| Tag | Content |
|---|
EnhancerAtlas ID | HS050-06093 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:226314500-226316950 |
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 | AGAGTCCCAG TGCTAAAACT GAGAGTCCTG GGCAAACTGG AACAATTGAT CACACAATAA 60
AGTGGGGGTT CTTGGGCTGG GTATGGAGGC TCATGCTTAT AATCTCAGTG CTTTGGGAGG 120
CCAAGGTGGA AGGATTGCTT GAGCCCAGGG CTTCAAGACC AGCCTGGACA ACATAGCAAG 180
ACCCTATCTC TACAAAAGAA AAAACAAGCA CACACTTGTA GTCCCAGCTA CTTGGGAGGC 240
TGAGGCAGGA GGACTGCTTA AGGCCAGGAG GTGGAGGTTG CAATGGGCTA TGATGGCACC 300
TCTGCACTCC AGCCTCAGTG ACAGAGCAAA ACCTCATTTT GAAAACACAC ACATGAGGGG 360
CGCTGGGAAT AGCCGCTCAT GTCGGCTGAC GGAGCGGTGT GGGGCCGCAT GCGAAGCTGC 420
CTCCGCGCCT TCCCCGAGCG GCTGGCCGCC TGCGGGGCCG AGTAAGGACT TCTGCGCGCG 480
GGAGTTCGAG GCCCTGCGGA GCTGCTTCGC CGCCGCGGCC AAGAAGACGC TGGAGGGAGG 540
CTGTTAGGAG GGACTCTGAG CTTCACACCT GTCTGCTGCC GTGGTTGCAG AGCCCTAGTC 600
CTGATGGCCC CCGGTGGCAT ACATTGAATG CCTAGGGCAG AAAGGAAGTG GGAATGGCGA 660
AGATGTGACG TGCCTCGGTG TTAGATACTG TTTCTTCTTA ACAAGTTGAG GCGTGGGTAG 720
AGCAGGAACT GGTTTTCCAG CATTGTGTCC GTAAACCTGA GTCAGAATAA GATGTAACAG 780
AAGCCAGATA AAGACTCTGT CAAATCCTGC AAAAAAAAAA AAAAGAAAAA AAAGAAAACA 840
CACACACACA CACATGCACA CAATGCATAA AGTGTTTCTG AAACTTTGGT GTGCATGAGA 900
GACACCTGGG GACTTACAAA AACACAGATG GCTGGCCCCA CCCTAGAGTT TCTAATTTAG 960
TAGGTCCAGG GTGGGGTCCG GTAATTTGCA TTTCTAACAA GTTTCCTGAT ACTGCTGCTG 1020
TTGCTCTTGG TTGGGGCCCA AACTTCCAGA ACAACTGGTC TGAATGAAGG GCTGGGTCCG 1080
GGACCTGCAA GTCCCACTGT GCTGCTTGCC CCGGTACCTC CTCCTAAGTC TGGCCCAGCA 1140
GGAAACGGAG CGCGGGTCAA AGTCCTCTCA CAGTCAACCA GGAGAAACCT GTGTCTTCCT 1200
GGCAGGGTGG CTGGGTGCTA TGGAAACAAG GCTCAGCCCA GAAGTGCCCA GCCTCCTTCC 1260
CAGAAGCAAC TTCAGCCTCT AGGGGAGGAG TGAAGTGAAC AAACAAACGG AAGGGCAGAG 1320
CTCAGTTCCT GGATGGAAGC GGCACCTGCA TGGAAGCGCC CTCAGCAACC TCAGGGCCCA 1380
GACTTCCGGG AAAGTCTCAC AGGGCCCCTG GCTTGAGTTT TGGAGCTGGA AGGGAACTTT 1440
GCAATCTTGG TTCAACTTTT TGTTTTATTT TCTGAGATGA ATCCTCGCTC TGTTGCCCAG 1500
GGTGGGGTGC AGTGGCGCAA TCTCGGCTCA CTGCAACCTC CGCCTCCCGG GTTCCAGCGA 1560
TGCTCCTGCC TCAGCCTCCT GAGTAGCTGG GATCACAGGT GCCTGCCACC ACGGTTGGCT 1620
AAATTTTGTA TTTTTAGTAG AGATGGGGGT TTCACCATGT TGGCCAGGCT GGTCTCGAAC 1680
TCCTTACCTC AGGTGATCCG CCCACCTCTG CCTTCCAAAG TGCTGGGATT ACAGGCATGA 1740
GCCACCGTGC CCGGCCCAGT ACATCTTTTA ACTGGGCTGT GAATGACACG ACTTGCTAAG 1800
ACCTGCCCAC TAAGAATGAG CTGCAGCCAG CACAATGTTG TCCGCTTCCA GCCACTTTCC 1860
TAGATACTCC TCCATTCCTC AGATTCCAGC CCCCACCCCA GCCTGGAACG CCCACAGTGC 1920
TTTTATCACA GCTCTTAACT CCACTTGGTT CCCCAAAGCT ATGAGCCCAC ATACCACCTC 1980
CCAGGGCTAC AACACTTTGG GTTTCTCAGA CACTGTCAAC ACTAAGCAGC ATGAACTGCA 2040
GGACACACAG GACAGCTGGA GAGGGGCAGT GAGTCACTGT GTCATAGTCC TGCCCAAATT 2100
CCAATGTTGA AATTGCAGAA GCCTGGGGCC CACCCTAGAG AATCTGATTC AGCAGGTTGG 2160
AGGGGGGGCC CAGGCACTGA TATTTTCAAG AGCCCTGGGT GATGTGGATG CCGATAGCAC 2220
TGGCTGCATG CTGAGAAACA CTGCCGATAG CATCATCTTC CACAGAAGGC CACCCAGGAA 2280
GAGATGATGA GGTGACAGAA CTTCATCACC CAACTCAAGA AGGCTTGGGA GGAAGGGGTA 2340
ATTTATTGGT TCTAAGCCCA GACCATGGAC AAAACAGAGT GCTATGGTTC AAATGTCCCC 2400
AGCAATGTTC ATGTTGAAAT GTAATTGCCG TTGTGATGGT GGCATTGGCA 2450
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