Tag | Content |
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EnhancerAtlas ID | HS056-10870 |
Organism | Homo sapiens |
Tissue/cell | GC_B_cell |
Coordinate | chr3:37010730-37012300 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr3:37011156-37011174 | GGAAGAGAGGGAGGGAGG | + | 6.14 | EWSR1-FLI1 | MA0149.1 | chr3:37011152-37011170 | GGAAGGAAGAGAGGGAGG | + | 6.73 | EWSR1-FLI1 | MA0149.1 | chr3:37011148-37011166 | GGAAGGAAGGAAGAGAGG | + | 7.82 | EWSR1-FLI1 | MA0149.1 | chr3:37011144-37011162 | AGAAGGAAGGAAGGAAGA | + | 8.2 | RFX5 | MA0510.2 | chr3:37011491-37011507 | TGTTGCCAAGGAAACC | + | 6.1 | RFX5 | MA0510.2 | chr3:37011491-37011507 | TGTTGCCAAGGAAACC | - | 6.23 | ZNF263 | MA0528.1 | chr3:37011145-37011166 | GAAGGAAGGAAGGAAGAGAGG | + | 6.11 | ZNF263 | MA0528.1 | chr3:37011201-37011222 | GGAGGAGGAGAGAAGGAGTGG | + | 6.35 | ZNF263 | MA0528.1 | chr3:37011149-37011170 | GAAGGAAGGAAGAGAGGGAGG | + | 6.78 | ZNF263 | MA0528.1 | chr3:37011235-37011256 | GGAGGGGGAGGAGGAGAAGGA | + | 6.7 | ZNF263 | MA0528.1 | chr3:37011226-37011247 | AGTGGAGAAGGAGGGGGAGGA | + | 6.92 | ZNF263 | MA0528.1 | chr3:37011221-37011242 | GGAGGAGTGGAGAAGGAGGGG | + | 6 | ZNF263 | MA0528.1 | chr3:37011241-37011262 | GGAGGAGGAGAAGGATAAAAG | + | 7.18 | ZNF263 | MA0528.1 | chr3:37011192-37011213 | GGGGGTGGAGGAGGAGGAGAG | + | 7.37 | ZNF263 | MA0528.1 | chr3:37011238-37011259 | GGGGGAGGAGGAGAAGGATAA | + | 7.37 | ZNF263 | MA0528.1 | chr3:37011195-37011216 | GGTGGAGGAGGAGGAGAGAAG | + | 7.38 | ZNF263 | MA0528.1 | chr3:37011153-37011174 | GAAGGAAGAGAGGGAGGGAGG | + | 7.61 | ZNF263 | MA0528.1 | chr3:37011198-37011219 | GGAGGAGGAGGAGAGAAGGAG | + | 7.64 | ZNF263 | MA0528.1 | chr3:37011229-37011250 | GGAGAAGGAGGGGGAGGAGGA | + | 9.38 | ZNF263 | MA0528.1 | chr3:37011232-37011253 | GAAGGAGGGGGAGGAGGAGAA | + | 9.68 | ZNF740 | MA0753.2 | chr3:37011184-37011197 | GGGGGGGGGGGGG | - | 6.03 | ZNF740 | MA0753.2 | chr3:37011187-37011200 | GGGGGGGGGGTGG | - | 6.44 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr3 | 37010977 | 37011113 | chr3 | 37011163 | 37011850 | chr3 | 37011455 | 37011827 |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I036968 | chr3 | 37010223 | 37012549 |
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Enhancer Sequence | AAAGGAGAAA TGGGGTGGTA TTAATTAGTT AAATCCTTAT TAATCATAAG CAATAAGTAG 60 ACAATGCCTA CAGTTGATAA ATTAAGAATT AGCAATATAC AGAAATATAT ATGAAACCAA 120 AATAACTAAT GAAAGAAAAG GAGGCTGGGC ACGGTGGCTC AGGCCTGTAA TCCCAGCACT 180 TTGGGAGGCA GAGGCAGGCA GATCATTTGA GTCCCGGAGT TTGAGACCAG CCTAAGCAAC 240 GTAGTGAGAC CTCATCGCTA CAAAAAAACA GAAAAATTAG CTGGGTGTGG TGGTGTATGC 300 CTGTATTCCC AGCTACTTCA GAGGCTGAGG CAGGAGAATC AGTTGAGCCC AGAAGGTGGA 360 AGCTACAGTG AGCCAACAGA GTGAGACCAT CTCAAAAAAA ATTTAAAAAA ATGAAGAAGG 420 AAGGAAGGAA GAGAGGGAGG GAGGGAGCGT GGGCGGGGGG GGGGGGGTGG AGGAGGAGGA 480 GAGAAGGAGT GGGAGGAGTG GAGAAGGAGG GGGAGGAGGA GAAGGATAAA AGGTTACAAG 540 TGGTTGTTAC TAGGAATGGG GGAGAAGAGA AGTGGGTAAT GGCACTGAAG CTTTTTATTA 600 TGTCTTTCAG CATTCTCTGA TTGTTCTTAA ACCATCAACA GATCTCAGTA TGTAGACTAA 660 AAGGGAATAT TTGGTGAAGA GATCTTCTTT CACTATTGTA CACTTGCTAT GGACATGTCC 720 ATGCCTGCTG CCTGGCAGGC ACCATTCATT AAGTAGGCCC CTGTTGCCAA GGAAACCAGC 780 TCTTCACTGA TACCAAAGAT AATGCAGAGG CCTGCCGCTC ACCAAGCAAC CTTCCTCATG 840 AGCTATGCCC CCACCTTCCT GAACTGTCTC TTGCTCCTGT TTGATACTGT CATGCTGCAC 900 GAAGCTTACA CTTGCTATCT CTCACTTCCC TCTTAGTCAT CTGTGATGCT GGCTAAGGGA 960 GCTAGGCCAG TCAGCAGTGA CCTGTTGCCC TTGGTTTATT ATAAGCAAAC TGTTCACAAG 1020 AAATGAACTT CTGTTGTTTT ATAAATGATA TGCATCACAG AACACAGAAT AATATCAAAA 1080 CCACATTAGT TTTTTCATAC TTGCTTCATT GACCCCAGGG GAAGAGGGGA GAGCAGGGAG 1140 AGGACTTTCT CTTTTTTTAA ATACTAATTA TATTGAGGTA TAAAGAACAT ATAGTAAGTT 1200 CACAGACCTT AAGTATACAG TTTGATGAGT TTTGGCAAAT ATGTATACCT GTGGAACCAA 1260 CACCTCAGTC AAGATATAAA TACTTACATC AGCCGGGCGC AGTGGCTCAT GCCCGTAATC 1320 CTAGCACTTT GGGAGGCCAA GGCAGGTGGA TCATGAGGTC AGGAGATCGA GACCATCCTG 1380 GCTGTCCACT AAAAATACAA AAAATTAGCC AGGCATGGTG GCACATGCCT GTTGTCCCAG 1440 CTACTCAGGA GGTTGAGGCA GGAAAATCGC TTGAACCCGG GAGGCAGAGG TTGCATTGAG 1500 CCGAGATAGC ACCACTGCAC TCCAGCCTGG GCAACAGAGA GAGACTCCGT CTCAAAAAAA 1560 CAAAAAACAA 1570
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