Tag | Content |
---|
EnhancerAtlas ID | HS042-48877 |
Organism | Homo sapiens |
Tissue/cell | Fetal_brain |
Coordinate | chr9:134606510-134608160 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MAX | MA0058.3 | chr9:134606637-134606647 | AGCACGTGGT | - | 6.02 |
|
| Number of super-enhancer constituents: 39 | ID | Coordinate | Tissue/cell |
SE_00686 | chr9:134606247-134608316 | Adipose_Nuclei | SE_04525 | chr9:134606414-134608321 | Brain_Anterior_Caudate | SE_09150 | chr9:134602020-134613269 | CD14 | SE_10404 | chr9:134599070-134613095 | CD19_Primary | SE_10884 | chr9:134591844-134615384 | CD20 | SE_12120 | chr9:134606082-134613193 | CD3 | SE_14804 | chr9:134606083-134613399 | CD4_Memory_Primary_7pool | SE_16701 | chr9:134601791-134611990 | CD4_Naive_Primary_8pool | SE_17150 | chr9:134606063-134613218 | CD4p_CD225int_CD127p_Tmem | SE_17952 | chr9:134601452-134615329 | CD4p_CD25-_CD45ROp_Memory | SE_18769 | chr9:134601534-134615309 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19472 | chr9:134602036-134615436 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20363 | chr9:134601294-134613216 | CD56 | SE_22914 | chr9:134601848-134613223 | CD8_primiary | SE_27117 | chr9:134606526-134611391 | Esophagus | SE_30786 | chr9:134606415-134610798 | Fetal_Muscle | SE_31710 | chr9:134606758-134608062 | Gastric | SE_32578 | chr9:134599803-134613266 | GM12878 | SE_33628 | chr9:134605461-134610903 | H2171 | SE_36750 | chr9:134606498-134610470 | HMEC | SE_36915 | chr9:134602036-134616473 | HSMMtube | SE_38234 | chr9:134607748-134613138 | HUVEC | SE_40722 | chr9:134606610-134608765 | Left_Ventricle | SE_42566 | chr9:134606682-134613188 | Lung | SE_44033 | chr9:134602118-134608169 | MM1S | SE_49262 | chr9:134606092-134608233 | Right_Atrium | SE_50405 | chr9:134606039-134613162 | Sigmoid_Colon | SE_52037 | chr9:134606112-134612282 | Skeletal_Muscle_Myoblast | SE_52732 | chr9:134605999-134613197 | Small_Intestine | SE_54202 | chr9:134601963-134613163 | Spleen | SE_58352 | chr9:134520171-134620333 | Ly1 | SE_58881 | chr9:134579557-134620273 | Ly3 | SE_60383 | chr9:134599961-134620084 | Ly4 | SE_60991 | chr9:134494570-134620113 | HBL1 | SE_61989 | chr9:134594251-134616125 | Toledo | SE_62218 | chr9:134495530-134621458 | Tonsil | SE_63796 | chr9:134606096-134612370 | HSMM | SE_64992 | chr9:134606662-134610348 | NHEK | SE_66603 | chr9:134606093-134608710 | Jurkat |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TCTCAAAGAA AAGCTCTGTG TCTTAGTCTC CTCCTCTGTA GGATGAGAAC AGTTAACAGT 60 ACCTTTCTCC TATTGTAAGG ATTAAATGCA ACCACAAGTG TAAAATATAC AGAAGCGAGC 120 CTGGTACAGC ACGTGGTAAG TGCCTAATGA ACATCAGCTA CTACTATTAT TTGTATTTAT 180 TATTGAAAGG AGGGGTTGAG AGTAGCCAAT TCCATGACTC ATGAACAATC ATCCATCTAT 240 TTATTCAGAA CCATCACTTG AAGGAGGATG GGCGCATGTG ATAACCAGCA AATAAATACA 300 ACCACTGTTT CCAACCAGGG GTTTTGTTTG TTTGCTCGTT TGGGGTCAGC TAAGTGGCTA 360 TTTAACACGG TCACATTCCA CTGGATGTCA GCTGTCCTCT CTTCTCATTC CATGTCCTTC 420 CTTCTCTCAG TTACTGTCAG TGTCACACTC CTGCTCCGTT TTTAACAATA CAGTGTGTGG 480 CTGGGAATCG CATCTGTCAG GTCCACATCA GTGGCACAAA TTTTAAAAGC TATAGAGCAA 540 ATGCCTGAAA TCCGCCCCTC TGAACCCAGC CCTGGGCAAA CCACACAGCA TCCTGTGCTC 600 AGTGCTCCAT TTCTACGCTT TAAAAGCACT GCAGAATCGC CTGATCACAA AACTTAATAT 660 GCAGTAAAGT CACTGTGTGG TTTGGGCAAG CCAGTGAAAA GCAAAGAGAA AGCTGCTGCT 720 AAGGGACTGT GGGGACAGAA GTCTAAGCTG TTACAGGAGT CGTGGTGTTC CGGGAAGCAG 780 CAGTCCAGAC TGCAGGGTGG GACTTGGGTT CAGAGAATTG TCACCTGTCT TTCAAACTAC 840 AGCCTGGGAG AAGAAAGTGG GAGAAAGGAA TTGTGACCAG CAGACAGCAG ATTTCTAATA 900 AATTCAGATG AACCTCCCCC CCTGTACCTT AGCTCACAGA GGAGGGGGAA GTAGCAAGAA 960 AATACTGCCC ATGCCTCTTG ACAAAGAAGG AAGGGGGTGC CAGAGGCACA CCAACAGCCT 1020 GCACCCCAGC CCTAGACAGC ACACGCTGCA CAGTCATCCT GGGAAAAGAG AGTAATGCTG 1080 CAGGAAGCCA GTCCTAAATC ACATTCAAAG GCCAACTGAA AAAAAAAAAA ATAACAAGTA 1140 GGGACAGGGA TTCCTGGGAT GGTGCTCATT ATGGGTGTCA GGCTGAGTAG AGCTGGCACA 1200 GGCCTTGGTT TGTAAACACA GGGCAGAACG AGCATTACCT AAGAGCGCTT TGCTCCTGCA 1260 CATCCCAAAG AACCAGGCAG TCACTACAAG TGGAAGCTCA AAGAACATGC ACTCAAGTGG 1320 AAGCTCAAAG AACGTGCACT CAAGTGGAAG CTCAAAGAAC GTGCACTGAC CAATGGATGC 1380 GGCATCAGAA CCGAGTGGCG GCTCAGCCTT CACGGTGTCC TGGCGTTCTC CCAGTGGTGT 1440 TCTGGGAATT TGATCCTAAC CTCATCATTA GTGTTCAGAG GACTACAGGA AAACACAGAA 1500 CCCCCAACTA ACTGCACACC ACTGATCAGA TATTGGTCCT ACTAATGTAC CAAGAAACAT 1560 CCTAATTGGC AATTTGAAAC CACAATAAGC TACGTCTAAA GATAATTTGA GACTTGGAAC 1620 CAGAAACTAA AATTCATTCT ATGATAATAT 1650
|