| Tag | Content |
|---|
EnhancerAtlas ID | HS145-04931 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr11:113316960-113319730 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr11 | 113317502 | 113318217 | | chr11 | 113318774 | 113318957 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I113445 | chr11 | 113316422 | 113319671 |
|
Enhancer Sequence | AGTTCCCCAG GCACTCTCTT CATCCAAACT CCTTAGAGTC ACGTCTGCTG AAAAGACCAG 60
TTTCTACCCC CGGCGCTGAG TCAGACACAG AGTTGCTGTC AGAACTGGAG AAAACACAGC 120
AGTCATAGTA ACGGTAGCTC CTGTTTATTG ACTGTTCACC GTATACTGGA CACTGTCTTG 180
CACACTGTAC ACACCTTTGT CCTAATTCTA AAAGCAACCT TAAAAGGGAA ACATTACTAA 240
TCCTTTTTCA CAGATAATGC CAATGGGGCC AAGGGAGTTC CTTTAATAAC CTATGTCAAC 300
TAGGAAGTGG CAGTGGAGGA TGGAAGACTG GGTTTGTCTA GTTGCAAAAC CTCTGTTTCC 360
ACAGTGGCAA TGAGGCACCC CCTACTAACA TTAACATACT GCAAATGCAA GATGGGATAT 420
TTGGAAATAG TTTACCCATG TTGCTGCTAA GCCTCATAAT AATCCTGTAA ATTCAATCCC 480
ATGTCCCCAC TGTACAGTAC ACATTGATGC AAGTAGTTGT GAAAATGAGA AACAGAGAGA 540
AGTCCTGTGG AGGCACGTGG CTGTAAGAGC ACCATTTAGG AACTCAGTGT TGGTGGCGAG 600
TGAGGATGAG GCCAACACTG ACAGTAAGGC ATATTCCCTG TGTTTCCAAA GTGGGAGGGG 660
TCTTCAAGGA ACCATCACAC CATTGCCACA GGAGCTGATG GCTGATAGGA CAGAATTCCT 720
AACTTGCTGC TGTGGGCTTC ATCTGCAGTC TTGACTCCTA AGCAGCACTC ACACCAGACA 780
AGAAGAGGGC TGCACAAATG CTGAACAAAC TCAGATCTGT GTAGATGCCC TCAGGGAACT 840
TGGGATCCTC TAGCATGTCA TAGCCCTTGC AAGTCCAAAC CTGCCCACTT CTGCTCCAGC 900
CTCCAAAGAC AGCAGCCCCA CCCTCCCCGG GGCCTGGGGT AAAGTCGGGA GGCCCGCTGG 960
GCTGCACGGC CACACTCTGT TCTGTTGTGC CCATGTCTGT CCCTGCTGCT GCTGCCCTGG 1020
AATTGCTCAG GCTCCGTGAT GTTGTTCTTT AAATCATAAA ATCCTCTCCC CGCTCCTGTG 1080
CCTTTCCTGG GGGAGCTCTC TCGGGCTTTT AATTGAATTT GCAGTTTCTG GCACACCCCT 1140
GTTACACAGA ATGCTTGGTA TGGGCAGATG GAAGTGCCCA TGAGAATCAA AACAAGGAAA 1200
CTTTGACAGG ATTCAAGGCT TCCATACCAC CCTCTGAAAA AAAAAAAAAA AGGAGAGAAA 1260
GAAAGAAAAG AAAGTGCTGC TTGTTCCAGC ACCTGCAGAG GATGCGAGCC AGCCAGCAAA 1320
TTCACTACTC ACCTTGCATA TGAACGAACA AACACACACG GGTTTGGTGG GCAACAGAGA 1380
AGGCAGGCGG AACTCTGGGG TGTGAGTGGT CCATGAAGCA AGACAGACAG ACATGGGGCG 1440
GGGTGTGTAG GGACTGAATT CTGACAGGCA GTCAGCATCT GGCTTCTGGC CCCTGCTCTG 1500
CCCCACATTT CCAACCATGT GACCTCAAGC AAGTGGCTTC CCTCTTCTGG CCCTGGATGT 1560
CCTTTTGTAA CAAACATGTG TGGCCACATC AGAGGACACA CAAGGCTTCC TCCCACCAGT 1620
CCTAAGATTC TAATCTGCCA TGATGCGATC TCCAGCCTTG TCCATGTTGA GGGGCCAGTA 1680
GCTGAAGGAG GGAGCTCAGG GTGCCCAGGC CCTCCCTGCT TGTCAGTCTG GGGACAACTG 1740
TCTATTGTGG TTAAAGCAGG TGTCTGAGGC CATGATGAAG GTAAGATCCC ACAAAGGGAT 1800
ACTGAGGGGG CTCTAGATGG TGTCTGGCAG CAGAGAATGT AGTCAGAGGA CCTTCAGGCT 1860
AGGAAGTCAT CATCACTCTG CGAGATGGAA CCACGAAACA GGGAGTGAGT GAGTCACCAG 1920
AGATAATGAG CTCCGAGGCA GGAAGATGCA GGAGTCTAAT GACGTTCTTT TCCTGTCCTG 1980
ATGAGATCTC TTGTCCATAG GCCAGTAGAG CACCCAAGCC CAGAGCAATG GGTAAGGGGG 2040
TCTGACTTCA ACCTGGGGCA GCCGCTCCTT GGAAGGAACC AGGCAGCAAC TGTGATTCCA 2100
GCATCCCAGC CCAGCCCAGA TGCACGGTGG CTGAAAACCA CGCCTCAAGC TCCGGGGGAA 2160
CTCCCTGGCT ATTCTTGGAA ACACAGAGAC TCCTGGCTCC CTGTCAGAGC TGCTCCCCAC 2220
TCTAAAAAGC CCAGGAGTCA CTGCTACAAT ATTTTTCCTT CTGAAGGAGG TGGCATCTCA 2280
GTAATTGCAA CGTGATGCTC TCTTGACAGC AGTATTAATC ACCTGTCTTC ATCTCAGCCC 2340
CAGCCATGAG AGAGGAACAG GAGGAAGACA GAGCCAGAGG GCCTGGTGTT GTTCACTGTC 2400
CTCATCCAAG GGCACGGGTA CAGCAGTCTA TTCTGTCTCT TCCTCAAGCT CATTGTCACT 2460
TCCGAGAGGG GACTGGGGTC AGGCCTCATT CGGGTTCCCT AGAGTGGAAA GGATTGGTAA 2520
GGAGCTGGGT AGCTCTCCTT GGCCACCTCT AAAGGAGCTG CACCACACTG GGCCTGCGAA 2580
GAGGAGACCA GGCCCACAGA CCCAGGCAGG ATGGAGGAGA TGGGAGGGGT CAGCAGGGGG 2640
CCAAATTCAA GAGTTTCTTC TCAACCCTAC CTTTAGCCTG CCTTCCTGAC CATCCTGCAC 2700
ATGCCCACCA AGTCCACCTC CCAAAGCCAT GGCTTCAGGC TCATGTCACC GCCTCGCTCA 2760
AAATATCTTC 2770
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