Tag | Content |
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EnhancerAtlas ID | HS128-21411 |
Organism | Homo sapiens |
Tissue/cell | MCF-7 |
Coordinate | chr8:38794260-38796520 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF4G | MA0484.1 | chr8:38795601-38795616 | TGCACTTTGACCCCT | - | 6.21 | Hnf4a | MA0114.3 | chr8:38795599-38795615 | GCTGCACTTTGACCCC | - | 6.78 | NR2C2 | MA0504.1 | chr8:38795601-38795616 | TGCACTTTGACCCCT | - | 6.3 | PPARG | MA0066.1 | chr8:38795905-38795925 | GTGGGGCAAGGTCACCCCCA | + | 6.34 |
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| Number of super-enhancer constituents: 28 | ID | Coordinate | Tissue/cell |
SE_01112 | chr8:38793267-38796600 | Adrenal_Gland | SE_02046 | chr8:38792906-38797424 | Aorta | SE_02449 | chr8:38792819-38797453 | Astrocytes | SE_03039 | chr8:38792819-38796540 | Bladder | SE_09752 | chr8:38792854-38797628 | CD14 | SE_10253 | chr8:38792914-38797711 | CD19_Primary | SE_10916 | chr8:38778152-38824593 | CD20 | SE_20358 | chr8:38793003-38797733 | CD56 | SE_25987 | chr8:38789829-38797700 | Duodenum_Smooth_Muscle | SE_26945 | chr8:38792798-38796597 | Esophagus | SE_30474 | chr8:38792683-38797435 | Fetal_Muscle | SE_35181 | chr8:38791545-38797788 | HeLa | SE_37318 | chr8:38792814-38797748 | HSMMtube | SE_40765 | chr8:38788682-38797591 | Left_Ventricle | SE_42292 | chr8:38789499-38797614 | Lung | SE_43830 | chr8:38792904-38796597 | MM1S | SE_44905 | chr8:38792860-38797384 | NHLF | SE_45759 | chr8:38791665-38797652 | Osteoblasts | SE_48823 | chr8:38792663-38796524 | Right_Atrium | SE_49720 | chr8:38793346-38796420 | Right_Ventricle | SE_50238 | chr8:38792759-38796543 | Sigmoid_Colon | SE_51979 | chr8:38793035-38796553 | Skeletal_Muscle_Myoblast | SE_52798 | chr8:38792885-38797648 | Small_Intestine | SE_53542 | chr8:38792660-38797616 | Spleen | SE_54989 | chr8:38791683-38797578 | Stomach_Smooth_Muscle | SE_56232 | chr8:38793215-38796134 | u87 | SE_62854 | chr8:38792840-38824305 | Tonsil | SE_63754 | chr8:38793035-38797448 | HSMM |
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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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| Number: 1 | ID | Chromosome | Start | End |
GH08I038934 | chr8 | 38792014 | 38798166 |
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Enhancer Sequence | TGGAGCAGGC ACCACTGCTG ACCCGTGATG CAGCGGTGAT AAAAAGGCCG GGAGATTTAG 60 AGCCTCCCCA GGAAGAGGAA CTCTTTGTAC AGTGAGGAGA GCCAGGTGGC ACCCCGCCAG 120 CACTGAGGTT TCGGAAGTCC TGTGCTCCCC ACACACCCTC ACTGCAGGCC TCTTGGGAGC 180 CTCTTCTGCC CTGCACATCC CCTTTCATCC TCAGGGGCTG GAGGCCTGGG GGCCCCTGAG 240 CCAAGGGTCT ATCGGCTCCA TCTTGTAACA AGCTTTGGGA GTCTTGTACC CTGGCTGGTC 300 AGGAGATGAA CCTGAAGGGG ACTGGGGGAC TCTGGAGGAG AGGCCACCCT TGGCTGGAGG 360 GGCAGCCCGC CCCTGTGCCT GTGGTATGCA GGCAGAGTCT GGCAGACACA GCCCAGTACA 420 AAGGCACAAG ATGCAGGGCA GCGTCAGGGC GGATTAAAGA GGGAGAGAAT GACCTCAGGG 480 AAGGAGGAAG GGCCTTTTCA AGTCCAGCCT TGCTAGCACA GCTGCCGGCA ATTTGTGCAT 540 GCCTTGTGGT GAGAAATGTG GCTGCCTCCC CGGGCCAGAG CAGCCAGAGG CCCAGGCCTG 600 CCCGCCCTCC CTGGCTTGTC CTCATCTTGC TGAGAGCTCC TGAGGTCGTT TCTCCAGGAG 660 GGTCGGAGAT GGAGAATTGA GAGCAGAGGA GCAGAGAACC TCGCAGTAAT AAAGGAAAAC 720 TGAAACCCTC TCCTGTGTGA GAGGGTTTGG GAAGCCTTTT TTTTTTATTT TTGGTTGGGG 780 AAGAATGAAT TCAGTCTCCT GCTGAATCAT GATTTATAAA TGCAGCTCAG ATGAGGGTTT 840 TAGAGTTCTC AGCCTTGGAG GCTGCGTCAT TTAGAAAGGG TGACCTGCCG TTTAGCCCCT 900 TCCCGAGAAA GGCAGGGCTG GATGGGCATT TTGCAAAACC CACAGCTGCC ACTGGGTCGG 960 GTTACACAGA GCTCAGAGCC TTTAACTCCT GCCTGACTCC CTGCCAGAAA GCAGGGGTTT 1020 TTCCCAGAAT GACATTTAGC CTCAGAGGCG CTGGACTCCA GCTCAGCATT CCAGGTCATT 1080 ATTTGTTAAC TCTTAGGTAT TCCTTCTTGG AGGAGAGCGC TTGCCACCGT GTCAGGTGGC 1140 CTGGCCAGAG GGCTGCGTGT GGGCTGGCTG TTCAGGGTGT GTGCTTCTCT GCTGTCTGCT 1200 GAGGGCCAGT GATGGGAAGA TGAGGACGGG CGTGTGGCCC TGGCCCTTTG GAGAGACAGA 1260 GATGAAAGTG ATGATTGGAT GTCATCCAGA GCATCAATGG CAACAGAACC AGTTCTTAGC 1320 AAACTAGAAA ATAATTAAAG CTGCACTTTG ACCCCTGCCT CCACCCGCCG ACTGCACAGC 1380 CAACCCCGCT GTCCCACCCC CAGCTGTGTC CCAGTTGTCA GGGCCTTGCT TTCAGCCACC 1440 TCTCAGAAAG AACTTGTAGG GGCTCATGGA TCCTTTTTTG AGACTGATGA AATGCATGGA 1500 TGCCTTCTCC AGGTAAATGC ATAGGTGTAC AGACACACCC TGCTTTTGCC TATAATTTCA 1560 GGGAGCCCAT TGACCTCCTG AAGCTGGTCC AGAGACCCCC ATCCCATGTA GGTGGCTGCT 1620 ATTCCCCTGA TCCTGATGCC ACCTTGTGGG GCAAGGTCAC CCCCAGATAC CAGGGCAGAG 1680 GCCGCAGCAG AGCTAGGAGA CCTTGTTTTG CTGCCACTGC TTCTGCCAGA GGGGCCCCAG 1740 CTCCTCTTCC GGCCATGGGC AGACAGGGTG GGGCTGGCCC TAGCCGTGCC TGGCCGCTGA 1800 CGAGCTTGCA GCTCCTGTGG TCTGTGTTTG ATCTGATAAG CGCAAGTTCC TGAGAGTCTG 1860 TTGAGCTGTG GAGCAGCCCT GTCTGCGTCA CTCTACGGGG GACCTGTGCC CACTCCCTGC 1920 TCACATCCCT GACCTCTGCT CGCTGCTGGG GTGTTCACAG GACCCACCAG TCAACCACTG 1980 CTGGGTAGCG CCTCTGCTGT GGCCACCTCG GCTGTGTGGA TGGCTGCACT TTGGTGGCCT 2040 CACTGGAGTC AGACGGTCGG GTGACCTCAC CCGCCTGCAG CCACGCCTCT TCATGAGAGG 2100 AGGTGAAGCC ACCACGTCTC CATGATAAGT TAGATTTCCT TCTTGGCCTT TCTTTTTCTT 2160 TTTTTTTTTT TTTAAATTTG AGACAAAGTC TTGCTCTGTC ACCCAGGCTG GAGTGCAATG 2220 GTGCAATCTC GCCTCACTTC AACCTTTGCC TCCTGGGTTC 2260
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