Tag | Content |
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EnhancerAtlas ID | HS069-00239 |
Organism | Homo sapiens |
Tissue/cell | GM18951 |
Coordinate | chr1:36652930-36654450 |
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 | CATCTTGCCC AGACTGGTCT TGAACTCCTG GCCTCAAGTA ATCCTCCCGC CTCAGCCTCC 60 CAAAGTGCTA GGATTAATTA CAGGCATGAG CCACCGCACC AGGCCTCTTC TTTTTTTTTT 120 CTCTTTGAGA CAGGGTCTCA CTCTGTCACC CAAGTTGGAG TGCAGTGGCA CCATCATGGC 180 TCACTGCAGC CTCAACCTTC TGGGCTCAAG GGATCCTCCT GTCTCAGCCT CCTGAGTAGC 240 TGGGAATACA GGCACACACC ACCATGCCTG GTTAATTATT TTTAATTTTT TCCTGTAGAG 300 ACAGGGTCTC GCTATATTAC TCACACTGGT CTTGAACTCC TGGACTCAAG TGATCCTCCT 360 GCCTCAGCCT CCCAAAGTGT TGGGATTACA GGTGTGAGCC AGGACAGCAA TTTCTTATGC 420 AAATGTGGTG CTCACAGGAA GGGTCTGATC CCACAGCTCA GGAAAGAGGA GCCAGGAGGG 480 AAGGAGGGAA GAACACAGAA GTTCTAGGAG AGACTCAGCC TTTAGGAGCC TGGAGTGTGG 540 CTCCTCTGAG ACAGCAGGGC CCTAGGGGGC AGTGAGGGCT TTGGAAGAAC TGGCCCAGGC 600 TGCAGGGAGG TAGCCTCCAG GTCTGATTTC CTGGTTTCCA GCTGGAGATT GAGGAATGTC 660 CGGTCTGTTC CAGGCCCTGA CTGAGCCTGA AGAGAGCGGA GGTGGAGGCA GAAGCCATCC 720 CCTCTGGAGA TCCCTCCCTT TCCCCATCTC TGCCCTTTCC CCAGTAGGGC CAGACTAGGC 780 AGGGCCAGAG GAAGGCAGCA AAATGCCCTT CCCTCCTCCC CTCTTCATCC CAGTCGCCAA 840 CGCTCCTGAA CTCCAGCTCT GTTACAACAC CCCCGCCCCT CAACACACAC ACAATCTTTC 900 TTTAACAGGA CTCCCCAGCT CCACTGTGTG TGCCCGTGGG CCCTCTCAAA GGAACATTCA 960 GTCCAACCCG AAGCCTGTGC CCTGCTTCCC AATGAATGGC GATCTCGCTC CACCTGGTGG 1020 TTACATGAGC ACATTGGCAA GGCAGTTGAG GTTGGAACTG CCAGGTCCAC CATGGACCAG 1080 ACCACAGGCC TATGGCTGAT GTCCTGGCTG CAGGAGATGT GTGCTCTACT CTAGACTTGG 1140 CCAGTGACTC ACTCTATAAC TAGGCAACCC TCCTGACCTC TGTGAGCTTC AATTTCCTCA 1200 TCTGCAAATT AGGGCTAGTG ATATGGGTAA GGTATTCCTT GAACAAACAC ACAGAATAAG 1260 AGTCTTAGTT GCAAGGTCCC CTTCCCACCA TGAGGGGCCA TGATATCCTG AGGTAGCTCA 1320 ACATCACCTC CTGTGTACTG CCAGTCCCTT CCCCAAACCA CTCCACTTTG GGACAGCCGT 1380 ATTAGACATG TCCCAATGTG GCCAGAACAT TGAGCTCTAA TTGACCAACA GGGCATGGAG 1440 TGCAATGGCG TGATCATGGC TCATTGCAGC CTGGACCCCT CGGGCTTGAG TGGTTCTCCC 1500 ACCTCAGCTT CCTAAGTAGC 1520
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