Tag | Content |
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EnhancerAtlas ID | HS197-13754 |
Organism | Homo sapiens |
Tissue/cell | ZR75-30 |
Coordinate | chr22:23643420-23646030 |
Target genes | |
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) |
Gata1 | MA0035.3 | chr22:23645132-23645143 | ACAGATAAGGA | - | 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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Enhancer Sequence | AGGCAGGGAT TTCAGTGAGC CAGGGTCGTG CCACTGCACT CCAGCCTGGG GGACAGAGCG 60 AGACTATCTC AAAAAAGACA GAAAAAACCT GAAGAAATTC CTAATGGCAG CAAGGCTCCA 120 ATTTCCCCAG CTCTGCCAAC TGTGGTGACT CCCTCTCTGG CCCAGGATGT GCAGGAGCAC 180 TGGGACTGTG TCTCAGGGCC CCCGTCCCTG TTGCGCTGCA CTCGGCTAGG CTGCAGACTA 240 GCCCTCCAGC AATGTGTCCC ATACCCCGTC CCATGAATCT TGGATGGATG TTGATGCCTT 300 CACCTTGAAA AATCCCTCCC TGAAGATACA GATTCAATGT CCCCTGCTCT GTGAAGGCTT 360 CTCTGTCCCG TGACCTCACT TCCCAAGTAA CCGTGCCATC TGAGCCACCA GTCAATCTGG 420 GCCAAAGCCT GCCCTGGCTC TTGGCACATT TGCCACATCC TTCCTTTCCA GCTTCTCTGA 480 TCTAGACCAT GAAGGCTGGG GAGAGGGGTC TTCTTGTTCT TGGGGACCCC CCCGCCAGGC 540 ATGGCACACA GGAAGCCTTC CATGACTAGG GTGGCACAGC GGGTTCCTGG TGTCTGAGGA 600 TGGACCAGGA TGGCCTCGCT CACTCAAATG GCTCATTCAG GCTCGGGGCT GGCTTGGAAG 660 GGACACCCGA CTTGGGTCCT CTTGCACCTG CCCACACACA AGGACTTCAA TTTGTGCTGT 720 CAGTGGCTCT TTTCTGGACT GTGGGCACCA CCACAGCTTT GTCCCTGCTG TACTGTGTAT 780 CCCCTTGCCT TTCTGGCTTG TGGCTCTGAA CAAAGCAGGT CACCCATCCC AATTTCTAGA 840 GCCCCCCCAC CGCCACCCCC ACCCTCATGG AGCCTCTATC GTGCAAGAAG GGAGGTGGGG 900 ACCTGGCAAG TCATCCAGGA CAGGCATTTG AAGAGCAGGA GCCAAAATCT GAGACTCGGG 960 CAAGTGGTTC CTAAACCCAG CTCATCAGCA CCATTAAGGG GAGCAAAAAA CCAGACCGGG 1020 CCAAGCCCCC AGCCCAGAAG ATCCCGACTC CTGCTGCCCA CAGACAGGCA CATGAGCAGC 1080 TTTGCTGAGG ACTCCTTTCC ATCCCAGACC CCTGCCCTTG GGGCCTGCCA GGGACCTCTG 1140 CCCTCATGGT TGGATCTGGA CACTCCCGGG ATGCTGCGGC TTCTCTACCT GCTGCAACTG 1200 CCTCACCTCA CGGGAGGGTC TCTCTACGCA ACTTCTGAGT CGAGGTGCAT AAGCAGTGTG 1260 GGGGCTGTAG GCCCCTGTAG CTGGCTGCAG AGAGCCAAGC GCCTCCCACA CGGTACAGCA 1320 CAGAAGGCTC CTGGTGTCAC TGGGAAAAGC CCAGATTCAA AAAGGCTGGG CTCCGGAGTC 1380 ATGCACATCC TCTCTCAGGT ATCCCTGTGC AGAAAACAGT GTCCACGGGG GAGAAAGAGG 1440 CCAGGCTGGT GTCGCAGAGC GCCAATGGCA TAGTCACCAC CACTCCTCCG ACTTACTTCC 1500 TCCTGGGATC CCACAAACAA GCCCCCCAGC TGGGAGCCTG GACCTCCAGG GACCAGGGCA 1560 GCCGCCACCT ACTTGGCGTG AGTCATGAAT GCCCTTCACA CAGCAATCAG ATTCCTTCCT 1620 GTCTAGCCAT GGTTCCCACC CATCACTCCC ACTGACACAG GGACCAGGGG CTGGAGCCAG 1680 ATAGTGCCTG CTCCATCGCC TCCTCACAAA CGACAGATAA GGATGAGAAC AGCAGCAAAC 1740 GCTGACCCCC CACCCGTGAG AGCATAAGTC ACTCAACCGT CAAGGCTGCA TGGCCCCCCC 1800 CACCCCAATT TAATTCACCT GTGAGAGGGC AAGTGCCTGG CTCAGCAATT TCTAGTGCAT 1860 GTAACAGTAC TTGCTTTGTG CCAATATGTA TTTTACTATA TATATATAAA CTCTAGATCC 1920 ATTAAACAAT GTATTATTAC ATAACTTATA GAGGTATGTT TTATGTCTCT GTCTGGGTAC 1980 TGGAGATACC ACAGAGAATG AACTGGACAA AGCCCTGTCC TCCACGTTTA CTTTCCAGCA 2040 GCAGAGACAA ACATAAGCCA AAATAAAGAT CACGTCACAG GGGACGTGAT GGGAGTCGGA 2100 GGAGGTATGG TCAGGTAAGG CGGATACCGT CATGAAGGCA CCAAGAATCC TCATTTGTAT 2160 TTCAAGGATT ATCTGAGGGC CACGTAGGTC TTGTCCACAC AGCCATTCAC CCATTCAGGG 2220 GGGTCTCTGA TGTGCCTGGG GGGCATTCCG AGATGAATGA GACATGCATG GTCCATGTGG 2280 CAGAGGCACC AATAGGAGAG AAACTTATGT ATGTAGCCTC TTAAACAGAC TTGGAGAGGG 2340 GCAGGCCCCA GGGGGTCTCT TGCAGCAGGA ACACAAAATG AGTGATGTTT GTTTTGAACC 2400 AATATTTGGG GAAGATATGA AGATGTAAAC ATCATGAAAA TGTAAGATCA CATGAGCAAA 2460 TTCTTACACA GATTCCACGG GATTCTTCTT GAAGCACACC GCCATCAACA TGGATAGTGA 2520 TACAGGTCCT CCTTGCTCTA TTGAGAGCCA CTTTTGGACC CTTTATTTTT AACTTTTGTA 2580 CCATGAAATG CATCCATTTT TATAACCGAA 2610
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