| Tag | Content |
|---|
EnhancerAtlas ID | HS108-11657 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr13:114012890-114015120 |
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: 1 | ID | Chromosome | Start | End |
| GH13I113358 | chr13 | 114012803 | 114013755 |
|
Enhancer Sequence | AGTAAGACAG ACAACGTGGT ACTGAAAAAA AGGTAGACAA ATGAAATAAT GGGATATGAT 60
AAGGAATCCA CAAAGAGACC CACACAAACA GAACCAATTG CTTTTTGATA AAGATGCAAA 120
GGAAATTTAA TGCACACAGA ATAGTCCATC TACAAAAGAA TGACTAAAAT AAAAAAACAC 180
CAACAATATG AAGAGCTGGC AAGAATGTGG AGCAATTAGG ACACTCATAT ATTTGTGGTG 240
GGAATGCAAA ATTTACAGCC ACATTGGAAA GGCGGTTTGT AATTTCTTAC TAGTTAGTTA 300
AACATGCACT TGTCACACGA CCCAGCAATC CCATGCGGTG TTTAGTCAAG ATAAATGAAG 360
ACCAAGTTCA CACAAAAACC TGTAGGTGGA TGTTTATAAT GTCGGCTTAC ACATTCCAAA 420
TGTCTTCTGC TGATGAATGG GTTTTTAAAA ATTGTAGTAC ATCCGTAAAT GAAGTACCTC 480
AGCAATAAAA AGGAAGGAAC TATTGACACA TACAAGGTCC TGGATGGATC TCCAACGCAT 540
TAGGTGAAAG AAACCAGACT CAAAGGCTAC AATCTGCATG ATTCCACTAA TGACACCATA 600
GAAATGGCTG AACTACGGGA ATGGGGAAGA GCTCAGTGAT GTGAGCAGTG GGCTGACTTC 660
AAAGGACAGG ATTGTTGAAG GCGACAGAAT CTTGACTGTG GTGATGACTG CCTAGCTGCG 720
TGTTTGTCCA AATTCACAGA ACCATATACT GTTAAGAGTG AATTTTACTG TAAATTGTTA 780
AAATTATTTG ATAGGCCAGG TGCAGTGGCT CATGCCTGTA ATCCCAGGAG ACTCCATCTC 840
TACAAAAAAA CCCTTAAAAA TTAGCTGGGC ATGGTGGTGC ACACCTGTAG TCCCAGCTAC 900
TCTGGAGGCT GAGGCGGGAG GATTGCTCCT CTAGGCTGCA GTGAGCTATG ATCGTCCCAC 960
TGTCCTCCTG CCTGGGTGAC AGAGCAAGAC CCTGTCTCGA TAATAACAAT AATATCAAGG 1020
TTGTATTTAA GAGAAAGGTC GAAATGGCTA AATGCACCAG CTCTGGAGTC AGACACTCTG 1080
CTCCGCTATG ACTTGCAGGC TCCAGACCCT GAGCGTGCCT TGGTTTCCTC ATCGTAAAGT 1140
GAACAGAAGG CACCGAGCCT GCACCCAAGG CCCCCGAGCA GCTCTGGCAG TTGGAGCAAC 1200
ACCCGGAAGC TTCACGGAAC AAAGAATTCT GCGACTTTTT GATAAGTTTG TTATCTGGAT 1260
TTACACTGTT TCTTTATAGA AGAAAGAAAA TTGTTTACTT GTCCTCACAG ACTGACACTT 1320
TCCCAAGGGC AGGGCTAACG CACAGAGCAT CACTAATGTT TGGAGAAGTA TAAAATATCA 1380
AGTCAAAACA GTTGGGAAAT TTTTAAAAAG AAGCTACATC CAGAGAACTG ACGTCCATCT 1440
GTCTACCCTG ACAAAGTTAG GCAAATCCCC AGTTTTTCGG TGTATCTTTG AAAATATGTT 1500
TTCTCGATTT AACTTAGGTG GTGTTAATAT TCTAAGCCAC CAGGAAGGAG GTCTCAAAGA 1560
AGCCAACGGC CCTGAAGCTG CTTCCCTGCA GACGTCTATT CTCGAGATGG AGAATGAAAT 1620
AGGAATCCAA CAGGACTAAG TTTGTTGAAT TTAGTCTTTC CAGGGAGGAA GAGGAAGCTG 1680
TCTTCCTAAG GGCTCCTGGT GGATATTTGC TATGGAAAAA GGAAAATACA ATATTTATTG 1740
TACCCACCAA GAGTGTGATC AGGCAGAATA CATAATAACT GTCCCTTAAG ACATGTGGAA 1800
TGCTGAGATT GGTAGATGAT TGTGTTCCTG GAGACTTTAA CATGGGGAGT GCAGATGAAA 1860
ACCCTCCAAA AGGAGAGGAA AGAACTCTAT CACTGTCAGC CTGGAATACC TGGCAGGAAG 1920
AAGTGGTATT CCCATTTTTG GAATAACTCG TCCACTCCAG TTTTATACCC GACCCTCTGC 1980
TCTTGGGGCT TTGCCAGTGC TCATGGGCAC CCTGACGGTC ACACTGGGAC CCAGGCCCCA 2040
GGCCAGTAGA GACACGCGAT CACTGACTCC ATGTGCCTCC CACCGGAGTC ACCAGCATCC 2100
CTACTCCCTG CAGAACAGGC CCACAGCCCT GTGGCTCCCA CCCCTCAGGC TGAGGCTCAT 2160
ATAGGATCAA AGAGATATAT TTGCTCACAG ACCCATTTAT GCCAGTGATG CTTGCTACCA 2220
TAATTACATG 2230
|
