| Tag | Content |
|---|
EnhancerAtlas ID | HS059-04305 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr1:226314570-226316900 |
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: 7 | Chromosome | Start | End |
| chr1 | 226314917 | 226315002 | | chr1 | 226315055 | 226316024 | | chr1 | 226316027 | 226316129 | | chr1 | 226314646 | 226315237 | | chr1 | 226315631 | 226315825 | | chr1 | 226315308 | 226315548 | | chr1 | 226316204 | 226316800 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I226126 | chr1 | 226314498 | 226317175 |
|
Enhancer Sequence | CTTGGGCTGG GTATGGAGGC TCATGCTTAT AATCTCAGTG CTTTGGGAGG CCAAGGTGGA 60
AGGATTGCTT GAGCCCAGGG CTTCAAGACC AGCCTGGACA ACATAGCAAG ACCCTATCTC 120
TACAAAAGAA AAAACAAGCA CACACTTGTA GTCCCAGCTA CTTGGGAGGC TGAGGCAGGA 180
GGACTGCTTA AGGCCAGGAG GTGGAGGTTG CAATGGGCTA TGATGGCACC TCTGCACTCC 240
AGCCTCAGTG ACAGAGCAAA ACCTCATTTT GAAAACACAC ACATGAGGGG CGCTGGGAAT 300
AGCCGCTCAT GTCGGCTGAC GGAGCGGTGT GGGGCCGCAT GCGAAGCTGC CTCCGCGCCT 360
TCCCCGAGCG GCTGGCCGCC TGCGGGGCCG AGTAAGGACT TCTGCGCGCG GGAGTTCGAG 420
GCCCTGCGGA GCTGCTTCGC CGCCGCGGCC AAGAAGACGC TGGAGGGAGG CTGTTAGGAG 480
GGACTCTGAG CTTCACACCT GTCTGCTGCC GTGGTTGCAG AGCCCTAGTC CTGATGGCCC 540
CCGGTGGCAT ACATTGAATG CCTAGGGCAG AAAGGAAGTG GGAATGGCGA AGATGTGACG 600
TGCCTCGGTG TTAGATACTG TTTCTTCTTA ACAAGTTGAG GCGTGGGTAG AGCAGGAACT 660
GGTTTTCCAG CATTGTGTCC GTAAACCTGA GTCAGAATAA GATGTAACAG AAGCCAGATA 720
AAGACTCTGT CAAATCCTGC AAAAAAAAAA AAAAGAAAAA AAAGAAAACA CACACACACA 780
CACATGCACA CAATGCATAA AGTGTTTCTG AAACTTTGGT GTGCATGAGA GACACCTGGG 840
GACTTACAAA AACACAGATG GCTGGCCCCA CCCTAGAGTT TCTAATTTAG TAGGTCCAGG 900
GTGGGGTCCG GTAATTTGCA TTTCTAACAA GTTTCCTGAT ACTGCTGCTG TTGCTCTTGG 960
TTGGGGCCCA AACTTCCAGA ACAACTGGTC TGAATGAAGG GCTGGGTCCG GGACCTGCAA 1020
GTCCCACTGT GCTGCTTGCC CCGGTACCTC CTCCTAAGTC TGGCCCAGCA GGAAACGGAG 1080
CGCGGGTCAA AGTCCTCTCA CAGTCAACCA GGAGAAACCT GTGTCTTCCT GGCAGGGTGG 1140
CTGGGTGCTA TGGAAACAAG GCTCAGCCCA GAAGTGCCCA GCCTCCTTCC CAGAAGCAAC 1200
TTCAGCCTCT AGGGGAGGAG TGAAGTGAAC AAACAAACGG AAGGGCAGAG CTCAGTTCCT 1260
GGATGGAAGC GGCACCTGCA TGGAAGCGCC CTCAGCAACC TCAGGGCCCA GACTTCCGGG 1320
AAAGTCTCAC AGGGCCCCTG GCTTGAGTTT TGGAGCTGGA AGGGAACTTT GCAATCTTGG 1380
TTCAACTTTT TGTTTTATTT TCTGAGATGA ATCCTCGCTC TGTTGCCCAG GGTGGGGTGC 1440
AGTGGCGCAA TCTCGGCTCA CTGCAACCTC CGCCTCCCGG GTTCCAGCGA TGCTCCTGCC 1500
TCAGCCTCCT GAGTAGCTGG GATCACAGGT GCCTGCCACC ACGGTTGGCT AAATTTTGTA 1560
TTTTTAGTAG AGATGGGGGT TTCACCATGT TGGCCAGGCT GGTCTCGAAC TCCTTACCTC 1620
AGGTGATCCG CCCACCTCTG CCTTCCAAAG TGCTGGGATT ACAGGCATGA GCCACCGTGC 1680
CCGGCCCAGT ACATCTTTTA ACTGGGCTGT GAATGACACG ACTTGCTAAG ACCTGCCCAC 1740
TAAGAATGAG CTGCAGCCAG CACAATGTTG TCCGCTTCCA GCCACTTTCC TAGATACTCC 1800
TCCATTCCTC AGATTCCAGC CCCCACCCCA GCCTGGAACG CCCACAGTGC TTTTATCACA 1860
GCTCTTAACT CCACTTGGTT CCCCAAAGCT ATGAGCCCAC ATACCACCTC CCAGGGCTAC 1920
AACACTTTGG GTTTCTCAGA CACTGTCAAC ACTAAGCAGC ATGAACTGCA GGACACACAG 1980
GACAGCTGGA GAGGGGCAGT GAGTCACTGT GTCATAGTCC TGCCCAAATT CCAATGTTGA 2040
AATTGCAGAA GCCTGGGGCC CACCCTAGAG AATCTGATTC AGCAGGTTGG AGGGGGGGCC 2100
CAGGCACTGA TATTTTCAAG AGCCCTGGGT GATGTGGATG CCGATAGCAC TGGCTGCATG 2160
CTGAGAAACA CTGCCGATAG CATCATCTTC CACAGAAGGC CACCCAGGAA GAGATGATGA 2220
GGTGACAGAA CTTCATCACC CAACTCAAGA AGGCTTGGGA GGAAGGGGTA ATTTATTGGT 2280
TCTAAGCCCA GACCATGGAC AAAACAGAGT GCTATGGTTC AAATGTCCCC 2330
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