Tag | Content |
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EnhancerAtlas ID | HS091-09427 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr12:12889580-12890980 |
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) |
FOXF2 | MA0030.1 | chr12:12889639-12889653 | TTAACATAAACAAT | + | 6.03 | ZNF263 | MA0528.1 | chr12:12890533-12890554 | CCTCTCCTCCTCCCCTTCTCC | - | 6.17 |
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| Number of super-enhancer constituents: 45 | ID | Coordinate | Tissue/cell |
SE_02384 | chr12:12889367-12891080 | Astrocytes | SE_03015 | chr12:12889561-12890025 | Bladder | SE_04457 | chr12:12889399-12890487 | Brain_Anterior_Caudate | SE_05723 | chr12:12889250-12890996 | Brain_Cingulate_Gyrus | SE_06515 | chr12:12889295-12890622 | Brain_Hippocampus_Middle | SE_07055 | chr12:12889264-12890612 | Brain_Hippocampus_Middle_150 | SE_09887 | chr12:12889463-12890550 | CD14 | SE_10399 | chr12:12889466-12890156 | CD19_Primary | SE_11298 | chr12:12889288-12891024 | CD20 | SE_11994 | chr12:12889317-12890964 | CD3 | SE_13418 | chr12:12889451-12890667 | CD34_Primary_RO01536 | SE_14411 | chr12:12889291-12890783 | CD4_Memory_Primary_7pool | SE_15395 | chr12:12889422-12890889 | CD4_Memory_Primary_8pool | SE_16327 | chr12:12889289-12890803 | CD4_Naive_Primary_8pool | SE_16955 | chr12:12889358-12890444 | CD4p_CD225int_CD127p_Tmem | SE_17376 | chr12:12889323-12890851 | CD4p_CD25-_CD45RAp_Naive | SE_19332 | chr12:12889413-12891128 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20110 | chr12:12889323-12891107 | CD56 | SE_20780 | chr12:12889241-12890995 | CD8_Memory_7pool | SE_21484 | chr12:12889406-12890424 | CD8_Naive_7pool | SE_21956 | chr12:12889267-12891152 | CD8_Naive_8pool | SE_24059 | chr12:12889693-12890061 | Colon_Crypt_2 | SE_25539 | chr12:12889286-12890978 | DND41 | SE_25894 | chr12:12889266-12890640 | Duodenum_Smooth_Muscle | SE_26782 | chr12:12889510-12890129 | Esophagus | SE_27782 | chr12:12889424-12890846 | Fetal_Intestine | SE_31002 | chr12:12889358-12890247 | Fetal_Thymus | SE_31618 | chr12:12889585-12890095 | Gastric | SE_32681 | chr12:12889248-12890518 | GM12878 | SE_34820 | chr12:12889520-12891049 | HeLa | SE_42460 | chr12:12889585-12890140 | Lung | SE_44374 | chr12:12889461-12890977 | NHDF-Ad | SE_44929 | chr12:12889526-12890707 | NHLF | SE_45697 | chr12:12889295-12892730 | Osteoblasts | SE_47372 | chr12:12889267-12891175 | Panc1 | SE_50256 | chr12:12889478-12890056 | Sigmoid_Colon | SE_52464 | chr12:12889382-12890237 | Small_Intestine | SE_53337 | chr12:12889493-12890332 | Spleen | SE_55147 | chr12:12889567-12890034 | Thymus | SE_56035 | chr12:12889371-12890742 | u87 | SE_61268 | chr12:12866751-12890857 | HBL1 | SE_61621 | chr12:12866181-12890888 | Toledo | SE_62220 | chr12:12864939-12895381 | Tonsil | SE_66441 | chr12:12889534-12890218 | Jurkat | SE_67164 | chr12:12889427-12890439 | MM1S |
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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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| Number: 1 | ID | Chromosome | Start | End |
GH12I012733 | chr12 | 12886055 | 12890944 |
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Enhancer Sequence | CAATAGGACG TGGGAAAGAA AGTTCAAGCT TTCGCCTTGA TAGTTCTCCA TGATGCTGCT 60 TAACATAAAC AATCGAGTTT TCAAAAACCA AAACTCTTGA TTTCATTAAG TAAGGAGGGT 120 GTAATGTGTA GTGCTTGGGC CGTTAGAGGG GATGTGGTCA CAAGTGGTAT ATCTGAGGCT 180 TTTGAAGGAG TGCATTCAAG GAAGAGCCCT GCTTGGTGTC AGCTACTGAA CCAGAGATCC 240 GAAGAAGTGG ACCTCGCCAG CCTCCTGCTC CACCCCGCTA CCAGTCTTAG CTGGAGCTCC 300 CTTTTCTTTG TCATACTCAG CCAGTTGCTC ATTGCTGTTT TAGAGTCTGG CCCATGTTTT 360 GCTCTTTGGC TGTGCGATTG GCGTGAATCT TCTAAGCAAA TGAATAGCTT AGAGGTGAAT 420 ACTGAATCTT TTGCTTCAAG TAGCTCAGCA TTTTTGTCTT TCATTTTTAC TAAGTGACTA 480 GATTCAGTAT TCGAAGATGT TTTGGCCAAA TGATTCATTA TTTATTTGGC TTTAGAAAGA 540 GACTTCAAAA GGATAATAGA AATAAACAAC CCAGAGGTTT TTTTTTTAAA TTGAAGATTA 600 ATAAAAGAGA GACCTCTGCT GGCTACAGTG GGGTAACAAC CTAGAGTTGG CCACTGACTC 660 CACAGGAAGC TATAATGGCT GTGACCCACC CCATACGCTT TTACAGTTGT CAGCAAATTG 720 ATCACTATTT GTTCACTTCT TCAGCAATCA ACTCAAGTTC TTTTGGAGTT CATTGAAGTG 780 AGGTATAATT CCCAGTCCAA TCACCACTGT TTCTGTTTCA ATCTTTAGGA AAAGTATTAG 840 TCTTTTATAT TTCTCGAACA TAATAGCTTT ACATATGAGC CCCTGCCAAA CTGAGACCTG 900 AAATAATTCC TGCATCTTAC CTTCTCTGTT TCCTTTCCCC TTTTTTGCCT CCACCTCTCC 960 TCCTCCCCTT CTCCAGTAAA ACAAAATAAA ACAAATCTAC ACTCAAGAGA GAGTACTGAT 1020 AGAAAGTGAG AAGGAGGGAG CTGGGCGCTT ATCTTTGGCA TATCCTCAGC TGAGGATCCA 1080 AGCTGGGGGG CCCAGGGTTG GTGTTAACTA CCTGAGTAGA GCTGTAGTTC CTACTGATGT 1140 CTTCCGTGGG ATTTGTTCAA CCGTGGGAAT GTGGCTGCAC GATAGTGGAG CAAGATTCAG 1200 TGAATGCTTC AGAATATGGA GGGTCGTTAT CTAGGGGGAG GAAGGGGACT GAATGTTCTC 1260 TTGAGACCTT TTGTTGGCAA CAACAATAAT GAGTGCCTAC TATGTGCCAG GCCCTGGACT 1320 AAGTACCTTA AATACCTTAA TTCTGTTTCC TGCTTTTCTT CTCTCTTCAC AGTCTTAAGA 1380 ATGTCTTTCT ATGAGAAAAA 1400
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