| Tag | Content |
|---|
EnhancerAtlas ID | HS091-22328 | Organism | Homo sapiens | Tissue/cell | HepG2 | Coordinate | chr18:47364170-47365510 | Target genes | | | | 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 |
| GH18I049837 | chr18 | 47364058 | 47365194 | | GH18I049839 | chr18 | 47365501 | 47365650 |
| Enhancer Sequence | AACTGAAATA AAAGCACAGT TAGAGAAGCT TGCATTCCCC ACTAACAATG CAAAGATTGG 60
ACCACTCAAA TCATTTAGTG CTCCGGGCTT TAGCAATGAT ACCATCCAGA GGTGTGCAAT 120
GTTGACATGC TTAGGAACTT ATAACATTTG GCAAAAAATT TCTAATGTGT TGATTTCTGT 180
ATGGAATAAA ACAGCTGTGG ACAGCATTTT CATTTAATTT ACTGGCAATT AGACAAAGAT 240
GATGGGCATG TACCAGCTCG ATTTGGTATC GCCTGTGCTG AAGTCCACAG TTTGAGAATT 300
GAGCAACCTG GGTGTCATCC TCGTCCAGCC ACTGACTATG TAAATAAGAG CTTCATTGGT 360
CCGTCATACT TACTAAGCAG CCATTACCTA TGCACCAGGG GCTTTATGTT CAGTATCTCT 420
TTCAATCTTC CAACAACTCT ATAAAGTACT ACCCATTTTT ATGAGGAAGT TGAGGTATAA 480
AGCGGTTAAA TAACTTGTCT GAGGTCACAC TGATAGGGAG TGGCAGGGCC AGGATTTAAA 540
CCCAAGTCTG TCTGACTCCA GAACTGCTGC TATTAACCTT CACATTATTC TGAGTATCTC 600
CAGCTTGATA TGTCAGTTCT CCCTCTGTCT GGTGCCTTAT AAAAAGATTT CCAGACAGGA 660
AGGAGGGTTT GGAATGAACC TCATTTCAAG TAATGTATTT CTAGATTGGT CCTTCTTGGG 720
ATTCACTCAT AACCTACTTG TGTTGTAAGA ACCTGGGGAA AGCATTATGA ATAGGTCCAG 780
GTACACTTTC CTTCCCAGCC TTTGCAGAGC ACAGTGAGTA ATGCATCTAC ACATAATTTT 840
TCTTCCGATT GAAAATGTAA CTGCTCTCAT TTCTCAATTC TGATTTCATG TTCAGTGCCC 900
AAGTACACTG CTTGGTTCAA AGCAAGTGTC TAATAAATAC TGATGCATCG TGCCGACTGC 960
TGTGTCCTTT CGCATGAACA CTCCTGCTTT TTTCCATGAA TCAAGTTCAT AATAGGTTAA 1020
GAGGGTTATG CTTTTTCACT GTATATGCAT TTGTACCTTT TGAGTTTACA TTTATTATGT 1080
ATTAAAATTT GGGAAAAAAT ACAACATATT ACAGAAAAAG AGATAAAGGG AAAGTCATCT 1140
ATGCCTCTTG CACTGTGTCA AATACTTTCA CAGCTTTTTA AGCATGATGT GCACACCTCA 1200
GTTCTGCCTT CACTGGAAGG TTCTGGCTTT CTGGAGGTCA TGGCTAAGAT ATCTGGTTCC 1260
CGAAAGGCAG AGGGTGCTGA CCACGCCTTC CCCTCATTTC AGACACCATG ATGAGTGATG 1320
TAGCTCTCCT GCTGCCAGCT 1340
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