Tag | Content |
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EnhancerAtlas ID | HS006-21983 |
Organism | Homo sapiens |
Tissue/cell | Astrocyte |
Coordinate | chr2:105876730-105878920 |
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) |
NFAT5 | MA0606.1 | chr2:105877856-105877866 | AATGGAAAAT | - | 6.02 | NFATC1 | MA0624.1 | chr2:105877856-105877866 | AATGGAAAAT | - | 6.02 | NFATC3 | MA0625.1 | chr2:105877856-105877866 | AATGGAAAAT | - | 6.02 | NKX2-3 | MA0672.1 | chr2:105878271-105878281 | ACCACTTGAA | + | 6.02 | Nr2f6(var.2) | MA0728.1 | chr2:105877992-105878007 | AAGGTCAGGAGTTCA | + | 6.04 | STAT3 | MA0144.2 | chr2:105878903-105878914 | CTTCCCAGAAG | - | 6.14 |
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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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| Number: 1 | ID | Chromosome | Start | End |
GH02I105260 | chr2 | 105877161 | 105878721 |
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Enhancer Sequence | GTGGCATGCG CCTATAATCC TAGTTACTTG GAGGCTGAGG CAGGAGGATC CCTTGAACCC 60 GGGAGGCGGA GGTTGCAGTG AACTGAGATC TTGCCACTGC ACTCCACCCT GGGTGACAGA 120 GTGAGATTCT GTCTCCATAA AAAAGGAAGA AAATTCTGAC GTATGCTACA ATATGGGTGA 180 ACTTTGAGGA CATTATGTCA AGTGAAATAA GCCAGTCACA AAAGGACACA CACTGTGTGA 240 TTCCACTTTT ATGAGACACC TAGAATAGTC AAGCTCATAG AGATAGAAAG TAGAATGGTG 300 GGTGTCAGGG GCTGGGGAGG GAGAAACAGG GAGTCAATGT TTAATGGGGA CAGGGTTTCT 360 GTTCGGGATG ATACAAAAAG TTCTGGAGAT GCATGGTGAT GATGATTGCA TAACAATGTA 420 AATGTATTTA TGCCACAGAA CTACACACTT AAAAATTGTT AGAATGATAA ACTTAATGTT 480 ATGTATATTT TACCACAATA AAAAAAATAC TATGAAAATG GCAAGAATAT TAACATACAT 540 GCAAAATGCA CTTAAATATA GCCAGGCCAG TAATATGATA ACCTGTCTTT TTTGGGGAGG 600 GCATAAAATT TGAGTTTCTG ACTATGTTTA CTCATATAAA GGGAATACAT TCTTGTAAAC 660 TGACTGAAGT CAAAGAAACT GAATCTCTTT TGAGGTGTAC ATCATTATGT CTTGTAAACA 720 ACTGAGAAAT GCTCTCCTGT ACTCTGTGTT AAGAAAGTAA GTTTAGGATT TCAGTTATAT 780 TCGTTTATAA GCTTCAGTCA ATAGCTGCCT GTAAGTCAGC AACATATTAA AAAACAGTTT 840 GGAAATAGTT GGTGGGGTTT TACCATAATG TGCTGGCTGC AGAGGCGGGA GTGAGGGAGG 900 GTAGGCCAAC TGACCACCCC AGTTCTATCA TGCACATTGC TGTGGAGGTA AATCATAAAC 960 ATGTGTGGGC AACCAGACAG AGGCAGGGGC TGGGTGAGTC AGCTCAAAGC ACGTAGCGTC 1020 ATCTTAGCTC ACATTCCTGT TGAGGTCAGG TTGGGGATTG GCCACCCCAG CTTCGTTGCA 1080 CACACATGGA TTCCGAAAGG GAAAAACTGA TATTTCAAGC AAGACAAATG GAAAATGTTC 1140 TCTAGAGAAA GAGGAAGGAC TTGTGAAACC TAGAGCACAT GAGAAAAGGC AAGGGGAGCC 1200 GGGCACAGTG GCTCAAGCCT GTAATCTCAG CACTTTGGGA GGCCGAGGTA GGAGGATCAC 1260 TTAAGGTCAG GAGTTCAAGA CCAACCTGGC CAACATAGTG AAACCCTATC TCTACTAAAA 1320 ATACAAAAAT TAGCTGGGCA TGATGGCATG TACCAGTAGT CCCAGCTACT CGGGAGGCTG 1380 AGGCAGGAGA ATCGCTTGAA CCCGGGAGGT AGAAGTCACA GTGAGCCGAG ATCACGCCAC 1440 TGCACTCCAG CCTGGGCGAC AGAGCAAGAC TCCATCTCAA AAAAGGACAG GACAGGCAAG 1500 GCAAGGCAAG GCAGAGGCTG GAGGAAAAGG GGCAACTGAA AACCACTTGA AAAAAGGTAT 1560 GTGTAGACCA ACTCCTCTCC TGGGTCCAGC TGGAACCGGG ATTGAGGAGT AGAGTGGGCT 1620 AGAGTCACTT TCCAAATCAA GGAACCATGC AATGAGATTC CGGAGTGCTC AGACACACCT 1680 GTGGGGGCAC ATCTGTGGGA TGTGTGCATG AGTCCCTGTG CTGGGTGCTT TCAAGGGCCA 1740 CCTGAGACCC TGGTCCTAGA GGACATCTTT TGGTAATGAA GACTGAGACC ACACTGCTAC 1800 CCTGCCCTGA CTTCCATTGC TTGGAACAGA AGGTTAACAC GAGAAGGGAA CTCAGATACT 1860 GCCCAGCTCC ACCTCCTGCT TATGGACGAT GCCACTGATA TGGTTTGGAT GCGTGTCGCC 1920 CTCCAAATCT CATGCTGAAA TTAACCTCCA GTGTTGGAGG TGGGGCCTAG TGGGAGGTAT 1980 TGGAACCCGG GGACGAATCC CTCACGAATT ACCTCCCCGT GGTAAAGAGT GAGTTCTCAC 2040 TCTGTTAGTT CACGTGAGAG CTGGCTGTTT AAAGGAGTCT GGCACCTCCT CCTCACTGTC 2100 TCTCTCCAGC TCTTGCCATG TGATGCATCT GCTCCCCCTT GGCCTCCCAC CATGGCTGGA 2160 AGCTTCCTGA GGCCTTCCCA GAAGCAGATG 2190
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