Tag | Content |
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EnhancerAtlas ID | HS196-31350 |
Organism | Homo sapiens |
Tissue/cell | ZR75-1 |
Coordinate | chr9:38022910-38024680 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXC1 | MA0032.2 | chr9:38023152-38023163 | TATGTAAATAT | + | 6.62 | NKX2-5 | MA0063.2 | chr9:38024655-38024665 | CTCAAGTGGT | - | 6.02 | ZNF263 | MA0528.1 | chr9:38023656-38023677 | TTTTCCCCCCTTTCCTGCTTT | - | 6.14 |
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| Number of super-enhancer constituents: 41 | ID | Coordinate | Tissue/cell |
SE_00446 | chr9:38023728-38028204 | Adipose_Nuclei | SE_01843 | chr9:38023547-38028728 | Aorta | SE_02310 | chr9:38023662-38027951 | Astrocytes | SE_03893 | chr9:38021633-38029096 | Brain_Anterior_Caudate | SE_04803 | chr9:38021731-38029328 | Brain_Cingulate_Gyrus | SE_05785 | chr9:38021183-38028964 | Brain_Hippocampus_Middle | SE_06784 | chr9:38021571-38027567 | Brain_Hippocampus_Middle_150 | SE_07767 | chr9:38021510-38029133 | Brain_Inferior_Temporal_Lobe | SE_23246 | chr9:38022664-38023963 | Colon_Crypt_1 | SE_26555 | chr9:38022184-38028472 | Esophagus | SE_27864 | chr9:38023794-38027403 | Fetal_Intestine | SE_28791 | chr9:38023108-38024990 | Fetal_Intestine_Large | SE_31580 | chr9:38022209-38024845 | Gastric | SE_33929 | chr9:38022707-38028095 | HCC1954 | SE_34811 | chr9:38023130-38028698 | HeLa | SE_36884 | chr9:38023288-38028023 | HMEC | SE_38030 | chr9:38023941-38028420 | HUVEC | SE_38998 | chr9:38022657-38029283 | IMR90 | SE_41666 | chr9:38022126-38024768 | LNCaP | SE_42283 | chr9:38021564-38028766 | Lung | SE_44329 | chr9:38023994-38024970 | NHDF-Ad | SE_44779 | chr9:38023356-38028059 | NHLF | SE_45758 | chr9:38023295-38028397 | Osteoblasts | SE_47196 | chr9:38021414-38029507 | Panc1 | SE_47459 | chr9:38022519-38023618 | Pancreas | SE_47459 | chr9:38023627-38023902 | Pancreas | SE_47459 | chr9:38024022-38024499 | Pancreas | SE_47459 | chr9:38024502-38024749 | Pancreas | SE_48861 | chr9:38023882-38027897 | Right_Atrium | SE_51847 | chr9:38023705-38024936 | Skeletal_Muscle_Myoblast | SE_55662 | chr9:38023553-38028534 | u87 | SE_57367 | chr9:38023283-38024836 | VACO_503 | SE_57926 | chr9:38023678-38023917 | VACO_9m | SE_57926 | chr9:38024256-38024472 | VACO_9m | SE_57926 | chr9:38024480-38024699 | VACO_9m | SE_63571 | chr9:38023691-38024985 | HSMM | SE_64986 | chr9:38023280-38027960 | NHEK | SE_65279 | chr9:38021466-38023716 | Pancreatic_islets | SE_65279 | chr9:38023979-38024746 | Pancreatic_islets | SE_67542 | chr9:38023553-38028534 | u87 | SE_69063 | chr9:38022163-38023946 | H9 |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I038021 | chr9 | 38021749 | 38029286 |
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Enhancer Sequence | GGGCTTCTGC TTTGGGGGGA AGGTCAGCTG GCTGGATGCC ACACTCAGTA TCTTTCTAGT 60 GCACATACAG TGCAAAGCCC AGACTCAACT TGGACGTAGA GGTCTGAGCT GCCCCAAGCA 120 GAGCCCTGGC TTTAAGGACT GGCTAAGTGG GTTGCAGAAC CCCTGCCATG GCGGAGGCAG 180 GCAGCATTTC CAAAGTCCCA AGGCTGACCG GTGGCAGCTG GGCTGCAGCA GCTGCCCGAG 240 GCTATGTAAA TATACAGAAA GGCAGCTGGC AGTGCAGAAA GGATGCCGCC AGGCAGGGAC 300 AGTCCAGGCA AGTGGAGCTC TGGAACTGGT TCTGCTACAC CCTTGCTGGG TAACTCCGTG 360 CAACCTGTTT TCTCTGAGTT TCGGCAGGTC ACCTGTGAAG TGGAGCAGGG TGGTTTGCCT 420 TCTCAGCTTC ACATAAACGT TGTAAGGAGC AAATAATCAG ATGATCCAAG GATGTGTCAG 480 TAATTTATAA AGAAAAGGCC GTGTCCTTGT TACAGAGCAG ATGGCACCTC CAGGATGAAG 540 GTAAGTGCGG TGAGGGGCAA AAGCACTTTC AGGCAGGGTC TCTGCCCACG AGAAGATGAA 600 AATCTGGTAG GGAAGACAGG ACAAAGACGT GAAAAGAAAC CCCCGCCAAG GCCCCGGTGA 660 TTACCAGGGA AAATGGGTAC AATTATGCAT GACAACAGCT GTCCTATTTC TCAAACACAA 720 AAAGGAAAAT GTTTGTGAAT GCCCTTTTTT CCCCCCTTTC CTGCTTTGGG TAAGATTCAT 780 GCCCTAGTTG GGGCACCTGG CAAAGTGGTG GAGAACCTCT CATAACTCTC GAGGCACTTC 840 CGCCTGTGTG CTGGGAGACA GAAGTGTGAC TTGCCTATGG CCAGCATCCA GGGCCCTGAG 900 GGGTCCACAG CACCAGGCTG TTACACCACT CAGGGATATG GGACACCCAT GCAGGTACAC 960 ACACAAGCGC CCCCTACTCG CCTCTTCCTG TCCTCAGCTT TGACTATCAT CATAGACCAA 1020 CTCTCCTTAT AGGCACGCCA ATAAATCACT GCTGACATGG TAAGGAAATT AATTTAGGGA 1080 AGATTAATTA GCTACATTCA TGCACTCAGC TGCAACTGCT GGAAATCAGA CGGTGGGGAG 1140 GTTGGTTTTC CACTCCATTT AGGATTGGTT TGCTTTCTAC CTTCTAAGAT CTGGCTTGCC 1200 TCAAAGTTCA AAGCCCCCTC TTGCATCATG AAGGCCCCTG CCAAGTACTC CGCCCACATG 1260 CCTTCAGGGG CAGGGAGCTC ATGATGTGGC AACACAGTCC TCTGGGACGG CCATCACCAC 1320 TAAAGTGTCT TCCCTACACT GAGCTGAAAT CTGTCTCCCA GCAGCCACTA TCCGTTTTTC 1380 TACTGACCTA AGGTGTTCTG TCCTAAATGC TCCTTTACAG ACCTGACAGT GACCTGCCCC 1440 ACATGTCAGG AGGCTGGGAG TGTGGGGGGT TAAAGTGGTC ACCACTGGTC TTTCCAGTCC 1500 TGCCCCTCCC ACGGCCACAG CTGCTTGCCT AGACACCTGC AGGCTCCGAC TTGTTAGGAA 1560 AAACACATTC CAAATTCCAG CCTCTGTCAG CTCCTCTCAA GCCTGCTTGC TCAGCCTCTC 1620 TCTCTCCGTC ACACACACAC ACAGCCCACT GTCTTCCAGC TTCACCCCCT CAGAGTGAGC 1680 TGTGGGTCCT GGGTAGGAGG CTGCTGGGAA CAGAGCCTGG CTCCACCCTC TGTTTACCCC 1740 AGAACCTCAA GTGGTAGAGA CAGGCTTTTC 1770
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