Tag | Content |
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EnhancerAtlas ID | HS042-19249 |
Organism | Homo sapiens |
Tissue/cell | Fetal_brain |
Coordinate | chr17:37040920-37043680 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr17:37041162-37041177 | TGAACTCCTGACCTC | - | 6.22 | RFX1 | MA0509.2 | chr17:37042471-37042487 | GGTTGCCATGGAAACC | + | 7.07 | RFX1 | MA0509.2 | chr17:37042471-37042487 | GGTTGCCATGGAAACC | - | 7.09 | RFX2 | MA0600.2 | chr17:37042471-37042487 | GGTTGCCATGGAAACC | - | 7.58 | RFX2 | MA0600.2 | chr17:37042471-37042487 | GGTTGCCATGGAAACC | + | 7.65 | RFX5 | MA0510.2 | chr17:37042471-37042487 | GGTTGCCATGGAAACC | - | 7.49 | RFX5 | MA0510.2 | chr17:37042471-37042487 | GGTTGCCATGGAAACC | + | 7.5 | SOX10 | MA0442.2 | chr17:37041352-37041363 | TGCTTTGTTTT | - | 6.02 | ZNF263 | MA0528.1 | chr17:37043459-37043480 | TCCTCTCCCCCACCCTGCTTT | - | 6.15 |
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| Number of super-enhancer constituents: 23 | ID | Coordinate | Tissue/cell |
SE_01869 | chr17:37041107-37042219 | Aorta | SE_04550 | chr17:37041217-37043246 | Brain_Anterior_Caudate | SE_06121 | chr17:37040932-37044381 | Brain_Hippocampus_Middle | SE_08151 | chr17:37040990-37043157 | Brain_Inferior_Temporal_Lobe | SE_19419 | chr17:37041258-37042819 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20407 | chr17:37041868-37043049 | CD56 | SE_22571 | chr17:37041198-37043140 | CD8_primiary | SE_23506 | chr17:37041139-37044448 | Colon_Crypt_1 | SE_24046 | chr17:37041309-37042184 | Colon_Crypt_2 | SE_24046 | chr17:37042719-37043159 | Colon_Crypt_2 | SE_24046 | chr17:37043169-37043889 | Colon_Crypt_2 | SE_27795 | chr17:37039457-37044351 | Fetal_Intestine | SE_28678 | chr17:37038937-37044257 | Fetal_Intestine_Large | SE_31542 | chr17:37041115-37044397 | Gastric | SE_42353 | chr17:37041080-37044562 | Lung | SE_50172 | chr17:37041116-37044569 | Sigmoid_Colon | SE_52400 | chr17:37038709-37044606 | Small_Intestine | SE_53492 | chr17:37041098-37041748 | Spleen | SE_59348 | chr17:37019329-37056453 | Ly3 | SE_62887 | chr17:37023359-37058235 | Tonsil | SE_65628 | chr17:37041277-37043501 | Pancreatic_islets | SE_68729 | chr17:37041065-37042402 | H9 | SE_68729 | chr17:37043286-37044499 | 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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| Number: 1 | ID | Chromosome | Start | End |
GH17I038876 | chr17 | 37032836 | 37043967 |
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Enhancer Sequence | CGTGAGCCAC CACGTCCGGC TTTTTTTTTT TTTTTTTTTT TGAGATGGGG TCTCTCTCTG 60 TCTCCCAGGT GGAAGTGCAG AGGTGTGATC TCGGCTCACT ACAACCTCCG CTTCCCGGGT 120 TCAAGGGATT TTCCTGCCTC AGCCTCCTGG GTAGCTGGGA CTACAGGCGT GTGTCACCAC 180 GCCCGGCTAA TTTTTGTATT TTTAGTAGAG ACAGGGTTTT GCCACGTTGG CCAGACTGGT 240 CTTGAACTCC TGACCTCAGA TGATCCGCCC GCTTCGGCCT CCCAAAGTGC TGGCATTTCG 300 TGCCCGACCT GTATCATATA CCTTTGAAAA GTTCAGAGGG ATAGGCAGCT CCTAAGCAGG 360 TGTGGCTGAG AGGCCCCAGA ATATCTCTCA TAATGGCCGA GCTTGGAAAC GAGTTGGGTT 420 TGAAGGATGA AGTGCTTTGT TTTGCACCCA ACCTGCCAAG CACATCTTTC CCCAGAACTG 480 AGTGCTGGAG GTGGCTGGGG TCCATCTGGC CTCCCCTTCG CTGTCTGGGC AGCTGTGGTG 540 TAGAGGAGAA TGCCTTGGGC AAGGTCTCTG TCCTTGACAC TGGACCTCAG TTTCTTCATC 600 TGTAAAACGG CACAATGAGA ATGCCAGCCT AAAGCTGTGT GGTGGGTTTT GAGAGAGAAT 660 GTGCACAGGA CTCAGTGTGC CAAGATGTTG CTTTGTGTCT CTGTAAATTG TCCTGAAGCC 720 CGAGGCTGCT GCCAATAGCT GCCTGTTTGC CCTGCCCTAT CCCTGTCCAG TCCCTGTTCC 780 TGCCCCGCTT CTTCCTGTCC TACATGCCTC TCCCTGCAAA CTCCCCAGAG CAGCTGATAG 840 CAGGGAGGAA GGGTGGGTGG GGCACCTGCA GAGAGCCCAC CACCCACTTG GAATGATTAA 900 CAAGGGGCCA GTACAGGCTG GCCTATGGGA CAAAGGACAG CTGTGCTCTG GACTCTGCCC 960 TGCACCCAGC TGATCACCTG TCCCTCATTC CTCGCCATGG CCCAGTCTGT CATGGGGTTG 1020 GGTTCCAGCG GAGTCACCAG CTGGGACGGG TGGCCCCTGG TCTGTCTTAG CACCCATGTT 1080 GGCATGCACA CATTTCCAGC CATCCCTGCT GGGATCTAGG GGTAATGGAT GGGATGGGCA 1140 GGAAGGGAAA AGGTAGAATT CCCAAAAATT GTTTCTGGAG GGAGGTCAAA TCAGTTGGAG 1200 CTTTCTTTGA AGCCCGGCAT GCTGGTGGGG GGAGGGGTGC AGCACTGATG TTCTCATGCC 1260 TTTGCTTCTA GAAACAAACC CGTGACACTT GTCCTCCTCA CCTAAATTAT CCAGAAAGAT 1320 CCTATAGACA CAGTCTCCTG ACTTTGCCCT CATGGGCTTC TCCTTAGTTG AGGACCCCCT 1380 TGCTGTCTGT GCCTCTTCCT CAACCCCCGT AGACCTCTCT CTCTCTCTCA CTCATTCTCT 1440 CTCACTCGCT CTCTCACTCT CACTCTCTCT CTCTCTCTCT CTGTCTCGCT CTCGCTCTCT 1500 CCTCACTCTC TCTCTCACTG TTGCTGCTCT CCTGCCTGGA GCTGAAGATG AGGTTGCCAT 1560 GGAAACCTGA AGCGTAGTGA GCCGGGAGAG GGAAAGGCAG AGTCGTCTCG CCAGGGCTGG 1620 GGGCTGGGGA CTGGGGACTG TGGGCTGTGG GGAGGGGACA GGGTTGACCC AGCAAGAGGA 1680 ATATAGCCCA AGCTGTCTGC CTGCCTTCCT CTGCCTGGGG TTGGGCTTAG TGGGCAGGGG 1740 AAGGAGCTTG GAGGCTCTGG AGTGCCTCTT TAATCTAGTT AATCTGATGC AGGATTAAAA 1800 TCCTCCCTCA CTCCTGCCAA ATTAAGCTGA GCTCACATCT GGGCTGGCTC ACCCCCACTT 1860 CCCTTCTGAT GGGATTAGCA CTCCAGCTGT CGGGGGCTGA GACTAGGGGG AAGGGTGCTT 1920 CTGAAGAGGA TGAAGTACCT GCCAACCCCA CCCAAGGTGC CTGCTGCATG TTGGAGGGGC 1980 TCCCGAGACC GTCTGGTGGG TGTAGGGTGA GCAGAGGGAC ACAGTGTGGG GTGCAGGGGG 2040 TGTGTGGACA TGGCCTCAAT GCAGCTGCTG CCTGGGTGTC TTGGAGGCGC CCATCGGTGC 2100 AGAGGGCACA TCTATATATT CATCGTGTGT GAGGCACAGT GCAGTGTGTG TAGGAACTTC 2160 AGACTGTGGA ATGGGTGGGG CACGTCAGGT GCACCTGTCT GGCGGTCTTT GGGCACTGGA 2220 GCTGGCCTCT GTTTTATTTA TTTATTTAAT AAAAACAGGC TCTCGCTCTG TAGCTCAGGC 2280 TGGTCTCAAA CTCCTGGCTC AAGAAATCTG CCCTCCTTGG CCTCCCAAAC TGCTGGGATT 2340 ACAGGCGTGA GCCACTGCAC CCAGCCTGGC CTGTTTTAAC CCTGTGCATT CTGGCCAATG 2400 AGAAACCCCA GGGTTTTGCA GACCGGGTCT GGAGGATGTG TTTGCCCTGC TTGCCTCTAG 2460 CCCTCCCCAT CAAATGCTAA CCAGCCTCAT CTTCTCAGAA TTGAGTCTTC GAGTGCTGGG 2520 CCAGAGCTGC CCGGAGGTCT CCTCTCCCCC ACCCTGCTTT TGCCACATGT GCCTCTACTT 2580 CCATGTGCTT GCCTCACCAC AGCCCCTGCC CATACAGTCT GCAGAATGGC TCTGATGTTG 2640 GGAGGAGGGT CGTCTCGTCT CTGAAGCGCT CCCTCTTAGG GCCTCAGGGC CTGCCAGCCC 2700 TGCTAGAGAT CTTCCCTTTC TGGTCTCTAG GAACAGACTC GTGGTTGATC ATCCCTTGGC 2760
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