| Tag | Content |
|---|
EnhancerAtlas ID | HS091-23764 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr19:30262180-30264600 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2C | MA0497.1 | chr19:30262199-30262214 | TTTTATTTTTAGTTT | - | 6.1 | | NFAT5 | MA0606.1 | chr19:30262332-30262342 | ATTTTCCATT | + | 6.02 | | NFATC1 | MA0624.1 | chr19:30262332-30262342 | ATTTTCCATT | + | 6.02 | | NFATC3 | MA0625.1 | chr19:30262332-30262342 | ATTTTCCATT | + | 6.02 | | NKX2-5 | MA0063.2 | chr19:30262261-30262271 | CTCAAGTGGT | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr19 | 30262498 | 30263197 | | chr19 | 30263933 | 30263987 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I029771 | chr19 | 30262701 | 30262870 |
|
Enhancer Sequence | ACCATGCCTG GCTTTTTATT TTTATTTTTA GTTTTTGTAG GGATCTCACC ATGTTGACCA 60
GGTTGGTCTC CGACTCTTGG GCTCAAGTGG TCCTCCCGCC TTGGCCTCCC AAGTTGCAGC 120
AATTACAAGG CGTGATCCCC TGTGCCTTGC CAATTTTCCA TTTTAGTGGA TCCTGCTCAC 180
TTGGGTTTCT ATGGCAGTCA TAGCTTCACT CAGTTAAGAT TGAGGCATGC CCTGCCTCCT 240
ACCTGGACCC CATGGAAGGC CTCCGGGATG AGACTTGTGG GTTGAAGTGT GTCCTCCAGA 300
AAGACATATG GAAGTCCTGA CCCCCAGTAC CTGTGACTGT GGCCTTATGT GGAAATAGCG 360
TCTTTGCAGA TGTAATCAAG ATGCAGTGGG GTCATACTTG ATTAGGGTGC TTTCTAAATC 420
CAATGACCGG TGGATTGGAT TGAGGGGAAT TATAGTTCGA TCAACTCCTA TGGAGAGGGG 480
GATTTGGTTA GAGACACAGA GACACGCAAA CAGGGAAGAA GGCCTTGTGA AGACAGAGGC 540
AGAAAGTGGA ATGACGCAGC TACAGCAGAG GAAGGCCAGG GATCCCCGGA GCCACCAGAA 600
GCTGGAGGAG GAGAGGAGGG ATTCCTCCCT GGAGCCTCCA GGGGGAGCAC GACCCTGCCG 660
GCACCTTGAT TTCGGGCTCA GCCTCCAGAA GCATGGGAGA ACAAATATCT GCTGTTTTAA 720
AGCCACCACG TCTGTGACAA TTTGTTACGG TGACCACAGG AAAATAATCC AGGGACTGCA 780
TCTAGAATTT ACCATGTGCC TCATGCCACT ATCACTGGCA CAGGCTGAAG CCTTTCTCCT 840
TTTTCCTCTG GAGAAGACCA TCTTCTCCTC CAGTAGTCTA AGCAGTTCTC AGCCCAGGGA 900
TTCCAGCAAG TGTCTCAAAG CCACACACTC GGAGAGACGA CGGCCACATG ACCTGGCTCA 960
GCAGGTGGCT CTGCTGCCTT TCACAGGAGT TTGCCTCTCT GTTCAGGGTG CCACACAGGG 1020
ACAGCCTTGG GGCAGACACT CTGCTGTTTA TTATTATTAT TATTATTGAG ACATAGTCTC 1080
ACTCTATCAC CCAGGCTAGA GGGCAGTGGC ATGATCTCGG CTCACTGCAA CCTCCGCCTC 1140
CTGGGTTCAA GCAAGTCTCC TGCCTCAGCC TCCCGAGGAG CTGGGATTAC AGGTGTGCAC 1200
CACCACGTCC ACTAATTTTT GTATTTTTAG CAGAGACGGG GTTTTGCCAT GTTGGCCAGG 1260
CTAGTCTCGA ACTCCTGGCC TCAAGTGATC CACCCGCCTC AGCCTCCTAA AGTGCTGAGA 1320
TTACAGGAGT GAGCCACTGT GCCGAGCCTA GCTGTTTATT ATTATTACAT TTTTTAAGAG 1380
ATAGGATCTT GCTATGCTGC TCAGACTGGT CTCAAACTCC TGGGCTCAAG TGATCCTCCT 1440
ACCTTGGCCT CCCAAAGTGC TGGCATAACA GGCATGAGCC ACCGTGCCCA GGCAGCCTTG 1500
CTAAGCACAC CTTGCACTCC TGCTGCACTA CTCCTGTGTG AGGCCATGGA GACATCTGCT 1560
ACATTGTAGA TACTATTGGA TACTTTTCAA GTATCACACA GCCTACAATT TCCAACAGTG 1620
CACTCCATTC AGCTCCCATG GGACGGATGA GTGTCACAGG GCAGCTCCAC ACGCAGATCA 1680
GGGAGAGGGT GGATATCACC CCCATCTTCC TGTGGCTCTG AGAAAAGGGG TGGGTGCCCG 1740
GCGTCAGGGC AGCTGACTTC ACCCAGGAGG GGCCACCTGC CCAGTTACTC GGGCCTCCAC 1800
TTCCCTGCAC TCAGGGCACT TTGTTGGAAG AGGGCTTGTC TGGCCATGAA TGGCCTGAAA 1860
GCTGCGAGAA TGGCTTAACA CACCTGAAGA AGGGACATGT ATATGCTGGG GGCTGGCACT 1920
CTCCCACATT AGCTCTTTTG CACCATTGTC ATGGGGATCT TGGGGCTCAG AGAGGAAAGT 1980
GACCTGCATG AGCTCATGCA GAGGCATGTG GCAGGACCAT CGCTTGAACC TGGCACTGGA 2040
GGGCCCTGGG CTCAGCACCT CGGGCACCTA GAGTGAGGGC ATCCCCAAGG TCCATGTGAC 2100
CCAGAGCACG GCTCCGGCCA CTCCCTCCCG GAAATGGATC GGTGAACAGA GAGGCTGAGG 2160
ACCTCTTGCA ATGCTGCCCA GACTGCATGG AGAAGCCCGT GGAGACATCT GCTACGTTGT 2220
AGATACTACT GGACATTTTT CTTTTTTTTT CTTTTCTTTT TTTTTTTTTT TTGAGATGGA 2280
GTCTCGCTCT GTCACCCAGG CTAGAGTGCA GTGGAGCGAT CTCGGCTCAC TGCAAGCTCT 2340
GCTTCCCGGG TTCACGCCAT TCTCCTGCCT CAGCCTCCCG AGTAGCTGGG ACTACAGGCG 2400
CCCGCCACCA CACCCGGCTA 2420
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