Tag | Content |
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EnhancerAtlas ID | HS118-00230 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr1:21573860-21575160 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESR2 | MA0258.2 | chr1:21573868-21573883 | AGGACAGTGTGACCC | - | 6.59 | Nr2f6(var.2) | MA0728.1 | chr1:21574885-21574900 | TGAACTCCTGACCTC | - | 6.22 | Nr5a2 | MA0505.1 | chr1:21574877-21574892 | GCTGGCCTTGAACTC | - | 8.25 | RARA | MA0729.1 | chr1:21574882-21574900 | CCTTGAACTCCTGACCTC | - | 6.73 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_29228 | chr1:21573489-21574963 | Fetal_Intestine_Large | SE_47523 | chr1:21573390-21574080 | Pancreas | SE_47523 | chr1:21574909-21575207 | Pancreas | SE_65263 | chr1:21573259-21574086 | Pancreatic_islets | SE_65263 | chr1:21574794-21575555 | Pancreatic_islets |
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| Number: 2 | ID | Chromosome | Start | End |
GH01I021246 | chr1 | 21573260 | 21574086 | GH01I021247 | chr1 | 21574196 | 21575150 |
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Enhancer Sequence | AAGGGAAAAG GACAGTGTGA CCCTGTGGGG CTGCTCCTCC TCACAGCCCA GGGCTCTAGG 60 ACGGGCTTCT ACAGGAAGCA AAGGAAAGAG CTTGGGCTTG GCGCCATCTG ACAGCGCACC 120 GGGCAGAGAG TCAAGCGGAG CCTGGCGGGC TTTTGTCAGA GATGCTGTAG GTAGAATTCT 180 AAGGAGTCCA ACACCAAAAT TTAACCTGAA ATGGAATGAG GATGCAATGA GAAGATGCAG 240 CAGCTGCCGC TACCATTCAG CAAGCGTCTC CTGTGTGCCA GGAGCCGTGG CAAATGATTG 300 ATGCATATGA TTCCACCTGG TCCTCACGCG AGTCCAAGCA GTAGGTACTA TTATCCCTGC 360 TTCATGGATG AGGAGACTGA GCTTTAGACA GGCCTGAAAC AGTTGAGCTT GTAGACTCTG 420 CAGCCAAACT GCCTGGGCTC ATCTTCTAGC TCTCTTCCTT GCTAGCTGTG TAACCCTGGG 480 TAAGTTAATG CATCCTTCTG GGCCTCAGTA TCTTGTCTGA GAAGTGGGGA TCACCATAAT 540 AACAGAACCC ACTTCACTGG GTTATTTGTG AGGACTGAAC AAGCTTATGC TGTTTGTTCT 600 ATTCAACATG GGATTCTGTA AGTAACATCA GTGAACTTCT ACATGATTGG TAAATTCAGG 660 AAGACAGCAG CATAACTTCT GAGCTGCATT GGTCCGAAGG TGATATTTCT CAGGCATGGG 720 ATCGGGAAGG GTTGAACATT AACTTTCAGC AAGAAAGGAA AAGCCCTCAG CTCAGCTAAT 780 GCACACAGCA GGCTGGTCAG CTCTACTTTT TTTTTTTTTT TGAGACGGAG TCTCACTCTC 840 TTGTCCAGGC TGGAGTGCAG TGGTGCCATC TTGGCTCACT GTAACCTCTG CCTCCAGGGT 900 TCAAGTGATT CTCCTGTTTC AGCTTCCCGA GTAGCTGGGA TTACAACAGG CACCCACCAC 960 CATGCCCACT TAATTTTCGT ATTTTTAGTA GAGATGGGGT TTTGCCATCT TGGCCAGGCT 1020 GGCCTTGAAC TCCTGACCTC AAGTGACCCG CCTGCCTCAG CCTCCCAAAG TGCTGGGATT 1080 ATAGGCATGA GCTACCGCAC CCAGCCTGGT CTGCTCTATT TTAAGATGAC TGAAAATGAG 1140 CGCTCGCGCC TGGGGCTTCC TCTCCTCACA GAGGCGCCTT CCAGACCTGT AACTCTCAGC 1200 CTCCAGCAGG TTGCACTTTC TCTGTGACCC TAAAGGCGCT TGTTCAGAGC TCTCTTTTTC 1260 TTTTCTTTTT TTTTTGAGAT GGAATCTTGC TCTCATGTCT 1300
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