Tag | Content |
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EnhancerAtlas ID | HS093-15098 |
Organism | Homo sapiens |
Tissue/cell | HL-60 |
Coordinate | chr19:11204930-11206460 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
JUN(var.2) | MA0489.1 | chr19:11205882-11205896 | AAGAAATGAGTCAT | + | 7.12 | JUN(var.2) | MA0489.1 | chr19:11205887-11205901 | ATGAGTCATTTCCT | - | 8.12 | SREBF1 | MA0595.1 | chr19:11205756-11205766 | GTGGGGTGAT | - | 6.02 |
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| Number of super-enhancer constituents: 35 | ID | Coordinate | Tissue/cell |
SE_01022 | chr19:11203682-11206319 | Adrenal_Gland | SE_12085 | chr19:11204949-11207773 | CD3 | SE_14622 | chr19:11198676-11207877 | CD4_Memory_Primary_7pool | SE_17142 | chr19:11204971-11207608 | CD4p_CD225int_CD127p_Tmem | SE_19715 | chr19:11204867-11207840 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20994 | chr19:11198676-11207604 | CD8_Memory_7pool | SE_22774 | chr19:11204855-11208057 | CD8_primiary | SE_23239 | chr19:11203891-11206070 | Colon_Crypt_1 | SE_23239 | chr19:11206100-11207601 | Colon_Crypt_1 | SE_24095 | chr19:11204989-11205979 | Colon_Crypt_2 | SE_24095 | chr19:11206049-11206285 | Colon_Crypt_2 | SE_24928 | chr19:11205061-11206082 | Colon_Crypt_3 | SE_24928 | chr19:11206201-11206876 | Colon_Crypt_3 | SE_26902 | chr19:11204916-11207828 | Esophagus | SE_28429 | chr19:11198835-11207741 | Fetal_Intestine | SE_29308 | chr19:11199027-11207595 | Fetal_Intestine_Large | SE_29905 | chr19:11204956-11208148 | Fetal_Muscle | SE_31737 | chr19:11204927-11207763 | Gastric | SE_34726 | chr19:11198191-11208606 | HeLa | SE_36050 | chr19:11204941-11207563 | HMEC | SE_38264 | chr19:11198668-11208150 | HUVEC | SE_40068 | chr19:11198411-11207591 | K562 | SE_42817 | chr19:11199051-11207805 | Lung | SE_44493 | chr19:11205013-11206118 | NHDF-Ad | SE_44932 | chr19:11205113-11207883 | NHLF | SE_47693 | chr19:11204994-11205972 | Pancreas | SE_47693 | chr19:11206022-11206280 | Pancreas | SE_49361 | chr19:11205119-11206191 | Right_Atrium | SE_49361 | chr19:11206197-11207709 | Right_Atrium | SE_50772 | chr19:11198863-11207767 | Sigmoid_Colon | SE_52540 | chr19:11198883-11208401 | Small_Intestine | SE_54059 | chr19:11198844-11207806 | Spleen | SE_57847 | chr19:11205007-11205595 | VACO_503 | SE_64571 | chr19:11204940-11207695 | NHEK | SE_65732 | chr19:11198652-11207882 | Pancreatic_islets |
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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 | CTGCCTCAGC CTCCTGAGTA GCTGGGATTA CAGGCATGCA CCACCACGCC CGGCTAATTT 60 TGTATTTTTC GTAGAGATGG GGTTTCTCCA CATTGGTTCA GGCTGTTCTC GAACTCCCAA 120 CCTCAGGTGA TCCACCCGCC TCAGCCTCCC AAAGTGCTGG GATTATAGGC GTGAGCCCCC 180 GAACCCGGCC ACTCCCAGCT AAGTTTAAAT TTTTTGTTTG TTTGTTCGTT TGTTTTTATT 240 TTTTGAGACA GAGTCTCCCG CCCAGGCTGG AGCGCAGATC ACTGCATCCT TGACCTCCCA 300 GGCTTAAGCC ATCCTCCCCA CTCAGCCTCC CAAGTAGCTG GGATTACAGG TGTGTGCCAC 360 TATGCTTGGC TAAGTTGTGT ATTTTTTGTA GAGATGGGGT TCAAGGGATT CTCGCTTTGT 420 TGCCTCGGTT GGTCTCAAAC TCCTGGGCTC AAGCAGTCCT CCCTCCTCAG CCTCCCAAGG 480 TGCTGGGGAA ATCCACTTTT GAAACATTGT CTGGAGAGTT GCCCAGGTGG TAGATCACAG 540 AAATAGGTCA TCGTGGGGTC CTTCCCATGG GTGCAGTCTT GAGCCACCTG TGGCCAGCAA 600 ATATTTGGAG AATAATAGTC AGGGGAGAGC TTGAGGTCCA GGGAAAGGTT TTGTTTTTCT 660 TCAGGGAAAG GTTTTTATTG TTCTTTATCC CTCCTTAAAG GACCTTCAGG TGTTACTGAC 720 ATTCCCGGTC TACCCAGTGG CACATTTAGT TTGTAAGCTG GGCCCTCGTA CAGAGGTAGG 780 GAGGTGAGAG CATTGGATTA GTGGTCACCA AAGCTGCGGT CACCTAGTGG GGTGATCAGA 840 GGCTCCTCCC TTAAGATCTT GATTGCCAAC GCCTCTGGCC CAACTTTCCT TTTTATTTAT 900 CGCAAGCCTC CTGGAATCTC AATTGCTTTT TGCCCACCCG GTGTGTCAGC ACAAGAAATG 960 AGTCATTTCC TCCTTTAAGC ACAGTTGAAA TTGAGCTGTG AGTCAGTGAG GTGTGTACGA 1020 TATTGTCAAA GCGGGGTGTG TACAGTATTG ACAGATCTGT AGTTGGGCAA GAGAATTATC 1080 AGAGTTTGTG ACCACAGCAG ATTCCAAAGC TCGACTCATT TTCTTCTCTC TTCCTTCCCT 1140 TTTTTCTTTT CTTTTTTTTT TTTTTTTTGA CAGAGTCTCG CTCTGTTGCC CAGGCTGGAG 1200 TGCAGTGGCA CAATCTGGGC TCACTGCAGC CCCTGCCTCC TGGGTTCAAA TGATTCTCAT 1260 GTTTCAGCCT CCCGAGTAGC TGCAATTACA GGCATTCGGG TTCAAGTGAT TCTCCTGCCT 1320 CAGCCACCTG AGCAGCTGGG ATTACAGGCG CCCGCCACCA CGCCCGGCTA ATTTTTGTAT 1380 TTTTAGTAGA GACGGGGTTT CACCATGTTG GCCAGGCTGG TCTCGAACTC CTGAACTCAG 1440 GTGATCCGCC CACTTCGGCC TCCCAAAGTG CTGAGATTAC AGACGTGAGT CACCGCGCCC 1500 AGCCTGTTCT GTTCTTTAAT TCTCAAAACA 1530
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