Tag | Content |
---|
EnhancerAtlas ID | HS110-02741 |
Organism | Homo sapiens |
Tissue/cell | KATO3 |
Coordinate | chr2:85145940-85148030 |
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 |
|
| 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 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH02I084918 | chr2 | 85145334 | 85148597 |
|
Enhancer Sequence | GATGAATAAG CTTCTATTAT GATATATAAG TCACTGGGTT TTTGTTTGTT TTTGTTTTCT 60 TTTTTTGTTT TGTTTTGTTT TTGTTTTGAG ACGGAGTCTC TCTGTCACCC AGATTAGAGT 120 GCAATGGTAC CATCTCAGCT CACTGCAACC TCCCCCTCCT GGGTTCAAGC GATTCTCCCA 180 CCTCAGATTC CAAAGTAGCT GGGATTACAG GCACCTGCCA TCATGCCCAG CTAATTTCTG 240 TATTTTTGTA GAGATGGGGT TTCACCATGT TGGCCAGGCT GGTCTTGAAC TCCTGACCTG 300 AGGTGATCCG CCTGCCTCAG CCTCCCAAGG TGCTGGGATT ACAAGCGTGA GCCACCACGC 360 CTGGTCGTGT TTTTGTTTCC TGAGACAGAG TCTCACTCTG TCACCCAGGC TGGAGTGCAG 420 TGGTGCCATC TCGACTCACT GCAACCTCCG CCTCCCAGGT TCAAGTAATT CTCCTGCATC 480 AGCCTCCGGA GTAGCTGGGA CTACAGGTAC TGCGCCACTA TGCCCGGCTA ATTTTTGTAT 540 TTTTAGTAGA GATGGGGTTT CACCATGTTG GCCAGCCTGG TCTCAAACTC CTGACCTCAG 600 GTAATCCATC CGCCTTGGCC TCCCAAAGTG CTGAGATTAC AGGCGTGGGC CACCATGCCT 660 GGCCAGACAG TCCAATATTT TTAAATCAGC CATAAATCTA TGCACCGAAT AATGTCTCTC 720 TCTCTCTCTC TGACACATAC ACACATACAC ACATGCGCAC GCGTGCACAC CCACACATTG 780 TTACCACTTA GAAGAGTGCC AGGCCCAGAT GGTTTCACAG ACGATTGCTT TCAAAGCTGC 840 AAGAAAGCAA TAACTTCAAT ACCTCAAAAT TTGTTTCAGT AGTTAGAAAA GGACATATGC 900 TTCCTGTGAT GGTTAATTTT AGCTGTCAAC TTGACTTGAT TAAGTAATAC ACTAGTCTCC 960 CCTTATCCAT GGAGGGTATG TTCCAAGATC CCCAGTGGAT GCCTGAAGCC ACACATGTAC 1020 CGAACCCTGT ACACACCTAT GATAACGTTT AATTTATAAA TTAGGCACAG TAAGAGATTA 1080 ACAACTAATA ATAAAATAGA ACAATTAAAC AGTTGAACAC AAGCACTGTG ATGCTGTGAC 1140 AGTCACTCGT AACTGAGATG GCTGCTAAGA GACTAGCTAA CGGGTGAGTA GTGTATACAA 1200 CGTGGAAACA CTGGACAAAG GGATGAGTCA CATCCTGGGA GGGACAGAGT GGAATGCCAT 1260 GAGATTTCAT CATGTTACAC AGAACGATGA GCCATTTAAA ACTTACGGAT TGTTTATTTC 1320 TGGAATTTTT AATTTAATAT TTTCAGACCA AGGTTGACCA GGAGTAACTA AAACTACAGA 1380 AAGCAAAACT GAATAAAGTG GGGAGTCGAG AACCTAGAGA GCTGGTAAAG CATTCTTTCT 1440 AGGTGTGTCT GTGAGGGTGT TTTCACAGGA GATTGGCATG TGAGTGGGTG GGCTGACTGA 1500 GGAAGATCTG CCCTCAGTGT GGGCGGACAA CATCCAATTG GCTGTGGGCC CAGATAGAAC 1560 CAAAAGGCAG AGAAAAGGCA AATTCTTTTT TTCTCTCTCC TGAAGCTGGG CCATCCTTCT 1620 TCTTCTGACC TTGGACATCA GAACTGCAGG CTCCCTGGCC TTTGGACTCT GGGTCTTACA 1680 TTAGCAGCCC CCAGGTTCTT GGCCTTTGGC CTTGGACTGA GAATTACACT ATCAGCTGCC 1740 CTGGTTCTGA GACTTTAGGA CTTGAACTGA GCCCCACTGT GGTATTCCAC GGTCTCCAGC 1800 TTACAGACAG TCTGTCGTGG GACTTTTCAC CTCCCTAATC TCATGAGCCA ATTCCCCTAA 1860 TAAATCCCCT CTCATATATC TATATACAGT CGCCCCTCAT ATCTATGGGA GATGGGTTCC 1920 AGGTTATGTT GCCCAGGCTG GCCTTGAACT CTTGGGCTCA AGCTATCCTC CCATCTCAGC 1980 TTCCCAAGTA GCTAGGACTA TCATATTCTT TTTTTTTTTT TTTTTTTGAG ACGGAGTCTC 2040 GCTCTGTCAC CCAGGCTGGA GTGCAGTGGT GCGATCTCGG CTCACTGCAA 2090
|