Tag | Content |
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EnhancerAtlas ID | HS131-05458 |
Organism | Homo sapiens |
Tissue/cell | ME-1 |
Coordinate | chr2:136893260-136894880 |
Target genes | |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myod1 | MA0499.1 | chr2:136894455-136894468 | AGAAACAGCTGCT | - | 6.28 | NR3C1 | MA0113.3 | chr2:136893996-136894013 | CAGGACATCATGTACTA | - | 6.12 | NR3C2 | MA0727.1 | chr2:136893996-136894013 | CAGGACATCATGTACTA | - | 6.1 | RUNX1 | MA0002.2 | chr2:136894309-136894320 | TTCTGTGGTTT | + | 6.32 | SPIC | MA0687.1 | chr2:136894054-136894068 | CAAAACAGGAAGAA | + | 6.03 |
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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 | chr2:136892763-136895721 | 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: 4 | Chromosome | Start | End |
chr2 | 136893351 | 136893858 | chr2 | 136893951 | 136894400 | chr2 | 136894653 | 136894791 | chr2 | 136893434 | 136894485 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I136124 | chr2 | 136881661 | 136899089 |
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Enhancer Sequence | TTCTCAAGTT TTAGCACAGT ATGGTATAGT TTGCAAGGAA GGAAAGTAGC ATTTAAGGAG 60 GGCCCATTGT GTGTCTGTCA CTTTGTGTGC AAGAGGTAAA AGCTACTGTG TTACTGAAAG 120 GAATGGGAAG CCATACAGTT AGGGCAGTGC CACAGGCTGG AAATCAGGAT AGTGGTTGTA 180 TTTTTGTCTC CACTGCTGAG TGGGTGTGTG ATTTTGGGTG AATCTCTAAA CTTCCTCTGG 240 GCCTGACCTG ATTTCCTCAT CAGTGGAATG AAGGTATTCC ACTCCAGCAT CTTCCAGCTC 300 TGTCATCTAC TTTTTCCTGT GGCCTTGCAG GCCATCTGGT TGTTGTTGAA CTGGTGGGAA 360 GACAACTGCA GAAGTTAGTT CAGGGGTTAA ATCTGGAAAC CCAATGTGGA AATGAAACCG 420 CAGCCCTGAA TACATTAAGT GCTGGGTTAG TTGGAGACTA AGGAAAGAAA GTCCCTGAGG 480 AATGAGCCCA TGTGAGCTTT AGCGCCTCTG TGCCCACTAC CAGGAGCCCC CAGTGCAAGC 540 TATCAGCCAG GGAGGAACAG TGTTTGCTCG GGCTTTGCTC TGTGGGCATG CAGAGCTTCC 600 ACCCGGCAGC ATCTACACCT GCGGTCTTGT AACCTAGCTA CAGAAATAGC AAGTATGTGC 660 GCAGAAGGCA AGTTGATGAG CTAGACAGTG GGTACAGACA CTTACAGCAG AACTTTGGTG 720 CTGAAAACAC CTAGTTCAGG ACATCATGTA CTAACTCAAG GGTGCCTCCC CCTTTTTGTC 780 TCTCTTAAAT TTTTCAAAAC AGGAAGAAAC TTTTCTTCAA CTGCAGGCAC CAATAACCTA 840 TGACCTTCTA GAGAGATCAT TTTGGAAACC ATCTAAGAAA GCTACCCTCA CTGAGGGGAT 900 GCTAGTCACT CTTTTCCCCT CTCCCCACAA CTCCCCACCC TCCTTTTTTT TTTGTAACTC 960 TGGGCTTCTG GCAACAGTTT GGAAGGTTGG CACAAGGCCA TCTGAAACCA CAGTGGGGTG 1020 TTAGGTAATC TGTTCTCATT AAAATGCTGT TCTGTGGTTT AATTTTCAAC GGTTTCTTTG 1080 CAGCTTGAAA ACACACATAC TATATTTTTT GAGGTAAGGA GAGATGGCTG TTACAGAGGC 1140 AAAAAGGCGG GAAGATGGGG TACCCCTAAG ACACTTCCTG GTATGTTTCC AGAAAAGAAA 1200 CAGCTGCTTT CATTCTAGAG GGGGCAAATT GAGCCTAAGG CAGCATTTAG GGAGCTTCCT 1260 GGACATAACT GACTCTAGGG ACAAATGCTT CAAACACATC TGAAAACTCT CCAGATTGAA 1320 AGGATCAAAT CATATGACCA TTCCCCCACT TAGTCATTGA ATTGAGCACT TTTATTGACT 1380 GTCTACCAAG TGCCAGGCAC TGGGAGACAT TTCAAATCAC ACCTGAGGAC AGAGAGACAG 1440 AAACCACTGC CCAGCAGGAG ATCACCACCA GGTGGTTGAT GACAAATAGG GCGGTGCAGT 1500 ACAGTGGGGT AAGCAAGCTG CTTGTTTCTT CTCATCCTCA CCTTCATGGA ATTCCCACCT 1560 TTTGAAGTGT ATCAGTGAAG ATAGCAAACT AAAGCCCAGG GTTATCATTT CTTTCTAAAA 1620
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