Tag | Content |
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EnhancerAtlas ID | HS056-03635 |
Organism | Homo sapiens |
Tissue/cell | GC_B_cell |
Coordinate | chr12:111155130-111157610 |
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) |
SPI1 | MA0080.4 | chr12:111156225-111156239 | AACTTCCTCTTTCC | - | 6.31 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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Enhancer Sequence | AAGCCAGCTG GTACATGAGG TTGAGTTTTG GGTCTTTTCC TCAAGATAGG AAAATGGAGA 60 CATAGCACTT CAAACCCACT TTGTTTGTTT AAGAGTCTCG CTCTGTCGCC CAGGCTGGAG 120 TGCAGTGGCG TGATCTCGGC TCACTGCAAG CTCCACCTCC CAGGTTCACG CCATTCTCCT 180 GCCTCAGGCT CCTGAGTAAC TGGGACTACA TGCGCCCATC ACCATGCCCG GCTAATTTTT 240 TCTATTTTTT TTAGTAGAGA CAGGGTTTCA CCGTGTTAGC CAGGATGGTC TCGATCTCCT 300 GACCTTGTAA TCCGCCTGCC TCAGCCTCCC AAAGTGCTGG GATTACAGGT GTGAGCCACC 360 ATGCCCGGCC TCAAACCCAC TTTCTGGAAG TTTTCTTTAA TGTCTTCTAT AGACCCAAAC 420 ATGAGGAAGA CATTCCTTCT TTGTTCTGAT GCAGATCCTC AGCTTTGTCC CTTCTACTAA 480 TTTCAGGTGA TACTTGGATT ACATGGCCCT TGTCTCCGTG TCTCAATTCA CATGGTGTCT 540 GCAAACTGCC AAAATAAACC TAAGATTTTT CATGCAGCAC TTCCCTGCAA TGGTTCCTTT 600 GTGTTTTTTG GTATCATGAT GCCTTAACTT GGTAGCTTGT ATCTTCACTT CCCAGCAAAC 660 TGAATTCCCT TTCAAACGCT CATCATGGAC CCACATTGAG AAATTTGATT GATATTCCTT 720 TCCATCAGTT TAAATCATGT GCCTTCTTCA TGGCTCAGCA TTCAGTAATT TTTTCCTAGT 780 CCCTGTGTTC CATATCCCAT TTATGTGTAT GTTACTCGAG AACTCTGGCC TTAAATCAAG 840 GTACTTCAAG AACAAGGGTT ATATGTGAGC ATCTGTGCTG TCCACTGCAA CTAGACATGG 900 GCAGGCCTAG TTTGTGTACC AAATCAGCAA TTTCTATGGG AGGGTATTAC ATAGATGATT 960 GAGCGACTAA GGATGCCTAG CACCTGCCTT TCTGTATGGT TTTGTAATGG TGCTGTCATC 1020 TTGTGACCCA GAATACTTGA CAAAAACAAA ACCAAACCAA AACACTTAAT AGAATAGTAT 1080 CACACTAATA ATTACAACTT CCTCTTTCCT AGTTACTTCT TTTGCATATG CTGAAAACAT 1140 CCATGATGGT GTTCCCTTAT GCAGTAAATG CTCAGACATA CTTAGCTATC CATGGCTTGG 1200 TATCAGGTGC AAAGCAAAGC AAAGGCAAGT GACACTTCAA ACTCAGCCAA CCGAGATGTG 1260 CAAAGACACG AAAGAACTGG GATCGATAAG ATAACCAAAA GCAAACATTT AGCAAATACC 1320 ACCGAGTTGA GCATTCTAAA GACACCACAC AACTTCACTC AAGATTCACA ATGTGAGACG 1380 GCTTCTGCTA TGGACGTTTC ATAGCTAGGA ACACAGTGGC TCAGCATTCA GGTCACTCAC 1440 TCAAATCAGG TAGGAGGGGC CAAGACTTGG GTTATCACAC ACATCTCAAG TTCTGCTGTC 1500 AAACAGATTT CAAACTGAGT CTCTCCTAAT GATCTCAGGT CCTAAAACCA AAGATTAATC 1560 TTGTCTTCTA CTTGACCAAT GTTCCTTAAG AAAAATTTGA GCCAGATACC ACACTCCAAT 1620 AATGATATAA TCCTTAGTAC TTGATAAATG TTCCTTAAGA AAAACTTGAG CCTGATACCA 1680 CACTCCAATA ATGATATAAT CCTAGTAGAG CAGCCCAATT TTACTTTATA GCATTTTGAA 1740 ATCCTAGTAT CAATTCATTA ACATTCAGGA CATAAAGATG TGCAGAATTT GCCTTTGACA 1800 CAATTATCAT TCACTGTTTT CTTCCTATAG TCAAAGAAGT CTGGGAGAAT ATTACGTAAA 1860 AGTGAAACAG CACAAGTTTG GATATTGTCA ATGTGGAGCA GGCAGGTAAT GAGGTCCCCC 1920 TTCCCTCTTT GATGGGAGCA TGGCAGGGTC CAGATGCCTC AGGACCGGGG CTTGTTAGCA 1980 GAGGGGAGTC CATGGCCCTG TGCTCTTCTG TGTCCTTCAA AGAGTTCCTC GCTAGGTCCT 2040 CTGCCAACGC CCTCAGGGAG ACCACTTTGT AACAGGAAAA AAAGCTTTTC AAATGACATG 2100 CTCTTCACTC ATTTTTAGCG TACCTTTGAG AAATTAAGAT ACATACTTGT GACAAAATAT 2160 GACATGATAC TGTGTTCCAT ATAAACCAGG GAAGGGGGAA GAGATCAAAG AACTGTGCAT 2220 GAAAATATAG GTGGCTGACT CAGAAAACAA AGTGAGCTGC TTTCAAATTC GCCACTAAGT 2280 TCAAGTGAAC CCAGACAGTA AGAAAACTAT GGACACAGAT TAATCCCCAT CTCCCCAAAT 2340 GGTAGAGGAG GATCGTTCCA CCTCATCACT CTATTACACA AATAGATGTC TCCAGGTTAC 2400 AACTCAAAGA GTATTAGTAT CTGTATTATA ATCCATCTTT GGAAAACAGA CTATTTGAAA 2460 GAAGCAAAAC CAAAATGCAA 2480
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