| Tag | Content |
|---|
EnhancerAtlas ID | HS034-31104 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr9:131929050-131931160 |
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 | 131930838 | 131930916 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I129166 | chr9 | 131928464 | 131931823 |
|
Enhancer Sequence | AGCAGAGCAT GGTTTGTCTT GAGCTCTATG TGGCTTTGGA GGCTGAGCTT GGAACTGCCA 60
GCCTGGGCTT TGGACGGGCA CCCTGGGTAG GGGTGGTCCT GGGTAGAGAT GGCCCTGGGA 120
ATCCCTCCGG TGCTTGGCCT TGTGCCTGGT GGTCCACAGT CTCACAGTCA CTCATCTGAT 180
ATTTAACAAC TTACAATGAG GAGTGCTCCA CAAGGAACCC TCACATAGCT TGGGATGCTC 240
TCCCATGTTC CGTCTTTGCT GAGGGTCCCT TGGATGGGTG TGTTTGTGGG GCATAGTCTC 300
TGGGGGAAGA GGGGCAGATC CTGGATTGGT CTGGAGCCCC AGCTGGCCCC GCACAACTAG 360
GAAAACTGGT TGGGGCGGCT GACTCAGGGT GTGTTTATAC TGGCGTACTC CCCGCCCCCT 420
CCCTCCCTCA GGCACCCTCC CCTCCCGTCC CTGACCCGGG AGAGGAAGGA AGTTCCTATA 480
ACGTTCATAG TTGCCACTAG TTCTGCGTGT TGTGCATTGG GCACGGAGCA GGAAGACCTT 540
CACAGGTTGT AACTGGTCCC AGCTTCCTTT GAGGAGACTG AGTCTCAGAA AAGTCAGGCT 600
GCTCCCTCGA TCCTACAGGG GCAAAGCTGG GATTGGAATC CAGCTCTGAC TGATGCCCCG 660
GATGGAACTC TCATCCACTG TGATTAGAAT ACAATCTGAG CACCTCCTGC TTTTCTTTCT 720
GGCCCCATCT CCTGCCTCTC CCACTTGCCC TCTCTCTCAG CCAGTTCTAT GAACATGCTA 780
AATTTATTCA TTTTCTTTTT TTTCTCTCTC TCTCCTTTCT TTTCTTCTTC TTTTTTTTTT 840
TTTTTTTTTT TTGCCGGAGT TTCGTTCTTC TTGCCCTGGC TAGAGTGCAA TGGTGTGATC 900
TTGGCTCACT GCAACCTCCG CCTCCCGGGT TCAAGCGATT CTCCTCTGTC AGTCCCCCAA 960
GTGGCTGGGA TTACAGGTGC ACACACCAGC ATGCCCAGCC AATTTTTGTA TTTTTAGTAG 1020
AGACAGGGTT TCGCCATGCT GGCCAGGCTG GTCTCACCCT GACTTCAGGT GATCTGCTCG 1080
CCTTGGCCTC CCAAAGTGCT GGGATTAAGG CGTGGGCCAC CGCGCCTGGC CTCATGTGTT 1140
TAGTCTTCAC CTTTTCCGTT CCTTCTGCCT GGAATGCTCC TCCACCGTTG TTTGTCCAGC 1200
TGCTATGGTA GAGACTTCTA GCGCTCATCC ATGTGTACTC GCCTTTCCTT CCCAGTTACC 1260
CAAGAAAACT GCTTTTCCCA GCCCCCTTGC AGTTAGATGA GGGCCTGGGA CTCATTCTGG 1320
CCAATGTGCT CTGAGTGTGA GTGAGGAGAA TCACTTCCAG GCTGAGGCCA TGAAGAGCCC 1380
TTGCAGGACT CCCCAGCTCT CATTCTGTGC CACGGTGGAG ATTCTGGAAG CCTTGTGTTG 1440
AGATAGACGC AGGCTGAATT GCTGAGTCAC CGTATGGAGG GCAGCAGCCT AGGAGACCTG 1500
GCAGTCTGAC TCAGACTTTG CATGGTCAAG AAACAAATCC TTTCTACCTG CTGGAGATCT 1560
TAAAAGAGAA AGAAATCCTT GTGTTAAATC TTTGAGATGC AGGGATTAAT TTGTTACTGC 1620
AGCATAGCCT GTCGTATACT AATAGAGCTG ATCTGTTCAG GTGTCAGTTG AAATATCACC 1680
TTCTCTGATC AAAATATCTA AACTGGTGCC ACCCCCACCC CCTCCCCCTC CAACCAGTCC 1740
TTTCTTTTTT TTTGAGACTT TTTTTTTTTG AGTCTCGTTC TGTCATCCAG GCTGGGGTGC 1800
AATGGTGCTG TGATCTTGGC TCACTCCAGC AGCTGCTTCC TAGGTGCAAG TGATTCTCCT 1860
GTCTCACTTT CCGAGTAGCT GGGATTACAG GCACGCGCCT CCACGCTAGG CTAATTTTTG 1920
TATGTTTGGT AGAGACGGGG TTTCACCATG TTGGCCAGGC CGGTCTTAAA CTCCTGGCCT 1980
CAACTGATCA GCTCACCTCG GCCTCCCAAA GTGCTGGGAT TACAGGCATG AGCCACGGGC 2040
CCTTACCAAT TTTTCTAGCA CTGTGTTTAT TTTCCTGAAA CACTTATCTA CTTGTTTGTT 2100
GCCTTGTGTA 2110
|
