| Tag | Content |
|---|
EnhancerAtlas ID | HS050-33073 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr19:14480190-14481750 |
| | Number of super-enhancer constituents: 30 | ID | Coordinate | Tissue/cell |
| SE_09406 | chr19:14478232-14481823 | CD14 | | SE_10220 | chr19:14478598-14482703 | CD19_Primary | | SE_10950 | chr19:14476858-14488102 | CD20 | | SE_11837 | chr19:14478601-14482680 | CD3 | | SE_12943 | chr19:14479917-14481545 | CD34_Primary_RO01480 | | SE_13526 | chr19:14479807-14481830 | CD34_Primary_RO01536 | | SE_14178 | chr19:14479980-14481674 | CD34_Primary_RO01549 | | SE_14416 | chr19:14476656-14487705 | CD4_Memory_Primary_7pool | | SE_15577 | chr19:14479962-14481976 | CD4_Memory_Primary_8pool | | SE_15810 | chr19:14478599-14482778 | CD4_Naive_Primary_7pool | | SE_16317 | chr19:14478290-14482541 | CD4_Naive_Primary_8pool | | SE_16867 | chr19:14478594-14481828 | CD4p_CD225int_CD127p_Tmem | | SE_17503 | chr19:14476715-14487840 | CD4p_CD25-_CD45RAp_Naive | | SE_17824 | chr19:14476749-14487778 | CD4p_CD25-_CD45ROp_Memory | | SE_18377 | chr19:14476938-14484541 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19159 | chr19:14476884-14482672 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_19988 | chr19:14476779-14487673 | CD56 | | SE_20741 | chr19:14477018-14484906 | CD8_Memory_7pool | | SE_21447 | chr19:14476843-14487364 | CD8_Naive_7pool | | SE_21965 | chr19:14476706-14483904 | CD8_Naive_8pool | | SE_22295 | chr19:14476865-14487666 | CD8_primiary | | SE_23938 | chr19:14480357-14480766 | Colon_Crypt_2 | | SE_23938 | chr19:14480953-14481235 | Colon_Crypt_2 | | SE_30750 | chr19:14480083-14481558 | Fetal_Muscle | | SE_42847 | chr19:14480091-14481630 | Lung | | SE_50325 | chr19:14479009-14481603 | Sigmoid_Colon | | SE_52719 | chr19:14480057-14481648 | Small_Intestine | | SE_53468 | chr19:14479863-14484766 | Spleen | | SE_55331 | chr19:14480009-14481804 | Thymus | | SE_62560 | chr19:14458771-14497116 | 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 |
| GH19I014365 | chr19 | 14476230 | 14487618 |
|
Enhancer Sequence | CATTTATTTA TAGAGATGGA GTCTTGCTAT GTTGCCCAGG CTGGTCTCAA ACTCCTGGCC 60
TCAAGTGATC CTCCCACCTC GGCCTCCCAA AGTGCTGGAA TTACAGGCGT GAGCCACCGC 120
ACCTGGCCTG TGGTTTTGAT TTGCATTTCC CTAATGATTG GTGACTTTGA GTATCTTTTC 180
ATAGGCCTAT TGGACATTTG TCTGGCCTGG AATTTTAACA ACTCTGTTTC AAAGGAAGCA 240
CAGAGTGTGG GTGTCAATCT CCTTGCCAAT GTCAGGGCCG CCTGACCTCG TGGATAGCAG 300
GCAGCCCAGA GCTGGCTCCT CGGGCCGGAC AGAAGCTGGG CATGAGAGGC TGTCGTGGGA 360
GTGACAATTC CACTAGGGGA ATGCCAGATT GCCACTGAAC TTTGTCACTA AGACCCACAC 420
CAAAGGCCCC AGAAAGCCCC AGTGACACTT TTGCCCCTAG ATAGGAGGGT ACCGACAGGA 480
AATGCTGTCA GAAAAATGCC TCCTTGTACA CTCAAAAATG GCTTTTGCCG TCTGCCCAGA 540
GGGGCCCCTC TCCCCCTGAC TCACCGTAGC AGCGCGTGGA GGACAATTTT GGCTGTGACA 600
ACGTCACGCC CGCTGCGGGG AGTTGATCTG CAAGCCACAA ACGTCATTCA TTCCTCTCCA 660
CCTCCAGGAT TTGGAACATC TCCCCGGACC ACAGATTTTT CCTTCAATCA ACTTGCTTTT 720
CCTTTAAAAA AAAAAAAAAA ACTTAAATGA ATTTATTTGG GAAGGAACTT TTATGCCACC 780
ACCACAAAAG GAAACAAAAG GAAACCAGGG CCATTTCCAT AAGTAGAAAG CAACAGCAAA 840
AGGACCTATA TTTGTAGGGG TGGGGGTGAA ATTAAACTTG CTTCCTGCTG TCGCCTGGTT 900
GAAGCCTCAA GAGCCGGGAC TAGGGTAGGG AGAGGGAGGT GCCCAGGCGT AGAATATAAT 960
GAGTCGCTCA CTCGCAGGAC CCTGGGATCC ACAGCCTCAC CCTCCAGTGA AGCTCTGGAT 1020
CAAAGAGACT GCTCTTTTTG TTTAAAAAAA AAAATTGAAA GGAGACAAAA AGGGAAAGAA 1080
ATAGGCCAGG CGCAGTGGCT CACGCCTGTA ATCCCAACAG TTTGGGAGGC AGAGGCGGGA 1140
GGATCGCTAG AGCTCAGGAG TCCAAGACCA GCCTGGGCAA CATAATGAGA CCCCTGTCTC 1200
ATTATAAAAA AGTAAAGAAA AAAAATGGGG AAGGAAATTA AAAACCGAAA GCGACGACTG 1260
AAGTGTTTAG AGGTGTCAGA GATATAGCTG TGAAAAACTC AGACTTCTTT TTTTTTTTTT 1320
TTTTTTTTTT GAGACAGAGT TTCGCTCTGT CGCCCAAGCT GGAGAGCAGT GGCGTCATCT 1380
CGGCTCACTG CAACCTCTCT GCCTCCCAGG TTCAAGCAAT TCTCCTGCCT CAGCCTCCTG 1440
AGTAGCTGGG ATTACAGGCA TGCGCCACCA TGCCCGGCTA ATTTTTGCAC TTTTAGTAGA 1500
GGCAGGATTT CACCATGTTG GCCAGACTGG TCTCAAACGC CTGACCTCAA GTAATCCACC 1560
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