Tag | Content |
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EnhancerAtlas ID | HS047-22793 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr22:36814770-36817380 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MSC | MA0665.1 | chr22:36816599-36816609 | AACAGCTGTT | + | 6.02 | MSC | MA0665.1 | chr22:36816599-36816609 | AACAGCTGTT | - | 6.02 | MYF6 | MA0667.1 | chr22:36816599-36816609 | AACAGCTGTT | + | 6.02 | MYF6 | MA0667.1 | chr22:36816599-36816609 | AACAGCTGTT | - | 6.02 | Zfx | MA0146.2 | chr22:36816890-36816904 | CCCGCCTCGGCCTC | + | 6.01 |
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| Number of super-enhancer constituents: 26 | ID | Coordinate | Tissue/cell |
SE_01080 | chr22:36815052-36816054 | Adrenal_Gland | SE_09195 | chr22:36815068-36816039 | CD14 | SE_23071 | chr22:36815208-36815913 | Colon_Crypt_1 | SE_23071 | chr22:36816162-36816817 | Colon_Crypt_1 | SE_23740 | chr22:36815198-36815895 | Colon_Crypt_2 | SE_23740 | chr22:36816245-36816671 | Colon_Crypt_2 | SE_24731 | chr22:36815495-36815926 | Colon_Crypt_3 | SE_24731 | chr22:36816226-36816782 | Colon_Crypt_3 | SE_27650 | chr22:36814561-36817422 | Fetal_Intestine | SE_28644 | chr22:36814534-36817532 | Fetal_Intestine_Large | SE_31378 | chr22:36814781-36815933 | Gastric | SE_31378 | chr22:36816180-36816888 | Gastric | SE_37504 | chr22:36814759-36817554 | HSMMtube | SE_40597 | chr22:36815120-36816847 | Left_Ventricle | SE_42094 | chr22:36814585-36816153 | Lung | SE_42094 | chr22:36816173-36816849 | Lung | SE_47757 | chr22:36815488-36815856 | Pancreas | SE_50050 | chr22:36814593-36816138 | Sigmoid_Colon | SE_50050 | chr22:36816153-36817226 | Sigmoid_Colon | SE_52340 | chr22:36814707-36816100 | Small_Intestine | SE_52340 | chr22:36816150-36816885 | Small_Intestine | SE_53283 | chr22:36814653-36816958 | Spleen | SE_58448 | chr22:36724049-36832686 | Ly1 | SE_62151 | chr22:36773097-36852649 | Toledo | SE_63127 | chr22:36801020-36866853 | Tonsil | SE_65459 | chr22:36815057-36816054 | Pancreatic_islets |
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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 |
GH22I036418 | chr22 | 36814698 | 36817466 |
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Enhancer Sequence | AAAAAAAAAA ATAGCGACTG GGTGTCACTA TGTTGCCTAC ATTGGTCTCA AACTCCTCGG 60 TCTCCCAAAG CGCTGGGATT GATGTAGGAG GTGGGACTCG ACTCTGGAGG TGGGGCTCAC 120 ACATTGAACC AAATCAAGGA CTAGCTAGGC TGGGCGCTGT GGCTCAAGCC TGTAATCCCA 180 GCACTTTGGG AGGCTGAGGC GGGTGGATCA CGAGGTCAGG AGTTCGAGAC CAGCCTGGCC 240 AACCTGGTGA ACCATCATCT CTACTGAAAA TAAAAAAATT AGCCAGGCAT GGTGACGGGT 300 GCCTGTAGTC CCAGCCTCTC GGGAGGCTGA GGCAGGAGAA TAGCTTGAAC TCGGGAGGCA 360 GAGGTTGCAG TGAGCCGAGA CCATACCACT GCACTTCAGC CTGGGTGACA GAGCGAGACT 420 CTCTCTCAAA AAAAAAAAAA AAAAAAAAAA GAGAAAAAGA AAAGGAAGAA CAGAAGAACA 480 GAAGAGAAAG GGCACCCCAC ACACATCCAT TCCTCTCTTC CTCCGTTAAA CCGGAGCCAG 540 GGGCTGGGGC TGGGTGTGTG TGCTCCTGCC TTCCCAGGCT CTTGCTTGTT TTCAAAGGAC 600 CAGAGAAATG TCTGGAGGAC TGCTGCTTCA GTCCACGTGA CCAGGATGAA AGTCATTAAC 660 AAAAGGCCAA TGTTTGGGGA AGAGCCTTTG CCCTCCTTTC AGGGCCTCAG CTGGGGCTCA 720 GGGAGATAAG GCGGGAGCAA AAATAAAACT GAAAATGTGT TTACTCTGAG ATGAAAGTGC 780 ATTGCTAAAC GCTAGCCGCG AGGACTTGTA TACAAAAACC ACATGTCTGG GGGTGTTCTG 840 GAATGTCACA AACTGCAATG GCAAGAAAAG GCAGCAGGCA GGACCAGGAC TCTGCTCCGT 900 GGGAGCCCCC TCTGGTGCCC TGGCTCTGTC ACCTCCTAGG GTCTGTGATC TCTCAAACCG 960 GACCTCAGAC AGCCTGAGCA GCCCACCCAG CCACGTGAGC CACCGTGCCC AGCCTGATTT 1020 CTTTCTTTCT TTTGTTTTCT TTCACTTTTT AAACAGAGAC CAGCAGGCCA GGTGCGGTGC 1080 CTCACGCCTA TAATCCCAGC ACTTTGGGAG GCTGAGGCAG GTGGATCACC TGAGGTCAGG 1140 AGTTTGAGAC TAGCCTGGCC AAGATGGTGA AACCCCATCT CTACTAAAAA TACAAAAAAT 1200 TAGCTGGGCG TGGTGGCGGG TGCCTGTAGT CCCAGCCACT CGGGAGGCTG AGCCGAGATC 1260 GCACCACTGC ACTCCAGCCT GGGAGACAGA ATGAGACTCC GCCTCAAAAA AAAAAAAAAA 1320 AATTAGCCTG GCGTGGTGGT GGGTGCCTAT AATCCCAGCT ACTCGAGAGT CTGGGGCAGG 1380 AGAATTGCTT GAACCCGGGA GGCAAAGGTT GCAGTGAGCT GAGATAGCGT CATTGCACTC 1440 CAGCCTGGGC AACAGAGCGA TACTCCGTCT CAAAAAAAAA AAAAAAAAAA GCCATGAGTG 1500 AGTTACTCTT GCGAGCAGCC CTCTCGAGCT GGAGTTTGAC TCCTGGAAGA TGGGATGCCA 1560 CTGTGACTGA GCAAACATAG GAATAGCTGT TCCACTAAAG TCTCACAAAG CCACTGGCCG 1620 GAGGAATTTC TCTAGGGACT CCCAGGAGCA GCTGAGGAAA CATGAAGGAG TGGACATTCC 1680 CAGAAGCCAA AGAAAAGTCG TTTGGTTACA GAGACTGGTG TCTGTGTTCT TCTAGAAAAC 1740 ATGGGCTCTG CTGAGATCAG GGAAGACTCT GACAGGAGCC ACCAGGCAGA ATCCTCCAGA 1800 CAGACTAGAA TGAGTACAAA GGAGAACAGA ACAGCTGTTG CTGGGCGTTT GGACTGAACA 1860 GACCTTTCTC ACGTGTTGTT TTTATTTATT TATTTGGAGA GAGTCTTGCT CTGTTGCCCA 1920 GGCTATAGTG CAGTGGTGAG AACTTGGTTC ACTGCAACTT CCACCTCCTG AGTTCAAGCT 1980 ATTCTCCTGC CTCAGCTTCC TGAGTAGCTG GAATTACAGG AGTGAGCTAC CATACCTGGC 2040 TAATTTTTGT ATTTTTAGCA GAGACGGGGT TTCAGCATGT TGGCCAGGCA GGTCTCAAGC 2100 TCCTGGCCTC AAGGGATCCA CCCGCCTCGG CCTCCCAAAG TGCTGGAATT ATAGGCATGA 2160 GCCACCACAC CCAGCCTGTT ATTATTTTTT AATTTGAGAT AAAACAGAAG CCATGTACCT 2220 TTGAATTATT CTAACCAAAA GTCTCCTGTT GGGACTTACA CAGAACCACT AACTGTCAAG 2280 TGTCTGCTGG AAGCCTCAGT TTCCTCATGT GTAAAGTGGG GAAAATAATA GTGCCTGCCT 2340 CCTAGGACTT AAAGTTGTTT GTGAGAAATG CTTAGTGCTG GGCATGGTGG CTCATGCCTC 2400 TAATGCCAGG GCTTTGGGAG GCCAAGGTGG GAGGATTGCT TGAGACCAGG ATTCTGAGAC 2460 CAGCCTGAGA AACATAATGA GACCCTATCT CTACAGATTT TTTTTCCATG AGGCATTTTA 2520 TTTGTAAATA TGTGTATTAC ATCCCTAGAA AAAGAATCCC AGGATTTTCC CTCCTGTGTG 2580 GTTTTGTCTT GCTTCTTCAT GGTCCATGAT 2610
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