Tag | Content |
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EnhancerAtlas ID | HS061-04846 |
Organism | Homo sapiens |
Tissue/cell | GM12892 |
Coordinate | chr11:116704010-116705030 |
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) |
RFX1 | MA0509.2 | chr11:116704406-116704422 | TGTTGTCATGATTACA | + | 6.14 | RFX1 | MA0509.2 | chr11:116704406-116704422 | TGTTGTCATGATTACA | - | 6.14 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_28896 | chr11:116695808-116712530 | Fetal_Intestine_Large | SE_35354 | chr11:116702196-116705541 | HepG2 |
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Enhancer Sequence | ACAGGACAAT AAGTTTGCTG ATACTTTGAT AAACTGTTAG GTGCTGCACA ACATGACTTG 60 AGTGTGTGCC CCATGCCAGC CACTATGCCT GGCACTTAAG TTGTCATCAG AGTTGAGACT 120 GTGTGTGTTT ACTCAAAACT GTGGAGCTGA CCTCCCCTAT CCAGGCCCCC TAGCCCTCTT 180 AGGCGCACGT GAAGGGAGGA GGCCGGATGG GCTAGAGGTT GGAGTAAGAT GCAACGAGGC 240 ACTATTCTTG GCTCCACCAC TTGATATCAG CCTCAGTTTC TTACATGTAA AGTGGATACA 300 ACCGTACCCC CTCCACCGTA GGTTTGCCGT GAGATTGAAA TGAGAGAGCG TTCGAACCGT 360 TTGGCACAGC ACCTGCACGT AAAGATGCTT GATCAATGTT GTCATGATTA CAGTTGAGCT 420 GACTGGGCCC TTGGGACCCG GACTGGAGTG GTGGGGGGCA GTGTCCTGGG ACCAAAAAGA 480 AGCACAAGGT CTCCCAATAG AGGCTGCTTC CTTTGTGTCC CCACCACCCG AAAGATGTCA 540 GGTCAGAGAG CCCGAGAGCT GCAGATGGCT TGAGTAGGGC TCCACTCTTC AGATCAAAAA 600 ACTGTGGCCC GGAGAGGCGA AGGCACTTGG CCAGCATCAC AGAGCCAGCA CGTGGCAGGG 660 CCAGACCTTG AGCCCAGGTC AGCTGCGTGT ATTCTGCTCA GTTGGTGCAG AAAACAGTTT 720 TGTCACTCCT ATGTCAGGTG TTAGGGACTC CTTTACAGAT CTCAGTGGCA TCAGTACATC 780 CAGCCCCACC TGGAGACTGC TTTCTCTCTG AAAATTCCCC AGGGCTTCTC TCTGGGCTGA 840 GAGATCTCAG CACCCGTATC TAGAAAATGT TCCCACCCAG ACCTGGCTGG ATGACTGCTG 900 TTGTAGCTCT GGAAGGTTAG GAACTAAAAA GCCCACTCCT TTACCTAGGG TAGCTAAGAT 960 ACACTGGAGA TGGGGACATG GGGATGGGGC CGATTATCCA GGGGCCTGCA TGAGGGGGCA 1020
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