Tag | Content |
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EnhancerAtlas ID | HS092-22477 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr19:13271290-13271960 |
Target genes | Number: 32 | Name | Ensembl ID |
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| Number of super-enhancer constituents: 15 | ID | Coordinate | Tissue/cell |
SE_11152 | chr19:13260138-13284995 | CD20 | SE_17360 | chr19:13270598-13276927 | CD4p_CD25-_CD45RAp_Naive | SE_27635 | chr19:13271249-13272060 | Fetal_Intestine | SE_28568 | chr19:13271245-13272063 | Fetal_Intestine_Large | SE_34050 | chr19:13271406-13271838 | HCC1954 | SE_34633 | chr19:13271191-13281627 | HeLa | SE_47439 | chr19:13271203-13272118 | Panc1 | SE_52361 | chr19:13271296-13271903 | Small_Intestine | SE_60135 | chr19:13260128-13279366 | Ly4 | SE_62354 | chr19:13259874-13293454 | Tonsil | SE_67827 | chr19:13271482-13271874 | u87 | SE_68590 | chr19:13260276-13279271 | TC71 | SE_68591 | chr19:13260276-13279271 | TC71 | SE_68592 | chr19:13260276-13279271 | TC71 | SE_68593 | chr19:13260276-13279271 | TC71 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH19I013160 | chr19 | 13271200 | 13285018 |
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Enhancer Sequence | GAGAATTGCT TGAGCCCGGG AGGCAGAGGA TGCAGTGAGT CAAGATCACA CCACGGCACT 60 CCAGCCTGGG CAACAGAGTG AGACTGTCTC AAAAAAATAA ATAAATAAAT AAATAACCTT 120 GAATTATTTT GCCACACTGT CCCAGAATAT GGAAAATTCT GCTTCTGGAA GAGGGACAAA 180 CTCCTATGAT GATCTGCAAG GCCCTGCTTG ATCTGGGGCC ATCCCATCTC TGGATGAATC 240 ATGCATCACC CTCTGGCCAC ATGGACCTGC TTTTTGTTCC TCATACTTCC ACAGCCTTCT 300 CAGCCACATG GCCTTTGGAT ATGCCGTGAC CTCCTGAAGA TCTTTCAGCT TCCTTGCTCA 360 CCTAGTGAAG CCAGCTCAGC TCAAGGGGCA AATCCTCAGG GAAGTGTTCC CTGTCTAACC 420 CTCTTTTGGC CTAAGGACTG CTTTATTTTA TTTTTTATTT TTATTTTTTG AGATGGAGTC 480 TCTCTCTGTC ACCCAGGCTG GAGTGCAGTG GTGCGATCTC AGCTCACTGC AACCTCCACC 540 TCCCGGGTTC AAGTGATTCT CCTGCCTCAG CCTCCCGAGT AGCTGGGATT ACAAGCTCCC 600 ACCATCACAC CTAGCTAATT TTTGTATTTT TAGTAGAAAT GGGGTTTCAC CATGTTGTCC 660 AGGATGGTCT 670
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