTTTA ACTGGGCTGT 2040
GAATGACACG ACTTGCTAAG ACCTGCCCAC TAAGAATGAG CTGCAGCCAG CACAATGTTG 2100
TCCGCTTCCA GCCACTTTCC TAGATACTCC TCCATTCCTC AGATTCCAGC CCCCACCCCA 2160
GCCTGGAACG CCCACAGTGC TTTTATCACA GCTCTTAACT CCACTTGGTT CCCCAAAGCT 2220
ATGAGCCCAC ATACCACCTC CCAGGGCTAC AACACTTTGG GTTTCTCAGA CACTGTCAAC 2280
ACTAAGCAGC ATGAACTGCA GGACACACAG GACAGCTGGA GAGGGGCAGT GAGTCACTGT 2340
GTCATAGTCC TGCCCAAATT CCAATGTTGA 2370
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