Tag | Content |
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EnhancerAtlas ID | HS127-16970 |
Organism | Homo sapiens |
Tissue/cell | Macrophage |
Coordinate | chr2:85145780-85148050 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOS | MA0476.1 | chr2:85147161-85147172 | GATGAGTCACA | - | 6.14 | Foxd3 | MA0041.1 | chr2:85147247-85147259 | GATTGTTTATTT | + | 6.62 | HNF4G | MA0484.1 | chr2:85147639-85147654 | TGGCCTTTGGCCTTG | - | 6.47 | HNF4G | MA0484.1 | chr2:85147595-85147610 | TGGCCTTTGGACTCT | - | 7.58 | JUN(var.2) | MA0489.1 | chr2:85147162-85147176 | ATGAGTCACATCCT | - | 6.21 | JUND | MA0491.1 | chr2:85147161-85147172 | GATGAGTCACA | - | 6.14 | Nr5a2 | MA0505.1 | chr2:85147876-85147891 | GCTGGCCTTGAACTC | - | 8.25 |
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| Number of super-enhancer constituents: 29 | ID | Coordinate | Tissue/cell |
SE_10467 | chr2:85145440-85148104 | CD19_Primary | SE_14858 | chr2:85146216-85148097 | CD4_Memory_Primary_7pool | SE_15828 | chr2:85146211-85147858 | CD4_Naive_Primary_7pool | SE_17329 | chr2:85144702-85148021 | CD4p_CD25-_CD45RAp_Naive | SE_18307 | chr2:85145257-85148272 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19290 | chr2:85146834-85148007 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_22056 | chr2:85146279-85147703 | CD8_Naive_8pool | SE_24195 | chr2:85147396-85147781 | Colon_Crypt_2 | SE_27502 | chr2:85146415-85148139 | Esophagus | SE_32545 | chr2:85146405-85147995 | GM12878 | SE_34685 | chr2:85144533-85148900 | HeLa | SE_35873 | chr2:85145245-85148284 | HMEC | SE_37561 | chr2:85145355-85148665 | HSMMtube | SE_39196 | chr2:85146289-85148051 | IMR90 | SE_43289 | chr2:85146287-85148018 | Lung | SE_45342 | chr2:85146235-85148013 | NHLF | SE_47378 | chr2:85146394-85148070 | Panc1 | SE_50337 | chr2:85146275-85148041 | Sigmoid_Colon | SE_52528 | chr2:85146343-85148031 | Small_Intestine | SE_54030 | chr2:85146413-85147977 | Spleen | SE_55507 | chr2:85147282-85147950 | Thymus | SE_55909 | chr2:85145260-85146133 | u87 | SE_55909 | chr2:85146272-85148271 | u87 | SE_57573 | chr2:85146370-85147966 | VACO_503 | SE_58212 | chr2:85146543-85147124 | VACO_9m | SE_58212 | chr2:85147243-85147947 | VACO_9m | SE_65145 | chr2:85146145-85148023 | NHEK | SE_67823 | chr2:85145260-85146133 | u87 | SE_67823 | chr2:85146272-85148271 | u87 |
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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 |
GH02I084918 | chr2 | 85145334 | 85148597 |
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Enhancer Sequence | GAAGCCCAGC TCCCACTCCC ACCCAGGGCC ACGAAATGAC ACTAGGGATG GAAACTGATG 60 TAGGATGGTG CAGCAGAAAG CATTAAGGTG ACTGGGATCT CAGAGTTGCT ATACCAGGCG 120 TGGACTACTC CTTCCAGACA TCTTTAATCT TTATCAGGAA GATGAATAAG CTTCTATTAT 180 GATATATAAG TCACTGGGTT TTTGTTTGTT TTTGTTTTCT TTTTTTGTTT TGTTTTGTTT 240 TTGTTTTGAG ACGGAGTCTC TCTGTCACCC AGATTAGAGT GCAATGGTAC CATCTCAGCT 300 CACTGCAACC TCCCCCTCCT GGGTTCAAGC GATTCTCCCA CCTCAGATTC CAAAGTAGCT 360 GGGATTACAG GCACCTGCCA TCATGCCCAG CTAATTTCTG TATTTTTGTA GAGATGGGGT 420 TTCACCATGT TGGCCAGGCT GGTCTTGAAC TCCTGACCTG AGGTGATCCG CCTGCCTCAG 480 CCTCCCAAGG TGCTGGGATT ACAAGCGTGA GCCACCACGC CTGGTCGTGT TTTTGTTTCC 540 TGAGACAGAG TCTCACTCTG TCACCCAGGC TGGAGTGCAG TGGTGCCATC TCGACTCACT 600 GCAACCTCCG CCTCCCAGGT TCAAGTAATT CTCCTGCATC AGCCTCCGGA GTAGCTGGGA 660 CTACAGGTAC TGCGCCACTA TGCCCGGCTA ATTTTTGTAT TTTTAGTAGA GATGGGGTTT 720 CACCATGTTG GCCAGCCTGG TCTCAAACTC CTGACCTCAG GTAATCCATC CGCCTTGGCC 780 TCCCAAAGTG CTGAGATTAC AGGCGTGGGC CACCATGCCT GGCCAGACAG TCCAATATTT 840 TTAAATCAGC CATAAATCTA TGCACCGAAT AATGTCTCTC TCTCTCTCTC TGACACATAC 900 ACACATACAC ACATGCGCAC GCGTGCACAC CCACACATTG TTACCACTTA GAAGAGTGCC 960 AGGCCCAGAT GGTTTCACAG ACGATTGCTT TCAAAGCTGC AAGAAAGCAA TAACTTCAAT 1020 ACCTCAAAAT TTGTTTCAGT AGTTAGAAAA GGACATATGC TTCCTGTGAT GGTTAATTTT 1080 AGCTGTCAAC TTGACTTGAT TAAGTAATAC ACTAGTCTCC CCTTATCCAT GGAGGGTATG 1140 TTCCAAGATC CCCAGTGGAT GCCTGAAGCC ACACATGTAC CGAACCCTGT ACACACCTAT 1200 GATAACGTTT AATTTATAAA TTAGGCACAG TAAGAGATTA ACAACTAATA ATAAAATAGA 1260 ACAATTAAAC AGTTGAACAC AAGCACTGTG ATGCTGTGAC AGTCACTCGT AACTGAGATG 1320 GCTGCTAAGA GACTAGCTAA CGGGTGAGTA GTGTATACAA CGTGGAAACA CTGGACAAAG 1380 GGATGAGTCA CATCCTGGGA GGGACAGAGT GGAATGCCAT GAGATTTCAT CATGTTACAC 1440 AGAACGATGA GCCATTTAAA ACTTACGGAT TGTTTATTTC TGGAATTTTT AATTTAATAT 1500 TTTCAGACCA AGGTTGACCA GGAGTAACTA AAACTACAGA AAGCAAAACT GAATAAAGTG 1560 GGGAGTCGAG AACCTAGAGA GCTGGTAAAG CATTCTTTCT AGGTGTGTCT GTGAGGGTGT 1620 TTTCACAGGA GATTGGCATG TGAGTGGGTG GGCTGACTGA GGAAGATCTG CCCTCAGTGT 1680 GGGCGGACAA CATCCAATTG GCTGTGGGCC CAGATAGAAC CAAAAGGCAG AGAAAAGGCA 1740 AATTCTTTTT TTCTCTCTCC TGAAGCTGGG CCATCCTTCT TCTTCTGACC TTGGACATCA 1800 GAACTGCAGG CTCCCTGGCC TTTGGACTCT GGGTCTTACA TTAGCAGCCC CCAGGTTCTT 1860 GGCCTTTGGC CTTGGACTGA GAATTACACT ATCAGCTGCC CTGGTTCTGA GACTTTAGGA 1920 CTTGAACTGA GCCCCACTGT GGTATTCCAC GGTCTCCAGC TTACAGACAG TCTGTCGTGG 1980 GACTTTTCAC CTCCCTAATC TCATGAGCCA ATTCCCCTAA TAAATCCCCT CTCATATATC 2040 TATATACAGT CGCCCCTCAT ATCTATGGGA GATGGGTTCC AGGTTATGTT GCCCAGGCTG 2100 GCCTTGAACT CTTGGGCTCA AGCTATCCTC CCATCTCAGC TTCCCAAGTA GCTAGGACTA 2160 TCATATTCTT TTTTTTTTTT TTTTTTTGAG ACGGAGTCTC GCTCTGTCAC CCAGGCTGGA 2220 GTGCAGTGGT GCGATCTCGG CTCACTGCAA GCTCTGCCTC CCGGGTTCAT 2270
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