Tag | Content |
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EnhancerAtlas ID | HS098-30694 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr2:85146280-85148010 |
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: 27 | 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 | chr2:85146272-85148271 | 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 | chr2:85146272-85148271 | 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 | ACAAGCGTGA GCCACCACGC CTGGTCGTGT TTTTGTTTCC TGAGACAGAG TCTCACTCTG 60 TCACCCAGGC TGGAGTGCAG TGGTGCCATC TCGACTCACT GCAACCTCCG CCTCCCAGGT 120 TCAAGTAATT CTCCTGCATC AGCCTCCGGA GTAGCTGGGA CTACAGGTAC TGCGCCACTA 180 TGCCCGGCTA ATTTTTGTAT TTTTAGTAGA GATGGGGTTT CACCATGTTG GCCAGCCTGG 240 TCTCAAACTC CTGACCTCAG GTAATCCATC CGCCTTGGCC TCCCAAAGTG CTGAGATTAC 300 AGGCGTGGGC CACCATGCCT GGCCAGACAG TCCAATATTT TTAAATCAGC CATAAATCTA 360 TGCACCGAAT AATGTCTCTC TCTCTCTCTC TGACACATAC ACACATACAC ACATGCGCAC 420 GCGTGCACAC CCACACATTG TTACCACTTA GAAGAGTGCC AGGCCCAGAT GGTTTCACAG 480 ACGATTGCTT TCAAAGCTGC AAGAAAGCAA TAACTTCAAT ACCTCAAAAT TTGTTTCAGT 540 AGTTAGAAAA GGACATATGC TTCCTGTGAT GGTTAATTTT AGCTGTCAAC TTGACTTGAT 600 TAAGTAATAC ACTAGTCTCC CCTTATCCAT GGAGGGTATG TTCCAAGATC CCCAGTGGAT 660 GCCTGAAGCC ACACATGTAC CGAACCCTGT ACACACCTAT GATAACGTTT AATTTATAAA 720 TTAGGCACAG TAAGAGATTA ACAACTAATA ATAAAATAGA ACAATTAAAC AGTTGAACAC 780 AAGCACTGTG ATGCTGTGAC AGTCACTCGT AACTGAGATG GCTGCTAAGA GACTAGCTAA 840 CGGGTGAGTA GTGTATACAA CGTGGAAACA CTGGACAAAG GGATGAGTCA CATCCTGGGA 900 GGGACAGAGT GGAATGCCAT GAGATTTCAT CATGTTACAC AGAACGATGA GCCATTTAAA 960 ACTTACGGAT TGTTTATTTC TGGAATTTTT AATTTAATAT TTTCAGACCA AGGTTGACCA 1020 GGAGTAACTA AAACTACAGA AAGCAAAACT GAATAAAGTG GGGAGTCGAG AACCTAGAGA 1080 GCTGGTAAAG CATTCTTTCT AGGTGTGTCT GTGAGGGTGT TTTCACAGGA GATTGGCATG 1140 TGAGTGGGTG GGCTGACTGA GGAAGATCTG CCCTCAGTGT GGGCGGACAA CATCCAATTG 1200 GCTGTGGGCC CAGATAGAAC CAAAAGGCAG AGAAAAGGCA AATTCTTTTT TTCTCTCTCC 1260 TGAAGCTGGG CCATCCTTCT TCTTCTGACC TTGGACATCA GAACTGCAGG CTCCCTGGCC 1320 TTTGGACTCT GGGTCTTACA TTAGCAGCCC CCAGGTTCTT GGCCTTTGGC CTTGGACTGA 1380 GAATTACACT ATCAGCTGCC CTGGTTCTGA GACTTTAGGA CTTGAACTGA GCCCCACTGT 1440 GGTATTCCAC GGTCTCCAGC TTACAGACAG TCTGTCGTGG GACTTTTCAC CTCCCTAATC 1500 TCATGAGCCA ATTCCCCTAA TAAATCCCCT CTCATATATC TATATACAGT CGCCCCTCAT 1560 ATCTATGGGA GATGGGTTCC AGGTTATGTT GCCCAGGCTG GCCTTGAACT CTTGGGCTCA 1620 AGCTATCCTC CCATCTCAGC TTCCCAAGTA GCTAGGACTA TCATATTCTT TTTTTTTTTT 1680 TTTTTTTGAG ACGGAGTCTC GCTCTGTCAC CCAGGCTGGA GTGCAGTGGT 1730
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