Tag | Content |
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EnhancerAtlas ID | HS110-02742 |
Organism | Homo sapiens |
Tissue/cell | KATO3 |
Coordinate | chr2:85172870-85174520 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr2:85173278-85173296 | GGAGGGGAGGGAGGAGGG | + | 6.27 | RREB1 | MA0073.1 | chr2:85172930-85172950 | TGGTGGGGGATGGGGTGGGG | - | 6.83 | ZNF263 | MA0528.1 | chr2:85173261-85173282 | GGAGGTGAGAGGGGAAGGGAG | + | 6.02 | ZNF263 | MA0528.1 | chr2:85173231-85173252 | GGGAGAGGGGAGGGGAGAGGA | + | 6.15 | ZNF263 | MA0528.1 | chr2:85173229-85173250 | AGGGGAGAGGGGAGGGGAGAG | + | 6.19 | ZNF263 | MA0528.1 | chr2:85173243-85173264 | GGGAGAGGAGGGGAGAGGGGA | + | 6.33 | ZNF263 | MA0528.1 | chr2:85173236-85173257 | AGGGGAGGGGAGAGGAGGGGA | + | 6.51 | ZNF263 | MA0528.1 | chr2:85173246-85173267 | AGAGGAGGGGAGAGGGGAGGT | + | 6.83 | ZNF263 | MA0528.1 | chr2:85173292-85173313 | AGGGGAGGGGAGGGGAGGGGA | + | 6.91 | ZNF263 | MA0528.1 | chr2:85173241-85173262 | AGGGGAGAGGAGGGGAGAGGG | + | 6 | ZNF263 | MA0528.1 | chr2:85173219-85173240 | AGGGGAGGGGAGGGGAGAGGG | + | 7.01 | ZNF263 | MA0528.1 | chr2:85173224-85173245 | AGGGGAGGGGAGAGGGGAGGG | + | 7.1 | ZNF263 | MA0528.1 | chr2:85173297-85173318 | AGGGGAGGGGAGGGGAGAGGA | + | 7.1 | ZNF263 | MA0528.1 | chr2:85173271-85173292 | GGGGAAGGGAGGGGAGGGAGG | + | 7.23 | ZNF263 | MA0528.1 | chr2:85173275-85173296 | AAGGGAGGGGAGGGAGGAGGG | + | 7.34 | ZNF263 | MA0528.1 | chr2:85173280-85173301 | AGGGGAGGGAGGAGGGGAGGG | + | 7.56 | ZNF263 | MA0528.1 | chr2:85173284-85173305 | GAGGGAGGAGGGGAGGGGAGG | + | 7.86 | ZNF263 | MA0528.1 | chr2:85173287-85173308 | GGAGGAGGGGAGGGGAGGGGA | + | 8.75 |
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| Number of super-enhancer constituents: 17 | ID | Coordinate | Tissue/cell |
SE_10467 | chr2:85172755-85174410 | CD19_Primary | SE_14858 | chr2:85173160-85174371 | CD4_Memory_Primary_7pool | SE_17329 | chr2:85172940-85174409 | CD4p_CD25-_CD45RAp_Naive | SE_18307 | chr2:85171711-85174762 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19290 | chr2:85172506-85174415 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_24195 | chr2:85173090-85174241 | Colon_Crypt_2 | SE_25084 | chr2:85173093-85174407 | Colon_Crypt_3 | SE_27502 | chr2:85172693-85174600 | Esophagus | SE_32545 | chr2:85164283-85174534 | GM12878 | SE_34685 | chr2:85171658-85174793 | HeLa | SE_35873 | chr2:85172149-85175081 | HMEC | SE_47378 | chr2:85172889-85174696 | Panc1 | SE_50337 | chr2:85171737-85174482 | Sigmoid_Colon | SE_52528 | chr2:85172218-85174434 | Small_Intestine | SE_54030 | chr2:85173005-85174218 | Spleen | SE_59563 | chr2:85151112-85174538 | Ly3 | SE_64856 | chr2:85172724-85174623 | NHEK |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 85173321 | 85174019 | chr2 | 85173188 | 85173797 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I084944 | chr2 | 85171482 | 85174859 |
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Enhancer Sequence | AAAAGAAATG CACAGAGCAT CATAGAGTCC AGGGCAGGGG TCCCTGACCA AGCTCGGGAA 60 TGGTGGGGGA TGGGGTGGGG ACATCAGTGG AGTTTTTTGG GGTTTTTTGT TTTGCTTTGT 120 TTGAGACAGG GTCTTGCTCC GTCACCCAGG CTGGAGTGCA GTGGTGTGAT CATAGTTCAC 180 TGCAACCTTG AACTCCTGGG CTCAAGGGAT CCCCCGGCCT CAGCCTCCTG AGTAGCTGGG 240 ATTACAGGCA TGAGCCACCA CACCCAGTCA ATAGACTTTT CTTGATGTGG GTGACACCCA 300 AGCTTTAAGT TTGAAGACTA AAGGAGAGCT GGCACACCAA CAGTATACGA GGGGAGGGGA 360 GGGGAGAGGG GAGGGGAGAG GAGGGGAGAG GGGAGGTGAG AGGGGAAGGG AGGGGAGGGA 420 GGAGGGGAGG GGAGGGGAGG GGAGAGGACA CAGCAGGCTG GTAGGGCAGC TTTGAATATG 480 GCTCAGAGGC GAGGCGAGCA AGGTCTGAAT CACTTCTGCT CCAAGTCCAG GCCCACATTA 540 CTTCTTATAC GGACAAGAGG CCAGTAACTG CTCTACCCAC ACATTCTCCT CCCCTACCAT 600 CAGAAAAATC TCCCTAAAGC TCAAATTTGA CTTCCTGTCT CCCCTGCTTG CTACCCTCTG 660 CTGGTTCCCC TTTCTGATCT GTGGTGTCTC AGCTCCACCT CTGTTCATAA ACTTCATATG 720 GTGCCTTCAA AAGTATTTCC GTCTCTGGAC CTTCATCCCT GCACTACTGT CTGCCTGGAA 780 TTTCCTGCCC TGCCTTGGTT GATGAGGTGG ACTCCTATTC ATACTTCAGA GTGACTCAGA 840 TGTGACTTGT TCCACAAAGT CCCCACCCAC TTGCACTCAC CTCCGTGGTG CACGTATTCC 900 AGGGCCGTGA GCTTCACCTC TCTGCACGTC TCCCTCCTGC TACAGCTGTG AGGGTGCAGA 960 CCTCCTCTGC TGGCACCAGG GCCCGGCCTG CAGTGGGCCT TTGGCAAATG AGGAACTAGG 1020 GCTACCGGTA GGTGAAAATG CAGCTAATGC CCAGGAAGCT AGAAGCTGTT GGAACATTTC 1080 TGAGACCCTT TAGACCTGGA AATAGCTCTA TGTTAGAGGG TTGCTGATAG AGAAGGCTGG 1140 AAGTGAGGTC CCTCTGTCCC CAGCTCGCCT CAGACCCTGG TTCCAGATAC AGTTGCATGT 1200 GTTTCCAACC AAGACTCTGA CCTGGCTCCT CAACCAAACC TCCCCTGCGT CCATGGATCT 1260 ATCTGAACTC CCATTTATAA TCGTAAGAGG CTGTGGGTTA GAGGCGCTGT GCTAATGATG 1320 GCTGTATGGT TATTATGATT GTGAAGTTGT TATATTTTAC ATAGAATACA AGTTTATGTA 1380 CATTACGATT AAGACTAGTA AAGCTCTTTG GAACTTTAAA AACAAATCCC AGTCAGGCGT 1440 GATGGCTCAC GCCTGTAATC CTAGCTCTTT GGGAGTCCAA GGCAGGAGGA CTGGTTAAGC 1500 CCAATTCTCC AGGAGTTTGA GACCAGCCTG GGCAACATAG TAGGACCCCA TCTCTACAAA 1560 AAAATAAAAA TCAAAAAATT AGCCAGACGT GGTGGCATGC ACCTTTAGTC CCAGCTACTC 1620 GGGAGGCTGA GGCAGGAGGA CTGTTTGAGC 1650
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