| Tag | Content |
|---|
EnhancerAtlas ID | HS030-02372 |
Organism | Homo sapiens |
Tissue/cell | CyT49 |
Coordinate | chr1:226314480-226316950 |
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 | TCCGTCTAAA AAAAAAAGAG AGAGTCCCAG TGCTAAAACT GAGAGTCCTG GGCAAACTGG 60
AACAATTGAT CACACAATAA AGTGGGGGTT CTTGGGCTGG GTATGGAGGC TCATGCTTAT 120
AATCTCAGTG CTTTGGGAGG CCAAGGTGGA AGGATTGCTT GAGCCCAGGG CTTCAAGACC 180
AGCCTGGACA ACATAGCAAG ACCCTATCTC TACAAAAGAA AAAACAAGCA CACACTTGTA 240
GTCCCAGCTA CTTGGGAGGC TGAGGCAGGA GGACTGCTTA AGGCCAGGAG GTGGAGGTTG 300
CAATGGGCTA TGATGGCACC TCTGCACTCC AGCCTCAGTG ACAGAGCAAA ACCTCATTTT 360
GAAAACACAC ACATGAGGGG CGCTGGGAAT AGCCGCTCAT GTCGGCTGAC GGAGCGGTGT 420
GGGGCCGCAT GCGAAGCTGC CTCCGCGCCT TCCCCGAGCG GCTGGCCGCC TGCGGGGCCG 480
AGTAAGGACT TCTGCGCGCG GGAGTTCGAG GCCCTGCGGA GCTGCTTCGC CGCCGCGGCC 540
AAGAAGACGC TGGAGGGAGG CTGTTAGGAG GGACTCTGAG CTTCACACCT GTCTGCTGCC 600
GTGGTTGCAG AGCCCTAGTC CTGATGGCCC CCGGTGGCAT ACATTGAATG CCTAGGGCAG 660
AAAGGAAGTG GGAATGGCGA AGATGTGACG TGCCTCGGTG TTAGATACTG TTTCTTCTTA 720
ACAAGTTGAG GCGTGGGTAG AGCAGGAACT GGTTTTCCAG CATTGTGTCC GTAAACCTGA 780
GTCAGAATAA GATGTAACAG AAGCCAGATA AAGACTCTGT CAAATCCTGC AAAAAAAAAA 840
AAAAGAAAAA AAAGAAAACA CACACACACA CACATGCACA CAATGCATAA AGTGTTTCTG 900
AAACTTTGGT GTGCATGAGA GACACCTGGG GACTTACAAA AACACAGATG GCTGGCCCCA 960
CCCTAGAGTT TCTAATTTAG TAGGTCCAGG GTGGGGTCCG GTAATTTGCA TTTCTAACAA 1020
GTTTCCTGAT ACTGCTGCTG TTGCTCTTGG TTGGGGCCCA AACTTCCAGA ACAACTGGTC 1080
TGAATGAAGG GCTGGGTCCG GGACCTGCAA GTCCCACTGT GCTGCTTGCC CCGGTACCTC 1140
CTCCTAAGTC TGGCCCAGCA GGAAACGGAG CGCGGGTCAA AGTCCTCTCA CAGTCAACCA 1200
GGAGAAACCT GTGTCTTCCT GGCAGGGTGG CTGGGTGCTA TGGAAACAAG GCTCAGCCCA 1260
GAAGTGCCCA GCCTCCTTCC CAGAAGCAAC TTCAGCCTCT AGGGGAGGAG TGAAGTGAAC 1320
AAACAAACGG AAGGGCAGAG CTCAGTTCCT GGATGGAAGC GGCACCTGCA TGGAAGCGCC 1380
CTCAGCAACC TCAGGGCCCA GACTTCCGGG AAAGTCTCAC AGGGCCCCTG GCTTGAGTTT 1440
TGGAGCTGGA AGGGAACTTT GCAATCTTGG TTCAACTTTT TGTTTTATTT TCTGAGATGA 1500
ATCCTCGCTC TGTTGCCCAG GGTGGGGTGC AGTGGCGCAA TCTCGGCTCA CTGCAACCTC 1560
CGCCTCCCGG GTTCCAGCGA TGCTCCTGCC TCAGCCTCCT GAGTAGCTGG GATCACAGGT 1620
GCCTGCCACC ACGGTTGGCT AAATTTTGTA TTTTTAGTAG AGATGGGGGT TTCACCATGT 1680
TGGCCAGGCT GGTCTCGAAC TCCTTACCTC AGGTGATCCG CCCACCTCTG CCTTCCAAAG 1740
TGCTGGGATT ACAGGCATGA GCCACCGTGC CCGGCCCAGT ACATCTTTTA ACTGGGCTGT 1800
GAATGACACG ACTTGCTAAG ACCTGCCCAC TAAGAATGAG CTGCAGCCAG CACAATGTTG 1860
TCCGCTTCCA GCCACTTTCC TAGATACTCC TCCATTCCTC AGATTCCAGC CCCCACCCCA 1920
GCCTGGAACG CCCACAGTGC TTTTATCACA GCTCTTAACT CCACTTGGTT CCCCAAAGCT 1980
ATGAGCCCAC ATACCACCTC CCAGGGCTAC AACACTTTGG GTTTCTCAGA CACTGTCAAC 2040
ACTAAGCAGC ATGAACTGCA GGACACACAG GACAGCTGGA GAGGGGCAGT GAGTCACTGT 2100
GTCATAGTCC TGCCCAAATT CCAATGTTGA AATTGCAGAA GCCTGGGGCC CACCCTAGAG 2160
AATCTGATTC AGCAGGTTGG AGGGGGGGCC CAGGCACTGA TATTTTCAAG AGCCCTGGGT 2220
GATGTGGATG CCGATAGCAC TGGCTGCATG CTGAGAAACA CTGCCGATAG CATCATCTTC 2280
CACAGAAGGC CACCCAGGAA GAGATGATGA GGTGACAGAA CTTCATCACC CAACTCAAGA 2340
AGGCTTGGGA GGAAGGGGTA ATTTATTGGT TCTAAGCCCA GACCATGGAC AAAACAGAGT 2400
GCTATGGTTC AAATGTCCCC AGCAATGTTC ATGTTGAAAT GTAATTGCCG TTGTGATGGT 2460
GGCATTGGCA 2470
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