Tag | Content |
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EnhancerAtlas ID | HS197-20927 |
Organism | Homo sapiens |
Tissue/cell | ZR75-30 |
Coordinate | chr8:102153900-102156310 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RARA(var.2) | MA0730.1 | chr8:102155512-102155529 | AGGTCATCAGTAGGTCA | + | 6.19 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_29495 | chr8:102154317-102157549 | Fetal_Intestine_Large |
|
| Number: 1 | ID | Chromosome | Start | End |
GH08I101142 | chr8 | 102154610 | 102157203 |
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Enhancer Sequence | TCTAGCTCCA CAGAACAGTC TTCTGATTAC TAATGTGGCA TCCTGGCTAC AATTTTTTTT 60 TTTTTTTTGA GACAGAGTCT TGCTCTGCTG CCCAGGCTGG AGTGCAGTGG TGCAATCTCG 120 GCTCACTGCA ACCTCTGCCT CCCGGGTTCA AGATATTTTC CTGTCTCAGC CTCCCAAGTA 180 GCTGAGAGTA CAGGTGTGTG CCACCACACC CAGCTAATTT TTGTATTTGT TGTAGAGACA 240 GGGTTTCACC ATGCTGGCCA GGCTGGTCTC GAACTCCTGA CCTGAAGTGA TTTGCCAACC 300 TTGGTCTCCC AAAGTGCTGG GATTACAGGT ATGAGCCACT GCACCTGGCC CTGGCTGCTT 360 TGATACTAGG AAGAATTAGC CAGGTGGCTC CCAATGCTGG TCATTAATGT TCTGATCCCT 420 GAGAAGGGGC ATTCTCAGTT GTGAACAGAT GTACTGGTGC TCTGATCAAT TCTTTATTCT 480 CTGTGGATCT GGTTAAGTCA GTAGCTCAGA ACTGACCTAT TCTGGGTGTC CTGACAAAGT 540 GGAGTTCTGG GACTTGCAAA GCTGAAGTAG AAAAAGACCA CCTCCAGGTG CTGCCACCAG 600 AAAAGGCCCT TCCTGGGTAA CTGCTGGCTT CCCTGGATGG CAGGGGCTTT CAAACTTCTG 660 GCTGTGTAAC CTCCGAAAAG AAAATGAAAT GTCATACAAA TGCCCACTCT GCAGAGCCAG 720 TTAAAGGGGA GCCGTGCTAC CTGGGGGCTG GGGATGGGAG GCCGGGAGAC AGCTCCCATG 780 CATCCTGAAA GCCTCTCCCT GTGGTGGGCG CGGGCTTCTT GAAGATGGAC AGGCTCTGAC 840 CGCTTTTGTC CTCTCTCTGA GTCACAGGAT GAAGTCTTGG CCTCTGCCAT CTCCCAGTTC 900 CTCCCTGGGG GTGATAGAGG GAGCCACCCA CACAGAAGCT CCTACCCAGG GACTTGATTC 960 CTCTCAGTGC CACGCCTGGG GGTGCACCCA GGTGGGGCCC CTGTATTCAC TGCGGCGGTA 1020 GAAGGGCTGT GAGCAGGCTT TCCTGGTTAG GCTCTGTATT AGTCCGTGTG CGTTGCTTTA 1080 AAAGAATGCC TGAGACTGGG TAATTTATAA AGAAAGGAGG CTTATTTGGC TCGTGGTTCT 1140 GCAGGCTGTG CACAAAGCAT AGGCCCAGCA CCTGCTTCTT TCTGGTGAGG CCTCAGGAAG 1200 TTTCCAATCA TGGCAGAAGG CAAAGGGGAG CCAGAGTATT ACGTGGAGAG ACTGAAAGCA 1260 AGAGAGGGAG GAGGTGCCAG GCTCTTCTTA AACAACCAGA TCTCCTGTGA ACTCAGAGTG 1320 AGTGCTCACT CATCATCATG AGGACAGCAC TAAGATATTC ATAAGGGTTA TGCCCCCGCA 1380 ACCCTAACAC CTCCCACTAG GCCCACCTCC ACCGCTGGAG GTCACATTCC AACATGAGAT 1440 TTGGAGGGGA CAAACATCCA AACCATATCA GGCTCTTTCC TAATCATTTT TCTTTTGCAT 1500 CTTAAAAGTG AAGAGGAAAG AAGTCAGGCT AAGCCACAGT TAAATGGTCC ATGGGGGAAC 1560 AGTTAAAGCA AGCATCAAAA TATTAAAGAC ATAAAGAGCT TTCACTAATA CCAGGTCATC 1620 AGTAGGTCAG GCCACCGGCT TTCCACCCTT CATAAAAAAG GGAGGGGGCG ATTTCCTGTC 1680 CAGTTCTGAA GGGAGCATGC ATGGAGAATG CTGGAAAACC AGGCCTCTTA AGCTCAGAAA 1740 CAGTCTGTGG CCCCAGCAAG CCCCAGGGCC CGGGACCCCA AATGCAGAAG AAATGCCTAG 1800 TAGCCACAGG GCCCAGAGGG GTGTGCAGTA CTGGGAGACA GAGATGGCAC TAATTCCCAG 1860 GACAGTGGCG GCCACCAGGG CATGCCCAGG AGCTCAGGGG TCTTGGTGGT ACCCGGGAAG 1920 CTCCTTCCCT CACCCAGCAA GCAGCTGAGG CTGCGGAGAC CAGGTACCTG CTCAAGAACA 1980 TTCATCTGAC AAATACTCAT TATTGAGTGC CTACGGTATG CTGAGCTGTT CCAAGTGCTC 2040 TAGATGGGGC TGGCTGTGAT CAAAACAGAA AGCCCTGCCC TGAAGGACTG GGTAGACCTC 2100 AGAAATACCT CTTATAAGTG TGAGAGTTTG CTTTATGCTT TTCTGTGTAT AAATGGGCTT 2160 GCATTGCTTT GAAAATTAGG AAAAAGGTTA TTAAAGAATG TTATTAGAAA TTGTTTTTGA 2220 ATAAATATCC ACGAGGAAAT AGAAACATGA TAAGGAAATA CCAGCTAATT ACACATCCGC 2280 AAGTGCAGTG GACTCTGTAC TCTGATGAGG CCTCAGGAGG TGTGGTCAGA GAATCAACAC 2340 CAGATGGTCC TAGAAGAACT GATTGTGAAC TGTTATTGTC AAAGAAATCA TCATAGGAGA 2400 ACTGTAACTG 2410
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