Tag | Content |
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EnhancerAtlas ID | HS018-01499 |
Organism | Homo sapiens |
Tissue/cell | CD19+ |
Coordinate | chr1:158131700-158134580 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr1:158133328-158133349 | GGAGGAGGAAGAAGAGGAAGA | + | 10.16 | ZNF263 | MA0528.1 | chr1:158133358-158133379 | GAAGGAGGAGGAGGAAGAGGA | + | 10 | ZNF263 | MA0528.1 | chr1:158133361-158133382 | GGAGGAGGAGGAAGAGGAGGA | + | 11.13 | ZNF263 | MA0528.1 | chr1:158133367-158133388 | GGAGGAAGAGGAGGACGAGGA | + | 6.12 | ZNF263 | MA0528.1 | chr1:158133346-158133367 | AGAAGAAGAGGAGAAGGAGGA | + | 6.15 | ZNF263 | MA0528.1 | chr1:158133325-158133346 | GTAGGAGGAGGAAGAAGAGGA | + | 6.2 | ZNF263 | MA0528.1 | chr1:158133334-158133355 | GGAAGAAGAGGAAGAAGAAGA | + | 6.2 | ZNF263 | MA0528.1 | chr1:158133337-158133358 | AGAAGAGGAAGAAGAAGAGGA | + | 6.52 | ZNF263 | MA0528.1 | chr1:158133343-158133364 | GGAAGAAGAAGAGGAGAAGGA | + | 6.5 | ZNF263 | MA0528.1 | chr1:158133322-158133343 | GGAGTAGGAGGAGGAAGAAGA | + | 6.66 | ZNF263 | MA0528.1 | chr1:158133349-158133370 | AGAAGAGGAGAAGGAGGAGGA | + | 6.99 | ZNF263 | MA0528.1 | chr1:158133373-158133394 | AGAGGAGGACGAGGATGAGAG | + | 7.12 | ZNF263 | MA0528.1 | chr1:158133340-158133361 | AGAGGAAGAAGAAGAGGAGAA | + | 7.31 | ZNF263 | MA0528.1 | chr1:158133316-158133337 | GAAGAAGGAGTAGGAGGAGGA | + | 7.52 | ZNF263 | MA0528.1 | chr1:158133319-158133340 | GAAGGAGTAGGAGGAGGAAGA | + | 8.21 | ZNF263 | MA0528.1 | chr1:158133364-158133385 | GGAGGAGGAAGAGGAGGACGA | + | 8.28 | ZNF263 | MA0528.1 | chr1:158133331-158133352 | GGAGGAAGAAGAGGAAGAAGA | + | 8.4 | ZNF263 | MA0528.1 | chr1:158133352-158133373 | AGAGGAGAAGGAGGAGGAGGA | + | 8.56 | ZNF263 | MA0528.1 | chr1:158133355-158133376 | GGAGAAGGAGGAGGAGGAAGA | + | 8.92 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_59679 | chr1:158116838-158154200 | Ly4 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 158133418 | 158133510 | chr1 | 158132800 | 158133318 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I158162 | chr1 | 158132391 | 158133590 |
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Enhancer Sequence | ATGATTAGTG TATAAAACCA AGAAGAATAT GGACCAAGCC TGGAATATTT TTAAGGGAGT 60 ATTTGCATTC TGAGGATTTC TAACCTAAGT GAGAACCATG TGACTAAGTC TTTGGCTCTC 120 AATAGCTATT GGCTCATCTG GGCAACTCCT CTCATACTTC CATTGAAGCC AAAGTGTATT 180 AGGTCCACAG TTTAACATAT TTTAAAAGTA GGGCTTAATT AGAAAACATT TACTGAGTAC 240 TTGAGATGTG CCTGACCCTG TGCTTAGCAC TGAAGATATT GAGATAAATG GAGAAGTCTC 300 CATACTCCAG GAACTCACAG ACTAGTTAGG GAGACAGGAT GGTAGATAGT GGCAGTGTGA 360 TGAGAGCTGT AATAGAGGCA TGCACATGAT TCTATGGAAA AACAGAACTA TCACTTAGCT 420 CAGATTGGGT GAGGACTGGG GTTGATGAGA GAGGTTCCTG GATTAAATGG CGTGAGACTG 480 ATGAGTGACT TGAAATTAGC CTGCAGATGG GAATGGGTAG GTTGGAGAAG CTGGAATGTG 540 TTACTAAGAG AAATTGGATT AAGACTCAGC TAAAAAATAC CAAGTATCTA CTATGTTCCA 600 GGTGATTTAT ACACATTATC TAATCTCTTA CATAAGACTC ATATGAGATT CTGATTTCAT 660 AAATGAGAAA GCTGAGGCTC AAAGAGATTA AATGGCTTGC CCATAAAGTG GAAAAAAAAA 720 ACATGTTTTA AAGTCCTCTT TTAGTCCACA GTGTCTCCAC TTTTAAAAAA GATATAGTTA 780 AAGCTAATCT TCTAGCCCAA TTTCTCTTAG TGTCACTGTG AAAAATAAAA CTCTGTCATT 840 ATTGTTTGCA GGGATGTCTG GCCTCACTTT GGATAATCTG GACCTTTTCT GCTGCAAGCA 900 TACCACTAGA TAGAAAAGAG GACCTGTGAA ACATCTTCTC CACATTTCCC TTCCCTAGTG 960 GGAAGCTTAT TGTTTCAGAG TCAAGAACTT GGTTCCAGGC TACAGTCCCA TGGCTACCAT 1020 TCTCTAACTG TTACTTTGCA CTTCTAAGGT GTGTTTTTTT AAAATATGAT TAATAATGGT 1080 GCCTAACTTG TCAGGCTGTT GTGAGAATCA AAAGAGAAAA ATAAATGTAA ACTGCTTAAT 1140 GTATTGCTGG CACATAGAAA CTGCTCGAGA AATATTGGCG ATTAAAGTGT TATACACTTT 1200 AAAGTGAACA GGCAAATTCA CTTCCCTAAA CTCAAGTTTC ACTCATTGAT TTGAACCTTG 1260 GTTGACATTT CATCTTCTCT GAAGCCTACA CTGTGGATGT AGGCTGTGGA TGAAACAGAA 1320 ACTGACCACA GGGGTCAGGG CCAGGGCTCT GCCAGAGAAG CCAGCTAGAT AGAAACTCAA 1380 TTTTGATGCC ACTGTGGAAT ACTATAGGCA CATTTCTATT TGAGATGTGG GTGACTACCT 1440 AGTCAAGAGC TGAGAGAGGG ATGAGACAAT GAAGTAAAGA AGTGGAGGGA AAAAGAATGT 1500 GGAGAGGGAA GGAGAAATGG GATGACCTGG CTGGATACAG ATGCAGATGA AGGGCAGATA 1560 GAAAGAGAGA AGAATGAGAT AGGTAAATGA GAGTGGAAGA GGGATAGGGA GAGAGAGAAG 1620 AAGGAGTAGG AGGAGGAAGA AGAGGAAGAA GAAGAGGAGA AGGAGGAGGA GGAAGAGGAG 1680 GACGAGGATG AGAGTGTGAT GGGGGAGAAG GAATCCAGAG GAATGAAAGA TCCAAGAGAT 1740 AAGGCAACAT ACAGTTTTTA AAAAATCTCT GCAGGTGTAG CTAGGTGTCT ATTACATGAA 1800 ACTTACTCTT CAGAGGCATT TGCTTTGTAA ATTTGTGAGT CATGGAGTAG AAAAAGGAAG 1860 TTGACAAAAT GACAAGTGCT TCCTTTCTCT CCTTGAAATA AAAATTGGAG TTTCTGAGAA 1920 GGCACCCATT AAAACCAGTT TTTCTCCATT TTTTGGGTTC TCTATGAGCT TTGTTCCATT 1980 TCACTGGTGG TTATTGTCCT GATATGTCTT AGATTTCCAT CTTATTTGAA CCATAGATCA 2040 TGAAAGGTGA GCCCATGAAA TTAAACTTTT GTTAAAAAGT GGAAGAACTT CAGAATTGGA 2100 AGACCCCCGT CCATGCAGTA ATCTCTTCAA CAGCATATTT GGCAGATGAT CATCCAGGTC 2160 CAGTATGGAT ATCACTACTG GCAGAGTTCA CAAAAATCAG ACCATCCTTT ATTGGGTAAG 2220 TCTAACAGCT ATACAATTTT CAGTTGCACT AAAGTTTGCC TTTTGATAAC TTTCACACAT 2280 TGAGCTTAAT GTCACTAACC AAAGCAACTG AAAAGTGATT TCCCATTTCT TCCTGACAGA 2340 TCTTTAAATA TTGGCTAGTC TTTTAAATTG TTCTTCCTTT TGATGATTTA AGACCTTTCC 2400 TCATTCTGTA GGGCCTCTTC TAGGAAGGTT GTAATTGTAA ATGTTCTTCT TCAGTCAAAG 2460 TGCTCAAAAC AATACAATAT GAAACATCAT AGTGGACAAT TCATGGCAAC AAGGCAGAGT 2520 AAGATAATAG AGACTGCCCA CCCATCCCAA TGCATACTTC AAAGACTTGT AAATACTGAG 2580 TGAAATGTAA TCTAAAGATT TAAAACAACA CAGCTGAGCT CAAGGGAGCC TTCCTATAAC 2640 AAAGAGAAGT ATTAAATAGT GAGCAGACAG AGCAGCAGCT CACGGTGTCT TGGTACTGGT 2700 TTTGCCTAGG TGCTGGGGAC TGAGTTTCTA ATGTCCATGA AGGGACAGAA GACTTTACCT 2760 TGGGATAGTG GGAGGTGACA CTCTGCAAAA GAGGTCCCCT AAAACTATAT CCTCTAATAA 2820 GTGTAAAGTC TATTACAAAG GGACAAAAAA CCTTTGCCCA CTGGTCCTGG GAAGTGATGA 2880
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