| Tag | Content |
|---|
EnhancerAtlas ID | HS182-04210 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr11:76476100-76477940 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR1 | MA0112.3 | chr11:76477509-76477526 | AAGGTCACACTGACCAT | + | 6.19 | | ESR2 | MA0258.2 | chr11:76477510-76477525 | AGGTCACACTGACCA | + | 6.53 | | Nr5a2 | MA0505.1 | chr11:76477503-76477518 | AAGGTCAAGGTCACA | + | 6.37 | | TBX2 | MA0688.1 | chr11:76476500-76476511 | TTTCACACCTC | - | 6.14 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_26826 | chr11:76477083-76483151 | Esophagus |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 4 | Chromosome | Start | End |
| chr11 | 76476164 | 76476705 | | chr11 | 76476755 | 76477567 | | chr11 | 76477687 | 76477727 | | chr11 | 76477783 | 76477896 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH11I076766 | chr11 | 76477121 | 76477270 | | GH11I076767 | chr11 | 76477731 | 76477895 |
|
Enhancer Sequence | ATACCCCCAT GTGAACCAGT CTCTGGATGC AGGCTGGCCC TGGAGGGACC ATGGCATTAG 60
GTGAGGAGGC AATGACGGTG GTGGGAGGAG TCTCACCTGC AAGCTGCCTG CCATCAGCAC 120
TCTCAGCAGC GGAGGTGTGG GGGTAGGAGG CACAGGCATT GGCAGCACAT CGCAGTGCCC 180
GCTACAAAGA TGTCTTGGGT CAAGTAGGTC CTCAGGAATG TTTGTCGCAT GATGAAAAGA 240
ATAACTCCCC ATCACCTTCA AGGCACATTT TGAGTATCTG GTGTAGCACA CAGGCTCTTC 300
GTGATCCACC CCAAACATCC TCCCCATTCC GTCTTCCTCT CTCCCTCTCC CCACTCGCAC 360
CATATTGTGC TTCTTGCAGT TTCCCAAGCT CAACATGCTA TTTCACACCT CTATGCTTTT 420
GCACGTGTTA TTTCATCTGC CTGGACTGCT TTAAATGGAA AAAAAGAAAT CCTATTCTCT 480
TCTTCCAGCC AATTCCTACT CCTTCATCAA GACTCCAGCT AAGCTCTGCC TCCCCTGGGA 540
AACCTTCTAT TAATTCCTCC AAGTCTGGTG CTCCCACCTC ATGCAGAGCA CAGCCATTGG 600
GTTCTAATCT GCCCCCGGGC TCCTCCAGGC TCAGATCCAC AGGGCCTGGT TACTCCATTA 660
CTTAGGATGC ATTTGTGCTG GAAGAAGTCT TGGGGGATGG CAAGGGAGAA GAAATGGCAA 720
GTGTGAAGCC TGGAAGCATG GAAGTACCCA GTATGTCGGA GAAGGCTGAG CAGCGTCTCA 780
TACTGTTCAA CGCAACGGTT GTCGCCATCC TTTCCCCACT CATTCCCATC TTCACCATCA 840
TCATTGTTGT CATCAAGGCC ACACTTTCTG AGTGCTGACT ACATACCAGG CTCTGCGCCA 900
AGTGTTTTAG ACACACTTCC CTTTAATCCT TATTTTATCC TCACTATTAA TAACCTTCAA 960
AAGTAGGTAC TATTATTATC ACTGTTTTAC AGATACAGAA ACCGAAGTTC AAGCAGGTTA 1020
AGAGCTCTGC TCAAGGTCAC ACAGCTGGTT AATGATCTGT GTGACCCAAG GACACTCTCT 1080
GTTCACCACT CCAGCAGGGA GCTGGGCCAC ACTGATCTCA TCCCTTTCCA AGCCTCCCAC 1140
CCCATCACTG TCTGCCTGTC TAAGGAAACT CCTTTCCTAA ATGAAAGGAC ATGCCACTGC 1200
GAAGATGTGG GGTGGGCCCA GCCAGGGCAG CCAAGAGACC TGGGAGGGGT GAGGGAGAAC 1260
ATTCTGACCA CATTCGCCCT TCTAGATCCG ACCAACACAG GGTTTGATTC AGCTCCAGCC 1320
ACTGCATGTT GCTGGGAGAT CTTGTCCCCT CTTCACGTCT GCAAATAGGG AATCTGAAGT 1380
CCCAAAAGGG AAGGGCCCCA TCCAAGGTCA AGGTCACACT GACCATCAGG GGGTCAACTG 1440
AAACTACAGC TTAGACTCTG GGCTCCCAGA CCAGGGCCTC GCCCACTGCC AGCCTAACTG 1500
CAGCCAAGGC TAATTTTAAG GGATAATTTG AGGGTGCTGG GAAGAGTTCC TCCTCCCCAC 1560
ACAAGGGTGT ACCTCCCCAG GCTGCTGGTG ATACCTGGAA TCCCTCCAGA GGGCACAGGT 1620
CATGAGCCCT GGGTTCAGGC CCACCGTCTC CTCTCCATCC TCCCTGGGAC CCTCCTGCCC 1680
GGGCTTCCTC GCCTTAGGAA ATGCACAAGC AGCCAGGGGC TGGCTCTGAG GAGGCTGTGG 1740
AAGGAGGCTG CCCCCAAACC TGGGCACGCC AGGAACAGAG AGACAAACAA GAGGCAGCAG 1800
AGCCCAGTGA GAGGCTAGTA GCCACATTGG TTTTAATCAG 1840
|
