Tag | Content |
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EnhancerAtlas ID | HS177-18524 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH_RA |
Coordinate | chr5:139076280-139077630 |
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: 36 | 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 | chr5:139077255-139077604 | 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 | AGAAGACAGC CCCAGGAACT AAGTCCCAAA GGAGTGTTCT AACCAGAGCT TGTGGGAGAT 60 AGACGGGCCT CCTTGGGCGG CGGGGGGCTG TGACTGCGGA CTGCCCCGAG GTGCGAGCTG 120 GTTCAGTGTT CTAAGAAACT GAGAGAATGG AGGATGGGCA AGGCAGGTAG CAGGACCTGC 180 AGGAGCAGAA CGGGGAGGCT GGAAAGCCTG GGGCCAGGCC TGTGGTGGGC AGGGGAGGGT 240 GCATGATGAG GGGGTGGGAA CACGGAGCGG GTGAGTCACC GTTTCTGGGC CAGGCAGGCG 300 GCGGCTGCAG AGCGGGGGGC GCATTCCTGG CTGGCAGGGC GGCCGGCACT AATGTCTTTC 360 CCACATGGCC CCGAATTCCC CGCTCGGCAC GATCACACGG GCAAGACGCT CCCGCGGCCA 420 CCCCCGCCCC AGCTGCCTCC TTCCCACAGA GCAGGGAAGG GGGAGGGAGT GTGGTGGAGG 480 CTGGCGGAAC CGGCCCCTCC TGGGGCGGGG TGGGGGTCTC TAGCGTGGCC TCCCTGGGGC 540 CTGCGCCCAC GGTGTCGGCA CGCGATGAGC GACTCACAGG GCAGCTGCAG TCACAGTGAG 600 AGCAGGGCCG CGCTTGTGAA GCGGAGAAGG AAGGAGGCCG GGAACCGCCT TGGGTCTTTG 660 GCCACGTCTC TCCTTCCCTG GCCCCCATTC ACCCACCCCC GCCCTGGGTC AGGCTTTCCC 720 TCGCGCTGCG GCTGTCGGAG GGCCGCGGCC GGATAGGGAC AAGCGGCGGA GCAGCAGCAA 780 GTCCGGCCGC CTCCGATCCT ACGCCTTCTG GCCCTCCCCT CCTTCCCGAC CTCTGGGCCT 840 GGCTGGTGGG GGGCGGAGTG GGGAGTGGGG GGACTGTGCC GCTGCCGCTG CATCCGGCGG 900 GGGCCTGCTG GGGTGGTTCC TGGAAGAGGC CACACCCAGT CCCTCCCTCC GTGGGATGGA 960 GGCCAGCCCT TGCTAAGGCG AAGGGAACTA GGAGCGCCGC TCTCCCACGC AGCCCCTGTC 1020 CCCAGGCCAG GTCCTGGAGA GGGGGGAAAC TGAGGCTGCT GAGAGGGCGG CCCACCCAGA 1080 GCTCCCTGTG CTGGGAGAGG TTGGCCGCTG TCCCTCCCAG CTGGGCTCAG AGGCGCTAAT 1140 GAGAGTTAAA TGTAGGACGT GAGTCACCTC TAGGAGGGGG CTGGGACCAC CCCCAGATGT 1200 GGGTCCAGAC GCTCAGGCTT TTTCCTACTC CCCTGTGTGT CACCCCCTAC CCTTGGCAGG 1260 GTGGGGCATG AGTTCTGACC TTGCTGACCA GGCTCTGTCA CCCTGGACCA GCCTCACTTA 1320 AATGGCTGGC TGCCTCAGGA GCGGGTGCTG 1350
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