Tag | Content |
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EnhancerAtlas ID | HS095-00629 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr1:27843740-27845320 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:27844587-27844605 | TCTGACTTCCTGCCTTCC | - | 6.01 | KLF14 | MA0740.1 | chr1:27844309-27844323 | TACCACGCCCACCT | + | 6.59 | Klf1 | MA0493.1 | chr1:27843990-27844001 | TGGGTGTGGCT | - | 6.14 | PRDM1 | MA0508.2 | chr1:27844946-27844956 | GTGAAAGTGA | - | 6.02 | SP3 | MA0746.2 | chr1:27844309-27844322 | TACCACGCCCACC | + | 6.37 | SP8 | MA0747.1 | chr1:27844310-27844322 | ACCACGCCCACC | + | 6.32 | 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_07770 | chr1:27844238-27856992 | Brain_Inferior_Temporal_Lobe | SE_23188 | chr1:27843698-27847641 | Colon_Crypt_1 | SE_24033 | chr1:27843764-27844291 | Colon_Crypt_2 | 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: 2 | Chromosome | Start | End |
chr1 | 27844465 | 27845239 | chr1 | 27843903 | 27844052 |
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Enhancer Sequence | TCCAGCCTGG GCAACAGAGC AAGACTCTGT TTCAAAAAAT AAATAAATAA AAATGAATTG 60 TAATGGGGCA TAGAAGAGAA ACTCATTTTT GTTGGGGAGG TGGGGGTCCA GAGAGGCTTC 120 TTAGAGAAAA GGAACATCTG TGTTGGGCTC TGAAGGATGA AGAGTTCACC CGGAAAAGTG 180 GCAGAGGGCA TTCCAGGAGG AATGTATTTT GTGGACAAAG GCCCAGGGAT ATGGAAGGAT 240 ATGACCTGTT TGGGTGTGGC TGAACACAGA GTTGGCTGAG AGGAGTGGTA GGAAATGAGG 300 TTCGAAAGGC AGTTTTGAGG GCCTCCAGTG CCTTGCTATT GAGGGCAGAC TTTAAAGGAC 360 TGGGGAAACA GAGCAGGAGT TTAAGGGCTG GGAAGGGACA GGATTATACC TATTTTATTT 420 TTATTATTTA TTTATTTAGA GATGGAGTCT TGCCCTGTTG CCCAGGCTGG AGTGCAGTGG 480 TGCAGTCTGC TCACTGCAAC CTCCTCCTCC CAGCTTCAAG CGATTCTCCT GCCTCAGCCT 540 CCCAAGTAGC TGGGATTATA GGCATGCACT ACCACGCCCA CCTAATTTTT TTGTATCTTT 600 AGTAGAGACG GGGTTTTGCC GTGTGGGGCA GGCTGGGTCT CGATCTCCTG ACCTCGTGAT 660 CTACCCTCCA CGGCCTCTCA AAGTGTTGGG ATTACAGGCG TGAGCCACGG TGCCTGGCCT 720 TATTGCGCCT ATTTTAGAAA GGTGATTCTA GCCGCAGTGT GGAGCGTGAG CTGTACGAGG 780 AGAGCCTGGC TGTCGGGGAG CAGATCTGAG CACGCTCCTC ACCAGCCCTA GCTCAGGCTC 840 GGACCTCTCT GACTTCCTGC CTTCCCACGT GCTCTTGCCT CTGCTTAGAG TATCTTTCCC 900 TTGACTTTGC CTGGCTAACT CCTTGCCCAC CTTCAGGTCT CAGTTTAGCC AGCACTTCCA 960 CCCGGAAGCT CTACTAGACA CCCCTCCCAG TCCAGATTAG ATGCTCCTAC TTACTCCTCC 1020 TCTGTGCTTG CAGACCTGCC CACCTGCCTG CCTCGTCGAC TGGACTCTGG CCAAGGGCAG 1080 GGACTGTGTG GCACTGCTCA CTGCTGTATC CACAAGGCCC TAAGGCATAA TGCCTGGAGC 1140 CTCAATCCAT GATCGGTAGG GAACGAATGA ATGGCTAAGC CTGTTGGGGC AGGTGTGATA 1200 GTTTGAGTGA AAGTGACAGG GTCTGCGGTG GCAGCGAGGA GAGAAGAGAC ACGATAGAAT 1260 TGACGGGACC CAGGAATCAT GAGAGGAGAA CACAGGGAGA GAAGAAGGAG TTGGTGATGA 1320 CTCAGAGGTG TTTTTTTTTT CACCTGGGTA AGCCCTGTGC CTCTAACCAA GATAGGAGCC 1380 ATGGAGGAGG GGGTTGGAGG GAGGGAGGGA GGAGTAGGCC AGGGCAGAGG GGCAGGGCGG 1440 AGCCTTACCT TGGTAGGAGA CTGGGGCCCT GGCCCAGGCC GTTCCTTGGA GTATTCTTCC 1500 CTTCTGGGAT GCTGTGCACA CTGATGGATC CTCAGCAATG TCTGTGACTG TCCAAATGCT 1560 GCCACCTTGA CCACTCTAAC 1580
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