Tag | Content |
---|
EnhancerAtlas ID | HS145-21364 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr5:139076250-139077670 |
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 |
|
| 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 |
|
| 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 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH05I139683 | chr5 | 139062979 | 139081910 |
|
Enhancer Sequence | GGTAGCGGGA CGGGGGCGAT CAGTCTGGAG AGAAGACAGC CCCAGGAACT AAGTCCCAAA 60 GGAGTGTTCT AACCAGAGCT TGTGGGAGAT AGACGGGCCT CCTTGGGCGG CGGGGGGCTG 120 TGACTGCGGA CTGCCCCGAG GTGCGAGCTG GTTCAGTGTT CTAAGAAACT GAGAGAATGG 180 AGGATGGGCA AGGCAGGTAG CAGGACCTGC AGGAGCAGAA CGGGGAGGCT GGAAAGCCTG 240 GGGCCAGGCC TGTGGTGGGC AGGGGAGGGT GCATGATGAG GGGGTGGGAA CACGGAGCGG 300 GTGAGTCACC GTTTCTGGGC CAGGCAGGCG GCGGCTGCAG AGCGGGGGGC GCATTCCTGG 360 CTGGCAGGGC GGCCGGCACT AATGTCTTTC CCACATGGCC CCGAATTCCC CGCTCGGCAC 420 GATCACACGG GCAAGACGCT CCCGCGGCCA CCCCCGCCCC AGCTGCCTCC TTCCCACAGA 480 GCAGGGAAGG GGGAGGGAGT GTGGTGGAGG CTGGCGGAAC CGGCCCCTCC TGGGGCGGGG 540 TGGGGGTCTC TAGCGTGGCC TCCCTGGGGC CTGCGCCCAC GGTGTCGGCA CGCGATGAGC 600 GACTCACAGG GCAGCTGCAG TCACAGTGAG AGCAGGGCCG CGCTTGTGAA GCGGAGAAGG 660 AAGGAGGCCG GGAACCGCCT TGGGTCTTTG GCCACGTCTC TCCTTCCCTG GCCCCCATTC 720 ACCCACCCCC GCCCTGGGTC AGGCTTTCCC TCGCGCTGCG GCTGTCGGAG GGCCGCGGCC 780 GGATAGGGAC AAGCGGCGGA GCAGCAGCAA GTCCGGCCGC CTCCGATCCT ACGCCTTCTG 840 GCCCTCCCCT CCTTCCCGAC CTCTGGGCCT GGCTGGTGGG GGGCGGAGTG GGGAGTGGGG 900 GGACTGTGCC GCTGCCGCTG CATCCGGCGG GGGCCTGCTG GGGTGGTTCC TGGAAGAGGC 960 CACACCCAGT CCCTCCCTCC GTGGGATGGA GGCCAGCCCT TGCTAAGGCG AAGGGAACTA 1020 GGAGCGCCGC TCTCCCACGC AGCCCCTGTC CCCAGGCCAG GTCCTGGAGA GGGGGGAAAC 1080 TGAGGCTGCT GAGAGGGCGG CCCACCCAGA GCTCCCTGTG CTGGGAGAGG TTGGCCGCTG 1140 TCCCTCCCAG CTGGGCTCAG AGGCGCTAAT GAGAGTTAAA TGTAGGACGT GAGTCACCTC 1200 TAGGAGGGGG CTGGGACCAC CCCCAGATGT GGGTCCAGAC GCTCAGGCTT TTTCCTACTC 1260 CCCTGTGTGT CACCCCCTAC CCTTGGCAGG GTGGGGCATG AGTTCTGACC TTGCTGACCA 1320 GGCTCTGTCA CCCTGGACCA GCCTCACTTA AATGGCTGGC TGCCTCAGGA GCGGGTGCTG 1380 TGGGACCACA GGAGACTCTA AATCCCGGGA TAGGCCCAGT 1420
|