Tag | Content |
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EnhancerAtlas ID | HS007-10190 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr20:43969480-43972030 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESR2 | MA0258.2 | chr20:43970932-43970947 | AGGTCAGTCTGTCCC | + | 6.17 | EWSR1-FLI1 | MA0149.1 | chr20:43969809-43969827 | CCTACCTGCCTTCCTCCT | - | 6.15 | EWSR1-FLI1 | MA0149.1 | chr20:43971340-43971358 | GGGAGGGAGGAAGGATGG | + | 7.09 | FOXP2 | MA0593.1 | chr20:43970785-43970796 | ATGTAAACAAA | + | 6.14 |
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| Number of super-enhancer constituents: 33 | ID | Coordinate | Tissue/cell |
SE_00964 | chr20:43964885-43977614 | Adrenal_Gland | SE_01911 | chr20:43964890-43978032 | Aorta | SE_02392 | chr20:43969504-43977658 | Astrocytes | SE_23562 | chr20:43968306-43977650 | Colon_Crypt_1 | SE_24283 | chr20:43968580-43969997 | Colon_Crypt_2 | SE_24283 | chr20:43970212-43973779 | Colon_Crypt_2 | SE_26046 | chr20:43964321-43977082 | Duodenum_Smooth_Muscle | SE_26791 | chr20:43964902-43977688 | Esophagus | SE_28171 | chr20:43968612-43977361 | Fetal_Intestine | SE_29157 | chr20:43968321-43977386 | Fetal_Intestine_Large | SE_31528 | chr20:43964178-43978011 | Gastric | SE_33992 | chr20:43964899-43976782 | HCC1954 | SE_35002 | chr20:43964136-43977911 | HeLa | SE_35976 | chr20:43963799-43977058 | HMEC | SE_39008 | chr20:43964972-43977155 | IMR90 | SE_40831 | chr20:43963949-43977702 | Left_Ventricle | SE_41658 | chr20:43968300-43973685 | LNCaP | SE_42476 | chr20:43963996-43977803 | Lung | SE_44639 | chr20:43970127-43977753 | NHDF-Ad | SE_44896 | chr20:43969941-43977366 | NHLF | SE_45837 | chr20:43963257-43977959 | Osteoblasts | SE_47536 | chr20:43968320-43977079 | Pancreas | SE_48276 | chr20:43963617-43978083 | Psoas_Muscle | SE_48947 | chr20:43964906-43977636 | Right_Atrium | SE_49537 | chr20:43970173-43973703 | Right_Ventricle | SE_50902 | chr20:43968274-43977802 | Sigmoid_Colon | SE_51424 | chr20:43963960-43978125 | Skeletal_Muscle | SE_52708 | chr20:43964889-43977710 | Small_Intestine | SE_56644 | chr20:43969982-43977740 | u87 | SE_57011 | chr20:43970213-43977179 | VACO_400 | SE_58242 | chr20:43970204-43973793 | VACO_9m | SE_64465 | chr20:43964144-43977081 | NHEK | SE_69070 | chr20:43968795-43973708 | H9 |
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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 | CCCCAGCAGC GTACACTACT CGTAACTGTT CTTCCCCACC CCACCCACTT CTTAAGGGCC 60 AGACATTCCC CAGAATGGCT AAAACCTGGG GCCCACAACT GTGACTCTAC CACCCAGAGT 120 GGTTGTGCAT CAAGGCAGAT TCACAAGTGT GAGTTCTGCC ACTTCCTAAC TATATGAGCT 180 TGGGAGTTTA TTTCATCTCT GAAATCCTCA GTTTCCTCTT TTGTGACTAG GGCTGGTAGC 240 ACCTTGCAGG GTGATGAGGA TTAAGAGGAA TGCATTTGTG TGTGCAAGGG ACCCAGCACG 300 TGATCAATGA ATAGTGGCTG TGATTAACCC CTACCTGCCT TCCTCCTGGC CAGTGGGATC 360 AGTGCTCAAA GGATCAGAGG CCTGGGAAAA CTTGCAGAGG CAGTTCTGTT GCTGGAAGGA 420 AGCTAGCCTG GGGACAGGGA GATGGTGCTT TGCAAACTGT AAAGGAATAT AATCTATAAT 480 AGGTTATCAT TTTGCTTCTG AGCCCAGAGA CTTTTCAACA ACCAATCAGG TCCCTTCAGA 540 CTGTGAAAAA AAGATACAGA GATAGTCAGA GACCTGCCCA AGGTCACACA GCTTTGACCA 600 CCTGTCCTAA GCAGACAGAG GTAAAGACCA TTTTTATTTT CCCCGAAGGT GCAAATGACA 660 GTGACCAGAA ACACCTGAAA TTCTACTTGG GGACCTGGGT CCCCAGGGAC AAAATAAATA 720 AATAAAAATC TAGAAGGTAA AAAGAAACTA CACACCAATC CATGGTCTGG TGCTCTGGTG 780 CCTGAATGGT TAAACCAGGT CTGGGGGTGG GGGTGGAGTG AGGGTTCAAA TGTCGCCTTC 840 AAGGTCGGGT TACTCTGAAC ACAATCACTC AGGAGAGAGC CAGGCCTGGC ACTGCCTGCA 900 ACCAGCTTTT CACCAAGCCT CAGGGCAGCC CATTCCCACA GCAAGAACTC CAGGATCCTA 960 GGGTGCCAGC TAGAAATGGG GGAAGGGTTC AGGAGCCTCT GGATGTCTCC CTGCCAGGAG 1020 CTGACCCAGC ACCCTTGTTA CTAACTCCCT GGATGATCGT GGACAATTCC CTTCTCTGAG 1080 CCTCAGTTTT CCAATCTGTA AAAGACAGGT CTCAAAGAGA CAAGCCTCCC TCTGTCCCAG 1140 CCCAGTAACC AAGCTGGGCA TTGCTCCGAT TACCGGTGGA GACAGCCAGG AGGGGGCTGG 1200 CTCCCTCAGG GCCTCAGAGA CAGAGGTGCA TTGAAGTTGG AGCTTGTAAT CTAGGCAGCA 1260 GATCCGAAAT CCCTGCTGGA TCCGAGGGCT AGGGAGGCTC TCGGGATGTA AACAAACCTC 1320 CTGTGTTCTC AGAGCAGAGT AGAGAGCCCA CGCTGCAGCC TTATCTCAGC TGATTAGATC 1380 AGCCCTGGGT GCTGGCTTCC TGCCTCTTCC CAGCCTCCCT CACCGACCCC CAAGGAAGCC 1440 ATCCTCCAGA CCAGGTCAGT CTGTCCCACA GACGGCTCCG GCAGGGCTTC TCCAAGGCAA 1500 GGAGTATCCC CACTCTGGGT AGCCGGGCCA GCCATGTGCC ACATCTGCCC CCACGCCCAG 1560 AGGCTAGAGT GACACCGCCA GTCCCCGCAG GCCTGGCCAC TGACTGCTGG GCTTCACCAA 1620 GTCACTGTTT CCACACATAC CAGCCTCTCC CTGCCTCCCC TTTCCATTAC CCCAGGTGTC 1680 ACCTGACCAG CAGCCTCTTC TACTGTGCCA GAGAAAACTG GAGCAGCCGA GCTCCCGGGC 1740 CTGGAGGACA GGGGGAGGGG TGAGATGCAG CCTGAAGGGG TGGGGGCCGC TGAATAGGAA 1800 GGTCTGGGCT GAAGGTGGGG GTTGGGGGAA GCAGGAGGCA AGAACAAGGC TGGGAAGTGG 1860 GGGAGGGAGG AAGGATGGCT GTAGAAAGGT CAAAGCCAGA AAGAACTGCT GAGATCAGAG 1920 TGACCTTTTG GGGAGTACTG CAGCCCCCTG AAAAGGATAA AAAGGTCTAA ACCCCAATAA 1980 CTGTAACTCT TAGTTTACAT TTTCAACATA TGCACAGACA CCACCTCCCC AAAGCCAAAC 2040 TCTGGCCGGG TTAAGAACCC TCGTCTAGGT GCTAATAAAG CCAGAACTTT ACAAGTTTGC 2100 CAAACAGCGA TGATGACCTT TGAGTGCCAC AGGTGTTTTA TAGAGGACAC TGGAGTTCAC 2160 ATCAACAAAG TGACGTATTA ACTGTGTGTG TCCCTGGGTG AGCAGCAGAG CTAGGACGGG 2220 GGCTGGAGTT TTCTGTACCC TCTTTTTCAG TCACCCAGCC TTCAGCAGAT GGGACCAGAG 2280 AGGCCCCAGT GAGATGCAAG AATGTGCCCA AGGTCACCAC TGTGTTAGTT AATGACAAAC 2340 AAGCCCAAGA AGTCAGGCTT ATTCTTCTAA GGTTAAATGA GACCCCAACT GTTGACATAT 2400 GTGTTCTCTC TCCTCCCTCT CTAGGGCACC ATGCAGTGAA AACATACGAG AAACTGGCTT 2460 TTCAGAACAC TGTACCTTTT CTGTCCACCA ACACCCCACC CCTCAAAGTG CTATTTGCAA 2520 TCACTCAGCC TCCTTAAGGG TAGAAACTCT 2550
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