| Tag | Content |
|---|
EnhancerAtlas ID | HS136-06460 | Organism | Homo sapiens | Tissue/cell | Monocyte | Coordinate | chr15:31739760-31741490 | 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 |
| chr15 | 31740827 | 31741249 | | chr15 | 31739959 | 31740450 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH15I031447 | chr15 | 31739959 | 31741294 |
| Enhancer Sequence | CCAGGATAGT CTCGATCTCC TGACCTCGTG ATCCACCCGC CTCGGCATCC CAAAGTGCTG 60
GGATTACAGG TGTGAGCCAC TGCGCCCGGC CCATCTGGTT TTTTAATCGT AGCCATCATA 120
GTGGTTGTGA AGTGGTATCC CATATCCCAC TGTGGTTGAA TTTGAATTTT CCTGATGGTT 180
AGTGATATTG ACCTTCTTTT TTTTTTTTTA TTATACTTTA AGTTCTAGGG TACATGTGCA 240
CGAGGTGCTG GTTTGTTACA TTTGTATACA TGTGACTTGT TGGTGTGCTG CACCCATTAA 300
CTTGGCATTT ACATTGGGTC TATCTCCTAA TGCTATCCCT CCCCCCTCCC CCCACCCCAC 360
AACAGGCCCT GGGGTGTGAT GTCCCCCTTC CTGTGTCCAA GTGTTCTCAT TGTTCAATTC 420
CCACTATGAG TGAGAACATG CGGTGTCTGG TTTTTTTGTG CTTGCGATAG TTTGCTGAGA 480
ATGGTGGTTT CCAGCTTCAT CCACGTCCCT ACCTTCACAG CACGTCTACA CTGATGTTGT 540
GGCCAGGCAA CTTGGCACTA TAGCCTAGCC ACGTCGACAC ACAGACTCAG TCATCATAGT 600
TCACCCCTTG TCACCAGACG CATTTCCTTT AAACTGTACT TCATCTCCAA ACAGAGGCAT 660
TAAATAACAA GGTCATACTT CCACCTAGCA TGATACAACT ATTCTGCCTA CAACCAAAAA 720
TGCACTAACC CTTACCCCAG AAAAAGACAG AAAGTCCTTG AAGGACATTT ACTTTTCTTT 780
GATATCCTAT AACTTAAACA CTAAGATATA AAACTAATAC ATCTTATATG ATAAGGCAAT 840
AAGAGATGGA AGAAAACAAA TGTTTTTTCA AACACATACA CACAAACATA TTTGTAACAA 900
AATAAGGAAG AAGCACTTAT AACAGTTACA GTCCTTGTTT CTGTCACGTG GTCATAGCTG 960
GTATTTCCAG TTACCCTTGT CTTCTGTGCA TTCTGTATTC CCTTTGCCTT CAGTGAGCAC 1020
CTGATGAAGT GACCTGAACT TCATTATTAA AAGGTTTGGG CCATTAGTAG TTCTGCCTGC 1080
GTTGTGCTCT GTTTTTGTTT TTTTTTATGG ACTTTAATCA CAGGGCATGG TAGTATTAAG 1140
AGATGCTCTA AGGGAGCTCT TCTATTCCAC ACGTGTTCTT CCTTATCTTC TGTGTGCAGT 1200
AGCGGTCCGG TTTCCTGTTT GTACTCCAGA TCAGTTTCCC CAGCCAGTAC AGTAACTCTC 1260
TTCTTTGCCT GTTAGTTCAT TTGCACAAGG AGCTCAAAGT GGCCGGATGG CAGTCTTAAC 1320
TTCCAGTTCA ATGGAATCAG TATTGTGTCT CTTGGTGGAA GCATTCCTTG CTTTGGAACT 1380
AAAACCTCTA GATGAGCAGA GCACAGCACA AAGTTGCAGA GACAGGAAGC AAACAATGTC 1440
CTAGTGGTTA CTACGCGTAA TAGTGAATGG TGCCACTCCC ATTTCCATCC TAGATTCCTG 1500
GACTATTGAA GAAATCCTGA CTATCAGAGA AACAGCACCC TATATGGGAC ACAGATTCAG 1560
AGAATGCACA GCCTGCTGGA GAACCTTGCC CCAGCCCCAC AAGGTGTTGC CACCTAGTAG 1620
GTGCTGTAAC TGCATTTTCA AAAGGCCATT CCACCATTCT ATGAAGCCAG CTGCTTCAGG 1680
ATAGTCAAAA ACATAATAAG ATCAGTAGAT TCCACGAGGA TGAGCCAGGG 1730
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