| Tag | Content |
|---|
EnhancerAtlas ID | HS056-13002 |
Organism | Homo sapiens |
Tissue/cell | GC_B_cell |
Coordinate | chr6:470110-472050 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr6:470763-470776 | TTCTAGAATTTTC | + | 6.71 | | IRF1 | MA0050.2 | chr6:470819-470840 | CAGCGGAAAGTGAAAGCAGGG | - | 6.34 | | IRF1 | MA0050.2 | chr6:470152-470173 | TTTTTCTTTCTGTTTTGTTTT | + | 6.7 | | IRF2 | MA0051.1 | chr6:470823-470841 | GGAAAGTGAAAGCAGGGA | + | 6.33 | | Rhox11 | MA0629.1 | chr6:471064-471081 | ATTTTTAACAGCGGCAT | - | 6.3 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_58878 | chr6:468375-503300 | Ly3 | | SE_61068 | chr6:422752-507076 | HBL1 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr6 | 470998 | 471469 | | chr6 | 470501 | 471666 |
|
Enhancer Sequence | TTATTTTTAC TGTAGATCTT AGCAAGTTCA GCTTACAATT GTTTTTTCTT TCTGTTTTGT 60
TTTGAGACAG GGTCTGGCTC TGTCGCCCAG GCTGGAGTGT GATGGATCAG TTAAGGCTCC 120
TTGCAGCCTT GACCTGTGGG GCTCAATCAT CCTCCAGCCT CACCCCCCCG TACTTGGGAT 180
TACAGGCATA CCACCATGCC TGGCTACATT TTGTATTTCT TGTAGAGACA GGGTTTTGCT 240
GTGTTGCCCA GACTGGTCTC AAACTCCTGG GCTCGAGTGA TCTGCCCACC TCAGCCTCCA 300
AAACTGCTGG GATTCCAGGC GTGAGACACC GCACCTGGCA GCTTTTATTT TCTTAGGAAC 360
GTTCACCGTT TCACGTAAAG AAAGCCCTCG ATGGCTCCTC TCTGGCAATC TGAATTGCCG 420
GCATCACCGC TCCTGCACCT TGGTGCCATT TTCAAGGAAA ATACGGGTTC TTTGAACACA 480
CGCACGGCCA CCTGGAGAGT CGGCCTCATA AGGGACAGGG TTCCTCAGTG GCTGAGGGAC 540
AGGCAGCACC TCCATCGTGG ATCCCCTGGG CAAAGCGATG AATCACGTCC CCATGCAAGA 600
TTGCATCACA CTACTCAGAG CTGTGCACCT TTTAAAACCC AGGAATTATG TATTTCTAGA 660
ATTTTCCACT TAATAGATTC GGACCACGGT TGAGTGCGGG TCGCTGAAAC AGCGGAAAGT 720
GAAAGCAGGG ATAAGGGGGA CTGCTGCAGA TGCACTTCCT CTGGGTGTCA AGCAGCACAC 780
CTCTCCCCCT GCCCCGCCAG GGTGCGGAGG CTGGGCGGTG GCCCCCGTAC CAAGGGTGGA 840
GGGAGCGGCC AGGCCACCCT GCCTGTCCCT GTGGGGTGGC CTTCCACTGT TGAGGGTTTA 900
ACTGGACATA GTCCTGCACA CAAAGACAGG GCAGGCGGTG CTTACTGAAC CGTGATTTTT 960
AACAGCGGCA TCTTAGCCCG GGTGGGAGAG CCCCGGCGGG GCTCGAGGCT GCAGGTGGGG 1020
TTGCACACTC CCAGAGGCTG CCCCACCCCC AGCAATGGGG ATGTCTGGGC TGCCAGTTCA 1080
GCAGTCGCTG CTTATAAAAA GGAAACTTTA GTGTATGGTA TTTTCCTGAA TAGTGAGGAA 1140
AAAACCCCTG ATATCTTACA GTAGAAAATC TCTTCCTCAC CTTAAAGAAA TCCCTGGGGG 1200
TTGGGTGTGG GAGAGGGACA TTCCCCTGCC CGATGCTTCC GTCAGCCTAG CCTGACAGAT 1260
GCTTTGGTTA TGTAGTTTCC AGTCATCGGC TGTGGCATTC TCTGCAACAC CTCATTGTCC 1320
AGATGGTTTC CAGGCACACC TCTTAGCACC TCGCTCACTA CCATGCGCTC AACAAGCCAG 1380
GCTTCACCTC TGCCCACCTG CCTCCACTTC CTCCTCTTCA GTGAGCTGAG CCGTCCCTGT 1440
CCCACCTGGG GATGTTTTTC CACCATCAGG AGCCCCGTCC TCGGTCCCAT GCAGCAAGGC 1500
CCAGGCAGCG GGCTGGGTGG TAGAGAATCG CCCTGCTCTG TAAAATCTAT ACCCGAAGCC 1560
TGGTTGGAGA CACTTGGTTG CAGCCTTGGC CTAAGACTTG ATCGTGGAAC TTAATAAAAC 1620
AACTGAAGGT CCTTGCACAG GAAGAAATCA AACCGCCAAG TCCTAGTGTC AGGATTCGCT 1680
GTCTTCCAGG CTCAGTCTCC CGCATCACAG CTCGAAGCAG GAGTGCTGGG AGGCGACAAG 1740
CACGGGCTAT GGTGCTGCTG TGCAGGCCCG ACATCGGCAG GTGCTCAGAC GTTCAGATGT 1800
AGTTCTCTAA AGCAATGGGA TCCCACTGCT CTGGGGTTTG CAAATTGGTT CTGAGGGCAT 1860
TGCTGAAAAT TCAATAAACT CCCAGATGGA ATGTTCTAAC GTCCAGGCGG CAGAGCTCTC 1920
ATCTACTCTG AGGATGTGTG 1940
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