Tag | Content |
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EnhancerAtlas ID | HS073-14728 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr9:130788440-130789760 |
Target genes | Number: 13 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr9:130789360-130789381 | CACCCTGCCCTTCCCTCCTCC | - | 6.01 |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_12408 | chr9:130786434-130791563 | CD3 | SE_23006 | chr9:130786408-130791742 | CD8_primiary | SE_31243 | chr9:130786453-130792509 | Fetal_Thymus | SE_47183 | chr9:130787622-130790192 | Panc1 | SE_55460 | chr9:130787399-130790485 | Thymus | SE_62942 | chr9:130767703-130798071 | 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 |
GH09I128024 | chr9 | 130786483 | 130795931 |
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Enhancer Sequence | AACTTCTTGG CTCAAGCAAT CCTCCCTCCC CAGCCTCCCA AAGTGCTGGG ATTACAGGCA 60 TGAGCTACCG TGCCGGGCCT CTTCCTCCCA TTTGATAGCA GAAGAAACTG AGGCTCGGAG 120 ACACTAGGTG TGGAACACCG CAGGCACCAT GCATGCTGAG CACCGTAGCC ATGTGCAGGC 180 AGGAGCTGCT GTGGCCCCTG TGTCTGGGGC AGACGAGAGA GGAAGGAAAG AGGAGGCACG 240 GCCTCGCATG AGAGATTAAC TTGCGATGCC TCATTATCGC AAATTCATAT CTTTGAGGCA 300 GAACCAGAAA CAGGATGTGG GTTCCCCTTT AAGGGGCTGG TGCCTCACAT TGACAGGTAC 360 CATGGGACAC ATGTGAGCAT CATGGGACAG GTAGTGTCGG TAAGAGGTTG GCACCCAGGC 420 TTTGGAGTCA ACAGGCTCCT GGCTGTGTGA CTGCAGATTC GTGGCTTGAC CTCTCTGGGC 480 TTCTGAATAG CACGGGTTGT TAGGCCTGGT GGAACAGTGC TCAATAAATA GTGACAAGGT 540 ACTGAGCACT CCAACAAGTG TTGGAGGCAG GGGCAATTAT TTGCCAAAAG AGGCAAAGCC 600 TGTGGAGCGG CCTGGCCAGC TTTACCCCCG TCCCTGCTGC CACATCCATC CGCGGTCCTC 660 TGCCCGAGCC CAGCCCTACC AAGCAAACAC ACCATCAAGA GGAGGCAGGT TGCTATGGCA 720 GTACAGCTTC TGGAAAGGCC CTGGCCTCCC ACACAATATC CCTCCACTGT GGTGGCCCCA 780 GGCTTTTCCT GTGGAGGCTT CTGAGGTTGC TCCAGCCTGA GGCCAGCCTG GCCCAGATGC 840 TGACCCAGAC ACAGCTGTGT TCACATGACA CGGGTTTGCC GAGTACCTAC CAGGTTCACA 900 TGAGCAGGAC AGGCAAGGGC CACCCTGCCC TTCCCTCCTC CCAGGGCTCG ACCTGGGCCC 960 TGTAAGTGTC ACTTGCATTT AGGAGCTACA ATACAGCTCT CAGGAATGTC CTGAGTGTCA 1020 GGATGACAGG AAGAAAGGGA GAGCCCAGGT TCAAGAAAAG GACACTGGAT TGGGTGTTAA 1080 AGGCCCATGT CTCGGCCTAA CTCAGCCTTA GTGTCTCTGT GGTTGTGAGC AAACACCCAT 1140 TTCTCTCTGG GTGTTTAGAA CTGAGGGGAG TACATGGAGT TCTTTCAAAC TAGTCAAAAC 1200 AGAAGCCGAG CTGTGCACTC AGGAGGCAGG CAGCCCCTTG TTTTGGACTA TCGTCTATCA 1260 CTTACTCGCT GGGTGGCTTA AAGGAAGTTA CTCAACATCT CTGAGCCATT TCCTCATCTC 1320
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