Tag | Content |
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EnhancerAtlas ID | HS116-35446 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr9:130843730-130844880 |
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: 28 | 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_23076 | chr9:130843302-130843912 | Colon_Crypt_1 | 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_48196 | chr9:130842866-130843851 | Psoas_Muscle | 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 | SE_63942 | chr9:130842662-130844074 | HSMM |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I128077 | chr9 | 130839773 | 130845323 |
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Enhancer Sequence | GCTCACATGG ACGAATTGTG TGGCTCCCAC TGGCCAGTGT TGGGTTGCTT CAAAATTTTT 60 TGAACATTTT AGGTGATTGG GTTGTCACAT GCTGGCCTCC ATACCATATT CACCCCCTGC 120 TCCTTACTCT TGGTGCACAT GTCTAATCTA AAGGAGAATC ATGCTCTTAT AAGAGCAGAA 180 AAAGAAGAGA AATTAGGCCG GGCACGGTGG CTCATGCCTG TACTCCCAGC ACTTTGGGAG 240 GCTGAGGTGG GAGGATTGCT TGAGGCCAGG AGTTCGAGAC CAGTCTGGGC AACATAGGGA 300 GACCCAATCT CTACAAAAAA TTTTAAAAAA TTAGCCAGGC ATGCCTGTGG TCCCAGCTAC 360 TTGGGAGGTT GAGGTGGGAA GATCCCTTGA GCCTGGGAGG TTGAGGCTGC AGTGAGCCAT 420 GATCATACCT GCACTCCAGT CTGGGCAGCA GAGCCAGACC CTGTCTCAAA AAAAATAAAG 480 TAGAAATCCC ATATTTCCAA GCAGACCCTT GCTTCTGTAG AACTTGACTT GTTACATCTT 540 AAAATCCTAC ACTTAAGAGT TGGGTAAATT TTGTATGCCT CTAACTTTCT TGTAGAGAAA 600 AGAAAAAGAC ATCTTTAATA TGCATTCACC TTGAACTTGG GACCTCGAAG GGGACTGGCT 660 TTTCACCAGG AGTAAACAGA AGCCATCCAC AAGACTGAGG GTTTTCATGC CGGACTTCTC 720 TTTTCCTTCC ACAGTTACAG GAGTTTTCTT TAGGGAGTTT TTGTCAAAGC TAGATTTTCC 780 GGTTCTGTTT CCTAAAATGG AAATAGATCA TGGATTTCCT TTTTTCATTA TTGCAGTTCT 840 GTCATCTGCC ATACCTTAGT TTCATTTGTG CCAAATGAGG TGAGTTGTGG CTCCTCTTCA 900 TTGTCCAATT GTTGCTGAGT CACATCAGGT GGGCGTTTAA GAGTCCTGCC TTACAGCCTG 960 AAACTCCAGC CGCCCAGCGC AGGCAGCACA TAGGAGCTGA GTTTTTCCGT TGGCTGATTG 1020 GTTCATTCCA GCGGAGACTG ACATTCACCT GCTACAGTCC TGCCTCTGGA ATAGCCTGGC 1080 ACTGCCATAT ATCAGTATAT AAAAGAGAGT CTTCAAACTC TTGACTCCTG TACCACCCAA 1140 AAATAATTTT 1150
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