Tag | Content |
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EnhancerAtlas ID | HS101-23220 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr2:28861730-28863790 |
Target genes | Number: 12 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
JUN | MA0488.1 | chr2:28863314-28863327 | GTAATGATGTCAT | + | 6.48 | JUND(var.2) | MA0492.1 | chr2:28863313-28863328 | AGTAATGATGTCATG | + | 6.51 | Rxra | MA0512.2 | chr2:28862981-28862995 | TGAACTTTCACCTC | - | 6.01 | STAT3 | MA0144.2 | chr2:28862354-28862365 | CTTCCCAGAAG | - | 6.14 |
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| Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
SE_01568 | chr2:28861838-28863291 | Aorta | SE_09812 | chr2:28862086-28863417 | CD14 | SE_23318 | chr2:28861804-28864206 | Colon_Crypt_1 | SE_26630 | chr2:28862555-28863347 | Esophagus | SE_28044 | chr2:28862373-28863470 | Fetal_Intestine | SE_31986 | chr2:28862564-28863350 | Gastric | SE_35216 | chr2:28862226-28863847 | HeLa | SE_50302 | chr2:28862021-28863860 | Sigmoid_Colon | SE_52600 | chr2:28862061-28863547 | Small_Intestine | SE_65622 | chr2:28861725-28865114 | Pancreatic_islets |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I028639 | chr2 | 28862517 | 28863727 |
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Enhancer Sequence | CATAGAGGGC CAATATGGTG AAACCCTGTC TCTACTGAAA ATACAAAAAT TATCCAGGCG 60 TGGTGGCATG CACCTGTAAT CCCAGCTACT CAGGGAGGCT GAGGCAGGAG AATTGCTTGA 120 ACCCAGAGAT GGGGTGGAGG TTGCAGTAAG CTGAGATCGT GCCATTGCAC TCCAGCCTGG 180 GTGACAGGGC AAGATTCCAT CTAAAAAAAA AAAAAAAGCC ACTACAGGAT CAACTAAGAG 240 CTCCTAGAGA AAGAATAGGT AGGTAGAAAA GAGTGTAAGG CCAACTACCT AGCCCTGGGC 300 ATTCATTCCA GCTTTCAACT CCAGTGAGAG ATGAGAAGGA GAGTGTGGAG GTAGATGGGA 360 AATGAGAAAC AATGCTGTGT CCAGAGAGCT AAGAGAAGTC AGTGTTTCAA GAGAGACAGA 420 GCTGTCAACT TTGATGGATG CTTCTGAGAA GCCAAGCAAG TTGAAGACAA AAAAAAAAAA 480 AAATGATCTT TGGCTCTGCC CATATGGCGA TCGTTGGTGG CCAGGGCCAG AGCTTCCATC 540 CAGCGATGGA GACTGCAGAC TGGCTGGAGC GAGCAGCAGA GAGAAGGAGA GATTAGGAAG 600 TGCTGCCAGC ACCTATAGAC AGCTCTTCCC AGAAGTTATG AGAAGTAACA GCCACGGTCA 660 CTGGAGGGGA CATGGATCAA AGAAAGGGCA GGTGAAGGAG GGGAGATGTC GGAGCAGGTT 720 GTGTACTGAC GAGAAGGAAC CAGTAGAAAG GGAGAAACTG ATGCACTCAT CAAACCCTTG 780 TAATCACGAT CATCTTCTGT GTGAATTAGT TCTGGGTTCC TGGAATAGCA TCGGGAATCA 840 GCCGCGCTGA CCTTTAGCAT TTATTCTGTC ACTGTTACGA TAGACTTGAG TTTCCTCAGT 900 TCTTAAGAAA GTGGAAATAA TACTACCTTA TGTATGTAAG CCACCCCAAT CACACGTGCT 960 TTCATGCCAT CTTCTCATTT GATGCTCACA ACAAACCAAG GTGTCAGGAC AGGATGTCAT 1020 GCCTGTCCCT AACCTCAGAG AAGTAGCCAG CCCAGCACTG CACAGCTCGT TACCAGCAGA 1080 GCCTGGATCC CAGCCATCTG CCCATCGTGC TCAGTCTAGT CACCCTAGCA TCTCTCCCAG 1140 GAACAGAACT GCCCTCCCTC CTCCAATTGT GTTACTAAGG AACGGGTGTA AAAGGCCTTC 1200 AGACAACAGA AAGTGAGATC ATGGGCCAGG TGTGGTCATG AGCTCAGATA GTGAACTTTC 1260 ACCTCCCTCC CTGGCAATAC CCTGTGGTCA GGAGCAGGCA GATTACACAA AGAGTGGAGG 1320 CTAGACGTTC CAAACAGACT CTGAATAGGT GACAGTGCCA GGGGCTCATT CTTCTCAGTG 1380 CTGGCCACAG GTTGGGCCTG GCTGCTGGCT AAAAGGTGCC GGGGAGGGGG ATACAGCAGC 1440 TCCCAGCTCA TCCTCAGAGG GTCCTGGGAT CAAAGGTATT TACACCCAGG GATATTTCAG 1500 ATAAATCTTT TCATCTATGT GGAAAACATA CAAAGTGGCG CAAGTGAGAA ACTCCGATTT 1560 CCTAAGGTTG ACAAGTCAAG TGCAGTAATG ATGTCATGGT AACCAATATG TTTCCAAACT 1620 TTCCTAAGGT TGACTAGCCC CATGCACTTT GAGAAGTTGG TAAATAGGAT TGTCGTCGTT 1680 TTATAAAATT GAAAACACGG TGTCTTGCAA TCACAGCCAC TCACAAAGGA AGCCAGAGAT 1740 GGTCCCAGCC CCTCCGCAGA CTTCCTGTGG ACTCAGGACT GGTGGTCTCT CCTGGGCCTT 1800 GCTGTACCCG GCAAATCCAG GGGCACAGAC TCAGGGTTCT GCCCTGCCGA CAGATGCTGC 1860 CTAGCCTTCT GTGTGTCATA AGTCAACTCC CGCTCAGCCC CAGGCTGCTG GGTCCCTGCT 1920 GTGGGCCAAA AACCAGCCAC TTCGCTGGTT TCTATCCCCC ACCCCGTTCC CGAGGGAGGG 1980 GCTCTGGTGT GAGACACCCC CTCAGAGAGG AAAGTGTCTC CCAGCTTTGG AGAGAATCGA 2040 GGTGTCCTTT CTCTCTCTCC 2060
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