Tag | Content |
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EnhancerAtlas ID | HS145-07426 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr14:65173120-65175580 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxa2 | MA0047.2 | chr14:65173405-65173417 | CCAGAGTAAACA | - | 6.11 | HNF4G | MA0484.1 | chr14:65173466-65173481 | AGAGGCCAAAGGCCA | + | 7.46 |
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| Number of super-enhancer constituents: 36 | ID | Coordinate | Tissue/cell |
SE_01667 | chr14:65170138-65174210 | Aorta | SE_01667 | chr14:65174221-65176548 | Aorta | SE_03251 | chr14:65171174-65173727 | Brain_Angular_Gyrus | SE_03251 | chr14:65173978-65177141 | Brain_Angular_Gyrus | SE_03953 | chr14:65167393-65177259 | Brain_Anterior_Caudate | SE_04856 | chr14:65167380-65178363 | Brain_Cingulate_Gyrus | SE_05821 | chr14:65167078-65178630 | Brain_Hippocampus_Middle | SE_06781 | chr14:65167470-65178320 | Brain_Hippocampus_Middle_150 | SE_07938 | chr14:65167829-65178149 | Brain_Inferior_Temporal_Lobe | SE_08852 | chr14:65174039-65174305 | Brain_Mid_Frontal_Lobe | SE_19856 | chr14:65169671-65177140 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20478 | chr14:65170052-65178236 | CD56 | SE_22874 | chr14:65171327-65178287 | CD8_primiary | SE_23289 | chr14:65169420-65174658 | Colon_Crypt_1 | SE_23289 | chr14:65174718-65176023 | Colon_Crypt_1 | SE_24426 | chr14:65173694-65174003 | Colon_Crypt_2 | SE_26750 | chr14:65169114-65176429 | Esophagus | SE_27717 | chr14:65169061-65176549 | Fetal_Intestine | SE_28783 | chr14:65169016-65176598 | Fetal_Intestine_Large | SE_32308 | chr14:65169312-65174204 | Gastric | SE_32308 | chr14:65174691-65176389 | Gastric | SE_36148 | chr14:65168954-65176260 | HMEC | SE_47632 | chr14:65173298-65173732 | Pancreas | SE_47632 | chr14:65174732-65175628 | Pancreas | SE_49272 | chr14:65170129-65174244 | Right_Atrium | SE_49272 | chr14:65174275-65176530 | Right_Atrium | SE_50477 | chr14:65169120-65176913 | Sigmoid_Colon | SE_54434 | chr14:65170219-65177185 | Spleen | SE_57093 | chr14:65169032-65174194 | VACO_400 | SE_57093 | chr14:65174718-65176042 | VACO_400 | SE_57603 | chr14:65169365-65174567 | VACO_503 | SE_57603 | chr14:65174647-65176157 | VACO_503 | SE_57932 | chr14:65170543-65173862 | VACO_9m | SE_64475 | chr14:65169439-65176203 | NHEK | SE_65298 | chr14:65169344-65176523 | Pancreatic_islets | SE_68953 | chr14:65173162-65174205 | 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 | GGCCAATTCA CTTATCTTTT CTGACTCAGT TTCCACATAA ATAAAGTGGG ATTACTTGCC 60 TGCTCTTCCT CATAGGAGCT GTGGTGAGGA TCAAAGGAAG CCTCATTTGT GGAAAGTGCT 120 CCATAAACTC CTGTTAAAAC TAAAGGGCTC ACAGTGGCTC GGGAGGGAGT CTCCCAAGGG 180 TTTTACAATT TGCTGGCTAT GTCCCACGTG TGTGCCACAA GGAGACGTTA GATACCAGGA 240 GCCATTGTTG GATGTTTAAA ACACCCTGGT CTTAATATCT CAGCCCCAGA GTAAACATTT 300 GCCTTACCAA ATCCGCAGCT ATCCCACGGT CACTGTTTAC GCTGGAAGAG GCCAAAGGCC 360 ACGGCCTGCG GGATGACCAG GGCTGGAGGG GGAAGGCTCC TCTGTTGCAG AGGTATGCCT 420 TGCCCGTTCT CTTCTCCCAG CTCCCAGAAC CTTGTGAAGG CTCCAGCTGT AAGCCAGGGG 480 TGCTGCCACA AGCCCAGGCC GCCCTGGCCT TGGAGGGTTA AAAGTGAAGC CCTCTGGCTA 540 TTCTCTGTTG TGTTGGGGGT TGCAGGGACT CTGGGAGGGT GTTGCTTTTG CAGCTGCACT 600 GAGGGCTGTC TTCAGCTCCT CATCTGTGCC CCCTCCCCCA TCTCAGGCCG CCCCTCTGGC 660 CCAGGCCACT GCTCTGTCCC GCCTCTCTGG CCAGCTGCAA GTCCACAGGC CTTTGTTCCG 720 TGGCTGCAAA CCCGCCCTAC TCCATCCTCC CTCCTCAGCA GAAGCCCTCC AGCGGGGGCC 780 CTGGCAGCTG GAAATCACAA CTGCCAGGAG GAAGGGGCTA CTGGAGCCCC CAGCGGACCT 840 GGCAGATCCT CATTTCCTCT TGTCAAGCTC ATCTGGGCCC CACAACTCAC CTCTGGCCAG 900 ATTCCCACAC CGTCTTTTCT CATCTCTCCT TTCTTCTGCT GAATGGACGG ATCACCTTTT 960 CCTCCCAGTA CTCATGCCCC TTAGTTCTAT TTTAAAGTAC TCTATTCATT CATTTAATAG 1020 TTAAGGAGTT AGCACCTACT ATGTATGAAT GCCAGATGCA GAAGACACAG CAGTGAAGAA 1080 AATATACAAT AATTATTGAC CCAGTGGAGC TGACTTTAGC AGAAGTGACA ATAAACAAGA 1140 TTGAAATAGC AAGTGTGTTA GTGATAAACA GAAATAAAAA ATATGATAGG GAAGGTAGGT 1200 GTGAATTGTC ATGGAAGGGG TGAGGTGACA GTTTAGATAG GGTGGCCAGG GAGGCTTCCA 1260 GGAGGAAGGT ACTTTTGAGG TGATGCCTGA AGGCGGTATT TTTCTTCATC GCTGCCTTTT 1320 CTAACTTGAA GCCCAGTTCA TCCCACTGTG GCATCGAGGA ACAGAGTTTG GAGTTGGACA 1380 CACCTTGGTT TCAAATCCCT GGCTTGACAG CTCACTAGCC CTGTGGACTT TGATGTGGTG 1440 CTAAATTCCT TTGAGCTGTG TTTCTTACCC AACGTGGAGT TAGTCATCAT ACTTACCACA 1500 TGCGGCATCA TGGCAATGTA CAGTGAGATA ACGTATGTTG AATGCTTAGC AAAGACTATA 1560 GAGAGGTTCG ATAAACTATT TCTCCAACCA AATTCTGCAG GGGTAGCATG AGATATTTAA 1620 TGTCATTGCT AAGGACTGTA GGTGCAAAGC TTTTCATTTT AGATATTGGG CAGGAGTGGG 1680 GAATTAGAGG GAGGGGAAAA TAGAAAACCT TGGCAAAAAC TTTCTGGTTA GGGAGGCTTT 1740 CCTGCCCTAC CCTAGATTGC AGATGGCTGA GGACGTGGGA CTCCCAGGTA TGTCCTATGC 1800 CCACCCCCAT CCTACAGATA GGATGACAGG GGCAGCCCTG ACCACCCCCC TCTTGCTCTG 1860 GAATTCCCCC TGCTTCCAGC CAGACTCAAT GAATCACACC TTCTCCCTGA CCTCCCGACT 1920 CTGCCTCACA GCTGGGAAGG CTGTCCACCC CTCCCCCAGC CTCCGGCAGG TAAATTATGC 1980 CTGGAGGTCG GAAGCGGAGT GGGGCGGGGA CAAGGGGTAG GGAAAGTGAG GGAGGGGGCA 2040 GATGGTGGGT GGAGCTGTCC TAGGAAAGCC CAGAAGGGTG GCAGGAGGAT TCTGGTGGAG 2100 GCTTCGAGAT GGCTCGGAAG ACTTTGAATA AGGGTTCGCC AGGGACCAGA ATTTAAAGTA 2160 ACAGAGTGAC AGACACAATG AGAACTCAGG GTCGGCTGCC TAACTCCTAG CCGCTTCTAC 2220 CCAGCTGATC TGCTGAGTCT CCGACCCTCT CTGCTGGAAC CACGGGCCTA CAAAGGGAGG 2280 GGTTTAATCT AAAGTACCGC TGTCAAAGTT TGTGGTGAGT GGCTTCCTGG AGACCCTGCC 2340 CTAGTTCAGG AAGTGAGAGA TGGGCAGTGG AGGATGAGGC CTAGGGAAGT GGTCATGGCC 2400 AGTTCCACCC CCCCGCCCCA CCCCCCAAGT ATGTCGCTGC ACACTCGGCA GCCAGGCAGG 2460
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