| Tag | Content |
|---|
EnhancerAtlas ID | HS146-07717 |
Organism | Homo sapiens |
Tissue/cell | NHDF |
Coordinate | chr19:44268960-44270200 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr19:44269851-44269871 | TGGTTTGGGGAGGTTTGGGG | - | 6.99 | | RREB1 | MA0073.1 | chr19:44269841-44269861 | GGTATGTGGGTGGTTTGGGG | - | 8.75 |
|
| | Number of super-enhancer constituents: 28 | ID | Coordinate | Tissue/cell |
| SE_02767 | chr19:44268896-44270200 | Astrocytes | | SE_09619 | chr19:44267161-44274237 | CD14 | | SE_10575 | chr19:44268972-44272145 | CD19_Primary | | SE_11483 | chr19:44267220-44273841 | CD20 | | SE_13735 | chr19:44268644-44271503 | CD34_Primary_RO01536 | | SE_14657 | chr19:44268615-44271764 | CD4_Memory_Primary_7pool | | SE_18182 | chr19:44268629-44272248 | CD4p_CD25-_CD45ROp_Memory | | SE_18680 | chr19:44268558-44272624 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19217 | chr19:44268630-44272276 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_20985 | chr19:44268851-44271784 | CD8_Memory_7pool | | SE_23510 | chr19:44269009-44269976 | Colon_Crypt_1 | | SE_27247 | chr19:44268619-44271203 | Esophagus | | SE_31804 | chr19:44268953-44269991 | Gastric | | SE_31804 | chr19:44269997-44272081 | Gastric | | SE_32542 | chr19:44266723-44271779 | GM12878 | | SE_33868 | chr19:44268905-44271368 | HCC1954 | | SE_34298 | chr19:44256799-44272203 | HCT-116 | | SE_34813 | chr19:44268615-44271135 | HeLa | | SE_37675 | chr19:44268467-44270470 | HSMMtube | | SE_39921 | chr19:44268698-44269880 | K562 | | SE_50403 | chr19:44268818-44272859 | Sigmoid_Colon | | SE_53073 | chr19:44268934-44271511 | Small_Intestine | | SE_53761 | chr19:44268902-44273559 | Spleen | | SE_56117 | chr19:44266358-44271787 | u87 | | SE_59025 | chr19:44248893-44290143 | Ly3 | | SE_60730 | chr19:44257018-44289948 | DHL6 | | SE_62525 | chr19:44242576-44303622 | Tonsil | | SE_64692 | chr19:44268872-44270949 | NHEK |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr19 | 44269192 | 44269953 | | chr19 | 44269026 | 44270045 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I043762 | chr19 | 44266826 | 44273433 |
|
Enhancer Sequence | TCCTGGCCTC AGGTGATCTG CCTGCCTCGG CCTCCCAAAG TGCTGGAATT ACAGGCGTGA 60
GCCACCATGC CTGGCCAGAC CCAATATTAT TATCGTGATA GGGATAGGTT TATGAGGCTA 120
TAGGAGTATC AGACAGGGCC TCCTGGAGGA GGGGACATAT TAGCCGAGGC CTACAGGAGG 180
CGTAGGAAGG AGTGTTTGCC AGCTAAAAGG GAGTGGAGGC AAGGAAAGAG AGGTCCCAGA 240
AGAATGAGTT TGGCAGGGGC TTTGGCAACA CTGCCAGGAG AGCTTCTTGC AGGGGAAGGG 300
TGTCAGCAAT ATCTGGAGGT CTCATCCAGT TCCTTTCTTG AGTCCCCGCC TTTACTCCCC 360
AGGTGGGCTG GCCTCCAGAG GAAGGGCAGT TCGTGGCAGT GGGTGGCGGA GGCTCCAATT 420
TAGCTCTCAG GGATGAAGGG GCGAGGCTGG CTGTGGACTT TAAGGGAAAT CCAAAGATAG 480
CTCAACAGAA AAGGATGACT CGCAGCCTGA TCTTCCCCTC AAGAGGAGGG AAGCAAGAAT 540
GAATCAGCCT CTCAAGCTGG AATGAAGTTG CGGCGGGAAG TCAGTCCTCG GTTTGTGGCC 600
CAAGGCCACT CTGCCTCTGA CTCACCTTGC AGTGGGGCGG GATGGGTGTG AATCTGGGCT 660
CTCCAGCCCG TATTCCTAGC TTCCGGCTGG GGGCCTGAGG GGAGGCCTGG CTCCTCTTGA 720
AACCTCGGTT TCTACATCTG TGCAGTGGGG TAACGAGGGT CAGGAGAGTG GTTATGGTGA 780
CTTATAAACA GAGCTGGGCA CACAGTAGGG CCTCTGGAAG TGCCAGCCCC CCTCCTTTGC 840
CCCCTTCCCT TTCACATCCT CTCTTGAGCG GATGTGAAAC GGGTATGTGG GTGGTTTGGG 900
GAGGTTTGGG GCCTCTGTTA GTCTCTTGAT GAGTGAGTTG TCATCTAGAT TCTGGTAAGG 960
CATGAATAGA GGGAGAAAAG CAACAAAAAA TCAGAAAAAG GGCAGCCACG CATTGTGTGT 1020
GAAAATCAAA AACAATAATA AAAATGATTC TTGGCCAGGG ACAGTGGCTC ACGCTTGTAA 1080
TCCCAGCACT TTGGGAGGCT GAGGCGGGCA GATTGCTTGA GCCCAGGAGT TCAAGACCAG 1140
CATCTGCAAC ATAGTGAAAC CCCATCTCTA CTAAAAATAC AAAAATTAGC CAGGCGTGGT 1200
GGCAGGTGCC TGTAATCCCA GCTACTTGGG GACTAAGGCA 1240
|
