| Tag | Content |
|---|
EnhancerAtlas ID | HS018-12198 |
Organism | Homo sapiens |
Tissue/cell | CD19+ |
Coordinate | chr2:43439230-43441980 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Ar | MA0007.3 | chr2:43439677-43439694 | AGGAACACAATGTTCTT | - | 7.05 | | Ar | MA0007.3 | chr2:43439677-43439694 | AGGAACACAATGTTCTT | + | 7.1 | | IRF1 | MA0050.2 | chr2:43441415-43441436 | AAAAAAAAAAAGAAAGAAAGA | - | 6.25 | | NR3C1 | MA0113.3 | chr2:43439677-43439694 | AGGAACACAATGTTCTT | - | 6.92 | | NR3C1 | MA0113.3 | chr2:43439677-43439694 | AGGAACACAATGTTCTT | + | 7.26 | | NR3C2 | MA0727.1 | chr2:43439677-43439694 | AGGAACACAATGTTCTT | - | 6.53 | | NR3C2 | MA0727.1 | chr2:43439677-43439694 | AGGAACACAATGTTCTT | + | 7.31 |
|
| | Number of super-enhancer constituents: 20 | ID | Coordinate | Tissue/cell |
| SE_09435 | chr2:43435994-43442184 | CD14 | | SE_13409 | chr2:43439328-43440747 | CD34_Primary_RO01536 | | SE_20337 | chr2:43439372-43441120 | CD56 | | SE_23724 | chr2:43439967-43440356 | Colon_Crypt_2 | | SE_26557 | chr2:43439803-43440723 | Esophagus | | SE_27617 | chr2:43439694-43440826 | Fetal_Intestine | | SE_28536 | chr2:43439572-43440971 | Fetal_Intestine_Large | | SE_30898 | chr2:43439466-43440509 | Fetal_Thymus | | SE_42201 | chr2:43439348-43440800 | Lung | | SE_49954 | chr2:43439343-43440980 | RPMI-8402 | | SE_50052 | chr2:43439292-43440868 | Sigmoid_Colon | | SE_51530 | chr2:43439734-43440675 | Skeletal_Muscle | | SE_52337 | chr2:43439327-43440880 | Small_Intestine | | SE_53288 | chr2:43439337-43441237 | Spleen | | SE_55103 | chr2:43439326-43440734 | Thymus | | SE_59314 | chr2:43439248-43468696 | Ly3 | | SE_61450 | chr2:43354337-43468354 | Toledo | | SE_62203 | chr2:43354169-43468733 | Tonsil | | SE_65350 | chr2:43439707-43440435 | Pancreatic_islets | | SE_68698 | chr2:43441211-43443035 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH02I043212 | chr2 | 43439141 | 43441139 | | GH02I043214 | chr2 | 43441444 | 43442310 |
|
Enhancer Sequence | GATGGTGGGT GCCTGTAATT CCAGCTACTC AGGAGGCTGA GGCAGGAGAA TCGCTTGAAC 60
CCGGGAGGCG GAGGTTGCAG TGAGCCGAGA TAGTGCCATT GTACTCCAGC CTGGCAACAG 120
AGCAAGACTC TGTCTCAAAA AAAAAAAAAA AAAAAGATAA AAAAGAGGAA AAAATCAACA 180
TGAGGTTCCT TGTACCAAGG AATAGTGCAT CTTTGCCTCT TCTGAATGGC TGGGACACTC 240
CGCCCTCTTT GTGAGGGCCT GGGGCGGCAT CATGGCGCTG CCACTTATGC ACTGGGAGAC 300
CTCAGGCAAG CATCTTTCAT TCTCTGAGCT CCATTTTCCT CATCTGTCCA ATGGGAGCGA 360
ACAGGGCCAG TCTCACAGGG CAGATTGGTT TTGTCGTAGA AACAGTTACT GAAGCCCTTC 420
GAGGAGCCAG GCTTGGGGGC TGCAAGGAGG AACACAATGT TCTTGCTTTG AAGGAACTGA 480
CAGGGTAGAG AGGAAGACAG ACATAACCAG TTGTTGTGGG ATGCTGTGAT ATGTGCTCTG 540
ATAAAGGCCT GGACAGTGCC CCGGTGGGGC CAGGGTTGGG TGGAGAGGCT AGATCTGAGT 600
TTGAGATTCA GCCTGGGCTG ACCGCGGAGG GAAGAGGCGA GGAAGCAGGG GGTCACAAGG 660
GGATGTCCCA GGCAGGGGTG GAAGGAAAGT AAAGGGCCCA GAGTGTGAAC AGCATCTCTA 720
GGAATCCTTG GTGCTCCCGA GCAGCTAAGA AGCAAGGAGC ATAGGCAGAG GAGGGAGGTT 780
TTTCCGGATC CCAGAGCCTC CTTGGACTTG AACAGTGGGT GGTGGGACCC TGTGTAGCGT 840
CCTAGGGCAG AGAAGAGTAT GATCACCCAA GTGCTTTACA ACCTTGCTCT AGAGGAGTGG 900
TGGCCTGGAA GAGGACCAGC CAGGGCTCCT GGTTGACAAG GTGTCTGGGT GAGCGTGGGG 960
CAGGCCTGAG TTGCAGAGGA GCTAGAGACA AAGGGGGCAA AGTCAAGGCC TGGTTAGAAA 1020
GCAGAGTCAT GATGGTTGGG CAACCTATGA GGGAAGGGGT AGAGGGAAGT GAGAGAAAAG 1080
ACTGGGGAAG CGTGCCAAGT TCTGGCATGG GTTCCTTGAG AGATGTGGTG TCACATGCTT 1140
GGGGACAGGG ACAACTGGAG GGGTTGGTGT GAGGTGCATC TGGGAGGAGG TGGGTCCCAG 1200
ACTGCTGAGT GGGGCTGAGA GATGCCAGCA CGTGTGGGCA GTTAGGCAGA GCTCAGTCCC 1260
TTCCCCTCTC CACTGGCACT TTCAATCTGC CAGGTGGAGC AGTAGTTTGG GAATATTCTG 1320
GAGTCTCTTG GCTTTTGGAA GGAAGGAGAA CCAGCAAGGA CATCATGGGG GTATCCCAGG 1380
ACCTGCTGCT GGAAGCATCT TTCCTTCAGC TGTTGGTATT TTAATAGAAC ATTCTAGACT 1440
CACAGTGCTG TCCAACAGAA CTTTTGTGAT GACAGAAATG TTCTGTGCTG TTTAATGCAG 1500
TAGCCCCTAG CTCCATGTGG CAACTGAATA CTTAAAACGT AGCTATCTAG TATGGCTGAG 1560
GAAGTGAGTT TTACATTTTG CTTACTTTTA ATTAATTTAA ATCTAAATGG CTACACGCAC 1620
AGCTACAAAC CCTGGGAGTT TGGTGGGGGC AAACCATGGG GCCTTCCTGA TGCCCATCAG 1680
ATTGGATGCC TACTGATTAG AAGTGGAAAA ATACCCCAAA ATGGTAATAA CAAACAAACC 1740
ATAAATATTG CACTTTTTTT TTTTGAGACG GAGTTTCACT CTTGTCGCCC AGGCTGGAGT 1800
GCAGTGGTGC AATCTCGGCT CACCGCAACC TCCGCCTCCC AGGTTCAAGC GATTCTCCTG 1860
CCTCAGCCCT CTAGTAGCTG GGATTACAGG CATGCACCAC CATGCCCAGC TAATTTTGTA 1920
TTTTTAATAG GGATGGGGTT TCTCCATGTT GGTCAGGCTG GTCTTTTTTT TTTTTTTTTT 1980
TTGAGACAGG TTCTGGCCCA CATGGCAAAA CCCCGTCTCT ACTGAAATAC AAAAAATTAG 2040
CCGGGCATGA TGGCGGGCGT CTGTAATCCC AGCTACTCGC GAGGCTCAGA CAGGAGAATC 2100
ACTTGAACCT GGGAGGCGGA GGTTGCGGTG AGCCGAGATC ACGCCACTGC ACTGCAGCCT 2160
GGGTGACAGA GCAACACTCT GCGTCAAAAA AAAAAAGAAA GAAAGAAAAG AAAAGAAAAA 2220
AGAAAACTGA AGTTCAGATT TGCTTGAGGT CACGCAGGTA GGAGGCAGCA CTGGGCTGAG 2280
ATTTGATTGC AGTCCAATGG GAGCCCCTGC TTGTAACCCC TTAGGGCCAG GCCCTTCCAC 2340
AGCCATGGAG GTAATGCCTG CCCAAGCTCC CTCCGGTCCC AGCCCCTGCA GCGGCTCTGG 2400
ACCTACAGGG CTATTGTTGG CAAGCTCCTG CCTGTCAGCC CCACAGACTC TCTGGGCCCC 2460
CTCTGAGAAG CCTGCTGGAT GGAACATCCA GGGACCAGCC ATGCTGAGCC TCTCAGCCAA 2520
GAAGGATTTG GGTTTGCTTT GGTGAGAATC GACACCAACA GCCCTATTGG CACAGCGCAC 2580
GCTCAGGGAG GTGTCCTGGG TTCTTTCTTT TCCAAGTGCT AGGTAGAGAC CCAGAAACTG 2640
GCAAGTCTCC AGAGGGGTGC CCCTACCCCT TCTCAACCTT AAGTTTCTCA TCTATGGAAT 2700
GAGAGGGCTA CACTAAGTCA TGGGTTTTTA TTTTTTATTT TTTTTTGAAA 2750
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