| Tag | Content |
|---|
EnhancerAtlas ID | HS026-16045 |
Organism | Homo sapiens |
Tissue/cell | CNCC |
Coordinate | chr19:14473670-14475410 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr19:14474973-14474988 | GAGGTCAGGAGTTCA | + | 6.22 | | Nr2f6(var.2) | MA0728.1 | chr19:14475282-14475297 | GAGGTCAGAAGTTCA | + | 6.38 | | RARA | MA0729.1 | chr19:14475282-14475300 | GAGGTCAGAAGTTCAAGA | + | 6.88 | | SP4 | MA0685.1 | chr19:14474700-14474717 | GGCATGGGCGTGGCCAG | - | 6.02 | | ZNF263 | MA0528.1 | chr19:14474339-14474360 | GGAGGCTGGGGGTGGGGAGGG | + | 6.01 | | Zfx | MA0146.2 | chr19:14473762-14473776 | GAGGCCGAGGCGGG | - | 6.01 |
|
| | Number of super-enhancer constituents: 26 | ID | Coordinate | Tissue/cell |
| SE_09406 | chr19:14473828-14474954 | CD14 | | SE_10220 | chr19:14473866-14475110 | CD19_Primary | | SE_10950 | chr19:14472405-14476345 | CD20 | | SE_11837 | chr19:14473931-14475221 | CD3 | | SE_13526 | chr19:14473863-14474894 | CD34_Primary_RO01536 | | SE_14416 | chr19:14473373-14475234 | CD4_Memory_Primary_7pool | | SE_15810 | chr19:14473799-14474984 | CD4_Naive_Primary_7pool | | SE_16317 | chr19:14474075-14475239 | CD4_Naive_Primary_8pool | | SE_16867 | chr19:14473866-14475099 | CD4p_CD225int_CD127p_Tmem | | SE_17824 | chr19:14473345-14475249 | CD4p_CD25-_CD45ROp_Memory | | SE_18377 | chr19:14472467-14476404 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19159 | chr19:14473633-14475114 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_19988 | chr19:14472673-14475105 | CD56 | | SE_20741 | chr19:14473788-14475063 | CD8_Memory_7pool | | SE_21447 | chr19:14473803-14475032 | CD8_Naive_7pool | | SE_21965 | chr19:14473801-14474965 | CD8_Naive_8pool | | SE_22295 | chr19:14473360-14475242 | CD8_primiary | | SE_23938 | chr19:14474196-14474847 | Colon_Crypt_2 | | SE_30750 | chr19:14474014-14475011 | Fetal_Muscle | | SE_40289 | chr19:14473871-14475217 | K562 | | SE_42847 | chr19:14473903-14475159 | Lung | | SE_50325 | chr19:14473906-14475074 | Sigmoid_Colon | | SE_52719 | chr19:14473913-14475083 | Small_Intestine | | SE_53468 | chr19:14472613-14475254 | Spleen | | SE_55331 | chr19:14474221-14475011 | 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 |
|
Enhancer Sequence | CTCCAAGTAT TTTGCCCCAA GAATCTGGGC CAAAAGAAAG GAAACAAGGT GGCCGGGCGC 60
GGTGGCTCCC GCCTGTAATC CCAGCACTTT GGGAGGCCGA GGCGGGCGGA TCACGAGGTC 120
AGGAGATTGA GACCATCCTG GCTAACACGG TGAAACCCCG TCTCTACTAA AAATACAAAA 180
AATTAGCCGG GCGTGGTGGG GGGCGCCTGT AGCCCCAGCT ACTCGGGAGG CTGAGGCAGG 240
AGAATGGCGT GAACCTGGGA GGCAGAGCTT GCAGTGAGCC GAGATCGCGC CACTGCACTC 300
CAGCCTGGGT GACAGAGCAA GACTCCGTCT CAAAAAAAAA AGAAAAAAGA AAAAAAAGGA 360
AGGAACAAGG CTCAGAGAGG TCCAAGGAGT TGCCCTGGCG GTCCGGGGCC ACAGTGGCCT 420
TCATCCCCAG CTGAGATGTG TCCCCAGTCT AAGGCCACTC AGAGCCAGGC ACCTTCTCCG 480
GCTGCCTCCC AATCCCCGCC CCCCGCTTCC GTCCCAGCAC CCTCACCCCG CCCCCGGGCC 540
CCTTTGTCCT CCTCTTCGTC TTATTTCCAG AATTTCTCCT CCCTAGGGAA TCCAGTCCAT 600
GTGCTTTTGA TTCCTTTGTC CTGAACTCAT GCGGCATGAG CACCCCTGAA GCCTTATGTG 660
GAAAAATTTG GAGGCTGGGG GTGGGGAGGG GGTCACATTC CTCCCGGGGG TACAGAGCTA 720
CGTCGGCATC TCCAGGGCCC CCCAGCAGCA AGCAGGCATC CTCCCAGGCC AGGCCAGACC 780
GGACGCTGCC CAACACAGGC TTTCTTTGGG GCTTGGCCGG CGCCCGACTA CAGCCCCGGC 840
TCCAGCTGCC CTGCCTGTCC CCCGCCCCCA CGCCTCCCGT CCCAACCTCC CACACGTTTC 900
CTCCTAGAAG CCCAGACCCG TGGGACTTGG CCTCCCCCGC GCCTTCCCTC TCTACTCAGC 960
TCTGCAGCTC CTGTAGGCCT CCTCCCCGGG TGATCACAGA AGGACCAGCT CACCTTAGCG 1020
GGACAGGCAG GGCATGGGCG TGGCCAGAGC CTCGGGCAGG CATCCCAGGC TCCCTGGTGT 1080
CTCTCTCATC CGCTGGCCTC TGTGCCCTCT TCTCTTCCCC ACCCCCGCTC GTGGCCCCTC 1140
CTGCCTCTCC ATCGCAAAGT CCCCAGAGGA GTCTCCTTAA TCACTTGCTT TTGACTGAAT 1200
CCTGACCACC TGGACCCTGA TCTAGCTACT GAGGAGATAA AGTAACCAAC ACTTAAAAGC 1260
TAACCTTCAG GCATTCTGGG AGGCTGAGAC TGACGGATCA CTTGAGGTCA GGAGTTCAAG 1320
ACCAGCCTGG CCAACAAGAT GAAACCTCGT CTCTACTAAA AATACAAAAA AATTAGCTGG 1380
CGTAGTGGCG GATGCCTGTA ATCCCAGCTA CTGCGGAGGC TGAGGCAGGA GAATCGCTTG 1440
AACTTGGGAG GTGGAGATTG CAGTGAGCTG AGATCGTGCC ACTGCACTCC AGCCTGGGCA 1500
ACAAAGCAAG ACTCCGTCTC AAAAAATAAA AATTAGCTGG GTGTGGGGCC GGGCTTGGTG 1560
GCTCAAGCCT GTAATCCCAG CACTTTGGGA GGCCGAGGCA GGCGGATCAC CTGAGGTCAG 1620
AAGTTCAAGA CCAGCCTGGC CAACATGGTG AAACCCCGTC TCTACTAAAA ATACAAAAAA 1680
AAATTAGCCA GGCGTGGTGG CGCATGCCTG TAATTCCAGC TACTCGGGAG GCTGAGGCAG 1740
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