Tag | Content |
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EnhancerAtlas ID | HS116-28957 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr6:11770320-11771750 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF143 | MA0088.2 | chr6:11770369-11770385 | TAAAGCATTGTGGGAG | - | 6.09 | ZNF263 | MA0528.1 | chr6:11771003-11771024 | TCCCTCCTCTCTCCCTCCCCC | - | 7.57 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_02588 | chr6:11765381-11773718 | Astrocytes | SE_36227 | chr6:11765602-11774208 | HMEC | SE_46411 | chr6:11765481-11773791 | Osteoblasts | SE_64267 | chr6:11765490-11774168 | NHEK |
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| Number: 1 | ID | Chromosome | Start | End |
GH06I011765 | chr6 | 11765246 | 11773950 |
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Enhancer Sequence | GACTTCGAAA AAATAAAAAA AATTATCAGG TTTCTGAGCG TAGTTCAGAT AAAGCATTGT 60 GGGAGGTCAG AAGAGAGACA ATTATCTCCA GGTGGGAGAA TGAACGACCA CTTCACAAAC 120 CACCGCTGCC TGGTTCCCAC CCCCAGAGAT TCTAATGTAA TCAGTCTGGG GCTAGGGCCT 180 AGGGGTTGGG ATTTTTAAAA TCCTCCCAGG TGATTCTAAT CACGGGCAGC TGAGGCTGAG 240 AACCACCTGC CTGGAGGAAC TTCCGTTTGG AAATTCAGAC CCTGCAGTCT CAAGAGAGGC 300 GGGGCTGGGG AGATGCAGGC TGTTGAGCCC TCCTGTGGAA CAAGATTGCA GGAAAGGGAG 360 AGAGGAGAGG GGAGAACAGA AAAGCAGGCA GCAGACAGCA GGGAAAGGTC CTTGTCTAAG 420 GGACAGGAAG GGAAAGGGAC ATAAAGGTAC TAAAGAACGG CCGGGGGTAG AAGAGCCAGA 480 AGATAGGAAA TCATGGGCCC TGGGGTGGAG GAGCTTTCGA ACCAGAAAGG GGTGTCCCAG 540 GGAGGGGTGG GGCAACAGCT TTAAATGGCA GGAAGGGGTT GCCACCCTAA TACTTCTCAT 600 TATTGCTGGT GATTTTGACA TTCACACCCT CAGGGCTGCA GAATTTGGAT GTGTAGTCAT 660 TTGCACAGGG AGTTGGGAGA AGTTCCCTCC TCTCTCCCTC CCCCACCAGT AGCCTCGCCT 720 CACCCTGGTT TCACTTCCAG CCGCTCAGGC CGCAGCAGGC CAGGCTGCTG CTGTAGTTAG 780 GAAGAGCAGG CACAGGCTTG GGCCCAGGGG AAGAGGCCTG CGCTGTTCTA TCAGCAGGGC 840 AATTAATCCC ATCCTGAGCC TGGGCCAGGC CTTCCCTCTC TGGGGAGAGG CCGCCTCCGC 900 CCGGCGTGTG AAGTCCATGT GACCTGCTTT CCTCAGGCTG GAGCTTCCTA GAGTCATCGT 960 GAGTCAAGCT CCTCCTGACT TTCTCCTGCC TCTCCCAGTC ACAGGATGTG GAAATCGGAT 1020 TGGGGGAAAG AACGCATTAC TCAGATCCTC CGGGCCTTCT CCATCAATAA AAACTTGCTT 1080 TACACCTCCA ACTTGTCAAT CCCCTCTCCC TCTCCACCCC AGCTCACGGT TACTTCTCAG 1140 GCTTATGGCA CACGGGCCTC TCTAGGTGCC CACGGTGTGT GCCAGGCAGC CCTGTCGCCA 1200 TCGAGCTTAC TCAACATTGA GGCGTCTTTG TCCGAATTCA CCACAAGCAG GTGGAACCCC 1260 CGCGTGGGGG CTCAGGAGGG AGGCACTAGG GAGCCGCCAA GGAAAAGAAA CCTGCAAGAG 1320 CTGGGGCGTG AAGGGGCTGC CAGGAGCAGC TGGGGCACAC GGAGAGCGAG AGAGCCTCTC 1380 CCAGGCTCCA TGGGGAGGCT TCCAGGAGGG CAGCAGGGAC AGGTGTGGAT 1430
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