Tag | Content |
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EnhancerAtlas ID | HS182-11323 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr19:39178580-39180320 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF1A | MA0046.2 | chr19:39180298-39180313 | AGTTAATTTTTAATT | - | 6.49 | NFE2L1 | MA0089.2 | chr19:39179695-39179710 | ATATGACTCAGCAAT | + | 7.68 | OLIG2 | MA0678.1 | chr19:39179966-39179976 | ACCATATGGT | + | 6.02 | OLIG2 | MA0678.1 | chr19:39179966-39179976 | ACCATATGGT | - | 6.02 |
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| Number of super-enhancer constituents: 32 | ID | Coordinate | Tissue/cell |
SE_00117 | chr19:39172768-39180290 | Adipose_Nuclei | SE_09404 | chr19:39164511-39180526 | CD14 | SE_13490 | chr19:39179003-39180338 | CD34_Primary_RO01536 | SE_14624 | chr19:39179374-39180514 | CD4_Memory_Primary_7pool | SE_20865 | chr19:39170480-39179166 | CD8_Memory_7pool | SE_25779 | chr19:39179417-39180269 | Duodenum_Smooth_Muscle | SE_26525 | chr19:39179021-39179809 | Esophagus | SE_26525 | chr19:39179873-39180389 | Esophagus | SE_27614 | chr19:39164407-39180553 | Fetal_Intestine | SE_28533 | chr19:39164445-39201888 | Fetal_Intestine_Large | SE_34681 | chr19:39170836-39180506 | HeLa | SE_35812 | chr19:39168616-39191950 | HMEC | SE_36926 | chr19:39172838-39186932 | HSMMtube | SE_40018 | chr19:39179218-39180516 | K562 | SE_40594 | chr19:39179201-39180442 | Left_Ventricle | SE_42097 | chr19:39179722-39180563 | Lung | SE_44161 | chr19:39177919-39179043 | NHDF-Ad | SE_44161 | chr19:39179045-39180304 | NHDF-Ad | SE_44797 | chr19:39179102-39179721 | NHLF | SE_45660 | chr19:39172827-39180503 | Osteoblasts | SE_47114 | chr19:39164477-39226374 | Panc1 | SE_51136 | chr19:39179021-39180428 | Skeletal_Muscle | SE_51705 | chr19:39179204-39179729 | Skeletal_Muscle_Myoblast | SE_51705 | chr19:39179740-39180298 | Skeletal_Muscle_Myoblast | SE_53291 | chr19:39179735-39180329 | Spleen | SE_56725 | chr19:39178407-39179038 | VACO_400 | SE_56725 | chr19:39179083-39180391 | VACO_400 | SE_58038 | chr19:39179862-39180220 | VACO_9m | SE_62811 | chr19:39125155-39186863 | Tonsil | SE_63494 | chr19:39179071-39179729 | HSMM | SE_63494 | chr19:39179752-39180316 | HSMM | SE_64225 | chr19:39179057-39180305 | NHEK |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 4 | Chromosome | Start | End |
chr19 | 39178653 | 39178869 | chr19 | 39179034 | 39179144 | chr19 | 39179451 | 39180013 | chr19 | 39179503 | 39179787 |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I038673 | chr19 | 39164536 | 39206516 |
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Enhancer Sequence | GGCAAAGGAT TCAAATAGAC ACTTCTCCAA AGAAGATCTA CAAATGGTCA ATAAGCACAT 60 GAAAAGGTGT TCGATGTCAT TACTAATTAG GGCAAATCAA AACCATAACC ACTACAAATG 120 GTCAATAAGC ACATGAAAAG GTGTTCAATG TCATTACTAA TTAGGGCAAA TCAAAACCAT 180 AACGTGGTTG GGCCTGGTGG CTCATGTCCA TAATTCCAAC ATTTTTGGAG GTAGAAGTGG 240 GAGGATGGCT TGGGGCCACG AATTGGAGAC CAGCCTGGGC ATCATAGTGA GACCCTGCCT 300 CTACAGAGAA TTAAAATAAA AAATTAGGCC GGGTATGGTG GCTCATGCCT GTAATCCTAG 360 CACTTTGGGA GGCCGAGGCG AGTGGATCAC CTGAGGTCAG GAGTTTGAGA CCAGCCTGGC 420 AAACATGGTG AATGAAACCT TGTCTCTACC AAAAAAAAAA AAAAAAAAAA ACCCACAAAA 480 ATTAGCTGGA CATGGTGGTG GGCGCCTGTT GTCCCAGCTA GTGGGGAGGC TGAGGTGGGA 540 GAATCGCTTG AACCTGGGTG GGAGAGGTTG CATTGAGCCG AGATCACGCC ATTGCACTCC 600 AGCCTGGGCA ACAGGGTGAG ACCCTGTCTC TAAATAATAA TAAAAATGAG AAATTGGCCA 660 GGTGTAGTAG CATATTCCTG GGAGGCTGAG GTGGGCAGAT TGCTTGAGCC CAGGAGTTCA 720 AGGCTGCAGT GAGCTATGAT GACACCACTG TACTCCAGCC TGGGCAACAG AGTAAGACCC 780 CAACCCTAAA ACAAAAAAAA ACAGAAAACC ACAATGAGAT ACCACTGCAC ACCCACCATG 840 ATGGCTATAA TCAGAAAGTC AGATAATAAG TATTGACTAG GATGGGAGAA ATCAGAACCC 900 TCACATTGCT GGTCAAAGTG TAATGTGGTG CAGCTTCTTG GGAAAACAGT CTGGCAGTTC 960 CTCAAAATTT AAACATGTTT TGTATTTTTA GTAGAGACGG GGTTTCACCA TGTCACCCAG 1020 GCTGGTCTTG TCTCAGCCTC CCAAAGTGTT GGAATTACAG GCATGAGCCA CCACGCCCAG 1080 CCAAGTTCCT CAAATTTTTA AATATAAGAG GTATCATATG ACTCAGCAAT TTTACTCCTA 1140 GGTATATGCC CAAGGCAGTT GAAAACATGT CCACATAAAA CTTGTACATG AATATTCACG 1200 GTGGTGCTAA TATCCAAAAG ATAGAAGCAA CACAAATAAT GCCCATCAGC CAATGAATTG 1260 ATAAATAAAA TGTGGTATAT CCATACAATG GAATGTTATT CAGACAGGAA CGAAGTACTG 1320 GTACATGCTA CAACATGGCT GAACCTTGAA AACATGCTAA GGAGAAGCCA AACTCAAAGA 1380 TCATATACCA TATGGTTCCA CTTATATGAA ATGCCCAGAA TAGGTAAATT GCAAGAGACG 1440 AAAGAAAGGT AGGTTAGTGG TTGCCAGGGG CTGGGGGCTG GGTAGGAGGG AAGTGGGGTT 1500 GGAGAGTAAC TGTACCAGTT TTGCGGTGGT AGACATGTTC CTTGTATTTT TGGTTTTTTG 1560 TTTTGTTTTG TTGTTTTGAG ATAAGGTCTC ACTGTCGCCC AGGCTAGAGT GCAGTGGCGC 1620 TGTCATAGCT CACTGTAGCC TCGAATTCCC AGGCTTAAGT GTTCCTCCCA CCTCAGCCTT 1680 CTGAGTAGCT GGGACTACAG GCAAGAGTCA CCATACCCAG TTAATTTTTA ATTTTTTTTT 1740
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