Tag | Content |
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EnhancerAtlas ID | HS060-20125 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr2:136890780-136892080 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
JUN(var.2) | MA0489.1 | chr2:136891310-136891324 | TAGAGATGAGTCAT | + | 6.08 | JUN(var.2) | MA0489.1 | chr2:136891315-136891329 | ATGAGTCATACTTT | - | 6.14 |
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| Number of super-enhancer constituents: 28 | ID | Coordinate | Tissue/cell |
SE_09693 | chr2:136888096-136895457 | CD14 | SE_10164 | chr2:136881599-136898787 | CD19_Primary | SE_10920 | chr2:136869824-136900482 | CD20 | SE_11819 | chr2:136881224-136898565 | CD3 | SE_14424 | chr2:136885813-136898806 | CD4_Memory_Primary_7pool | SE_15399 | chr2:136885928-136897793 | CD4_Memory_Primary_8pool | SE_15801 | chr2:136885832-136897564 | CD4_Naive_Primary_7pool | SE_16281 | chr2:136885643-136897634 | CD4_Naive_Primary_8pool | SE_16890 | chr2:136885826-136897779 | CD4p_CD225int_CD127p_Tmem | SE_17313 | chr2:136878490-136899751 | CD4p_CD25-_CD45RAp_Naive | SE_17847 | chr2:136883846-136898991 | CD4p_CD25-_CD45ROp_Memory | SE_20024 | chr2:136882246-136897636 | CD56 | SE_20760 | chr2:136884316-136897171 | CD8_Memory_7pool | SE_21445 | chr2:136881276-136896276 | CD8_Naive_7pool | SE_21908 | chr2:136881090-136899486 | CD8_Naive_8pool | SE_22417 | chr2:136880590-136898694 | CD8_primiary | SE_25571 | chr2:136886017-136896348 | DND41 | SE_31158 | chr2:136882346-136892628 | Fetal_Thymus | SE_39512 | chr2:136890769-136897819 | Jurkat | SE_49980 | chr2:136890836-136897736 | RPMI-8402 | SE_50566 | chr2:136885976-136896239 | Sigmoid_Colon | SE_53724 | chr2:136886050-136896243 | Spleen | SE_55113 | chr2:136885784-136896094 | Thymus | SE_58729 | chr2:136863567-136896276 | Ly1 | SE_60681 | chr2:136863571-136895984 | DHL6 | SE_61433 | chr2:136863899-136926915 | Toledo | SE_62216 | chr2:136864010-136900323 | Tonsil | SE_66378 | chr2:136890769-136897819 | Jurkat |
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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 |
GH02I136124 | chr2 | 136881661 | 136899089 |
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Enhancer Sequence | TGTTGTAGAG ATGGGGTCTC ACTCTATTGC CCAGGCTGGT CTTGAACTCC TGGCCTCAAG 60 CAATCCTCCT GCCTCAGTCT CCCAAAGTGC TGTGATTGCA GGTGTGAGCC ACTGCACTCA 120 GCCAGCAGCC ACCCATTTCT TACAGCTGCT CCAGTGTGAG GGGGTAACAA AAGGCTGCTT 180 TCAAGGCAGC AGCCCAGCCC CCATGTTTCC TGCCTGGTCC CTGAGGAGTG CACAAGTGAT 240 CAGGAGAGAT TCTTCTTTTG GTCACAGGGA TCTTAATGAT CACTGGGACT TGGGCTGTTT 300 AAGATGTCAC TTAGAAGTTC AAATCTACTT CCAGATGGCT TCCAAGCGAG GGATGGCCTC 360 TACAGTGAGG CCAATCATGT GGTATATTCT TACCTAAGTG GGCCTTGCTG CCCTGCACAA 420 TGGCATCTCG GCCCATGGGC CAGCCTCGTA AGGTCTTTAA ACCTATGACC ACCAGGTGAT 480 CTTCTCTGGG GAGCAGCAGA ACTTCCATGA GTCTGTCCAG GGATCTTATT TAGAGATGAG 540 TCATACTTTT CTACGCTGTC AGCTCTAGGT TGAAGTAGAA TGTACCAGCA ACAGACTAGG 600 ATGACCTCGC AGCTAGCTGT CCATAGGAAT ACACCTCTTC TTTCTTCCAA CCTCTCAGTT 660 TCCTGGCGTT TCCTCTAAGT TAATGTCTTG CTAGAATGGT TTGAGTTGAC ATTAACTGTC 720 TGCTATGTTT TATGCAGCAC ATGGCCACCT ACCAAGTGGC ACTTTCCATT TTGGGTATGG 780 GGAGCAGGGT ATATTTTATA CCTCCAATCC CATTGTTCTT TATGAATCTT TGTTCCTTCA 840 CCCCTCACTT CCCAAATCGA TCACTTTGCT TCTTGATTAT GATATCCCTG TGGGTGAACC 900 CGTAGATAGC AGAAACTGAG CTGTCTCTGC TGTTGATAAT TTTAGCTCTT CTTGGAACTC 960 CTTTCTTTTT GCAAATGCCA ACCAGGTGTC CCCAAGTAAG AGATGATACT TGTTTGTTTG 1020 GTAAAGGCAC CCAGATAAGA AGAGTCAGAA TGAACAGCTC CAAAAGAGAA GTGGTTTCCT 1080 CGGTCACCGA CTCACCACAT TAAACATTCA CCCTGGCTCA CTGTCTGAAA TGAGTCAGTG 1140 GTCCTTTCAG AATTCCCTTT ACAACAGTGT TTCAAAGAAA TCTGTGACTG AGGTTGCAAA 1200 TCATTTTTTC TTCACTGCAG CTGACTATTT TGCATTTTCC CAAGGTGAAA CTCAGCCTGT 1260 CTTTTCAGGT GTTGAGAAAG AGAGTCAAAA CTTCAAAGTT 1300
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