Tag | Content |
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EnhancerAtlas ID | HS191-00671 |
Organism | Homo sapiens |
Tissue/cell | Trophoblast |
Coordinate | chr1:27844360-27845320 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:27844587-27844605 | TCTGACTTCCTGCCTTCC | - | 6.01 | PRDM1 | MA0508.2 | chr1:27844946-27844956 | GTGAAAGTGA | - | 6.02 | ZNF263 | MA0528.1 | chr1:27845122-27845143 | GGAGGAGGGGGTTGGAGGGAG | + | 6.7 |
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| Number of super-enhancer constituents: 30 | ID | Coordinate | Tissue/cell |
SE_02913 | chr1:27844536-27845036 | Bladder | SE_05196 | chr1:27845131-27856743 | Brain_Cingulate_Gyrus | SE_05814 | chr1:27844227-27851238 | Brain_Hippocampus_Middle | SE_06945 | chr1:27845183-27851030 | Brain_Hippocampus_Middle_150 | SE_07770 | chr1:27844238-27856992 | Brain_Inferior_Temporal_Lobe | SE_23188 | chr1:27843698-27847641 | Colon_Crypt_1 | SE_24033 | chr1:27844307-27845471 | Colon_Crypt_2 | SE_24711 | chr1:27843869-27847003 | Colon_Crypt_3 | SE_25901 | chr1:27844261-27845577 | Duodenum_Smooth_Muscle | SE_26518 | chr1:27843507-27857767 | Esophagus | SE_27625 | chr1:27843691-27857024 | Fetal_Intestine | SE_28547 | chr1:27843416-27856986 | Fetal_Intestine_Large | SE_29557 | chr1:27845136-27850991 | Fetal_Muscle | SE_31394 | chr1:27843780-27847429 | Gastric | SE_33477 | chr1:27843634-27857256 | H2171 | SE_34367 | chr1:27844425-27845418 | HCT-116 | SE_34755 | chr1:27843588-27845742 | HeLa | SE_35950 | chr1:27843632-27846014 | HMEC | SE_36974 | chr1:27845141-27851091 | HSMMtube | SE_39896 | chr1:27844247-27845283 | K562 | SE_40593 | chr1:27844098-27856916 | Left_Ventricle | SE_42106 | chr1:27844182-27851151 | Lung | SE_48567 | chr1:27844222-27851412 | Right_Atrium | SE_50130 | chr1:27844122-27851113 | Sigmoid_Colon | SE_51091 | chr1:27844267-27845360 | Skeletal_Muscle | SE_52467 | chr1:27843721-27848576 | Small_Intestine | SE_57160 | chr1:27844222-27845429 | VACO_400 | SE_62718 | chr1:27801410-27856116 | Tonsil | SE_65253 | chr1:27843908-27851025 | Pancreatic_islets | SE_66890 | chr1:27843634-27857256 | H2171 |
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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 | GTGTGGGGCA GGCTGGGTCT CGATCTCCTG ACCTCGTGAT CTACCCTCCA CGGCCTCTCA 60 AAGTGTTGGG ATTACAGGCG TGAGCCACGG TGCCTGGCCT TATTGCGCCT ATTTTAGAAA 120 GGTGATTCTA GCCGCAGTGT GGAGCGTGAG CTGTACGAGG AGAGCCTGGC TGTCGGGGAG 180 CAGATCTGAG CACGCTCCTC ACCAGCCCTA GCTCAGGCTC GGACCTCTCT GACTTCCTGC 240 CTTCCCACGT GCTCTTGCCT CTGCTTAGAG TATCTTTCCC TTGACTTTGC CTGGCTAACT 300 CCTTGCCCAC CTTCAGGTCT CAGTTTAGCC AGCACTTCCA CCCGGAAGCT CTACTAGACA 360 CCCCTCCCAG TCCAGATTAG ATGCTCCTAC TTACTCCTCC TCTGTGCTTG CAGACCTGCC 420 CACCTGCCTG CCTCGTCGAC TGGACTCTGG CCAAGGGCAG GGACTGTGTG GCACTGCTCA 480 CTGCTGTATC CACAAGGCCC TAAGGCATAA TGCCTGGAGC CTCAATCCAT GATCGGTAGG 540 GAACGAATGA ATGGCTAAGC CTGTTGGGGC AGGTGTGATA GTTTGAGTGA AAGTGACAGG 600 GTCTGCGGTG GCAGCGAGGA GAGAAGAGAC ACGATAGAAT TGACGGGACC CAGGAATCAT 660 GAGAGGAGAA CACAGGGAGA GAAGAAGGAG TTGGTGATGA CTCAGAGGTG TTTTTTTTTT 720 CACCTGGGTA AGCCCTGTGC CTCTAACCAA GATAGGAGCC ATGGAGGAGG GGGTTGGAGG 780 GAGGGAGGGA GGAGTAGGCC AGGGCAGAGG GGCAGGGCGG AGCCTTACCT TGGTAGGAGA 840 CTGGGGCCCT GGCCCAGGCC GTTCCTTGGA GTATTCTTCC CTTCTGGGAT GCTGTGCACA 900 CTGATGGATC CTCAGCAATG TCTGTGACTG TCCAAATGCT GCCACCTTGA CCACTCTAAC 960
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