Tag | Content |
---|
EnhancerAtlas ID | HS156-09858 | Organism | Homo sapiens | Tissue/cell | P493-6 | Coordinate | chr5:122774560-122777430 | SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 2 | ID | Chromosome | Start | End |
GH05I123438 | chr5 | 122774681 | 122774830 | GH05I123439 | chr5 | 122774999 | 122775065 |
| Enhancer Sequence | CAAACAGAAA ACAATTTTAA AAAGTATTTA GTTAAGGCTA GTTGCTGCTG CTTGCCAAAG 60 GCTCTTGAGC CTGAGGCTTG ATTTCTGTTT GTTTAGAAAA AAAAAAAAAA AGGTTAGGGA 120 GTAGGTAGGA GGAGTTAGCA TTTTAGCATA GTTAAAAGCG TTAACAAACT GGTACTGTTC 180 AAGGACTTCC TCAGAAGAAC TGCAAGCACA TTGAGTCACT TTCTGTATAT GATTCGATAT 240 TATTTTTACT ACCTCACTTC CTTTCCCGGG ATGCACACCC CTCTAGCAAA CACTTGCTGG 300 AGGAAGCTGC CCTGTGTAAA GCGTTAGGGA GCAGACCTGG CTGTTGCCCT AGGCCAGCCT 360 TGGAAACTGT TCAGGAATTG AGGAGTTACC ATGAACCCCT ACGCTCTATA ACTGAATGAC 420 ATGTTGGTCA GGGAATGCTC TCCCATCTGA TGAACTCTCC TGATACAGGC TGGCTTGTGT 480 TCCTCCAGAA TTCATCTGTT GAAGTCCTAA CCCCCAGAAC CTCAGAATGT GACTGTGTTT 540 GAAAATAGGG CCTTTGATGA AGTAATTAAG TTAAAATGAG GCCATTAGAG TGGGCCCTAT 600 GACTGGTTAC CTTGTAAAAA AGAGATTAGG ACACAGAGGA GAGACATGTG AAGACACAGG 660 AGATGACAAC CATCTGCAAG CCAAGAGGCC TCAGAAGAAA CCAGCCTTGC TGACACCTTG 720 ATCTTGGACC TCTAGCCTCC AGAATTGTGA GAAAATGCAT TTCTGTTGTT TAAGTCACAT 780 GTTCCATGGT ACTTTCTTAT GGCAGCCCTA GAAAACCAAT ACATTTCTCA AGTGGAACAA 840 CATTCAGAGA TACAGATTTT GTATAAGTGC TTTGACTTGC TTCCTGAAGT ATTACAGAGG 900 CGCTAAGGCC TAGACCACAT GTGGAGACCA TCTGGATTTG TTTCTTTGCT GGTATGGCGA 960 TTTCTAAGAT TCCTCGTGGA GATCATGCGT AGGGAGACAG CCAGTGAGTA CATGTGCATT 1020 GTTTAATGAC AGGATACATT CTGAGAAATG CATCGTTAGG CAAGTTCATC ATGTGCAAAC 1080 ATCAGAGAGT GCACTTACAC AAACCTAAAT GGTACAGCCT ACTACACACC CAGGCTATAT 1140 GATATAGTCT ATTGCTCCTA GCCTATAAAC CTCTACACAT GTACTGTACT GAATGCTGTA 1200 GGCAATTGTA ACATAATAGT AAATATTTGT GTATTTAAAC CTATCTAAAC ATAGAGAAGG 1260 TGCAGTAAAA ACATGGTATA AAAGAGAAAA TTGGCATACC TATTTAGGGC ACTTACCGTG 1320 AATGGAATTT GCAGGACTTG AAGTTGCTCT GGGTGAGTCA GTGAGCGGTG AGTGAATGTG 1380 AAGGCCTAGA ACATTACTGT ATACTACTAT CGGCTTTGTA AATACTGTAT ACTTAGGCTA 1440 CACTGTTTAT TTAAAAATTT CTTTCTTCAA TAATAAAGTA GCCTTAGCTT ACTGTGTTTT 1500 TTTTTTTATT TTATAAACTT TAAAGTTTTT TTTAGCTTTT GACTCTTTGT AATAGCTTGA 1560 AACGCAAATA TATCGTACAG GCTGTACGAA AAGTTTCCTT TCTTTATATT TTTATTCCAT 1620 AAACATTTTT CTATTTAAAT TTTTTAATTT TAAAACATTT TTTAAAAAAC TGAAACACAA 1680 ACACACACAC TAGTCTAGGC CTACACAGGG TCAGGATCAT CAGTATGACT ATCTTCCACT 1740 TCCACATCTT GTCTCACTGG AAGGTCTTCA GGGTCAATTA CACACATGGA GCTGTCCTCT 1800 CCTGTGGTAA CAATGCCTTC TTCTGAAATA CCTCCTGAAT GACCTGTCTG AGGCTGCTTT 1860 ACAGTTAACT TTTTTTTTAA TAAGTAGAGG GAGTAAACAC TAAAATAATG ATAAAGAGTA 1920 TAGCATAGTA AATACATAAC CCAGTAACAT ACTCATTTAT TATCAAGAAT TATGAATTGT 1980 ACATGATTGC ATGTATTATA CTTTTCTAAG ACTGGCAGCA CAATAGGTTT GTTTGCATCA 2040 GCATCACCAC AAACACTTGA GTAATGTGTT GCACTATGAT GGTACTACAG CTACAACATC 2100 ACTAGGCAGT AGGAATTTTT CAGCTCTATT ATAATCTTAT GGGGTCACTG TCATACATGC 2160 AGTCCATCAT TGACTGAAAT GTCATTATGC GGTACATGAC TGTGGAAGGA ACCTGTTCCA 2220 GTCAAGCAAT TAAAGGCAAT CCTGTGTATC ATTTAAATAA TCATGTACAT ACTTCAATGG 2280 TGGAAACAGC CCTACACTTA AATGGAGTTA TAAATCTGAT TGACAATATC CTCAGAGGTG 2340 TAGCTCTTGC CATAAGATGC AATTGGACCT TATTCCAAAA CGATGCCCCC ATAAAATCAT 2400 AAAATTAGCC ATAAATAAGA TAATAATCAG TTAGTCTACA TCAACTGAAA GCCACTATAC 2460 CAGGGTACAA ACTAAACACG CATGGCCCTA CATGCCAGGT GGGCCTGATG CCCAGTTGGG 2520 GTACTTTGAG GGTTAGTAAT TTGACTTCTG AGGGAGGCAG TAAATTTCTG TAATGGAACT 2580 GGAATCATCC CTTCTGGCAT AATTCCCTCT AGCTTCTGTT ATGGGTTAGA TCAACAATTC 2640 AGCTGACACA TTTGTCAATG ACACAAATCA AATGCTTTCC TGTATTCTGT TACTTCAACC 2700 TTCTTGAAAA CTGAGACAGT GCAGGACAGA AGAACATAAA AGAGATGCTA CTGCAGGAAC 2760 TAGATGACAC AGTGATGTCA GGAAGAACCA TCTGACTCAG CGCCACCCCA AGCCTAGGAG 2820 CTGTATGCCT GTGCTGTAGC CATACACATA AATCTGTAAT TATTTTAGTC 2870
|
| |
|
|
|