| Tag | Content |
|---|
EnhancerAtlas ID | HS017-05242 |
Organism | Homo sapiens |
Tissue/cell | CD14+_monocyte |
Coordinate | chr11:3885270-3888140 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr11:3888078-3888099 | AAAGTAAAAAAGAAATTAAAA | - | 6.04 | | Nr2f6(var.2) | MA0728.1 | chr11:3887875-3887890 | TGAACTCCTGACCTT | - | 6.04 |
|
| | Number of super-enhancer constituents: 27 | ID | Coordinate | Tissue/cell |
| SE_00449 | chr11:3885540-3890024 | Adipose_Nuclei | | SE_09198 | chr11:3884825-3889822 | CD14 | | SE_10362 | chr11:3885848-3887759 | CD19_Primary | | SE_10993 | chr11:3884379-3890001 | CD20 | | SE_12110 | chr11:3885856-3887721 | CD3 | | SE_13419 | chr11:3885364-3890218 | CD34_Primary_RO01536 | | SE_14480 | chr11:3885668-3890332 | CD4_Memory_Primary_7pool | | SE_17392 | chr11:3885033-3889786 | CD4p_CD25-_CD45RAp_Naive | | SE_18441 | chr11:3884978-3889989 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_20159 | chr11:3885069-3889498 | CD56 | | SE_20833 | chr11:3885478-3890360 | CD8_Memory_7pool | | SE_22458 | chr11:3884882-3889692 | CD8_primiary | | SE_26456 | chr11:3885852-3887731 | Duodenum_Smooth_Muscle | | SE_27094 | chr11:3886476-3887637 | Esophagus | | SE_31213 | chr11:3885563-3889506 | Fetal_Thymus | | SE_32623 | chr11:3885616-3889526 | GM12878 | | SE_39607 | chr11:3885151-3887587 | Jurkat | | SE_39945 | chr11:3885746-3889764 | K562 | | SE_48193 | chr11:3884524-3885672 | Psoas_Muscle | | SE_48193 | chr11:3885947-3887606 | Psoas_Muscle | | SE_48193 | chr11:3887609-3889785 | Psoas_Muscle | | SE_50421 | chr11:3886593-3887816 | Sigmoid_Colon | | SE_52832 | chr11:3886571-3887576 | Small_Intestine | | SE_53386 | chr11:3885915-3889308 | Spleen | | SE_55245 | chr11:3885489-3886164 | Thymus | | SE_55245 | chr11:3886405-3887356 | Thymus | | SE_61865 | chr11:3873734-3925165 | Toledo |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr11 | 3885483 | 3885527 | | chr11 | 3886861 | 3887784 | | chr11 | 3886702 | 3886770 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I003864 | chr11 | 3885382 | 3890036 |
|
Enhancer Sequence | GGCTATACCC AGCCATCATG CGTAACTCTG GTGTGGCCAA ACCAGGCTTT TATTCAAGGC 60
TTACTGTGGG CCATGGGGAG ACTGTTAATA AAGTCTGGGT GCTAATATTT GACCTCAGCT 120
CCAGCTGTAC TCTCTTATTG AGTATAACCA CCTCCCTAGC TTCACCTGCA GTCTTGAAAT 180
GGCTGAGCAA ATGGGCCTGG TCCCCACTGT ATTGGTTACT TATTGGTGTA TAACAAATTA 240
TGCCAAAACA GAGAGGGCTA AAATAATAAG TATTTATTAT CTCATAGATT CTGTGCATCG 300
GGAGTCTGGA TATAGCTTGA CTGGGTACCT CTGGCTCAGA GTCTCTCATG AGATGGCAGT 360
CAAACTGTTG GCTGGGGCTG AAGACTCTAT TTGGGGGGAG AGTGTTTGCT TTTAAGCTAA 420
TTCACATGGT TGTTGGCAGG CCTTGGTTCC TTGCCATATG GGCCTCTACA CTGGGCTATA 480
CTGGACATGA TGATTGGTTT CCCCTAGAAC AAGTGGTCCA AGAGAGCGCA AGAGAGAGTG 540
CCTAAGATAG ATACCTCCAT CTTTTTATCA TCTAATCTTG GAATTGATAG GCCATCACTT 600
CTTCTATATT GTGTTTGTTA GTAAGTCCAG CCCATCCTCA AGGTGAGGGA ATTACATAAG 660
GGCATGAACA CTAGGAGGGC AAGGACCGCT AGGGATCATC TTAAAGGATG CCTCTGAGAT 720
TGCCCAAGGG CCATGCTCTG GGGAACAATC ACTTCTAGGT TCTGTGGCCT TTTAGTTTTT 780
CTTTGACTTC CTTTGCTTAT GACCTAGAGT CTTGTGGAGT CTTTTTATAC TCCCTTTTAT 840
GTTGTGTCTC TTGGTTCATG CATTACTTCA TTGCTTTGAC ATGACCTATC CTTTTTTCCT 900
TCTCCCCGGA CTCCTGGGCT CCAATTAGAA ACTAGCTTTT TATCCTAGGC TGCAGTCCTG 960
CCTACCAACT TTTTTTGTTT CATACCTTCT ATTCTGGAGC CCATTGTACA GCCACTGACT 1020
TTGGAGCCTT TACTACTCCA ACTTGGCTTC TGAGAGTTAG ATTTGTAGAT GGCATTGAAT 1080
TGGGACTCAC AATGACAGAT GAAAAACTTC ATTCTGACTT TTTAGGCCAT TGGTGTTAGG 1140
TGCTAGGACT GAAATCCTAG TATGTGAAAG CTGGAAGGGG TTTTAGAGAC CATCTCTCCC 1200
AAACTTCTTA TTTACATATC AGAAGAACAA ACTTACCCAA GGTTTTGGTA AGCCAGGGCT 1260
AGAATATAAT TTTCTCTGAT TCTCATTCAT ATGTTGTTCT CACTCTGTTG TGGAGCCTGT 1320
CTACCCTAAT GGAGCCTGTT TGGGTTGTTA GGAGGTCTGG GACCTACACA GAGGAGAACC 1380
AGGAAGCAGT TCACAATATT ATATTATGTT CACCGAAATT GGTCTGGGTA CAATTAGGGA 1440
TATACAAAGT CAAATGTCAA GTGCTGCTTC TTTGGACCTA TCCAGCTAGA AAGCTTTTTT 1500
ATTAGGCACA GAAAAAGAAG CCCAGCAATA TCTGTTTCCT ATGGTGCCTA ATATATGCAC 1560
CCTATACCAC TCTCTTGACA ATATCTGTTC AGAGCAATGA GGAATCTGTT TGCTGGGATG 1620
TACAGTATAG GCATCTGAAG GAGACAGGTC AGAGCCTTAT GTTGTATGTC TCACCACTGA 1680
GCTGTTCAGC TGGCTCCATT ATGGATTTGG GGCCTCCACA GGCAGGGTAA ATGTATTAAA 1740
AACTTTGTGG GGTTACTCGT GGCCACCTGG AAAGTGCCAA GGGGAGGTTC TCTGGGCATT 1800
GAGAATTTGA CAACTTTGCC TGTGTTGATA CAACTTGCTA GAGCAGGCAA GACTTGAAGA 1860
GGGATGGCTG TGGTCCTGTC ATGTTTATCA GAGTGGAGCA GATTTCTTTT GTGTGAGAAG 1920
TCATGCAAGA AAAATCCGGA AATGAGCCAA CAGCACTTAA ACTTTTGTTT TCTGCTGGGG 1980
AGCATGGAAT AGAGAAGGTG CAGGTTCTAA AATTTCTGTA TGGGTGGTGG TTGCTTTCCT 2040
GACACAGAGT TCCAGCCCCA GACCACTTTA CTCACTTCAT CTCCCTCTGT TCCCCTTGCT 2100
GCATTCTTGG CAAGCCAAGC ATTTTTCTTT GTTCTGATCT GCAGAACAAA CTTTTATTTA 2160
TACTGCTTCA CTTTTGTTTT TACTTATGTC ATTTAACTTC CTTCAGAATG TCTTTATTAC 2220
CTGTCCTTCT TTATTTCTAC TTCCAGTCCT CTATGAAGTC TTTCCTGACA CTAATTCTAG 2280
CTGTGAGATA CTGCTGACCT GTGAACAAAC TCTGGTAGCA CTTACTATCT GCAGTGCTCT 2340
CTGTGCACTT CACACCCTGC TTACGCCACA AGAGGCAGCT TGCTATGTCT TTTTTTTTTT 2400
TTTTTGTGAC AGAGTCTTGC TCTGTCCCCT GGCTGGAGTG CAGTGGCGTA ATCTTGGCTC 2460
ACTGCAACTT CCGCCTCCTG GGTTCCGGTG ATTCTCCTGC ATCAGCCTCC TGAGTAGCTG 2520
GGATTACAGG TGCGTGCCAC CATGCCCAGC TAATTTTTGT ATATTTAGTA GAGACGGGGT 2580
TTCACCATGT TGATCAGGCT GGTCTTGAAC TCCTGACCTT GCGATCCGCC TGCCTCGGCC 2640
TCTCAAGATA TGTCTTTTAC AGCAAGCCAG TACCTAAGAG CACTGGGCAT TGGTTTGAGT 2700
TCTTGGTGAC AGTATGACAG TGTGATCCAA ACTGTCAAAT GACAGTTTCC TCACTTGAAA 2760
AATGGAGTTA TCAGCACCAT AAGAGAGGGT AAAGAAAGAA AGAAAAGAAA AGTAAAAAAG 2820
AAATTAAAAC TGTGCTTTAT TTATTATTAT TATTATTTTT GAATATTTCC 2870
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