Tag | Content |
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EnhancerAtlas ID | HS091-10120 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr12:57496700-57498240 |
Target genes | Number: 23 | Name | Ensembl ID |
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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) |
Nr2f6(var.2) | MA0728.1 | chr12:57497568-57497583 | TGAACTCCTGACCTT | - | 6.04 |
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| Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
SE_11234 | chr12:57495427-57497240 | CD20 | SE_14806 | chr12:57495469-57496934 | CD4_Memory_Primary_7pool | SE_14806 | chr12:57497460-57498149 | CD4_Memory_Primary_7pool | SE_17491 | chr12:57495513-57496963 | CD4p_CD25-_CD45RAp_Naive | SE_20397 | chr12:57495596-57497070 | CD56 | SE_22446 | chr12:57495650-57496971 | CD8_primiary | SE_28460 | chr12:57495537-57496941 | Fetal_Intestine | SE_28876 | chr12:57495521-57496948 | Fetal_Intestine_Large | SE_34392 | chr12:57495658-57496871 | HCT-116 | SE_50276 | chr12:57495574-57496938 | Sigmoid_Colon |
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| Number: 2 | ID | Chromosome | Start | End |
GH12I057101 | chr12 | 57495228 | 57497013 | GH12I057103 | chr12 | 57497461 | 57498149 |
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Enhancer Sequence | GGGCCTGAAG AGGGTGAGGA CAGGGGTTTC TTTTCTTTCT TTCTTTCCTT TTTTTTTTTT 60 TTTTTTTTTT TTTTTTTTTT TTTTTTTTTT TTTTTTTAGA TAGTATCTCA CTCTGTTGCC 120 CAGGCTGGAG TGCAGTAGTG CAATCTCAGC TCACTGCAGC CTCAGCCTTC AGGGCTCAAG 180 TGATCCTTCC ACCTCAGCCT CCTGAATAGC TGGAACTACA GAAATGTACC ACCTAATCCA 240 GCTAATTATT TATTTATTTA TTTTTGAGAC AGAGTCTCGC TCTGTCACTC AGGCTGGAGT 300 GCAGTGGCGC GATCTTGGCT CACTGCAAGC TCTCCCTCCC AGGTTCACGC CATTCTCCTG 360 CTTCAGCCTC CCGAGTAGCT GGGACTCAGG CGCCCGCCAC CATGCCTGGC TAATTTTTTG 420 TATTTTTAGT AGATACGAGG TTTCACCGTG TTAGCCAGGA TGGTCTCGAT TTCCTGACCT 480 CATGATCCGC CCGCCTTGGC CTCCCAAAGT GCTGGGATTA CAGGCGTGAG CCACCATGCC 540 CGGCCAATTT TTTATTTTTT GTAGAGATTG GATCTCCCTA TGTAGCCCAG GCTGGTCTTA 600 AACTTGCAGG CTCAAGCGAT CCTCCTACCT TGGCCTCCCA AAGTGCTGAG TTGTTTTGTT 660 TTGTTTTTGA GACATAGTCT TGCTCTGTCG CCCAGGCTGA AGGGCAGTGG CGCAATCTTG 720 GCTCACTGCA ACCTCCGCCT CCTGGGTTCA AGCGATTCTC CTGCTTAGCC TCCCGAGCAG 780 CTGGGACTAC AGGCCTGCAC CACCACGCCC AGCTAATTTT TGTATTTTTA GTGGAGACGG 840 GGTTTCACCA TATTGGCCAG GCTGGTCTTG AACTCCTGAC CTTGTGATCT ACCCACCTCG 900 GCCTCCCAAA GTGCTGGGAT TACAGGCTTG AGCCACCATG CCCAGCCGGA CAGGGGTTTC 960 TTAGTGAAGC AAGAAGTTTC CTCAGGGGAC TGGCTCTGAG CACTCAGAGA AGTTATTGGA 1020 CTCACACATC ATAATCAAAA AGCTCATGCC ATGTTATTAA ATGCGTTCTG AAGCTCAATC 1080 AGGGCCTCAC CGTAGAGAAG TGGTTATTAG TCATCGCTAT GGAACCAGAC CTCCAGGTTT 1140 CAAATACCAG CTCCAACACT TAGCTGTGTG ACTGGGACAA ACTACTTAAA CTCTCTGTCT 1200 CAATGTCCTT ATCTATAAAA TGAGGCTGAT AATACTGCCT ACCTCATAAT GTTATTGTGA 1260 AAACCAGACG TGTGTGTGCT GGCACGCATG TGCGTATGTA TCATTTAATA GAGTGCCCTG 1320 GTCTATAGGA AGTGCTTCCG AAGTGTTTGC TGCTATCCAC TACCATTCCC TGCCCTGTGC 1380 ACTCCATGCT CTTGCTCACC CCCACTCACC CGGGCCCCAG TGTGCATGAA TCCCAGACAC 1440 ATGGGGTATG GGGCAGTCAC AAGAGGTGAG GGTCCAGGGC CCTTGTGTGT GGCATTGGAG 1500 GAGGACTCGG GGTCCCAGAT TGGGGCAGGG CTGGGCCACG 1540
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