Tag | Content |
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EnhancerAtlas ID | HS098-12422 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr12:12889510-12891780 |
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) |
FOXC1 | MA0032.2 | chr12:12891449-12891460 | ATATTTACATA | - | 6.62 | 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 | AATAAATTTT ATTGTTTCCT CACTTTATCT AATATTAATT GAAATCCTTA GTCTTATGTT 60 GGGGTTATCC CAATAGGACG TGGGAAAGAA AGTTCAAGCT TTCGCCTTGA TAGTTCTCCA 120 TGATGCTGCT TAACATAAAC AATCGAGTTT TCAAAAACCA AAACTCTTGA TTTCATTAAG 180 TAAGGAGGGT GTAATGTGTA GTGCTTGGGC CGTTAGAGGG GATGTGGTCA CAAGTGGTAT 240 ATCTGAGGCT TTTGAAGGAG TGCATTCAAG GAAGAGCCCT GCTTGGTGTC AGCTACTGAA 300 CCAGAGATCC GAAGAAGTGG ACCTCGCCAG CCTCCTGCTC CACCCCGCTA CCAGTCTTAG 360 CTGGAGCTCC CTTTTCTTTG TCATACTCAG CCAGTTGCTC ATTGCTGTTT TAGAGTCTGG 420 CCCATGTTTT GCTCTTTGGC TGTGCGATTG GCGTGAATCT TCTAAGCAAA TGAATAGCTT 480 AGAGGTGAAT ACTGAATCTT TTGCTTCAAG TAGCTCAGCA TTTTTGTCTT TCATTTTTAC 540 TAAGTGACTA GATTCAGTAT TCGAAGATGT TTTGGCCAAA TGATTCATTA TTTATTTGGC 600 TTTAGAAAGA GACTTCAAAA GGATAATAGA AATAAACAAC CCAGAGGTTT TTTTTTTAAA 660 TTGAAGATTA ATAAAAGAGA GACCTCTGCT GGCTACAGTG GGGTAACAAC CTAGAGTTGG 720 CCACTGACTC CACAGGAAGC TATAATGGCT GTGACCCACC CCATACGCTT TTACAGTTGT 780 CAGCAAATTG ATCACTATTT GTTCACTTCT TCAGCAATCA ACTCAAGTTC TTTTGGAGTT 840 CATTGAAGTG AGGTATAATT CCCAGTCCAA TCACCACTGT TTCTGTTTCA ATCTTTAGGA 900 AAAGTATTAG TCTTTTATAT TTCTCGAACA TAATAGCTTT ACATATGAGC CCCTGCCAAA 960 CTGAGACCTG AAATAATTCC TGCATCTTAC CTTCTCTGTT TCCTTTCCCC TTTTTTGCCT 1020 CCACCTCTCC TCCTCCCCTT CTCCAGTAAA ACAAAATAAA ACAAATCTAC ACTCAAGAGA 1080 GAGTACTGAT AGAAAGTGAG AAGGAGGGAG CTGGGCGCTT ATCTTTGGCA TATCCTCAGC 1140 TGAGGATCCA AGCTGGGGGG CCCAGGGTTG GTGTTAACTA CCTGAGTAGA GCTGTAGTTC 1200 CTACTGATGT CTTCCGTGGG ATTTGTTCAA CCGTGGGAAT GTGGCTGCAC GATAGTGGAG 1260 CAAGATTCAG TGAATGCTTC AGAATATGGA GGGTCGTTAT CTAGGGGGAG GAAGGGGACT 1320 GAATGTTCTC TTGAGACCTT TTGTTGGCAA CAACAATAAT GAGTGCCTAC TATGTGCCAG 1380 GCCCTGGACT AAGTACCTTA AATACCTTAA TTCTGTTTCC TGCTTTTCTT CTCTCTTCAC 1440 AGTCTTAAGA ATGTCTTTCT ATGAGAAAAA CATTGAATAT ATGTAAAGAA CTTACAACAA 1500 GGCCTGCATA AAGTAGTAGC TATGCATGTG TTCACTATTT TATTATTATG TTTTTACTCT 1560 GGAATATGCT GCCACTCCTA CACATGAGGA GAGGCTCTCC CCATACTCAC CAGAGCAAGC 1620 AAGTCCTTTT TTTTTTTTTT TTTTTTAAGA CACATGGAGT CTTGCTCTAT TGCCCAGGCT 1680 GCAGTGCAGT GGCATGATCA TGGCTCACTG CAGCCTCGAC CTCTTGGGCT CAGGCAGTCC 1740 TCCTGCCTCA GCCTCCTGAG TAGCTGGGAC TGCAGGTGTA TGCCACCACA CCTGGCTAAT 1800 TTTAAATTTT TTAGAGATGG GGTCTCACTA TGTTGCCCTG GCTGGTCTTG AACTCCTTTG 1860 CTCAAGCAGT CCTCCCAACT TAGCCTCCCA AATCATTGGG ATGAGAAGCA TGAACCACTG 1920 TGCCTGGTTA ATTACATAGA TATTTACATA TCTACTATCT TAAAACGGTG TCCTTTTAAG 1980 AATTTCAAAT GATGCTTTAT AGTTTCTAAT ATGGTGCACT GGGTATACTG TTGATATTTA 2040 AAGTTTTGTG AATGATAAAT TTCCCTACTT CAGTAGTGCC ATAGAATTAA TTGATTCTTG 2100 TATCTGAAAT TTAATGAGTG CTTATGAAGT ATGCTGGACT GTGCTAGGTT CTGACAGCAT 2160 TTGAAAAGAA GTTTGACATC TGCCTGTCTG TCCCCTTTTG GCTGCCTATG AGGTGTGTAA 2220 GATGGCTGCA ATTTGAGGAG GCATCCTTTG TTCCTGAGGA TAGAAGGTGC 2270
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