| Tag | Content |
|---|
EnhancerAtlas ID | HS091-10167 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr12:58208010-58209750 |
Target genes | | Number: 24 | Name | Ensembl ID |
|
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 |
| chr12 | 58208254 | 58208659 | | chr12 | 58208078 | 58208252 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH12I057814 | chr12 | 58208242 | 58208646 | | GH12I057815 | chr12 | 58209061 | 58209210 |
|
Enhancer Sequence | TGGAAGGACA AGGGGTGGGT ATAGGCTACA TCCCCTCCCA CCTCCCTTCC CCATGAGCCT 60
CCCTCTCCTC TCTGTCATTC GGTGCAGGTG GTGGGGAGAA GGAGGGGAGA TGTTCTCAAT 120
GACCTTACAG GATGTGAGGC TGCCAGCCAC AGGGTTAACG TGGCCATCCC TCTGGCTTCT 180
GTGAGCTCTG CTTGCATCAC CCCGGATCTG AACCTTGGTC CCTATCCTGC TTTCCCTTGC 240
CCTATTCTCC ACTCTACTTC CCACCCGATC TCATCTCGCA CTATTGTGGG AAACCTGTGA 300
ACCACCTCCA GCCCTTTGCT GGATATAAAC GACCAAGTAC AAACCCTTCT CTGAGCCGTT 360
GTGCCAGCAC CTCCAACGCT CTTCCCAACG CTGACCACTG GGTGCTGGCC CAGGCCCATG 420
TAAGAAAGAA CACTTGGATT CTGTGGGGCC GTGGGAGGTG GAGGATAACA TTTGGAGAGT 480
GCCAGCGGTC AGCAGGGCTC TGTGCCAAGT GTCTTATATT TGGAGTCTGG GTCAGGGCCC 540
TGATTTATCA CTGCATGTAT GGCTTGGCCC TGGAGGACTG TTCACACAGC CTTGATGTAG 600
ATTTTCATCA CACTCCCCAA GTGAGGGAAA CTTGCGGCCA TACTTGTGTG TGTTCTATGT 660
AAAATGTGAT AAATGTTAAA TATACTGCAA ATCTGGTAAC CGTGTTTTAG TACTTGTTTT 720
TTGTTTTTGT TTTTGTTTTT TTTGAGAGGG AGTCTCCCTG TGTCTCCCAG GCTGGAGTGC 780
AGTGGCGCGA TCTCGGCTCA CTGCAAGCTC CGCCTCCCGG GTTCACGCCA TTCTCCTGCC 840
TCAGCCTCCT GAGTAGCTGG GACTATAGGC GCCTGCCACC ATGCCCAGCT AATTTTTTGT 900
ATTTTTAGTA GAGGTGGGGT TTCACTGTGT TAGCCAGGAT GGTCTCAATC TCCTGACTTC 960
GTGATCCACC CGCCTCAGCC TCCCAGAGTG CTGGGATTAC AGGCGTGAGC CACCGCACCC 1020
CGCCAGTACC TGTTAGTTTT TAAGGAAACT GGAAGCCTTC AAACAGTGGA AGTGACCTGG 1080
GACTCACAAT CTCTGCGAGG CTTGCTGGAG AGCTGACTCC CCCTCCTGGT TGAGGATAGT 1140
GAAGTGAGGC ATCATCGCTG GGTTTTAGGC AGCAGCAACT GACTGGGCTC AGGGCAGGGG 1200
TTGGGGGGAA TCCTCGTATC TGGCAGGTGG AGCTACCCAG GCCAGGGTGG TTCCCAGCTA 1260
TGGATTGCTG GAGCTCACAG CCGCACAGAG GGTCCCAAGC CCAAGAGGAG ACGGGCTGAA 1320
CAGCTCCTCA TCTCTGCAGT GCCCCCTCAC CTCTCCCCAT ATTTTGTAGG AGCCAGGGTG 1380
CCCCGTGGAA GACATGTTCC ATTTCTCTGA TGGAAGCTGC CAGGAGTCTG CTGAGTAGGT 1440
CCCACCTGTC TTTCCAGGGT GTTTCCTGCA AGTGCAGACT CACTGAGCAG GTGGCTGGCT 1500
AAAGGACAAG CCTGTTTTTG TCTGGAGCCC TGTTCTTCGG GGCTGAACAT TTCCTCCACC 1560
TGCCAACCAC CTGCTTTGAG CACCCAGGAG AGGTGAAGGA TGGGAAATAG GTACTTTGAT 1620
GCTGCCTCTC ATTCTCCTCA AACCATAGGC TAAGGGGTGC TGGCGGGCTG TTGCCTAGCA 1680
GCCCCAGGCA GCCAGACTGC TTCCAGATGC CAGTGGTCAC AAGTAAGGTG CCTCCAGCCC 1740
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