| Tag | Content |
|---|
EnhancerAtlas ID | HS145-02338 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr1:226314700-226317090 |
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 | 226315631 | 226315825 | | chr1 | 226315308 | 226315548 | | chr1 | 226316204 | 226316800 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I226126 | chr1 | 226314498 | 226317175 |
|
Enhancer Sequence | AAAACAAGCA CACACTTGTA GTCCCAGCTA CTTGGGAGGC TGAGGCAGGA GGACTGCTTA 60
AGGCCAGGAG GTGGAGGTTG CAATGGGCTA TGATGGCACC TCTGCACTCC AGCCTCAGTG 120
ACAGAGCAAA ACCTCATTTT GAAAACACAC ACATGAGGGG CGCTGGGAAT AGCCGCTCAT 180
GTCGGCTGAC GGAGCGGTGT GGGGCCGCAT GCGAAGCTGC CTCCGCGCCT TCCCCGAGCG 240
GCTGGCCGCC TGCGGGGCCG AGTAAGGACT TCTGCGCGCG GGAGTTCGAG GCCCTGCGGA 300
GCTGCTTCGC CGCCGCGGCC AAGAAGACGC TGGAGGGAGG CTGTTAGGAG GGACTCTGAG 360
CTTCACACCT GTCTGCTGCC GTGGTTGCAG AGCCCTAGTC CTGATGGCCC CCGGTGGCAT 420
ACATTGAATG CCTAGGGCAG AAAGGAAGTG GGAATGGCGA AGATGTGACG TGCCTCGGTG 480
TTAGATACTG TTTCTTCTTA ACAAGTTGAG GCGTGGGTAG AGCAGGAACT GGTTTTCCAG 540
CATTGTGTCC GTAAACCTGA GTCAGAATAA GATGTAACAG AAGCCAGATA AAGACTCTGT 600
CAAATCCTGC AAAAAAAAAA AAAAGAAAAA AAAGAAAACA CACACACACA CACATGCACA 660
CAATGCATAA AGTGTTTCTG AAACTTTGGT GTGCATGAGA GACACCTGGG GACTTACAAA 720
AACACAGATG GCTGGCCCCA CCCTAGAGTT TCTAATTTAG TAGGTCCAGG GTGGGGTCCG 780
GTAATTTGCA TTTCTAACAA GTTTCCTGAT ACTGCTGCTG TTGCTCTTGG TTGGGGCCCA 840
AACTTCCAGA ACAACTGGTC TGAATGAAGG GCTGGGTCCG GGACCTGCAA GTCCCACTGT 900
GCTGCTTGCC CCGGTACCTC CTCCTAAGTC TGGCCCAGCA GGAAACGGAG CGCGGGTCAA 960
AGTCCTCTCA CAGTCAACCA GGAGAAACCT GTGTCTTCCT GGCAGGGTGG CTGGGTGCTA 1020
TGGAAACAAG GCTCAGCCCA GAAGTGCCCA GCCTCCTTCC CAGAAGCAAC TTCAGCCTCT 1080
AGGGGAGGAG TGAAGTGAAC AAACAAACGG AAGGGCAGAG CTCAGTTCCT GGATGGAAGC 1140
GGCACCTGCA TGGAAGCGCC CTCAGCAACC TCAGGGCCCA GACTTCCGGG AAAGTCTCAC 1200
AGGGCCCCTG GCTTGAGTTT TGGAGCTGGA AGGGAACTTT GCAATCTTGG TTCAACTTTT 1260
TGTTTTATTT TCTGAGATGA ATCCTCGCTC TGTTGCCCAG GGTGGGGTGC AGTGGCGCAA 1320
TCTCGGCTCA CTGCAACCTC CGCCTCCCGG GTTCCAGCGA TGCTCCTGCC TCAGCCTCCT 1380
GAGTAGCTGG GATCACAGGT GCCTGCCACC ACGGTTGGCT AAATTTTGTA TTTTTAGTAG 1440
AGATGGGGGT TTCACCATGT TGGCCAGGCT GGTCTCGAAC TCCTTACCTC AGGTGATCCG 1500
CCCACCTCTG CCTTCCAAAG TGCTGGGATT ACAGGCATGA GCCACCGTGC CCGGCCCAGT 1560
ACATCTTTTA ACTGGGCTGT GAATGACACG ACTTGCTAAG ACCTGCCCAC TAAGAATGAG 1620
CTGCAGCCAG CACAATGTTG TCCGCTTCCA GCCACTTTCC TAGATACTCC TCCATTCCTC 1680
AGATTCCAGC CCCCACCCCA GCCTGGAACG CCCACAGTGC TTTTATCACA GCTCTTAACT 1740
CCACTTGGTT CCCCAAAGCT ATGAGCCCAC ATACCACCTC CCAGGGCTAC AACACTTTGG 1800
GTTTCTCAGA CACTGTCAAC ACTAAGCAGC ATGAACTGCA GGACACACAG GACAGCTGGA 1860
GAGGGGCAGT GAGTCACTGT GTCATAGTCC TGCCCAAATT CCAATGTTGA AATTGCAGAA 1920
GCCTGGGGCC CACCCTAGAG AATCTGATTC AGCAGGTTGG AGGGGGGGCC CAGGCACTGA 1980
TATTTTCAAG AGCCCTGGGT GATGTGGATG CCGATAGCAC TGGCTGCATG CTGAGAAACA 2040
CTGCCGATAG CATCATCTTC CACAGAAGGC CACCCAGGAA GAGATGATGA GGTGACAGAA 2100
CTTCATCACC CAACTCAAGA AGGCTTGGGA GGAAGGGGTA ATTTATTGGT TCTAAGCCCA 2160
GACCATGGAC AAAACAGAGT GCTATGGTTC AAATGTCCCC AGCAATGTTC ATGTTGAAAT 2220
GTAATTGCCG TTGTGATGGT GGCATTGGCA GGTGGGGCCT TTGCAAGGTA ATTAGGTTAT 2280
GAGGGCTCTG CCCTCAGGAA TGGATCCATG CCATCATCTC TGGAGTGGGT TCTTGATAAA 2340
AAGGATGATT CTGGACCACT TCCCTCTCAT GTCTCACATG CTTACCTCTG 2390
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