Tag | Content |
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EnhancerAtlas ID | HS076-57018 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr9:130843960-130845110 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXP1 | MA0481.2 | chr9:130844399-130844411 | GAGTAAACAGAA | + | 6.27 | NFE2L1 | MA0089.2 | chr9:130844640-130844655 | GTTGCTGAGTCACAT | - | 6.11 | NFYB | MA0502.1 | chr9:130844743-130844758 | CTGATTGGTTCATTC | - | 8.03 | RARA | MA0729.1 | chr9:130844358-130844376 | CCTTGAACTTGGGACCTC | - | 6.1 |
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| Number of super-enhancer constituents: 25 | ID | Coordinate | Tissue/cell |
SE_00502 | chr9:130842515-130845246 | Adipose_Nuclei | SE_01177 | chr9:130843251-130844078 | Adrenal_Gland | SE_02461 | chr9:130842784-130844254 | Astrocytes | SE_08626 | chr9:130842888-130844953 | Brain_Inferior_Temporal_Lobe | SE_13739 | chr9:130842723-130845240 | CD34_Primary_RO01536 | SE_20918 | chr9:130842521-130845206 | CD8_Memory_7pool | SE_25948 | chr9:130842821-130844886 | Duodenum_Smooth_Muscle | SE_26752 | chr9:130842612-130845490 | Esophagus | SE_27710 | chr9:130842720-130845037 | Fetal_Intestine | SE_28658 | chr9:130839467-130845132 | Fetal_Intestine_Large | SE_29715 | chr9:130842656-130845066 | Fetal_Muscle | SE_31462 | chr9:130843236-130844266 | Gastric | SE_31462 | chr9:130844545-130845011 | Gastric | SE_37200 | chr9:130842417-130845267 | HSMMtube | SE_42378 | chr9:130843058-130844267 | Lung | SE_42378 | chr9:130844524-130845076 | Lung | SE_44311 | chr9:130842647-130845056 | NHDF-Ad | SE_44961 | chr9:130842653-130844806 | NHLF | SE_46195 | chr9:130842646-130845010 | Osteoblasts | SE_46747 | chr9:130844461-130844863 | Ovary | SE_51250 | chr9:130842845-130844981 | Skeletal_Muscle | SE_52155 | chr9:130842863-130844196 | Skeletal_Muscle_Myoblast | SE_53470 | chr9:130843353-130844334 | Spleen | SE_55063 | chr9:130842491-130845159 | Stomach_Smooth_Muscle | SE_62896 | chr9:130823046-130858157 | Tonsil |
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| 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 |
GH09I128077 | chr9 | 130839773 | 130845323 |
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Enhancer Sequence | ACTTTGGGAG GCTGAGGTGG GAGGATTGCT TGAGGCCAGG AGTTCGAGAC CAGTCTGGGC 60 AACATAGGGA GACCCAATCT CTACAAAAAA TTTTAAAAAA TTAGCCAGGC ATGCCTGTGG 120 TCCCAGCTAC TTGGGAGGTT GAGGTGGGAA GATCCCTTGA GCCTGGGAGG TTGAGGCTGC 180 AGTGAGCCAT GATCATACCT GCACTCCAGT CTGGGCAGCA GAGCCAGACC CTGTCTCAAA 240 AAAAATAAAG TAGAAATCCC ATATTTCCAA GCAGACCCTT GCTTCTGTAG AACTTGACTT 300 GTTACATCTT AAAATCCTAC ACTTAAGAGT TGGGTAAATT TTGTATGCCT CTAACTTTCT 360 TGTAGAGAAA AGAAAAAGAC ATCTTTAATA TGCATTCACC TTGAACTTGG GACCTCGAAG 420 GGGACTGGCT TTTCACCAGG AGTAAACAGA AGCCATCCAC AAGACTGAGG GTTTTCATGC 480 CGGACTTCTC TTTTCCTTCC ACAGTTACAG GAGTTTTCTT TAGGGAGTTT TTGTCAAAGC 540 TAGATTTTCC GGTTCTGTTT CCTAAAATGG AAATAGATCA TGGATTTCCT TTTTTCATTA 600 TTGCAGTTCT GTCATCTGCC ATACCTTAGT TTCATTTGTG CCAAATGAGG TGAGTTGTGG 660 CTCCTCTTCA TTGTCCAATT GTTGCTGAGT CACATCAGGT GGGCGTTTAA GAGTCCTGCC 720 TTACAGCCTG AAACTCCAGC CGCCCAGCGC AGGCAGCACA TAGGAGCTGA GTTTTTCCGT 780 TGGCTGATTG GTTCATTCCA GCGGAGACTG ACATTCACCT GCTACAGTCC TGCCTCTGGA 840 ATAGCCTGGC ACTGCCATAT ATCAGTATAT AAAAGAGAGT CTTCAAACTC TTGACTCCTG 900 TACCACCCAA AAATAATTTT GAAAACAGCA TATCCCCTTG CACATTTTGT ACATCTGCTT 960 TATTATTTTT ATTTTATTTT ATTTTAAGAC AGTCTCGCTC TTTGCCCAGG CTAGAGTGCA 1020 GTGGCGCAAT CTTGGCTCAC TGCAACCTCC GCCTCCCGGA TTCAAGGGAT TCTCCTGCCT 1080 CAACCTCCCA AGTAGCTAGA ATCACCACGC CTGGCTAATT TTTGTATTTT TAGTAGAGAT 1140 GGGGTTTCAC 1150
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