| Tag | Content |
|---|
EnhancerAtlas ID | HS108-19828 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr19:16449050-16451920 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr19:16450509-16450524 | TGAACTCCTGACCTC | - | 6.22 | | Nr5a2 | MA0505.1 | chr19:16451112-16451127 | CCTGACCTTGAACTG | - | 7.26 | | RUNX3 | MA0684.1 | chr19:16449876-16449886 | AAACCGCAAA | + | 6.02 | | ZNF263 | MA0528.1 | chr19:16451818-16451839 | GGGGGAGGGGAATGGGGAGTG | + | 6.03 |
|
| | Number of super-enhancer constituents: 24 | ID | Coordinate | Tissue/cell |
| SE_02121 | chr19:16448235-16450623 | Aorta | | SE_11761 | chr19:16448597-16450448 | CD20 | | SE_11761 | chr19:16451218-16454619 | CD20 | | SE_14486 | chr19:16448358-16450704 | CD4_Memory_Primary_7pool | | SE_15424 | chr19:16448830-16450328 | CD4_Memory_Primary_8pool | | SE_15819 | chr19:16449013-16450244 | CD4_Naive_Primary_7pool | | SE_16376 | chr19:16448709-16450527 | CD4_Naive_Primary_8pool | | SE_17319 | chr19:16448094-16450433 | CD4p_CD25-_CD45RAp_Naive | | SE_19662 | chr19:16448483-16450678 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_20477 | chr19:16447136-16450765 | CD56 | | SE_20801 | chr19:16448268-16450591 | CD8_Memory_7pool | | SE_21459 | chr19:16448569-16450058 | CD8_Naive_7pool | | SE_22931 | chr19:16448097-16450690 | CD8_primiary | | SE_30197 | chr19:16449039-16450309 | Fetal_Muscle | | SE_31861 | chr19:16449060-16450155 | Gastric | | SE_37239 | chr19:16448480-16450955 | HSMMtube | | SE_38557 | chr19:16448117-16451385 | HUVEC | | SE_41301 | chr19:16448493-16450620 | Left_Ventricle | | SE_42601 | chr19:16448631-16450689 | Lung | | SE_45405 | chr19:16448360-16450644 | NHLF | | SE_49016 | chr19:16448672-16450633 | Right_Atrium | | SE_53383 | chr19:16448370-16450551 | Spleen | | SE_61491 | chr19:16432573-16510994 | Toledo | | SE_62295 | chr19:16434424-16512260 | Tonsil |
|
| | 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 |
| GH19I016337 | chr19 | 16448221 | 16451210 |
|
Enhancer Sequence | AGAGCAACAC ACAAAATCCA AGGATTCCTG GGATGACAGA ATTTCTGACC TCAAGGCCAA 60
GATGATGCTG GGTAGAGTGT GCAGCGTGTA GTGTAGACGG GGACTTGGAT CCGCTGGCCC 120
TGGCTGCCTG GAGATGCTGG GTAGAGCACG TAGTATGCAG CGTAGACAGC ATTCAGAGTC 180
CCTCAGCCCT GGCTGCCCCT ACCTCTGCCC CTTGCCCCTG GCCATGGCCC TGGGCGCACG 240
CCTGGCCCTC TCTGAGCCAC AGCTCCCTCC CACCAGGGCT GGTGAGAAAA GTAAACCGAG 300
AGTGCTGTTT CCTGCCACCC TGCTGGGTGC TCAGCCTCCC TCCACCCGCA TCCTCTCGAG 360
TGGGTAGAAT CCCAACTGGG GGCCCTCTGG CAGGGTCCGG GAGCTGGCAC ACGAGCAGGC 420
ACTCTGGCTC GGCCATGCAT CCGTCCATGG GCCACTCGCC GAGACACGTG GCTCTAAATG 480
GACACAGTCA TTCAGGAAAT AGCGCCTCGC CCACCGAATG CCAGGCGCCA CTCAGCAGGC 540
TGCTGTAACT CCGCAGGCTG CCTCCTGAAT TGCCCTCCAC TTTCAACCTT GACCCCAGGT 600
TGGCCTTTCT GGGGACTGTC CCAAGATCGA GAGACACACT TCACAGCCAA GCCCTCGTCT 660
GCAGCCTCGG AGCTATGAGA TGTTCCAGCT CCAGGGAAAA AACTCAGGAA TCAGAAGTCT 720
GGCCAGCCCC ATCCCACTCC TCTTGGCTTT AATGTAACTC AGAGGCACCG ATCCTGGCTC 780
TTGGGGCAGA ATTCTCCACA TTCCTGGTGT GTTTCCGTTG AACCCCAAAC CGCAAACACA 840
TCCTGACATC TCATTTCCTC AATGTGCCCT GGTGGTGACT CGGGCCACCT TGCCGGGAGC 900
TCGTTTTGAG TCATACAGAG ATTTGTCGAA GGAAGGGTTT CTCATCTCAG AAGTTGGAGG 960
CCGTTCCCAC CAACCTCCCT CCCTGCATCT GTACAAGAAT TGCTGGCGGG GCTGCTATTC 1020
CCTGATGCTT GGATCTGAGC TCTCAGTGAC TCGGGAGGCA CTGGCCAGGG GCCCTGGACA 1080
AATCTAAGCT CAGTTCCTTA TGTCACCACT GTCAACCTCA GGCACGGGAA GGCGGCTCTC 1140
AGTCTCTTTC CTCCTCTGTA GAGCTGGGCT CTTAGCAGCT ATCTTGGCCG GGCTCTATCT 1200
CAAATGGATG GAATCTGGGC TATGCCTGAC ACATAGTAGG TGCTCAGTGA AGGAATGGTG 1260
CCCATTAGTG AGAGAGGGAG ACAGGGCTGG GCATGGTGAT GTGCACCCGT GGTCCCAGCT 1320
ACTTAGGAGG CTGAGGCAGA AGGATCCCTA GAGGCCAGGA GGTCGAGACA GCAATGAGCT 1380
ATGATTGCAC CGTTGCACTC CAGCCTGGGC AACAGAGCAA GACCCTGTCC TTAAAATAAT 1440
AATAGTAATA ATAATTTATT GAACTCCTGA CCTCAGGTGA TCCACCCGCC TCGGCCTTCC 1500
AAAGTGCTGA GATTACAAGC ATGAGCCACT GTGCCTGGCT GAATAATAAT CACTAAAAAA 1560
TTAATCTAAA CATAATTTCT AGGCTGGGTG CGGTGGCTCA TGCCTGTAAT CCCAGCACTT 1620
TGGGAGGCCA AGGCGGGCAG ATCACCTGAG GTCAGGATTT TGAAACCAGC CTGGCCAACA 1680
TGGCGAAACC CTGTCTCTAA TTTAAAAAAA AAAGAAAAAA AAAATTAGCC CGGTGTGGTG 1740
GTGCATGCCT GTAGTCCCAG CTGCTGGGGA GGCTGAGAAT TGTTTGAACC CAGGAGGTGG 1800
ACGTTGCAGT GAGTTAAGAT CATGCCACTA CACTTCAGCC TAGGCAACAG AGAGAGACCC 1860
TGTCTCTAAA TAAATAAATG AGAGAGAGAG AGAAAAAAAA TCCAAGGAAA CAAGCCCATT 1920
CATTCTACTT AATTCCGCTG GTCTCTGGGA GGCAGGTTGG GGGTGGAGAA ATTCCATGTT 1980
TTTACAGAAT CCTGACGTCA CCAGCAACTG CCCCACCAGG AGCTAACTTC AGCACGGGCG 2040
GAGGGAGGGT GTCTGCCCAC GACCTGACCT TGAACTGGGC CTTTCTTAAA TGTAAATGTG 2100
CATCTCCTTT GGTGCTTTTT TAAGTGGGAG AGGTCCCTGA AAGGTTGTTG CCTGGAGGAA 2160
AAGTTTTGGC AATTAACTTT TATTATTGTT TGCTTGCTTA AAGAAACTGG GGGCCCAGAG 2220
CAGTGAGTGG CTTATGCCTG TAATCCCAGC ACTCTGGGAA GCCGAGGCGG GCAGATCACT 2280
TGAGCCCAGG ACTTCCAGAC CAGCCTGGCC AACAAAAATT AGCCAGGCAT GGTGGAGTGC 2340
ACCTGTAATC CCAGCTACTC GGGAGGCTGA GGCAGGGGGA TCACTTGAAC CCGGGAGGCA 2400
GAGGCTGCAG TGAGCTAATA TTGCTCCACT GCACTCCAAC CTGCTGGGCG ACAGAGTGAG 2460
ACTGTCTCAA AAAACAATTG GGATGTTCAT CAAAGCACTA TTCATAACAG CCAAAAAGTA 2520
GAAACAACCC AAGTGTCCAT TAGAGAATGA ATAAGAAAAC TGTGATCCAT ACATACAATG 2580
GAATATTATT CAGCCATGAA AAGGAATGAA GCACTGATCC ATGCTACAAT GTGGATGAGC 2640
CCCCAAAACA TTCTGAGTGA GAGAAGCCAG ACGCGAAAGC CCACATAGTG TGAGATTCCA 2700
CTGATACAAA ATGCCCAGAA CAGGCAAATC CAGAGAGACA GGAAGCAGAT GAGTGGCTGC 2760
CAGGGGCTGG GGGAGGGGAA TGGGGAGTGG CTGCTGATGG GGACAGGGTC TCCTCTTGGG 2820
GGATGCAAAT GTTCTGGAAT TAGACAGAGG TGATGGTTGC ACAACATTGT 2870
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