Tag | Content |
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EnhancerAtlas ID | HS044-13270 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr9:38025690-38027400 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL2 | MA0478.1 | chr9:38026433-38026444 | GGATGACTCAT | + | 6.62 | JUNB | MA0490.1 | chr9:38026433-38026444 | GGATGACTCAT | + | 6.62 |
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| Number of super-enhancer constituents: 39 | 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 | chr9:38025987-38028588 | Colon_Crypt_1 | SE_24298 | chr9:38025998-38028126 | Colon_Crypt_2 | SE_26555 | chr9:38022184-38028472 | Esophagus | SE_27864 | chr9:38023794-38027403 | Fetal_Intestine | SE_28791 | chr9:38025361-38027128 | Fetal_Intestine_Large | SE_31580 | chr9:38025043-38027247 | 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_40993 | chr9:38025034-38027717 | Left_Ventricle | SE_41666 | chr9:38025120-38026517 | LNCaP | SE_41666 | chr9:38026590-38027990 | LNCaP | SE_42283 | chr9:38021564-38028766 | Lung | SE_44329 | chr9:38025101-38027892 | NHDF-Ad | SE_44779 | chr9:38023356-38028059 | NHLF | SE_45758 | chr9:38023295-38028397 | Osteoblasts | SE_47196 | chr9:38021414-38029507 | Panc1 | SE_47459 | chr9:38025870-38027469 | Pancreas | SE_48861 | chr9:38023882-38027897 | Right_Atrium | SE_51847 | chr9:38025100-38027768 | Skeletal_Muscle_Myoblast | SE_55662 | chr9:38023553-38028534 | u87 | SE_57367 | chr9:38025123-38028638 | VACO_503 | SE_57926 | chr9:38026010-38026363 | VACO_9m | SE_57926 | chr9:38026673-38027099 | VACO_9m | SE_63571 | chr9:38025065-38027814 | HSMM | SE_64986 | chr9:38023280-38027960 | NHEK | SE_65279 | chr9:38024925-38028685 | Pancreatic_islets | SE_67542 | chr9:38023553-38028534 | u87 | SE_69063 | chr9:38025056-38027553 | H9 |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I038021 | chr9 | 38021749 | 38029286 |
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Enhancer Sequence | TTCGGAACAG GGTGGTGCAC AGCAAGTGCT CAGTGTCAGG TGTGATCACC ATCAGCTCAA 60 CACACCATCC AGCCTGCAGA GTCTGGGTCT TGCCCAGGGT CACCTGGACA TCAGAAATCC 120 AGACTATCCC CCTCCCCATG TTGATGAGGA GCCACCAGAG GCTCCAAGTA ACAAATGACA 180 CAGCAGAACA CTCCTGAGCG GGTGACAGAA CTAGACTCCC ATCAAATCCC AACCAGGAGA 240 GGACCTATGT CATCTGTTGA ACTACATATT TACAGAGTGC CTCCCAAACT GGTTTTAGAC 300 AGCTTAATTC GAGGCATTTT TCTGCTTCTG ATAGGCACAG CCTGTTGGTC CCCCACCCCC 360 TTCCCAAGGA AGGATCAGGA ATGCCCGTGA GGCTTTCTCA CGGTAACGTA AGGCTCTGTA 420 CAGTAAGAAT AACTTCCAGT GTGCTCACAG GAAAAGTATG TAAAAGCAAA ACAGCAGCGC 480 CTGTGAGCCA AAGGCCTTTC CTGTGCAATG TGGTACCTTT CAAAGCCAGG CCTCTGTGCC 540 CCAGCCAAGG CCCGGGAGTC ACCAAGTGCA CCCTCTCTCT CGTGTGTGCT TCCTGTGCTA 600 GAAGCCAAGG TTAAAGGGGA GAAAGAGCTC AGGCCTGGAG GAGCACGAGA TCGGGCCAGC 660 ACAGTGCCTT TTAATGATCA GCTGCAGAGG CGCGGGAACC CGCACTAAGT GAAGGATCAT 720 TTCTCCCCGA ACGGGACCCA TTAGGATGAC TCATGCACAT TTCCCACAGG GGAGCTAAAA 780 GGCTGGGCCA GGCCCCTTTA AGGCACAAGC AGCACTAAAC AGCTGCTCTC CCCAAGAGTC 840 ACTCTCTCTT TATTGAGGAT AGGCAGCATC AGCCACAATT ACCAGCCCCA TGTTTGAGGG 900 CTCCCAATTA CATTCCGCTT AACACCAGGT GCTCCATAAA TGCTGATTCA CTTTTTAAAA 960 TAATGCTGTA TCCTCCAGCA ACCAAGCCTT GATGAACTCT TTCTCCTGTG CCGTCATCTA 1020 GGCTGGGAAA CCCTGAACCT CACAGGCCTG TTTCTCACAT GTACTCGGCG CTTTCTAATG 1080 TACAGGAAAC TTAGGGTGGC TAGGGCTTTG CGATGTCAAG CAGGTCTGTG ATGGTGTTTA 1140 TCGCTGTTCA GTCCGATCAC CTCGTGCCTC CACGTGCCAG GCAATGGGCT CTGTGCTGGG 1200 GATACAGAGG AGAGGAAAGG CAGGCCTCCT CCCCCTGCTC TTGCATTGCT TCCAGGTCCC 1260 CAGGGGAGAT GGGCATTATT CAGTTCACCT CCCCAAGGCA GGCTGGCATG TGCCAGGCAG 1320 GGTGAGTAAA TGCCTGGGTG AAGGGCCCTT CCCACCCTGC CCTGAATTGC AGCTATGTGT 1380 AGGCCTGTCT GCTTCCGCTC CACCAGGAAG GCAGGTTCTG GAGCTCTGTT TCCTTTTTAT 1440 TACAATATAG CACCTGGTGC ACAGCAGGGT CCCAGCAAGG TGTGCTGGGC TGAAACCAGG 1500 GGCAGGGCAG GGCAGGGCCT CCAGGGTGGT GGATTCCGGG CCCTGAGCTC CAATGCTTCC 1560 AAATTTCTCA CCAGCTATGG AGCTCTACTT TCTCTAAGCC TGAGCCCTCC CACTTTCACT 1620 GGGAAAACAT CTTCCTTCTG CGGTGCAGGA GAAGCTGAGT CAATGAACCA AGGGATACAT 1680 AGTGCCTGTC ACATTATGCT GGCATAGGCA 1710
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