Tag | Content |
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EnhancerAtlas ID | HS195-00048 |
Organism | Homo sapiens |
Tissue/cell | VCaP |
Coordinate | chr1:8241860-8243290 |
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) |
FOXP2 | MA0593.1 | chr1:8242600-8242611 | TTTGTTTACTT | - | 6.62 | IRF2 | MA0051.1 | chr1:8242750-8242768 | AGAAAGCGAAAGCATTCA | + | 6.14 |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_33918 | chr1:8241396-8243905 | HCC1954 | SE_34231 | chr1:8240249-8246041 | HCT-116 | SE_34786 | chr1:8240946-8245641 | HeLa | SE_47106 | chr1:8240454-8246507 | Panc1 | SE_57530 | chr1:8241904-8242444 | VACO_503 | SE_65889 | chr1:8242598-8243711 | Pancreatic_islets |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I008180 | chr1 | 8240803 | 8245776 |
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Enhancer Sequence | CGTAAGTTTC CAACATCTCA CTGTAGGGGA TACTGGAAAG TATGAGCGTC AAGATCATGT 60 ATCTTTTCCA GGAATCAAAG CACGTAGTGT GGCAATTCAG ATATGTTGGT TGCCTTGACT 120 CTTCTTCAAC AGAATTAACA GTTTTGGATC TTGAGAAAAT GTTATTTTCT GGCTAAGTAT 180 AGGGGTAAAA TGAAATCTTT GGGAAATTAG TGAATTCTCA TGATTTCTCA AAGCTTTTCT 240 TGGGTAACTC CAAGAGGCAG CCTGGTGGAG TGAAAGCATG GACTCCAGTG CCCCATTCTC 300 TAGCTGCGTG ATTTGGAGTA AATTCCTTAT CTCAGTGACT CTGTGTCTCC ATCTTGAAAT 360 TGAGAATAAT CACACCGGCC TGAGATTTTT TTACCATGTG AATGGAAGCA CGTGGCACAT 420 AGCAGGGACT GAATGAATGT GCCCATGTCC GCTCTCCCTC CTCTTTCTAG GGCTGCGGCC 480 TTGGTGATGT CAAGAACATT TTGTAAATAT TACAAGTAAG ATAAGGCATT GTGACTATTA 540 CTCGTTAAAA TCACTTTGTT TCCTGACTTA GGTGATTCAC TGCAACCCAG AGAAAGTTTT 600 GTGTTGTGTT CTGGCTGGCG AAACTTCTGC AAACAACGAA TGCTTCTTTT CATCAGCCTA 660 TTCTGCGTTG GTTGGTAGGA TGTCAGTCTA TAACCACATC AATTTCAGGT AATAACAAGT 720 GTGTGAGCTT TCTGAAGCTT TTTGTTTACT TATTTGTTTT AGGGTTGTTC AAGTGTGACT 780 CATGTAGTAG CACTGCATTC TTGAGAATTC ACAGAGATCG AAACACAGAT ATGAAACAGG 840 GCCAGAAAGA ATAAGGCGTT CCCAATATAT GAGAGTAAAA AAAAAGCACA AGAAAGCGAA 900 AGCATTCAAT GTCTGCATCC TGTATAGATG AGAAACTTAG CAGTATCCTC TTTTCTTTTT 960 GGACCAATCA TATGCTGATA AAACAGGGTC TCGCTGCTTT CCCCCCATTT TTAACATCTT 1020 CAAACATTCT GAGAGCCTAC GGGAATAGAG GCAAACAGGT TTGATGTGAC TGGTCATTTG 1080 GCCAAAGGTA TTTTACTCTG CGCTCAGCAT TTTGTTTCGT TCATGCTCTC TAGCAGTTTG 1140 GAATCTAAAA AGGAAAGATT AGATAGAGGA AGTGTGAAAA TGCATACGCA ATGTGGGAAA 1200 CCAGGCCATG AACTTGAGTT TTTAAATGCA TGGTATAAGG CCGGGCTCAG TGGCTCACGC 1260 CTGTAATCCC AGTACTTTGG GAGGCCGAGG TGGGCGGATC ACCTGAGGTC AGGAGTTCGA 1320 GACCAGCCTG TCCAACATGG TGAAACCCCG TCTCTACTAA AAATACAAAA ATTAGCCGGG 1380 CATGGTGGCA GGCGCCTGTA ATCCCAGCTA CTCGTGAGGC TGAGACAGGA 1430
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