Tag | Content |
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EnhancerAtlas ID | HS007-08084 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr19:13960890-13962020 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF16 | MA0741.1 | chr19:13961365-13961376 | GGGGGCGGGGC | - | 6.02 | KLF5 | MA0599.1 | chr19:13961366-13961376 | GGGGCGGGGC | - | 6.02 | SP3 | MA0746.2 | chr19:13961364-13961377 | GGGGGGCGGGGCC | - | 6.11 |
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| Number of super-enhancer constituents: 34 | ID | Coordinate | Tissue/cell |
SE_00394 | chr19:13948737-13963116 | Adipose_Nuclei | SE_00791 | chr19:13961433-13962030 | Adipose_Tissue | SE_02576 | chr19:13959489-13964991 | Astrocytes | SE_09068 | chr19:13961136-13961282 | Brain_Mid_Frontal_Lobe | SE_09068 | chr19:13961590-13962107 | Brain_Mid_Frontal_Lobe | SE_13342 | chr19:13948702-13962977 | CD34_Primary_RO01536 | SE_14690 | chr19:13956464-13962797 | CD4_Memory_Primary_7pool | SE_15885 | chr19:13960875-13961655 | CD4_Naive_Primary_7pool | SE_17782 | chr19:13943266-13962691 | CD4p_CD25-_CD45ROp_Memory | SE_24646 | chr19:13960770-13962750 | Colon_Crypt_2 | SE_27158 | chr19:13957065-13962903 | Esophagus | SE_27768 | chr19:13949302-13963575 | Fetal_Intestine | SE_28760 | chr19:13949189-13965110 | Fetal_Intestine_Large | SE_29787 | chr19:13956506-13962940 | Fetal_Muscle | SE_34630 | chr19:13946176-13967046 | HeLa | SE_36667 | chr19:13959473-13965372 | HMEC | SE_37011 | chr19:13948733-13965296 | HSMMtube | SE_38128 | chr19:13956463-13965113 | HUVEC | SE_39105 | chr19:13961475-13962948 | IMR90 | SE_41122 | chr19:13956563-13963049 | Left_Ventricle | SE_42413 | chr19:13956569-13963420 | Lung | SE_44426 | chr19:13956507-13962882 | NHDF-Ad | SE_45089 | chr19:13960639-13964642 | NHLF | SE_46491 | chr19:13955521-13964784 | Osteoblasts | SE_49032 | chr19:13957052-13962760 | Right_Atrium | SE_49472 | chr19:13960823-13962773 | Right_Ventricle | SE_51833 | chr19:13960791-13963307 | Skeletal_Muscle_Myoblast | SE_54944 | chr19:13956487-13963104 | Stomach_Smooth_Muscle | SE_56033 | chr19:13960695-13963675 | u87 | SE_58196 | chr19:13960880-13961346 | VACO_9m | SE_58196 | chr19:13961368-13962715 | VACO_9m | SE_63613 | chr19:13960696-13963563 | HSMM | SE_68219 | chr19:13949152-13977449 | TC32 | SE_68559 | chr19:13949281-13977291 | TC71 |
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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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Enhancer Sequence | AGGCCCACAC ATGCATAGAA CAGGCTTAGA ACATAGAACG TGCTCATTAA GTGTTAGCTA 60 GTTTGGGAGG TCGGCAGGGG TGGGGAGGAT GCAAAAAAGC CCTCATCACA GCGCTCCTGA 120 CAGCTCCCGC CAGGCCAGCT CCCCAAATCC CTTAGGAAAA TGGCCTCGAC CTCTCAGCTG 180 CAACTCTGGC CCAGCCGCCA TCTCCTGACC TGACCGCCCA CTTCTGGGGA GCCCCGGTGG 240 GTCTGGATTG GAGAGAGCCA CCCTCAGCCC TCCCCACCTT CATTGGACCA CAGCTGTCTC 300 CTTCACCATC ACCTCCGTGC CCACCAGGAT TACAGGCCTG ATCTGAACCC CTAATCTAGG 360 GAAGACTACG GAGTCCCAAA ATCCCTCTTA GCGCGCACCC CGGCCTGAGG CTCGAACCCA 420 GGTCCGCGCT GGAGGGCGGT GGCGGTTGCC GAGCAACGCG CTGTTTGTTG GCGCGGGGGG 480 CGGGGCCGGG GCCGGCGCGC GGTGACTCAC CGCGGCGTGA TGCGGACGGG CGCGGCGCCC 540 AGCAGCCTGG CCGGCGGCCC GATCTCGGCT GGCCTCGGCG TCCGGAGGGG CCCGGCGGCG 600 GGGGCGCCTT AGCCCCCAAG TGGGCGCCGG AGGCCCGTGG GGAAGCGGCG GAGCAGGTCC 660 CGGGCTCTCG GACTCGGTTC GAATCCCAGC CCTGCCTCTT ACTCTTGACT CTTGATCTGT 720 GACTTCAAGG CTCCTTGCCT CAGTTTACCC GTCAGTAAAA GAAGCGACAC TGGAGGGTGC 780 AGTAACCCAC CACTGGCATT TAAAGCAGCT GAGATGATCA CGCAGTGACA CTGCGGGGCA 840 GCAAGTTTGG GACACCCAGA TTCTGCACGT GAATCTCCTG TGTTAAACTC TGCAACCTCA 900 CGGAGAATCA ATTTCCGCAT CTGTTACAGG GCAGTAGCAA GAACAAACAC CCTGCCTCTC 960 GGGTGGTTTG AGAATCCCGT GAATTCATAG TGAGACAATG CGTGGCACAT TTCAGTACCA 1020 TGTCTGCTGC CCCACGGAGG GACGGGATGT AGGAGGTTTT CTCTGTGGTC CGAGCTCAGG 1080 AGGGCAAGGA GGTGAGGGCA AGACTGGAAC CCCTAGAAGT GGGTGGCAAG 1130
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