Tag | Content |
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EnhancerAtlas ID | HS051-25507 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr7:130692100-130693080 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EHF | MA0598.2 | chr7:130692444-130692456 | CACTTCCGGGTC | - | 6.07 | ELF1 | MA0473.2 | chr7:130692444-130692456 | CACTTCCGGGTC | - | 6.44 | ELF3 | MA0640.1 | chr7:130692443-130692456 | CCACTTCCGGGTC | - | 6.12 | ELF4 | MA0641.1 | chr7:130692444-130692456 | CACTTCCGGGTC | - | 6.52 | ELF5 | MA0136.2 | chr7:130692444-130692455 | CACTTCCGGGT | - | 6.32 | Gabpa | MA0062.2 | chr7:130692442-130692453 | GCCACTTCCGG | - | 6.62 | HNF4G | MA0484.1 | chr7:130692555-130692570 | AGGGACCAAAGTTCA | + | 6.78 | ZBTB7A | MA0750.2 | chr7:130692442-130692455 | GCCACTTCCGGGT | - | 7.52 | ZNF263 | MA0528.1 | chr7:130692361-130692382 | GAGGGAGGAAAGAAAGAAAAA | + | 6.05 | ZNF263 | MA0528.1 | chr7:130692420-130692441 | AGAGGAGGAGGAATTGGAAGG | + | 6.21 | ZNF263 | MA0528.1 | chr7:130692357-130692378 | AGAGGAGGGAGGAAAGAAAGA | + | 7.23 |
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| Number of super-enhancer constituents: 19 | ID | Coordinate | Tissue/cell |
SE_00305 | chr7:130691512-130699299 | Adipose_Nuclei | SE_04014 | chr7:130691838-130693316 | Brain_Anterior_Caudate | SE_08450 | chr7:130691663-130693636 | Brain_Inferior_Temporal_Lobe | SE_10895 | chr7:130691162-130702108 | CD20 | SE_12190 | chr7:130691865-130693199 | CD3 | SE_14401 | chr7:130691962-130693338 | CD4_Memory_Primary_7pool | SE_17149 | chr7:130691873-130694714 | CD4p_CD225int_CD127p_Tmem | SE_18091 | chr7:130691365-130698597 | CD4p_CD25-_CD45ROp_Memory | SE_18806 | chr7:130690797-130702081 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19100 | chr7:130691585-130699006 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_22355 | chr7:130691842-130694348 | CD8_primiary | SE_25633 | chr7:130691882-130693298 | DND41 | SE_25777 | chr7:130691568-130698289 | Duodenum_Smooth_Muscle | SE_32450 | chr7:130692075-130693187 | Gastric | SE_34275 | chr7:130690958-130702225 | HCT-116 | SE_36057 | chr7:130691913-130693168 | HMEC | SE_59181 | chr7:130691702-130725831 | Ly3 | SE_64469 | chr7:130691957-130694670 | NHEK | SE_68199 | chr7:130691685-130725839 | TC32 |
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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 |
GH07I131006 | chr7 | 130691491 | 130698830 |
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Enhancer Sequence | TACCTGCAAG GCAGCATGAA TAAAAATGTA AAGGCAAACT TAACTGTTAC AATAACATAT 60 CAGCTCTGAG TCTAAAGGAA AACGGGTGTT TGTCTAAGAA ATGTGCTAGA GAGAACCAGC 120 CAGTTTTAAT GTGCCTTAAG CAATGAAAAC CTGTTTCCTC CTTTCCTTCT TGTCCTTTTG 180 AAAAGACAAC ATGTCACAGG GAGACGTTTT TCTAACAGCA TCCATCCTGG TGACAAATGT 240 TTGCCAAGGG TGGGGAGAGA GGAGGGAGGA AAGAAAGAAA AAGAGAAGGA AGACGCCATC 300 TGCTGACGAA AGAGAAAAGA AGAGGAGGAG GAATTGGAAG GCGCCACTTC CGGGTCCGTG 360 TCTGAGAAAT ACAACGTATC ACCATAAGGC AGACTTCTAC TCAATATAAG GAAGAACTTT 420 ATAATAATTG GAGGAATTCA AAGGCAGAAT TGATCAGGGA CCAAAGTTCA AGCAGGGGGT 480 GGCGAGGTCT CCTCAGGCAG AATAATCTTT CGTAAGCTTC TCCCTCTTGA AGGAAGAACG 540 GCCCCAGTTC AAGTAGAAGA AAATACTGTG CTTATTATTT TTCTCTAATT CTTAAATGTT 600 TCAAATAGTC TCTATCTTGA TAATTCACGA TTCAAAGGAC TGAGACTGAA ACATCAAATA 660 AGCAAGCACA CAAATTTGCC TGACACCACC TGCCCCCACC CCTAGTCCCT GGGCCTTATT 720 TCTGGGCTTG CTGCTGGGCT CTCCACGGGC AGCTGGCTGC CATCGCTCCG CTGGAGGGCG 780 GTACCATGAG CACGGATGGG GCCCACATGG CAGGCAAAGC ACTGGAAATT GATGCCGCAC 840 CCCGCTGCTG CCTCTCAGTC AGCAACTGGC CAAAGCTGAT GTGTAAGTGA CCCATGTGGG 900 CTAACACTGA GGCCTGGTCC TTACACTGGC TCCCAGAGTG TCCAGCAAAG TTAGGCTCCA 960 ATTGTTTCCC TATCTCGCTT 980
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