| Tag | Content |
|---|
EnhancerAtlas ID | HS047-14655 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr17:43369810-43372210 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
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 |
|
| | 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 |
|
| | 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 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I045290 | chr17 | 43368028 | 43375075 |
|
Enhancer Sequence | CAGCTACTCT AGAGGCTGCG GTGGGAGGAA TGCTTGAGCC CAGGAGGTTG AGGCTGCAGT 60
GAGCTGAGAT TGCACCATTG CATTCTCCAG CCTGAGTGAC AGAATAAGAC CCTGTCTCTA 120
AAAGAAAAAA AAAGTCTAAG GGGTGTTCTG ACATCCAATT AGGCAAAAGC CCTTCAAGGC 180
TGGCTATGCT TCTTGTAACT GTACTTTCAT CCCACCTCAC ACCTCCCCAC CCCACTCTAC 240
CTCCAAAAAA GAAACTGACC TAAGCCCAGA GCCGATCCCA CTGTTCTCAG CCTCTTTACC 300
AGGGGAAATG AGATCTTAAG AACAGACCAA AAAGTCTCCA AACCTAACAG CAGTAGGGAA 360
TGCTCACAGG GAGCTCGATG TGAGCGTGAC CTCCTCATTT CTATTTGAAG AAGCTGAGGC 420
CTAATTCAGT GGAGACTTGC CCAAGGTCAC CCAACCCACG TGTGACAGGA CATGGCCAGG 480
ATCCAGACCC TAGGTTCTTT AGGCTATGAT GCCCACTCCC CAAGCTCCTG GGTTACAGGC 540
AAATGCAGGA GGGCACACTA AGGTCCTCCC TGGTCAACAG GCTCCTGAGG GAAGAGGTGG 600
GGCCCTGCAC ACAGTGCCTC CCCAGTGTAT AGCACAGGGG CCACAGACCA CGCAACTGAC 660
GCTGGCTGAA CGAGGGACTC AAAGGACAAA GATTGCTTTT CCATAACCTT TGGAGACAGG 720
ATGATCCCGA ATGCTGAGGA GGAAGAGAGA GTCCTGCCTG ATGAATGAGA AAAATGAGGC 780
CAGGTGGTGC AGTTGCTGCT CTGAGGGGCA CGTGGCTATT AGAGATCTGG CTGTGTGGGG 840
GCTCTGATAG CCTGTCTCCG CCTGGCATGG CCCAACGGAG GCTTCTGGAT AGGTCATCCT 900
GAGCTAGAAC TCCTCCAGAG GGGGTGCAGG GCATCCCGAG TCCCAGAGTT GTCCTTTCAT 960
ATTGGTGTTA GGTAGGCAGC TGTCCAGCGC CCCTCTGTGA GCACACCAGG CTCCCCTCTT 1020
CCCAGAGAAG TGGAAGCTGA GGCTGAGGCA GCCACGCTCA GAGACTCCTT TGCAGTTCCC 1080
CGATGACTCA TCCAACAGCC TGGCAGGCAG ACAGTAACAA GGAGGCTGTT GAGAAGCTGA 1140
CCCAGCAGAT GGCAGCTGAA CTTGTGAAGG ACATGGGGAA AACAGGCTGA CCCTCACCTC 1200
TCAGGGGCAC AAATCACGGC CTGGGAGCTG TAAAGCTCCT CCTGTGGCTG GCTTTTCTGT 1260
GCCACATCAC CATGACTCAG ACCCTCACCG ACAGCCTCCA AGTTCAAGAG GCTATTCTTG 1320
GGACACTTTG GCCTGACAGT GGCTCTCCCC AAACACCACC TCCCACACAG ACACACATGC 1380
ACACACACAC ATGCACACAC AGACACACAC ACATACGGAT GCACTTGCTC CCTCCCTCCT 1440
TTCCTAATTC TATCTGGACT CTGGTCTACA AAAATCATGG TTCTGTACTA AGTCCAGGAC 1500
TACTGGCCAG GGGGCCTTCC CAGCCCTGGA CTTTGGTCTC TGGCTGTCAC CCCAGCTCAT 1560
GGCCCTAACA CTTTGCCCCT TCTCCCTCCT GCAGCGTGTG GGGAGGACGA AGTGGGAGCC 1620
AGTTATGTCT CTGCCTTTGA AGGCAAGTCA AACTCCTGAT TCATTCCTCA GCCTAGACAC 1680
TCTCCTCAGC TTATTCACGC CCCAAAGGCA TTGGGCCCTC TACTCTCTGC ATAAGAGTTG 1740
AGGACACGAG CAGTGGCAAC AGCCAAACCC ACATGGCTCA CCCATAAGCC CAAGAAATCA 1800
GAAGAGGAAA GGAAAGGAGC AGAATTCACT CCATATTCTT TGAGGCCTGA TGCACAGACA 1860
CTGTTGGTTC TTTCTTCTGT GATGCCTCAG TGACCTCCTG GAGAAGCCTG GGGGATAGGA 1920
ATGATCTGGA CAGTACCAGA TCAACCTCTG GGCATAGCTG TATGAGGAGT TCTTAATCTA 1980
GGTTCAAGGA TGGATTCAGG GAGAAAAATG TAATTTGCAT TTTTCCAGGG AAGACTTGGT 2040
CCATAGCTTT CAACAGATTC TCCAAGGATC TGCCATTCCC CAGAAGGTTC CTCTAGTCTC 2100
CCTAGAAAAT CAGGGCCGGG CTAAATGCCT GATTCTGGCT CTATTCTTCC ACTCCGAGGA 2160
AAAGCTCTCC AATGCAGCAG TTTCCAATCT GACCACAGAT TAGAATAACC AGATAAGTTC 2220
TTTAAATGCA TTCCTCCTAG GCCTGCTGAA CCAGTCACTG GGCATTAGGC CCAGAATCTG 2280
TACTTTTGAC AAGTTCTCTG GATGATTCTG ATGCCAAAGG GCCAGAGACT GCCACCTGAC 2340
CCCTGCTCTG TACTCAAGGC GACACTGTCC AAAATGGTAG CCACTAGCAA CATGTGGCTA 2400
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