| Tag | Content |
|---|
EnhancerAtlas ID | HS056-01358 |
Organism | Homo sapiens |
Tissue/cell | GC_B_cell |
Coordinate | chr1:226314120-226316960 |
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 | GCCAAGATTG TGCCACTTTA CTCCAGCCTG GATGACAGAG CGAGATTGTC TCAAAAAAAA 60
AAAAAAAAAG AAAAAAGAAA AAAAAAAAGC CGGGCACGGT GGCTTATGCC TGTAATCCCA 120
GGACTTTGGG AGGCCAAGGC GGGTGGGTCA CGAGGTCACG AGATCGAGAC CATCCTGGCT 180
AACACAGTGA AACCCCGTCT CTACTAAAAA TACAAAAAAT TAGCTGGGCG TGGTGGCGGG 240
CACCTGTAGT CCCAGCTGCT CGGGAGGCTG AGGCAGAAGA ATGGCATGAA CCTGGGAGGT 300
GGAGGTTGCA GTGAGCTGAG ATCGCGCCAC TGCACTCCAG CCTGGGCGAC AGAGCAAGAA 360
TCCGTCTAAA AAAAAAAGAG AGAGTCCCAG TGCTAAAACT GAGAGTCCTG GGCAAACTGG 420
AACAATTGAT CACACAATAA AGTGGGGGTT CTTGGGCTGG GTATGGAGGC TCATGCTTAT 480
AATCTCAGTG CTTTGGGAGG CCAAGGTGGA AGGATTGCTT GAGCCCAGGG CTTCAAGACC 540
AGCCTGGACA ACATAGCAAG ACCCTATCTC TACAAAAGAA AAAACAAGCA CACACTTGTA 600
GTCCCAGCTA CTTGGGAGGC TGAGGCAGGA GGACTGCTTA AGGCCAGGAG GTGGAGGTTG 660
CAATGGGCTA TGATGGCACC TCTGCACTCC AGCCTCAGTG ACAGAGCAAA ACCTCATTTT 720
GAAAACACAC ACATGAGGGG CGCTGGGAAT AGCCGCTCAT GTCGGCTGAC GGAGCGGTGT 780
GGGGCCGCAT GCGAAGCTGC CTCCGCGCCT TCCCCGAGCG GCTGGCCGCC TGCGGGGCCG 840
AGTAAGGACT TCTGCGCGCG GGAGTTCGAG GCCCTGCGGA GCTGCTTCGC CGCCGCGGCC 900
AAGAAGACGC TGGAGGGAGG CTGTTAGGAG GGACTCTGAG CTTCACACCT GTCTGCTGCC 960
GTGGTTGCAG AGCCCTAGTC CTGATGGCCC CCGGTGGCAT ACATTGAATG CCTAGGGCAG 1020
AAAGGAAGTG GGAATGGCGA AGATGTGACG TGCCTCGGTG TTAGATACTG TTTCTTCTTA 1080
ACAAGTTGAG GCGTGGGTAG AGCAGGAACT GGTTTTCCAG CATTGTGTCC GTAAACCTGA 1140
GTCAGAATAA GATGTAACAG AAGCCAGATA AAGACTCTGT CAAATCCTGC AAAAAAAAAA 1200
AAAAGAAAAA AAAGAAAACA CACACACACA CACATGCACA CAATGCATAA AGTGTTTCTG 1260
AAACTTTGGT GTGCATGAGA GACACCTGGG GACTTACAAA AACACAGATG GCTGGCCCCA 1320
CCCTAGAGTT TCTAATTTAG TAGGTCCAGG GTGGGGTCCG GTAATTTGCA TTTCTAACAA 1380
GTTTCCTGAT ACTGCTGCTG TTGCTCTTGG TTGGGGCCCA AACTTCCAGA ACAACTGGTC 1440
TGAATGAAGG GCTGGGTCCG GGACCTGCAA GTCCCACTGT GCTGCTTGCC CCGGTACCTC 1500
CTCCTAAGTC TGGCCCAGCA GGAAACGGAG CGCGGGTCAA AGTCCTCTCA CAGTCAACCA 1560
GGAGAAACCT GTGTCTTCCT GGCAGGGTGG CTGGGTGCTA TGGAAACAAG GCTCAGCCCA 1620
GAAGTGCCCA GCCTCCTTCC CAGAAGCAAC TTCAGCCTCT AGGGGAGGAG TGAAGTGAAC 1680
AAACAAACGG AAGGGCAGAG CTCAGTTCCT GGATGGAAGC GGCACCTGCA TGGAAGCGCC 1740
CTCAGCAACC TCAGGGCCCA GACTTCCGGG AAAGTCTCAC AGGGCCCCTG GCTTGAGTTT 1800
TGGAGCTGGA AGGGAACTTT GCAATCTTGG TTCAACTTTT TGTTTTATTT TCTGAGATGA 1860
ATCCTCGCTC TGTTGCCCAG GGTGGGGTGC AGTGGCGCAA TCTCGGCTCA CTGCAACCTC 1920
CGCCTCCCGG GTTCCAGCGA TGCTCCTGCC TCAGCCTCCT GAGTAGCTGG GATCACAGGT 1980
GCCTGCCACC ACGGTTGGCT AAATTTTGTA TTTTTAGTAG AGATGGGGGT TTCACCATGT 2040
TGGCCAGGCT GGTCTCGAAC TCCTTACCTC AGGTGATCCG CCCACCTCTG CCTTCCAAAG 2100
TGCTGGGATT ACAGGCATGA GCCACCGTGC CCGGCCCAGT ACATCTTTTA ACTGGGCTGT 2160
GAATGACACG ACTTGCTAAG ACCTGCCCAC TAAGAATGAG CTGCAGCCAG CACAATGTTG 2220
TCCGCTTCCA GCCACTTTCC TAGATACTCC TCCATTCCTC AGATTCCAGC CCCCACCCCA 2280
GCCTGGAACG CCCACAGTGC TTTTATCACA GCTCTTAACT CCACTTGGTT CCCCAAAGCT 2340
ATGAGCCCAC ATACCACCTC CCAGGGCTAC AACACTTTGG GTTTCTCAGA CACTGTCAAC 2400
ACTAAGCAGC ATGAACTGCA GGACACACAG GACAGCTGGA GAGGGGCAGT GAGTCACTGT 2460
GTCATAGTCC TGCCCAAATT CCAATGTTGA AATTGCAGAA GCCTGGGGCC CACCCTAGAG 2520
AATCTGATTC AGCAGGTTGG AGGGGGGGCC CAGGCACTGA TATTTTCAAG AGCCCTGGGT 2580
GATGTGGATG CCGATAGCAC TGGCTGCATG CTGAGAAACA CTGCCGATAG CATCATCTTC 2640
CACAGAAGGC CACCCAGGAA GAGATGATGA GGTGACAGAA CTTCATCACC CAACTCAAGA 2700
AGGCTTGGGA GGAAGGGGTA ATTTATTGGT TCTAAGCCCA GACCATGGAC AAAACAGAGT 2760
GCTATGGTTC AAATGTCCCC AGCAATGTTC ATGTTGAAAT GTAATTGCCG TTGTGATGGT 2820
GGCATTGGCA GGTGGGGCCT 2840
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