Tag | Content |
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EnhancerAtlas ID | HS050-26902 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr16:85935440-85936620 |
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) |
HNF4G | MA0484.1 | chr16:85935762-85935777 | TGAACTTTGCCCTGT | - | 6.41 | Hnf4a | MA0114.3 | chr16:85935760-85935776 | AGTGAACTTTGCCCTG | - | 6.07 | REL | MA0101.1 | chr16:85935573-85935583 | GGGGATTTCC | + | 6.02 |
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| Number of super-enhancer constituents: 11 | ID | Coordinate | Tissue/cell |
SE_09646 | chr16:85931464-85953411 | CD14 | SE_10390 | chr16:85931996-85945829 | CD19_Primary | SE_11040 | chr16:85931423-85953891 | CD20 | SE_50844 | chr16:85931729-85939461 | Sigmoid_Colon | SE_58456 | chr16:85922137-85990238 | Ly1 | SE_59205 | chr16:85931527-85991956 | Ly3 | SE_60098 | chr16:85921948-85948021 | Ly4 | SE_60552 | chr16:85931020-85947991 | DHL6 | SE_61060 | chr16:85922118-86004487 | HBL1 | SE_61811 | chr16:85933046-85990530 | Toledo | SE_62266 | chr16:85921249-85999852 | Tonsil |
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Enhancer Sequence | CATATTTTGG GATGTTATGT CTTGTTACTG CTGATTGTTT CAAACTCGTT TGCCCAAAGA 60 GGTCACATTT TAATCAGAAG AACAAAAATG CTATTTTTTT TTTTTTTTGG GTGGGCGTCT 120 ATCCAGCTGT CTTGGGGATT TCCAGCACTG TTCTTGGAAA TGTTGGCTCT AAGTCGATAG 180 GTCATGCTAG TTCTCTCTCT CTTTCTCTGT GCTGTTGGGG AAGCTGTCTG CTTGGGTGAG 240 AGTGTTCTTC CAAAGGATGT CTTTGGGTGC CCTGGGATGG TTAGGTCCCT AGAGTGGGAC 300 ATGTTCTGGA AGAGGAGCCC AGTGAACTTT GCCCTGTTCG GTAGCTGCAG TTTATTTCCT 360 CACTCTTGTC CCTATCTTTC AGTTGGTCGT AGGAGTTGCC CAGGAAGGAA GTTTGGATAA 420 TAATAATGAC ATCTGGCATG TAAGGTCCAG GCCCTGTCTC AGTTGCTTTC CGTGTAGCAT 480 CTGAATTCTC TTACAACCAG TACAGGTAGT GTTTTGTTAG CTGCATCTGG GACTGGGTAG 540 CTGATGCCCT GAGTTTAAAT GCTGATCCAG CGTCTCCCAG CTGAGCGGTG GCGGGACTTG 600 AATGAGATCG CGGTTCTGTC TCATTCTCAA ACTGCTGCTC TTATCACTGT GAAGGAACAG 660 CTATTTAGAT GGGCTGGCCT GAGGGCCTCC TCTTTCCCAG ACGGCACGGA CGCAGTATTC 720 TATCAGGGAA TGTGGGGCCA GCTGGGCATC TGGTAGCCCA GTTGGTTCTT CGGATAATGG 780 GCTGCTCAGT GAAGGAACCT GGTGCTGTAA AAGTGATTCC CCCTCTCCTT CCAGTCTTGG 840 GCTAAAACTG GAGCTGTTCA CTGTGGTTGT ATCTGCCTGA AAGGAAAGGG CAGATGAAAG 900 CTGGAAGGAG CACAGCCAGC ACAGTGGGAG GGGCCTGCAG GGGGCTGCTG GTGGCTGCAG 960 GTTTCCCACG GAGCTTTCAG TTTGCACTCA GGGCTGTGAG GTCATGGAGG CCAGCATTGC 1020 CTTCTCATGG CAGGTGTCCC GGAGTCCCTG AATCTGTGGG TTTCCCCCAA GCCAGCACCT 1080 TTGCTGCAAA CCTCTGAGTT TCCTGTTAGC AGTTTTTGGG TTGCTGTGAT GAATGAGACA 1140 ATATCCGTAA TATCACAGCG TGTATTTCTG TCTTTCCAAG 1180
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