Tag | Content |
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EnhancerAtlas ID | HS093-18741 |
Organism | Homo sapiens |
Tissue/cell | HL-60 |
Coordinate | chr2:233939670-233941170 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Pou2f3 | MA0627.1 | chr2:233940898-233940914 | CCTCATTTGCATACCT | - | 6.01 | RREB1 | MA0073.1 | chr2:233940470-233940490 | TGATGGGGTGTGTGTGGGGT | - | 6.04 |
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| Number of super-enhancer constituents: 28 | ID | Coordinate | Tissue/cell |
SE_09311 | chr2:233937067-233942245 | CD14 | SE_10249 | chr2:233938234-233943474 | CD19_Primary | SE_10919 | chr2:233930549-233974717 | CD20 | SE_12194 | chr2:233939154-233941573 | CD3 | SE_13257 | chr2:233940185-233940957 | CD34_Primary_RO01480 | SE_13493 | chr2:233938656-233941304 | CD34_Primary_RO01536 | SE_14130 | chr2:233939137-233940122 | CD34_Primary_RO01549 | SE_15230 | chr2:233938611-233941940 | CD4_Memory_Primary_7pool | SE_16679 | chr2:233940019-233941540 | CD4_Naive_Primary_8pool | SE_18148 | chr2:233938745-233942140 | CD4p_CD25-_CD45ROp_Memory | SE_18751 | chr2:233938155-233942339 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19530 | chr2:233938930-233940217 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_19530 | chr2:233940273-233942107 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20168 | chr2:233938266-233952756 | CD56 | SE_21349 | chr2:233940044-233941773 | CD8_Memory_7pool | SE_22469 | chr2:233938254-233943493 | CD8_primiary | SE_32503 | chr2:233939090-233942003 | GM12878 | SE_43270 | chr2:233939678-233941239 | Lung | SE_50357 | chr2:233938442-233941346 | Sigmoid_Colon | SE_53149 | chr2:233939421-233941360 | Small_Intestine | SE_53617 | chr2:233938719-233941498 | Spleen | SE_58604 | chr2:233923957-233967222 | Ly1 | SE_59023 | chr2:233923916-233966682 | Ly3 | SE_59754 | chr2:233923674-233966318 | Ly4 | SE_60535 | chr2:233923765-233967375 | DHL6 | SE_61116 | chr2:233918458-233966992 | HBL1 | SE_61975 | chr2:233923768-233966412 | Toledo | SE_62364 | chr2:233923684-233967286 | Tonsil |
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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 |
GH02I233072 | chr2 | 233937424 | 233954276 |
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Enhancer Sequence | AAACACGATG ATGTTTCTTC CTACTTCCAC GGGCTTGTCC TCCCATATTA GAGTAGAACT 60 TCTCGTACTA CATCAGGGTT GACCTGGTCC AGAAATGCTC TTCTACTGAG AAGCACCTTC 120 CTGCCTCTTC TTTGCCTCCA CACTCAGCAC AGGGTGGGCA CCTGTCATCA CCCAGCACCT 180 GTGGGAGTCA CATGGGAAAT TTGCTGTAAG CCCCCCTTCA TTTGGGAATG GAACAAATCT 240 CATTTGTTAG CAGAAGGAAG TACTGTTGGG CCCAGTGCTA TCCTAACCCA GATCTCCAAT 300 GGGAATAATC CTGATCTGAT TACTCTGAAA GGTCATCCAG TCACTGGGAG GAGTCTCAGC 360 TGAGAGCCAG TGTTAGCGTA ACAAGGTGTT ACCAAATCAC CACAAAGAGC TGGGGAAGGG 420 CTGGGCGGGA CCCACTGCCC CTAAAGAGCA GTGAGCATGT TTTCCAGGTT ATGTTCCAGG 480 GCAGCAATTG CCAAACACTA TTTAGTTGTA GAATCTTTGC TTTAAACATT TTGCATGCAA 540 GATATTGTGT GTGTGTGTGT GCATGTGTAC ATACACACAT GCATGCATGC ATGTTACATG 600 TATACACATG TATGCATATG TTGTGTGTGC ACATGTATAT GTGTGTGTGT GTGTGTGTAT 660 ATAGGACCAG AGTGAAGTAC AAACTGCTGG TGGGGTGGCA GGCCAAGTGA GCACCTTCCT 720 CCACCGCTTG GCAGAGCCTC CACACCCGTG GAATACAGTT TGGTACTACT GCTCACCCAA 780 CGACTTGTGT GTGGCGGGGC TGATGGGGTG TGTGTGGGGT GGTGCTGTAT GTTTTCCCTT 840 GAAGGTTGAA ACTGATTCAG CCCTGGGGGT CAGAATGTCC AGCCCTGTGC ATTGGCTATG 900 CAGGGTCATT AACATCTGCT GAGATGTTAC TGTCTAAGGG GGAAGTATCT TCTTCCTGTT 960 ATACTAGCTT TTGAATTCTG ATCTGTTTTG GTAACATGGA GCTGTTTCTT TGTTTCAGTG 1020 TTTCTAGAAC ATCTTTGAAA AAGCCATAAA GGTTTGTCTG CCACACTTGA TTGAACCAAA 1080 AAGCCTTTCC TGTTCTGTGC GCCTGCCTCT GACTCTCCCT TCGTGATTAT GTTCTTTCTC 1140 TCTGTCTACA GGCTGATGTT TGGGCTGGCT GGAGCTCTTC CACAAGTCAG CTGCCCTCAG 1200 CCAAATAAGA GGCTGTTCTC ACCCCTCACC TCATTTGCAT ACCTACAGGA GGAAGTGCCA 1260 AGGGAAGAGA GCATTGAAAA ATAAGAGCAC AGCAGAGTTG AGCTATCTCC ACATTTGTCT 1320 GGCAGGCTCT GCAAAGGGGA TTGAGGCCAG TGGTTCTCTG TGTCCCAGAG GTGTCCCTGG 1380 GAGATGTAGT GTCACTGGAC TAGAGATTCA TCCTTGCTAT CTCTGATGCA AGACGATTGT 1440 ATCAATTCAG GCTCTGGAGG TAGGACAGGG AGCAGAAGGA TGGGGACTAA AGCCATGGAA 1500
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