Tag | Content |
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EnhancerAtlas ID | HS116-19088 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr2:106405980-106407650 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CDX2 | MA0465.1 | chr2:106406512-106406523 | TTTTATTGCTT | - | 6.32 | DUX4 | MA0468.1 | chr2:106406694-106406705 | TGATTGGATTA | - | 6.02 | MEF2A | MA0052.3 | chr2:106406756-106406768 | TCTATTTTTAGC | - | 6.92 | MEF2B | MA0660.1 | chr2:106406756-106406768 | TCTATTTTTAGC | - | 6.44 | MEF2C | MA0497.1 | chr2:106406755-106406770 | ATCTATTTTTAGCAG | - | 6.67 |
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| Number of super-enhancer constituents: 23 | ID | Coordinate | Tissue/cell |
SE_10292 | chr2:106405788-106408014 | CD19_Primary | SE_10910 | chr2:106379803-106410786 | CD20 | SE_11843 | chr2:106402382-106408086 | CD3 | SE_13211 | chr2:106405465-106407790 | CD34_Primary_RO01480 | SE_14420 | chr2:106405743-106410113 | CD4_Memory_Primary_7pool | SE_15409 | chr2:106405697-106408428 | CD4_Memory_Primary_8pool | SE_16297 | chr2:106405634-106409205 | CD4_Naive_Primary_8pool | SE_17245 | chr2:106405822-106408163 | CD4p_CD225int_CD127p_Tmem | SE_17337 | chr2:106387664-106410837 | CD4p_CD25-_CD45RAp_Naive | SE_17777 | chr2:106401720-106410545 | CD4p_CD25-_CD45ROp_Memory | SE_18243 | chr2:106389599-106421920 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19126 | chr2:106402155-106408453 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20619 | chr2:106405906-106407830 | CD56 | SE_21274 | chr2:106404971-106408410 | CD8_Memory_7pool | SE_21873 | chr2:106405876-106407817 | CD8_Naive_7pool | SE_21946 | chr2:106405766-106407854 | CD8_Naive_8pool | SE_22311 | chr2:106401712-106410582 | CD8_primiary | SE_37706 | chr2:106404902-106407752 | HSMMtube | SE_39779 | chr2:106405947-106407658 | Jurkat | SE_44057 | chr2:106405817-106407883 | MM1S | SE_53622 | chr2:106405877-106407797 | Spleen | SE_62262 | chr2:106353762-106421483 | Tonsil | SE_66643 | chr2:106405947-106407658 | Jurkat |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 106406623 | 106406870 | chr2 | 106407000 | 106407299 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I105788 | chr2 | 106405212 | 106408316 |
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Enhancer Sequence | TCTTTTGTTA CACATAAGAG AGTTCTTTCT AGTTGAAGAG ATGTTTCCCT GAGTCTTTCT 60 GATGAAAATG ATCCTCTTGC TACATAAAAT CCTTATAGGA GCAATAAAAC CTGCCTTCGG 120 AACCAGCTGT AAAGCACTTA TTGTCCATCA TCATCTGCTG GTGAGGACCT TGCTCCCCGG 180 CTTGTGATTC TCAAACCCCA ACTTAGGCTT GCTCCCGGTT AACGGGAGGG CTTTTTCTGA 240 CACAGACTGC TGCCCCACAC ACCCCCAGTT TCTGCCTCAG TGGTCTGGGG TGGGCCCCAG 300 TAATTTGCAT TTTTAAAAAG TCCCCAGGTG ATGCTGGTGC TGGCCAGGGC ACACCTCACC 360 ATCAGATAAC GAACAGGTTG GATATGAGTG GTCGCCAACT AAATGTTCAC GAATGGATGT 420 TGTGTTTTGC CATCACTGCC TGGAGGGGGC AGGGTAATCA GAGTCCAACA CTAGCGTGTT 480 CATGTATTGA GTGCAAGGGA GCAGAATTGG CTTGTCTTCA AAACATCTTA ATTTTTATTG 540 CTTCTACTTT GTGGAATGTT ACTTCCTATT TGTAGAACGA GAAGAATTAA AAGTTGATTT 600 GTGAGCTAAA AATACGGGCA GCCGTTTCTT CTTCATCAAA GCCCACAAAT AGACCTGAAC 660 ATTTAGACAT AAAAGTAAAC CGTTAGAAAT AGTGTGCATG TCATTAGGAT CTGTTGATTG 720 GATTAAAATG ACAGACTCGT TTCTTGGCTT CCTGCAGCTC TCGTCATTGC CCACCATCTA 780 TTTTTAGCAG ATCTTGCCCT GCTGACTCAG AGTGGGAACA GTTGCTGAGC CCTGGGCTTC 840 TCAATGCCAT AGGCTGGCAA GTAGCCTGAC TTCTAGGATG GGTAGCACTC TATGCCTGGG 900 CAGCAGGAGA GTCTGTGCCT GTGAGGAGAC CCCTCTGCAG GCAGCCTGGG AGCCCGGCCA 960 CCCCCGCCTG CCCCATTTCT TGTTACCTCA CCCACTGAGA GGAGCCACCT CTGGAGCCCT 1020 GGTTTCCTAG GCCCTTTGAG AAGTGTGCCA GGTGTTGCTG CCTGGAGTGT CATCACTTGA 1080 TGTGACATCT TACTGCATCC CCCGCACCTG TCCTCATCTT AGGTGAAGGC ATCAGGCCAG 1140 GCCCTTAGTG CCTCCTTCCT CTGTTCTGGG CACCCCTAGG GGAGAAGTGT ACATGGGTGG 1200 AGCTTGTCTT CAGGAGACTG TACCTGTTTC TTTAAGGCTG CTGTCCAGGT GGGTCTCTCG 1260 CTGCCAGCTG ATGCACATAG GCAAGACTTG GGTGGAGGGA ACGGCCTTTG AGCTGTGCCC 1320 GAAGAAGGAA GGGTGTGGCA GGTCAGCCCG AGGCAAGGGA GGAGAGTCCT CATCTGCAGG 1380 GCTTGGTGAG GAGCCAGCCA GAGTCCAACC CCTCCCCTTT ATATCACAGA TGCACACTGC 1440 TAGGGGAGTG CTCCTCGTGT TAGAACCTGC AAGAGTTGGA AGGCACTGCT TAGAGGTTGT 1500 CCGCTCCCAC TCAGGAAACT TTGGGGCTCT GGAAATGCCC ATGAGCAACA CAGCTGAGAG 1560 GGTAGGTACT GTATGTGGGA GCCACTTGGA AGCCCCTGCG GCCCTGGGCT CAGCCACTCT 1620 GCACCCTCAT TTTCTCATTT GTTAAATGAA GAGGTGACAG CGGAAGATCT 1670
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