Tag | Content |
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EnhancerAtlas ID | HS044-07769 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr2:219154230-219155360 |
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 | chr2:219154372-219154387 | AAAGATCAAAGTCCA | + | 6.98 | Hnf4a | MA0114.3 | chr2:219154373-219154389 | AAGATCAAAGTCCACT | + | 6.7 | IRF1 | MA0050.2 | chr2:219154360-219154381 | AAAAAAAAACTGAAAGATCAA | - | 6.34 | KLF4 | MA0039.3 | chr2:219154552-219154563 | CCACACCCTCC | + | 6.32 |
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| Number of super-enhancer constituents: 37 | ID | Coordinate | Tissue/cell |
SE_00326 | chr2:219145665-219158265 | Adipose_Nuclei | SE_03432 | chr2:219154454-219157349 | Brain_Angular_Gyrus | SE_06270 | chr2:219145735-219164206 | Brain_Hippocampus_Middle | SE_08985 | chr2:219155134-219155389 | Brain_Mid_Frontal_Lobe | SE_10092 | chr2:219146718-219159598 | CD14 | SE_11206 | chr2:219145902-219159097 | CD20 | SE_12180 | chr2:219148529-219157314 | CD3 | SE_12831 | chr2:219154485-219154601 | CD34_fetal | SE_12831 | chr2:219155247-219155405 | CD34_fetal | SE_14014 | chr2:219148910-219157816 | CD34_Primary_RO01536 | SE_15197 | chr2:219146865-219158111 | CD4_Memory_Primary_7pool | SE_16725 | chr2:219154813-219157847 | CD4_Naive_Primary_8pool | SE_17020 | chr2:219153033-219157989 | CD4p_CD225int_CD127p_Tmem | SE_17694 | chr2:219145927-219158488 | CD4p_CD25-_CD45RAp_Naive | SE_17933 | chr2:219145740-219158304 | CD4p_CD25-_CD45ROp_Memory | SE_18906 | chr2:219145938-219158335 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19423 | chr2:219148822-219157978 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20197 | chr2:219154274-219158091 | CD56 | SE_21204 | chr2:219148412-219158157 | CD8_Memory_7pool | SE_22529 | chr2:219146601-219158435 | CD8_primiary | SE_26022 | chr2:219146503-219160474 | Duodenum_Smooth_Muscle | SE_27110 | chr2:219153196-219162475 | Esophagus | SE_27658 | chr2:219148708-219161413 | Fetal_Intestine | SE_28578 | chr2:219146925-219161400 | Fetal_Intestine_Large | SE_30125 | chr2:219154218-219158006 | Fetal_Muscle | SE_32283 | chr2:219154277-219157757 | Gastric | SE_35648 | chr2:219153304-219159543 | HepG2 | SE_36018 | chr2:219146032-219158345 | HMEC | SE_45286 | chr2:219154286-219157309 | NHLF | SE_47526 | chr2:219154386-219157655 | Pancreas | SE_50394 | chr2:219149842-219160653 | Sigmoid_Colon | SE_51585 | chr2:219145632-219158203 | Skeletal_Muscle | SE_52542 | chr2:219149722-219160735 | Small_Intestine | SE_57570 | chr2:219154375-219154848 | VACO_503 | SE_57570 | chr2:219154969-219157318 | VACO_503 | SE_58066 | chr2:219154372-219154887 | VACO_9m | SE_64537 | chr2:219153043-219158397 | NHEK |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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Enhancer Sequence | GGCACATGCC TATAATCCCA GCTTCTCGGG AGGCTGAGGC AGGAGAATCA CTTGAACCCA 60 GGAGATGTAG GTTGCAGTGA GCCGAGACCA TGCCACTGCA CTCCAGCCTG GGCGACAGAA 120 AAAAAAAAAA AAAAAAAAAC TGAAAGATCA AAGTCCACTC TGCCAGTTTC TGATTCTGAA 180 TGAACAGCCT AACAGGAGGC TTCAGGGCAG AATGGCATGG CTCCCCAAGA ACCTACACCA 240 GGGGGTCACT ACTGATGTGC AACTGTTTCC AAGGACATCT TCAGAGGCAG AAGTACATGG 300 CATGTTCTCA GTATGGGGCT GTCCACACCC TCCCAAACTG TCCCCATAAT GCTGTCTGGA 360 CCCTACGGCC AGCTCTTCCT GGGTGATCAG TTACGCCCGA GCTAAACAGT ATATAACACT 420 CTAGGAAAGA AAGAGTAGGA GGCAGGAAGT CCACTGACCT GGGTTCATGA ACTAGCTGCA 480 GGAATCCAGG CAAATGACCT CCCCTGGCCT CCTTTTATCC CTAAATCAGC CCACGTGGGG 540 GAAAGGAGTA GGGACTTGTT TATGGGAGCC ACAGTGGAGA AACAGAATCA CCTAGCCAGG 600 CATTTCCCAG ACTGTTCTAA AGAACACGCC CCAGGAGACG TTAATGAATG AGTGCTGGAA 660 ACAGATGACT CTTGAGAAAC AATCCACACC CCCTTCTTGG AAATTCACAA TGGCATATTC 720 TGCCCCTGAG AAGTCCTGCA GTAAGCAACC CTGTTCAGCT TTGTTTAACC CAGTGTTCCT 780 TCAAACTCCC TTAAGCCTGA GCCACTTTTA TCGAGGCAAA CCTATTAACA CCCTGTGGGA 840 TGCTGACCCA GGCCACCTTT GTATTACAGA CACCCAACCC TGAGAATCAT TCATATCCTA 900 ACTCCTCGTC TCTTATAACC TCTGTGCGTA CACCCAGCTG CCCCTCAGAG CAGTCACATG 960 AAGTACTAGA CATGCCCTCT CACTCTCAGG GGGTCAGCCC AGTGCCAGGA TCTCTGGCGA 1020 GGGTCCTCCC CTTCCCCCAT TCCACACAGC TGCTATCCCA CCGTGGGATT TACTGCCAAG 1080 GGCCGGGGGA CATATCCAGC TACCACAGAA CCAGGAAACG GGCACCCCTA 1130
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