Tag | Content |
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EnhancerAtlas ID | HS184-20181 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr3:42054010-42056420 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr3:42055029-42055048 | CGGCCCGCAGGTGGCGGCG | + | 6.05 | JUN | MA0488.1 | chr3:42055944-42055957 | ATGACATCATCTG | - | 6.5 |
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| Number of super-enhancer constituents: 36 | ID | Coordinate | Tissue/cell |
SE_00063 | chr3:42053210-42058517 | Adipose_Nuclei | SE_01171 | chr3:42054332-42056059 | Adrenal_Gland | SE_01171 | chr3:42056113-42057025 | Adrenal_Gland | SE_01796 | chr3:42054165-42055170 | Aorta | SE_01796 | chr3:42055216-42057220 | Aorta | SE_02512 | chr3:42055179-42056224 | Astrocytes | SE_10226 | chr3:42053281-42057372 | CD19_Primary | SE_10922 | chr3:42051847-42059221 | CD20 | SE_23272 | chr3:42054002-42057196 | Colon_Crypt_1 | SE_24262 | chr3:42054204-42057031 | Colon_Crypt_2 | SE_24991 | chr3:42053973-42057170 | Colon_Crypt_3 | SE_25861 | chr3:42053527-42055150 | Duodenum_Smooth_Muscle | SE_25861 | chr3:42055368-42057453 | Duodenum_Smooth_Muscle | SE_26989 | chr3:42053970-42057177 | Esophagus | SE_29565 | chr3:42053750-42057409 | Fetal_Muscle | SE_36966 | chr3:42055096-42057639 | HSMMtube | SE_38230 | chr3:42054206-42055102 | HUVEC | SE_38230 | chr3:42055174-42057329 | HUVEC | SE_40683 | chr3:42053752-42057406 | Left_Ventricle | SE_42248 | chr3:42053783-42057505 | Lung | SE_44658 | chr3:42055202-42057431 | NHDF-Ad | SE_44918 | chr3:42054488-42055035 | NHLF | SE_44918 | chr3:42055221-42057239 | NHLF | SE_45733 | chr3:42054238-42057420 | Osteoblasts | SE_48185 | chr3:42054287-42057598 | Psoas_Muscle | SE_48670 | chr3:42053922-42057248 | Right_Atrium | SE_49555 | chr3:42054514-42055106 | Right_Ventricle | SE_49555 | chr3:42055109-42057064 | Right_Ventricle | SE_50309 | chr3:42053789-42057391 | Sigmoid_Colon | SE_51166 | chr3:42053575-42057505 | Skeletal_Muscle | SE_52625 | chr3:42053740-42057356 | Small_Intestine | SE_53513 | chr3:42053719-42057315 | Spleen | SE_54717 | chr3:42053746-42057466 | Stomach_Smooth_Muscle | SE_62800 | chr3:42053253-42125059 | Tonsil | SE_63663 | chr3:42055253-42056879 | HSMM | SE_65769 | chr3:42053879-42058280 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr3 | 42054046 | 42055050 | chr3 | 42055916 | 42056411 |
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Enhancer Sequence | TAATAGATGT TCCTCATTTT GGGTTTGTCC GATGTTTCAC TATCATGATT CAGGTTATGC 60 ATTGTCCCCA GGAATACTGC ATAGCTGATG TGGACATGAT ATCCATCTGC TCTCATTGGT 120 GATGTAAATT TTGATCACCT GGTTAAGATG CTGTCTGCCT GCCTCTTTGT ATAGTTACTA 180 TTTCCGCTTT TGCTACTAAC AGGTCTAAAC CATCTATGGG GAGACACATC AACCCAGACA 240 AATATCTGCC AGCCAGTAAC AGCCCCCTAG AGTAAGCATT CATGGATGAT TCTTGCCTGA 300 GCCAATCTTC ACTATACACT TGATGATCTC TTCAAGTCAA GTCTATGCCA GTATGAGAAA 360 TCAGGTTTTG CAGGGTTTAG TTTCCTTACA CCTTTGGTTC TGGTCTGAGT CTTCTTCAAG 420 TCCTCCCAAT GTCCTCTATG ACCCCTGGGT TGAAAAGAAG TAGACTCAGT AGCCTCAACT 480 GGAAATGAGA TCATGTGGGT TGTTCCCTGT TAAACCGTCC ACAAGTGATT TGCATAATAG 540 AGTGGCCTGT GAGCTCTTAC TTCCTGGATC GGTTCCTGAT CCCCTCTCTG CTGTCCGCCA 600 GCCCCCTGCC TGTCACCCTT TGGTGGCATC TTAGTCCAAC AGCCAGTTCC ATCCCCTCCA 660 GCCTTCCCCC CGTCCCCGGC TCCATCCTCC CTCCATTTAA GCCTAAGGGC GGCTTTGCTA 720 GGAGACAGCC CGCCCTGCAG GAACAGAACG CCTGGACTTC CACTGTGTTC ACGACAATCA 780 GCGCCCCGGG CCGCGGGGGT CCCATCCTTC TCTTAGACTG ACTCTGGAAG GACCCCGAGA 840 AGTGCTAGAA GTAAATAAGC GCTCGGGGAG GGATGTGATC AGCTTTTCCG GATCCAGGTC 900 TTTACCGGAT ACTTCTCTGT GCCCCACGGC GTGGGTAAAA GTGCAGGGGC AGCCGCGGGC 960 GAGGAAGGCG GGGCGCGGCT CCAGGCGACT AGGACGTGGC CGGCGGGCAT CCTGGAGGGC 1020 GGCCCGCAGG TGGCGGCGCG GGGCGGCGGG CGGGGCTGGG AAGGGGGAGG GCTCGGCGCG 1080 CGTCGGGCGG TGACGGCAGC GCGGAGGGGA GGTGCAAGCC GCCCGCTCGC GGGGGAGCCA 1140 TGGCGAGAGG CCGCGCGGCG GCGCCCGCAA CAGTGCCCGC GTCCGCAGCA GCGCCCCCGC 1200 CCGCCGCCCC GGGGCCCACC CGGCCGCCGC CCCCGCGCGC CCCGAGCCCT TGACGCCCGC 1260 GCGCCTCAAG CGAGGCGTCC CCCAGAGTGG GGCCGCGCGC GGGAGAGCCG GAGCGCAGCC 1320 TTAGCGTCCC CGAGAGTCTC GAACGCCCCG ACGACCCCCG CGTCTCGGAA CCCCGGACTC 1380 CGAGCCCAGG AGCGCCAGAG CGGCAGGCGG GCAGCAGGAG GCGGCGGCGC CAGAGCGGAG 1440 CCCCCGCGAG TGCCCCCGTG CCGCCCGGCC GGCTGCAGCG GAGGGAACCG AAGCCGCCGG 1500 GCGGCCGGGG CCGGGCCGAG AACGACGCGG AGGAAGCCCC CACCGAGGCC CCCCGGCACC 1560 GCGCCTGCTG CCGGGTTGCG CTCCGTGCAC CTCTTGCGGG TAAGCCAGGG GTCCGCTCAC 1620 CCGCGCCGCC TGCGCCTCGG GCCCAGGGGC TGGGGAAGGA CACGGGTGTT CTGGGAGTGT 1680 CCGCGTGAGA TAGTGGCGGC GTGAGAGGCC GGGCGCCGGG ACCCTGCGGG GACAGCCCTC 1740 CTAATGCACC GGCCGCACCT GCAGGAGGCC CTCGGAGCCC GGAAAAGTGC CCCTAGGGCA 1800 TCGTGTCGGC CACGCCGCGT GGCCTGGATT CCGCGCTCCG GCACTCCGAG GTGACAGTGA 1860 GGCGACCTTC AAAGAGCCTG GAGCTGAGCG CGGGCAGCAC CCCGATTCCC ACTCACCCGC 1920 AAAACTTGAT GAAAATGACA TCATCTGAGC GTGTCAGAGA GCAGAGAGCC TTTAGAGCCC 1980 TCCTTTGCAT CCTTGAGAGT TAACAAGTTT ACTTTGTCAC TTTCTTGACC TGATTTTTAA 2040 AGTTCTTTTC TAGTCTCCAA GGTCAAGCTC TTGCAGGTAA AAACAAATGT AATGAACTGT 2100 ATCGTTTCTT CTTTTGTAAA GTTGTGTTTC AGGAAAGATG TTAAAAGTCG GCCTGCTCTT 2160 GAGGCTGGTG CTGGGTGCCC CTTCCGCTTT AAGCTTGCCT GTTTTAGAAC CCGTGGCTGC 2220 ACTTGTTCAG ACACTGAAAT TAGCGTCCGC TTTGAGAGCC TTCAGAGTAT TCGTCGTTGG 2280 ACCGCTGATT TTTTTTTTTT TCTGATATGC TTCACTGGAA CTTTATTTGC TTCAAAAGTG 2340 TAAACGTTGT CAATACTGTC TGTGAGTGTG TATTCGGGAC TGGTAACCTT TTCTGGAGGG 2400 TCTTTTGTTT 2410
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