Tag | Content |
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EnhancerAtlas ID | HS088-01561 |
Organism | Homo sapiens |
Tissue/cell | HeLa-S3 |
Coordinate | chr1:36653170-36654580 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr1:36653934-36653953 | TCGCTCCACCTGGTGGTTA | - | 6.39 | EWSR1-FLI1 | MA0149.1 | chr1:36653404-36653422 | GGAGGGAAGGAGGGAAGA | + | 6.96 | Nkx2-5(var.2) | MA0503.1 | chr1:36654414-36654425 | CTTGAGTGGTT | - | 6.32 | PLAG1 | MA0163.1 | chr1:36653485-36653499 | AGGGCCCTAGGGGG | + | 6.02 | Pou2f3 | MA0627.1 | chr1:36653342-36653358 | TCTTATGCAAATGTGG | + | 6.09 | ZNF263 | MA0528.1 | chr1:36653739-36653760 | TCCCTCCTCCCCTCTTCATCC | - | 6.22 |
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| Number of super-enhancer constituents: 29 | ID | Coordinate | Tissue/cell |
SE_01636 | chr1:36652995-36654753 | Aorta | SE_02424 | chr1:36653204-36653930 | Astrocytes | SE_03303 | chr1:36653192-36654323 | Brain_Angular_Gyrus | SE_04066 | chr1:36652996-36654623 | Brain_Anterior_Caudate | SE_05024 | chr1:36652977-36656262 | Brain_Cingulate_Gyrus | SE_05887 | chr1:36652630-36656066 | Brain_Hippocampus_Middle | SE_06862 | chr1:36653091-36655960 | Brain_Hippocampus_Middle_150 | SE_07920 | chr1:36652680-36655845 | Brain_Inferior_Temporal_Lobe | SE_08864 | chr1:36653305-36654041 | Brain_Mid_Frontal_Lobe | SE_13759 | chr1:36653177-36653817 | CD34_Primary_RO01536 | SE_25992 | chr1:36652975-36654426 | Duodenum_Smooth_Muscle | SE_26652 | chr1:36653109-36654141 | Esophagus | SE_29723 | chr1:36653052-36654183 | Fetal_Muscle | SE_31707 | chr1:36653186-36654094 | Gastric | SE_35879 | chr1:36653010-36654413 | HMEC | SE_37181 | chr1:36653087-36654469 | HSMMtube | SE_38303 | chr1:36653082-36654537 | HUVEC | SE_42156 | chr1:36653020-36654669 | Lung | SE_44877 | chr1:36653214-36654241 | NHLF | SE_45971 | chr1:36653029-36654342 | Osteoblasts | SE_48111 | chr1:36653017-36654579 | Psoas_Muscle | SE_48599 | chr1:36653107-36654458 | Right_Atrium | SE_49470 | chr1:36653212-36654000 | Right_Ventricle | SE_50384 | chr1:36653079-36654371 | Sigmoid_Colon | SE_51235 | chr1:36652987-36654416 | Skeletal_Muscle | SE_52691 | chr1:36653137-36654296 | Small_Intestine | SE_54589 | chr1:36652224-36654880 | Stomach_Smooth_Muscle | SE_62466 | chr1:36605507-36654228 | Tonsil | SE_65351 | chr1:36653195-36654310 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 36653326 | 36654243 | chr1 | 36653182 | 36654200 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I036186 | chr1 | 36652330 | 36654510 |
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Enhancer Sequence | TGGGAATACA GGCACACACC ACCATGCCTG GTTAATTATT TTTAATTTTT TCCTGTAGAG 60 ACAGGGTCTC GCTATATTAC TCACACTGGT CTTGAACTCC TGGACTCAAG TGATCCTCCT 120 GCCTCAGCCT CCCAAAGTGT TGGGATTACA GGTGTGAGCC AGGACAGCAA TTTCTTATGC 180 AAATGTGGTG CTCACAGGAA GGGTCTGATC CCACAGCTCA GGAAAGAGGA GCCAGGAGGG 240 AAGGAGGGAA GAACACAGAA GTTCTAGGAG AGACTCAGCC TTTAGGAGCC TGGAGTGTGG 300 CTCCTCTGAG ACAGCAGGGC CCTAGGGGGC AGTGAGGGCT TTGGAAGAAC TGGCCCAGGC 360 TGCAGGGAGG TAGCCTCCAG GTCTGATTTC CTGGTTTCCA GCTGGAGATT GAGGAATGTC 420 CGGTCTGTTC CAGGCCCTGA CTGAGCCTGA AGAGAGCGGA GGTGGAGGCA GAAGCCATCC 480 CCTCTGGAGA TCCCTCCCTT TCCCCATCTC TGCCCTTTCC CCAGTAGGGC CAGACTAGGC 540 AGGGCCAGAG GAAGGCAGCA AAATGCCCTT CCCTCCTCCC CTCTTCATCC CAGTCGCCAA 600 CGCTCCTGAA CTCCAGCTCT GTTACAACAC CCCCGCCCCT CAACACACAC ACAATCTTTC 660 TTTAACAGGA CTCCCCAGCT CCACTGTGTG TGCCCGTGGG CCCTCTCAAA GGAACATTCA 720 GTCCAACCCG AAGCCTGTGC CCTGCTTCCC AATGAATGGC GATCTCGCTC CACCTGGTGG 780 TTACATGAGC ACATTGGCAA GGCAGTTGAG GTTGGAACTG CCAGGTCCAC CATGGACCAG 840 ACCACAGGCC TATGGCTGAT GTCCTGGCTG CAGGAGATGT GTGCTCTACT CTAGACTTGG 900 CCAGTGACTC ACTCTATAAC TAGGCAACCC TCCTGACCTC TGTGAGCTTC AATTTCCTCA 960 TCTGCAAATT AGGGCTAGTG ATATGGGTAA GGTATTCCTT GAACAAACAC ACAGAATAAG 1020 AGTCTTAGTT GCAAGGTCCC CTTCCCACCA TGAGGGGCCA TGATATCCTG AGGTAGCTCA 1080 ACATCACCTC CTGTGTACTG CCAGTCCCTT CCCCAAACCA CTCCACTTTG GGACAGCCGT 1140 ATTAGACATG TCCCAATGTG GCCAGAACAT TGAGCTCTAA TTGACCAACA GGGCATGGAG 1200 TGCAATGGCG TGATCATGGC TCATTGCAGC CTGGACCCCT CGGGCTTGAG TGGTTCTCCC 1260 ACCTCAGCTT CCTAAGTAGC TGGGACCACA GGTGCACACC ACCATGCCTG GCTAATTTTT 1320 AAATTTTTTG TGGAAACAGA TCTCGTTTTT TGTCCACGTT GGTCTTGAAA TCCTGGCCTT 1380 AAATGATCCT CCTGCCTCCG CCTCCCAAAG 1410
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