| Tag | Content |
|---|
EnhancerAtlas ID | HS195-07385 |
Organism | Homo sapiens |
Tissue/cell | VCaP |
Coordinate | chr9:131928970-131930860 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MAFK | MA0496.2 | chr9:131930506-131930525 | AATTGCTGAGTCACCGTAT | + | 6.06 | | NFE2L1 | MA0089.2 | chr9:131930507-131930522 | ATTGCTGAGTCACCG | - | 6.97 | | Nfe2l2 | MA0150.2 | chr9:131930509-131930524 | TGCTGAGTCACCGTA | - | 6.68 | | ZNF263 | MA0528.1 | chr9:131930757-131930778 | GCCACCCCCACCCCCTCCCCC | - | 6 |
|
| | Number of super-enhancer constituents: 24 | ID | Coordinate | Tissue/cell |
| SE_01377 | chr9:131928873-131930959 | Adrenal_Gland | | SE_26914 | chr9:131928223-131931145 | Esophagus | | SE_27869 | chr9:131928909-131930745 | Fetal_Intestine | | SE_28773 | chr9:131928727-131930857 | Fetal_Intestine_Large | | SE_30321 | chr9:131928839-131930038 | Fetal_Muscle | | SE_31776 | chr9:131928375-131931171 | Gastric | | SE_34379 | chr9:131928204-131931924 | HCT-116 | | SE_35053 | chr9:131928605-131931608 | HeLa | | SE_42081 | chr9:131928958-131929830 | LNCaP | | SE_42081 | chr9:131929901-131930683 | LNCaP | | SE_43197 | chr9:131928798-131930727 | Lung | | SE_46983 | chr9:131928949-131929438 | Ovary | | SE_46983 | chr9:131929455-131929836 | Ovary | | SE_46983 | chr9:131930089-131930539 | Ovary | | SE_47992 | chr9:131928939-131929430 | Pancreas | | SE_47992 | chr9:131929486-131929890 | Pancreas | | SE_47992 | chr9:131929957-131930610 | Pancreas | | SE_50677 | chr9:131928813-131930770 | Sigmoid_Colon | | SE_53874 | chr9:131928804-131930748 | Spleen | | SE_56721 | chr9:131928843-131931262 | u87 | | SE_57142 | chr9:131929046-131929865 | VACO_400 | | SE_57142 | chr9:131929927-131930596 | VACO_400 | | SE_57775 | chr9:131928926-131929839 | VACO_503 | | SE_57775 | chr9:131930005-131930538 | VACO_503 |
|
| | 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 |
| GH09I129166 | chr9 | 131928464 | 131931823 |
|
Enhancer Sequence | GCGGAGGTTT CGGTGAGCTG AGATCCTGGG CAACAAGAGC AAAACTGTGT CTCAAAAAAA 60
AAAAAAAGAA AAAAAAAAGC AGCAGAGCAT GGTTTGTCTT GAGCTCTATG TGGCTTTGGA 120
GGCTGAGCTT GGAACTGCCA GCCTGGGCTT TGGACGGGCA CCCTGGGTAG GGGTGGTCCT 180
GGGTAGAGAT GGCCCTGGGA ATCCCTCCGG TGCTTGGCCT TGTGCCTGGT GGTCCACAGT 240
CTCACAGTCA CTCATCTGAT ATTTAACAAC TTACAATGAG GAGTGCTCCA CAAGGAACCC 300
TCACATAGCT TGGGATGCTC TCCCATGTTC CGTCTTTGCT GAGGGTCCCT TGGATGGGTG 360
TGTTTGTGGG GCATAGTCTC TGGGGGAAGA GGGGCAGATC CTGGATTGGT CTGGAGCCCC 420
AGCTGGCCCC GCACAACTAG GAAAACTGGT TGGGGCGGCT GACTCAGGGT GTGTTTATAC 480
TGGCGTACTC CCCGCCCCCT CCCTCCCTCA GGCACCCTCC CCTCCCGTCC CTGACCCGGG 540
AGAGGAAGGA AGTTCCTATA ACGTTCATAG TTGCCACTAG TTCTGCGTGT TGTGCATTGG 600
GCACGGAGCA GGAAGACCTT CACAGGTTGT AACTGGTCCC AGCTTCCTTT GAGGAGACTG 660
AGTCTCAGAA AAGTCAGGCT GCTCCCTCGA TCCTACAGGG GCAAAGCTGG GATTGGAATC 720
CAGCTCTGAC TGATGCCCCG GATGGAACTC TCATCCACTG TGATTAGAAT ACAATCTGAG 780
CACCTCCTGC TTTTCTTTCT GGCCCCATCT CCTGCCTCTC CCACTTGCCC TCTCTCTCAG 840
CCAGTTCTAT GAACATGCTA AATTTATTCA TTTTCTTTTT TTTCTCTCTC TCTCCTTTCT 900
TTTCTTCTTC TTTTTTTTTT TTTTTTTTTT TTGCCGGAGT TTCGTTCTTC TTGCCCTGGC 960
TAGAGTGCAA TGGTGTGATC TTGGCTCACT GCAACCTCCG CCTCCCGGGT TCAAGCGATT 1020
CTCCTCTGTC AGTCCCCCAA GTGGCTGGGA TTACAGGTGC ACACACCAGC ATGCCCAGCC 1080
AATTTTTGTA TTTTTAGTAG AGACAGGGTT TCGCCATGCT GGCCAGGCTG GTCTCACCCT 1140
GACTTCAGGT GATCTGCTCG CCTTGGCCTC CCAAAGTGCT GGGATTAAGG CGTGGGCCAC 1200
CGCGCCTGGC CTCATGTGTT TAGTCTTCAC CTTTTCCGTT CCTTCTGCCT GGAATGCTCC 1260
TCCACCGTTG TTTGTCCAGC TGCTATGGTA GAGACTTCTA GCGCTCATCC ATGTGTACTC 1320
GCCTTTCCTT CCCAGTTACC CAAGAAAACT GCTTTTCCCA GCCCCCTTGC AGTTAGATGA 1380
GGGCCTGGGA CTCATTCTGG CCAATGTGCT CTGAGTGTGA GTGAGGAGAA TCACTTCCAG 1440
GCTGAGGCCA TGAAGAGCCC TTGCAGGACT CCCCAGCTCT CATTCTGTGC CACGGTGGAG 1500
ATTCTGGAAG CCTTGTGTTG AGATAGACGC AGGCTGAATT GCTGAGTCAC CGTATGGAGG 1560
GCAGCAGCCT AGGAGACCTG GCAGTCTGAC TCAGACTTTG CATGGTCAAG AAACAAATCC 1620
TTTCTACCTG CTGGAGATCT TAAAAGAGAA AGAAATCCTT GTGTTAAATC TTTGAGATGC 1680
AGGGATTAAT TTGTTACTGC AGCATAGCCT GTCGTATACT AATAGAGCTG ATCTGTTCAG 1740
GTGTCAGTTG AAATATCACC TTCTCTGATC AAAATATCTA AACTGGTGCC ACCCCCACCC 1800
CCTCCCCCTC CAACCAGTCC TTTCTTTTTT TTTGAGACTT TTTTTTTTTG AGTCTCGTTC 1860
TGTCATCCAG GCTGGGGTGC AATGGTGCTG 1890
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