Tag | Content |
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EnhancerAtlas ID | HS131-07655 |
Organism | Homo sapiens |
Tissue/cell | ME-1 |
Coordinate | chr5:139076170-139077690 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Klf1 | MA0493.1 | chr5:139077207-139077218 | GGCCACACCCA | + | 6.62 | RREB1 | MA0073.1 | chr5:139076961-139076981 | CCCCCATTCACCCACCCCCG | + | 6.5 | ZNF263 | MA0528.1 | chr5:139076727-139076748 | AGAGCAGGGAAGGGGGAGGGA | + | 6.26 |
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| Number of super-enhancer constituents: 37 | ID | Coordinate | Tissue/cell |
SE_03140 | chr5:139077222-139079757 | Brain_Angular_Gyrus | SE_03865 | chr5:139075665-139079795 | Brain_Anterior_Caudate | SE_04768 | chr5:139075791-139079817 | Brain_Cingulate_Gyrus | SE_05771 | chr5:139074803-139079842 | Brain_Hippocampus_Middle | SE_06683 | chr5:139075852-139079604 | Brain_Hippocampus_Middle_150 | SE_07722 | chr5:139075367-139079904 | Brain_Inferior_Temporal_Lobe | SE_08785 | chr5:139076058-139076350 | Brain_Mid_Frontal_Lobe | SE_08785 | chr5:139077255-139077604 | Brain_Mid_Frontal_Lobe | SE_13414 | chr5:139075806-139078377 | CD34_Primary_RO01536 | SE_25255 | chr5:139076350-139077533 | Colon_Crypt_3 | SE_27739 | chr5:139075790-139079429 | Fetal_Intestine | SE_28684 | chr5:139075714-139079698 | Fetal_Intestine_Large | SE_29581 | chr5:139075776-139079395 | Fetal_Muscle | SE_30930 | chr5:139075948-139078068 | Fetal_Thymus | SE_31417 | chr5:139075889-139079477 | Gastric | SE_33374 | chr5:139076434-139077140 | H1 | SE_33677 | chr5:139075744-139077639 | H2171 | SE_34346 | chr5:139075888-139078466 | HCT-116 | SE_36941 | chr5:139068133-139079024 | HSMMtube | SE_40547 | chr5:139075555-139079970 | K562 | SE_40649 | chr5:139075743-139079459 | Left_Ventricle | SE_42197 | chr5:139075725-139079407 | Lung | SE_45813 | chr5:139071957-139078550 | Osteoblasts | SE_47460 | chr5:139075818-139078710 | Pancreas | SE_48055 | chr5:139075785-139078204 | Psoas_Muscle | SE_48579 | chr5:139075882-139079587 | Right_Atrium | SE_49460 | chr5:139076628-139077101 | Right_Ventricle | SE_51090 | chr5:139075721-139079481 | Skeletal_Muscle | SE_53351 | chr5:139075859-139079558 | Spleen | SE_55117 | chr5:139076126-139077598 | Thymus | SE_55730 | chr5:139075803-139078946 | u87 | SE_58504 | chr5:139012442-139092243 | Ly1 | SE_59951 | chr5:139067745-139092302 | Ly4 | SE_63555 | chr5:139075583-139078253 | HSMM | SE_65250 | chr5:139075601-139078895 | Pancreatic_islets | SE_67548 | chr5:139075803-139078946 | u87 | SE_68692 | chr5:139075792-139079343 | H9 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr5 | 139076374 | 139076603 | chr5 | 139077054 | 139077268 |
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| Number: 1 | ID | Chromosome | Start | End |
GH05I139683 | chr5 | 139062979 | 139081910 |
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Enhancer Sequence | CACAGTGCTC TGCTTCTCGA GCTGAAGAGG TTTCATTGAC TCCTTTTTTC TGCACCTGCC 60 CTGTGCTCCT GGCCTGGTCC GGTAGCGGGA CGGGGGCGAT CAGTCTGGAG AGAAGACAGC 120 CCCAGGAACT AAGTCCCAAA GGAGTGTTCT AACCAGAGCT TGTGGGAGAT AGACGGGCCT 180 CCTTGGGCGG CGGGGGGCTG TGACTGCGGA CTGCCCCGAG GTGCGAGCTG GTTCAGTGTT 240 CTAAGAAACT GAGAGAATGG AGGATGGGCA AGGCAGGTAG CAGGACCTGC AGGAGCAGAA 300 CGGGGAGGCT GGAAAGCCTG GGGCCAGGCC TGTGGTGGGC AGGGGAGGGT GCATGATGAG 360 GGGGTGGGAA CACGGAGCGG GTGAGTCACC GTTTCTGGGC CAGGCAGGCG GCGGCTGCAG 420 AGCGGGGGGC GCATTCCTGG CTGGCAGGGC GGCCGGCACT AATGTCTTTC CCACATGGCC 480 CCGAATTCCC CGCTCGGCAC GATCACACGG GCAAGACGCT CCCGCGGCCA CCCCCGCCCC 540 AGCTGCCTCC TTCCCACAGA GCAGGGAAGG GGGAGGGAGT GTGGTGGAGG CTGGCGGAAC 600 CGGCCCCTCC TGGGGCGGGG TGGGGGTCTC TAGCGTGGCC TCCCTGGGGC CTGCGCCCAC 660 GGTGTCGGCA CGCGATGAGC GACTCACAGG GCAGCTGCAG TCACAGTGAG AGCAGGGCCG 720 CGCTTGTGAA GCGGAGAAGG AAGGAGGCCG GGAACCGCCT TGGGTCTTTG GCCACGTCTC 780 TCCTTCCCTG GCCCCCATTC ACCCACCCCC GCCCTGGGTC AGGCTTTCCC TCGCGCTGCG 840 GCTGTCGGAG GGCCGCGGCC GGATAGGGAC AAGCGGCGGA GCAGCAGCAA GTCCGGCCGC 900 CTCCGATCCT ACGCCTTCTG GCCCTCCCCT CCTTCCCGAC CTCTGGGCCT GGCTGGTGGG 960 GGGCGGAGTG GGGAGTGGGG GGACTGTGCC GCTGCCGCTG CATCCGGCGG GGGCCTGCTG 1020 GGGTGGTTCC TGGAAGAGGC CACACCCAGT CCCTCCCTCC GTGGGATGGA GGCCAGCCCT 1080 TGCTAAGGCG AAGGGAACTA GGAGCGCCGC TCTCCCACGC AGCCCCTGTC CCCAGGCCAG 1140 GTCCTGGAGA GGGGGGAAAC TGAGGCTGCT GAGAGGGCGG CCCACCCAGA GCTCCCTGTG 1200 CTGGGAGAGG TTGGCCGCTG TCCCTCCCAG CTGGGCTCAG AGGCGCTAAT GAGAGTTAAA 1260 TGTAGGACGT GAGTCACCTC TAGGAGGGGG CTGGGACCAC CCCCAGATGT GGGTCCAGAC 1320 GCTCAGGCTT TTTCCTACTC CCCTGTGTGT CACCCCCTAC CCTTGGCAGG GTGGGGCATG 1380 AGTTCTGACC TTGCTGACCA GGCTCTGTCA CCCTGGACCA GCCTCACTTA AATGGCTGGC 1440 TGCCTCAGGA GCGGGTGCTG TGGGACCACA GGAGACTCTA AATCCCGGGA TAGGCCCAGT 1500 GGACCCTGAG GACTTAGGGG 1520
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