Tag | Content |
---|
EnhancerAtlas ID | HS098-53334 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr7:130692120-130693180 |
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 |
|
| 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 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH07I131006 | chr7 | 130691491 | 130698830 |
|
Enhancer Sequence | TAAAAATGTA AAGGCAAACT TAACTGTTAC AATAACATAT CAGCTCTGAG TCTAAAGGAA 60 AACGGGTGTT TGTCTAAGAA ATGTGCTAGA GAGAACCAGC CAGTTTTAAT GTGCCTTAAG 120 CAATGAAAAC CTGTTTCCTC CTTTCCTTCT TGTCCTTTTG AAAAGACAAC ATGTCACAGG 180 GAGACGTTTT TCTAACAGCA TCCATCCTGG TGACAAATGT TTGCCAAGGG TGGGGAGAGA 240 GGAGGGAGGA AAGAAAGAAA AAGAGAAGGA AGACGCCATC TGCTGACGAA AGAGAAAAGA 300 AGAGGAGGAG GAATTGGAAG GCGCCACTTC CGGGTCCGTG TCTGAGAAAT ACAACGTATC 360 ACCATAAGGC AGACTTCTAC TCAATATAAG GAAGAACTTT ATAATAATTG GAGGAATTCA 420 AAGGCAGAAT TGATCAGGGA CCAAAGTTCA AGCAGGGGGT GGCGAGGTCT CCTCAGGCAG 480 AATAATCTTT CGTAAGCTTC TCCCTCTTGA AGGAAGAACG GCCCCAGTTC AAGTAGAAGA 540 AAATACTGTG CTTATTATTT TTCTCTAATT CTTAAATGTT TCAAATAGTC TCTATCTTGA 600 TAATTCACGA TTCAAAGGAC TGAGACTGAA ACATCAAATA AGCAAGCACA CAAATTTGCC 660 TGACACCACC TGCCCCCACC CCTAGTCCCT GGGCCTTATT TCTGGGCTTG CTGCTGGGCT 720 CTCCACGGGC AGCTGGCTGC CATCGCTCCG CTGGAGGGCG GTACCATGAG CACGGATGGG 780 GCCCACATGG CAGGCAAAGC ACTGGAAATT GATGCCGCAC CCCGCTGCTG CCTCTCAGTC 840 AGCAACTGGC CAAAGCTGAT GTGTAAGTGA CCCATGTGGG CTAACACTGA GGCCTGGTCC 900 TTACACTGGC TCCCAGAGTG TCCAGCAAAG TTAGGCTCCA ATTGTTTCCC TATCTCGCTT 960 CCCTTAAAAT GTTTCTTTCA CCTTCCAAAC AGATAACATA CATCTCTGTC TCAGCGGAAC 1020 TCAATCCAAG AAAACACCTC ACACCATGAT GATATAAAGA 1060
|