Tag | Content |
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EnhancerAtlas ID | HS155-06082 |
Organism | Homo sapiens |
Tissue/cell | Ovary |
Coordinate | chr17:43370010-43371760 |
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) |
HNF4G | MA0484.1 | chr17:43371336-43371351 | TGGACTTTGGTCTCT | - | 7.31 | MYC | MA0147.3 | chr17:43370615-43370627 | GGGCACGTGGCT | - | 6.18 | PAX5 | MA0014.3 | chr17:43370191-43370203 | GAGCGTGACCTC | + | 6.14 | RREB1 | MA0073.1 | chr17:43371155-43371175 | TCCCCAAACACCACCTCCCA | + | 6.67 |
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| Number of super-enhancer constituents: 29 | ID | Coordinate | Tissue/cell |
SE_01249 | chr17:43369797-43372371 | Adrenal_Gland | SE_04602 | chr17:43367359-43372240 | Brain_Anterior_Caudate | SE_11470 | chr17:43364690-43370274 | CD20 | SE_11470 | chr17:43370585-43396257 | CD20 | SE_15206 | chr17:43369767-43372845 | CD4_Memory_Primary_7pool | SE_18500 | chr17:43366366-43375242 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19630 | chr17:43370599-43371979 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_23493 | chr17:43370233-43371784 | Colon_Crypt_1 | SE_24167 | chr17:43370547-43371576 | Colon_Crypt_2 | SE_25878 | chr17:43364447-43377187 | Duodenum_Smooth_Muscle | SE_26725 | chr17:43369959-43372440 | Esophagus | SE_30018 | chr17:43370009-43372329 | Fetal_Muscle | SE_31611 | chr17:43370038-43372444 | Gastric | SE_32589 | chr17:43370933-43372485 | GM12878 | SE_34075 | chr17:43370326-43375105 | HCC1954 | SE_40748 | chr17:43363700-43375200 | Left_Ventricle | SE_41691 | chr17:43369983-43371993 | LNCaP | SE_44657 | chr17:43370169-43372693 | NHDF-Ad | SE_46201 | chr17:43369956-43372823 | Osteoblasts | SE_47195 | chr17:43366097-43378703 | Panc1 | SE_48714 | chr17:43365874-43374860 | Right_Atrium | SE_49545 | chr17:43369873-43372224 | Right_Ventricle | SE_50169 | chr17:43369845-43372240 | Sigmoid_Colon | SE_51970 | chr17:43369906-43372027 | Skeletal_Muscle_Myoblast | SE_54723 | chr17:43359357-43378642 | Stomach_Smooth_Muscle | SE_59053 | chr17:43370566-43412054 | Ly3 | SE_62481 | chr17:43366079-43396493 | Tonsil | SE_63770 | chr17:43369873-43372185 | HSMM | SE_65719 | chr17:43369005-43372029 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr17 | 43370974 | 43371161 | chr17 | 43370147 | 43370559 |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I045290 | chr17 | 43368028 | 43375075 |
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Enhancer Sequence | GTACTTTCAT CCCACCTCAC ACCTCCCCAC CCCACTCTAC CTCCAAAAAA GAAACTGACC 60 TAAGCCCAGA GCCGATCCCA CTGTTCTCAG CCTCTTTACC AGGGGAAATG AGATCTTAAG 120 AACAGACCAA AAAGTCTCCA AACCTAACAG CAGTAGGGAA TGCTCACAGG GAGCTCGATG 180 TGAGCGTGAC CTCCTCATTT CTATTTGAAG AAGCTGAGGC CTAATTCAGT GGAGACTTGC 240 CCAAGGTCAC CCAACCCACG TGTGACAGGA CATGGCCAGG ATCCAGACCC TAGGTTCTTT 300 AGGCTATGAT GCCCACTCCC CAAGCTCCTG GGTTACAGGC AAATGCAGGA GGGCACACTA 360 AGGTCCTCCC TGGTCAACAG GCTCCTGAGG GAAGAGGTGG GGCCCTGCAC ACAGTGCCTC 420 CCCAGTGTAT AGCACAGGGG CCACAGACCA CGCAACTGAC GCTGGCTGAA CGAGGGACTC 480 AAAGGACAAA GATTGCTTTT CCATAACCTT TGGAGACAGG ATGATCCCGA ATGCTGAGGA 540 GGAAGAGAGA GTCCTGCCTG ATGAATGAGA AAAATGAGGC CAGGTGGTGC AGTTGCTGCT 600 CTGAGGGGCA CGTGGCTATT AGAGATCTGG CTGTGTGGGG GCTCTGATAG CCTGTCTCCG 660 CCTGGCATGG CCCAACGGAG GCTTCTGGAT AGGTCATCCT GAGCTAGAAC TCCTCCAGAG 720 GGGGTGCAGG GCATCCCGAG TCCCAGAGTT GTCCTTTCAT ATTGGTGTTA GGTAGGCAGC 780 TGTCCAGCGC CCCTCTGTGA GCACACCAGG CTCCCCTCTT CCCAGAGAAG TGGAAGCTGA 840 GGCTGAGGCA GCCACGCTCA GAGACTCCTT TGCAGTTCCC CGATGACTCA TCCAACAGCC 900 TGGCAGGCAG ACAGTAACAA GGAGGCTGTT GAGAAGCTGA CCCAGCAGAT GGCAGCTGAA 960 CTTGTGAAGG ACATGGGGAA AACAGGCTGA CCCTCACCTC TCAGGGGCAC AAATCACGGC 1020 CTGGGAGCTG TAAAGCTCCT CCTGTGGCTG GCTTTTCTGT GCCACATCAC CATGACTCAG 1080 ACCCTCACCG ACAGCCTCCA AGTTCAAGAG GCTATTCTTG GGACACTTTG GCCTGACAGT 1140 GGCTCTCCCC AAACACCACC TCCCACACAG ACACACATGC ACACACACAC ATGCACACAC 1200 AGACACACAC ACATACGGAT GCACTTGCTC CCTCCCTCCT TTCCTAATTC TATCTGGACT 1260 CTGGTCTACA AAAATCATGG TTCTGTACTA AGTCCAGGAC TACTGGCCAG GGGGCCTTCC 1320 CAGCCCTGGA CTTTGGTCTC TGGCTGTCAC CCCAGCTCAT GGCCCTAACA CTTTGCCCCT 1380 TCTCCCTCCT GCAGCGTGTG GGGAGGACGA AGTGGGAGCC AGTTATGTCT CTGCCTTTGA 1440 AGGCAAGTCA AACTCCTGAT TCATTCCTCA GCCTAGACAC TCTCCTCAGC TTATTCACGC 1500 CCCAAAGGCA TTGGGCCCTC TACTCTCTGC ATAAGAGTTG AGGACACGAG CAGTGGCAAC 1560 AGCCAAACCC ACATGGCTCA CCCATAAGCC CAAGAAATCA GAAGAGGAAA GGAAAGGAGC 1620 AGAATTCACT CCATATTCTT TGAGGCCTGA TGCACAGACA CTGTTGGTTC TTTCTTCTGT 1680 GATGCCTCAG TGACCTCCTG GAGAAGCCTG GGGGATAGGA ATGATCTGGA CAGTACCAGA 1740 TCAACCTCTG 1750
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