| Tag | Content |
|---|
EnhancerAtlas ID | HS182-22156 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr9:131928920-131930820 |
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: 2 | Chromosome | Start | End |
| chr9 | 131929981 | 131930820 | | chr9 | 131928947 | 131929843 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I129166 | chr9 | 131928464 | 131931823 |
|
Enhancer Sequence | CTACTCGGGA CTCAGGAGGC TCAGGCAGTA GAATTGCTTG AACCTGGGAG GCGGAGGTTT 60
CGGTGAGCTG AGATCCTGGG CAACAAGAGC AAAACTGTGT CTCAAAAAAA AAAAAAAGAA 120
AAAAAAAAGC AGCAGAGCAT GGTTTGTCTT GAGCTCTATG TGGCTTTGGA GGCTGAGCTT 180
GGAACTGCCA GCCTGGGCTT TGGACGGGCA CCCTGGGTAG GGGTGGTCCT GGGTAGAGAT 240
GGCCCTGGGA ATCCCTCCGG TGCTTGGCCT TGTGCCTGGT GGTCCACAGT CTCACAGTCA 300
CTCATCTGAT ATTTAACAAC TTACAATGAG GAGTGCTCCA CAAGGAACCC TCACATAGCT 360
TGGGATGCTC TCCCATGTTC CGTCTTTGCT GAGGGTCCCT TGGATGGGTG TGTTTGTGGG 420
GCATAGTCTC TGGGGGAAGA GGGGCAGATC CTGGATTGGT CTGGAGCCCC AGCTGGCCCC 480
GCACAACTAG GAAAACTGGT TGGGGCGGCT GACTCAGGGT GTGTTTATAC TGGCGTACTC 540
CCCGCCCCCT CCCTCCCTCA GGCACCCTCC CCTCCCGTCC CTGACCCGGG AGAGGAAGGA 600
AGTTCCTATA ACGTTCATAG TTGCCACTAG TTCTGCGTGT TGTGCATTGG GCACGGAGCA 660
GGAAGACCTT CACAGGTTGT AACTGGTCCC AGCTTCCTTT GAGGAGACTG AGTCTCAGAA 720
AAGTCAGGCT GCTCCCTCGA TCCTACAGGG GCAAAGCTGG GATTGGAATC CAGCTCTGAC 780
TGATGCCCCG GATGGAACTC TCATCCACTG TGATTAGAAT ACAATCTGAG CACCTCCTGC 840
TTTTCTTTCT GGCCCCATCT CCTGCCTCTC CCACTTGCCC TCTCTCTCAG CCAGTTCTAT 900
GAACATGCTA AATTTATTCA TTTTCTTTTT TTTCTCTCTC TCTCCTTTCT TTTCTTCTTC 960
TTTTTTTTTT TTTTTTTTTT TTGCCGGAGT TTCGTTCTTC TTGCCCTGGC TAGAGTGCAA 1020
TGGTGTGATC TTGGCTCACT GCAACCTCCG CCTCCCGGGT TCAAGCGATT CTCCTCTGTC 1080
AGTCCCCCAA GTGGCTGGGA TTACAGGTGC ACACACCAGC ATGCCCAGCC AATTTTTGTA 1140
TTTTTAGTAG AGACAGGGTT TCGCCATGCT GGCCAGGCTG GTCTCACCCT GACTTCAGGT 1200
GATCTGCTCG CCTTGGCCTC CCAAAGTGCT GGGATTAAGG CGTGGGCCAC CGCGCCTGGC 1260
CTCATGTGTT TAGTCTTCAC CTTTTCCGTT CCTTCTGCCT GGAATGCTCC TCCACCGTTG 1320
TTTGTCCAGC TGCTATGGTA GAGACTTCTA GCGCTCATCC ATGTGTACTC GCCTTTCCTT 1380
CCCAGTTACC CAAGAAAACT GCTTTTCCCA GCCCCCTTGC AGTTAGATGA GGGCCTGGGA 1440
CTCATTCTGG CCAATGTGCT CTGAGTGTGA GTGAGGAGAA TCACTTCCAG GCTGAGGCCA 1500
TGAAGAGCCC TTGCAGGACT CCCCAGCTCT CATTCTGTGC CACGGTGGAG ATTCTGGAAG 1560
CCTTGTGTTG AGATAGACGC AGGCTGAATT GCTGAGTCAC CGTATGGAGG GCAGCAGCCT 1620
AGGAGACCTG GCAGTCTGAC TCAGACTTTG CATGGTCAAG AAACAAATCC TTTCTACCTG 1680
CTGGAGATCT TAAAAGAGAA AGAAATCCTT GTGTTAAATC TTTGAGATGC AGGGATTAAT 1740
TTGTTACTGC AGCATAGCCT GTCGTATACT AATAGAGCTG ATCTGTTCAG GTGTCAGTTG 1800
AAATATCACC TTCTCTGATC AAAATATCTA AACTGGTGCC ACCCCCACCC CCTCCCCCTC 1860
CAACCAGTCC TTTCTTTTTT TTTGAGACTT TTTTTTTTTG 1900
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