Tag | Content |
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EnhancerAtlas ID | HS134-36761 |
Organism | Homo sapiens |
Tissue/cell | Mesendoderm |
Coordinate | chr22:36821660-36823550 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr22:36823473-36823485 | AAACAAACAAAC | - | 6.32 | Foxd3 | MA0041.1 | chr22:36823477-36823489 | AAACAAACAAAC | - | 6.32 | Nr2f6(var.2) | MA0728.1 | chr22:36823258-36823273 | GAGGTCAGGAGTTCA | + | 6.22 | ZNF263 | MA0528.1 | chr22:36822757-36822778 | GGGGGATGGGGGGCAAGAGAG | + | 6.28 | ZNF263 | MA0528.1 | chr22:36822310-36822331 | TCTCCCTGCCCCACTTCCTCC | - | 6.45 | ZNF263 | MA0528.1 | chr22:36822329-36822350 | CCCTCCCCCTCCTCCTCTCTC | - | 6.86 | ZNF263 | MA0528.1 | chr22:36822295-36822316 | CCTTCCTCTTCCTCCTCTCCC | - | 6.89 | ZNF263 | MA0528.1 | chr22:36822289-36822310 | CTTTTCCCTTCCTCTTCCTCC | - | 6.95 | ZNF263 | MA0528.1 | chr22:36822333-36822354 | CCCCCTCCTCCTCTCTCCTCC | - | 7.35 | ZNF263 | MA0528.1 | chr22:36822301-36822322 | TCTTCCTCCTCTCCCTGCCCC | - | 7.85 | ZNF263 | MA0528.1 | chr22:36822292-36822313 | TTCCCTTCCTCTTCCTCCTCT | - | 8.22 | ZNF263 | MA0528.1 | chr22:36822323-36822344 | CTTCCTCCCTCCCCCTCCTCC | - | 8.39 | ZNF263 | MA0528.1 | chr22:36822326-36822347 | CCTCCCTCCCCCTCCTCCTCT | - | 9.3 |
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| Number of super-enhancer constituents: 14 | ID | Coordinate | Tissue/cell |
SE_01080 | chr22:36822232-36822985 | Adrenal_Gland | SE_09195 | chr22:36821805-36823234 | CD14 | SE_23071 | chr22:36822172-36823105 | Colon_Crypt_1 | SE_23740 | chr22:36822261-36822770 | Colon_Crypt_2 | SE_24731 | chr22:36822224-36822887 | Colon_Crypt_3 | SE_27650 | chr22:36821806-36823251 | Fetal_Intestine | SE_28644 | chr22:36821676-36823359 | Fetal_Intestine_Large | SE_40597 | chr22:36822213-36823332 | Left_Ventricle | SE_42094 | chr22:36821798-36823140 | Lung | SE_52340 | chr22:36821808-36823053 | Small_Intestine | SE_53283 | chr22:36821751-36823316 | Spleen | SE_58448 | chr22:36724049-36832686 | Ly1 | SE_62151 | chr22:36773097-36852649 | Toledo | SE_63127 | chr22:36801020-36866853 | Tonsil |
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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 |
GH22I036422 | chr22 | 36818448 | 36823730 |
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Enhancer Sequence | GCGTGGTGGC ACAAGCCTGT AGTCCCAGCT ACTCGGGAGG CTGAGGCAGG AGAATCGCTT 60 AAACCCGGGA GGCAGAGGTT GCAGTGAGCC GCGATCGTAC CACTGTGCTC CAGCCTGGGT 120 GACAGAACGA GACTCCGTCT CAACAAAACA AAACAAACAA CAAAAAAAGA AAGCTCAGGT 180 GATTTTTTCA ATTTCTTCTT CTTCTTCTTC TTTTTTTTTT TTTTTTTTTC CCAGAGACAG 240 CGTTTCACGC TGTTGCCCAG GCTGGTCTTG AACTCCTGGC CTTAAGCGAT CCTCCTGCCT 300 CGGCCTCTCA AAGTGCTGGG ATTACAGGAG AGGCACCGCA CCGGCCTCAG GTGTTTTCTG 360 GGCTTCTGTG CATTTCTGCT CCTCTCTGGG TTTCTGTCTA TCTCTGACTC TCCCTGTGTC 420 TCTCTCTTCC TCCCACACTC TTGCTGTCTT TCTCTGTGTA GTAACTTAAT TTCCCCCTCT 480 TGTTTCCTTT TCTCTTGTCT CTTTCTCTAT GCCTCTGACT GCTCATCTTC TGTTACCTTC 540 TGTCTCTGGT TCTCTCCTTT CTGTGTCTCA CTGTATTTTT ATTTATTTAT TTTTTTGGTC 600 TCTCCCAGTC TCTTCCAACT CCTTCTGCCC TTTTCCCTTC CTCTTCCTCC TCTCCCTGCC 660 CCACTTCCTC CCTCCCCCTC CTCCTCTCTC CTCCCATCTC TTTCCCTGCC CTGTCTCCCC 720 CTGGAGCTCC CACACAGGGA CCCAGCTGGC CTCTCAGAGA GAAGAGGCTC CCTGGAGGCC 780 CAGCAGGAAG TGCAGTTTCC CCTTTGACCT GTCAGCTGGC CACTGGGGAC GCAGCTTCCC 840 TCCCACTCCT GTCCACCAGG CAGCCTGTGA AGACTCCCTG GAGCTGGGGA TAGAGTTTTG 900 AATCTCGCCA TTTGAGGGGC TCTGAAGACA GGCTTTACCC GGAGTGGGAG AGAAGGGGAC 960 TGGGCTCCAG GGGAGGAGAA CCCCATTTTC ACGGGGCACC TCCTGGGTGC TGGTTCTCCA 1020 CCAGGTCCTG GGGAGAGGGA TTGTCAAAGG CCACAGTCCC TTTCTGAGAG ACAGAAAGAC 1080 ACAAAAGGGA AAGAGCCGGG GGATGGGGGG CAAGAGAGGT CTCTGTGGAG GCAGGGCTTC 1140 CGGGCCAGCC TGGATGAAAA GAACCACCCC CACACATTGC AGGGCTCCTA AGATATTTTT 1200 ACAGGGACTG AAGACCCTTA GGAGGGGCGG TGTGTTGTCA GAAAGTGTCC AGGAGTCGGA 1260 GTCAGAGGTC CGGCTTCCGA GTGCATTTCC ACCATGCTGT GTGCCACCTT GGCCATCTGG 1320 AGTAACCTCT CCCCGCCTGT TTGTGTCAGA GGCATTGGAA CCACAGCCAC TCCATCTTGA 1380 ATAGGGGCTG GGTAAAATGA GGCTGAGACC TACTGGGCTG CATTCCCAGA CGGTTAAAAC 1440 ATATCTCACA GGATGAGATA GGAGGTCAGC ACAAGATACA GGTCATAAAC ACTTTGCTGA 1500 TAAAACAGGT TGCAGTAAAG AAGCTGGCCC AAGGCCAGAT GTGGTGGCTC ACGCCTGTAA 1560 TCCCAGCACT TTGGGAAGTC AAGGCGGGCA AATCACCTGA GGTCAGGAGT TCAAGACCAG 1620 CCTCACCACA TGGAGAAACC CCGTCTCTAC TAAAAATACA AAATTAGCCG GGCATGGTGG 1680 CACATGCCTG TAATCCCAGC TACTCAGGAG GCTGAGGCAG GAGAATCACT TGAACCTAGG 1740 AGGCAGAGCT TGCAGTGAGC CGAGATGGCA CCATTACACT CCAGCCTGGG CAACAAGAGT 1800 GAAACTCCAT CTCAAACAAA CAAACAAACA AAAAAAGAAG CTGGCCCAAA CCCACCAAAA 1860 CCAAGATAGC AATGAGAGTG ACCTCTGGCT 1890
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