| Tag | Content |
|---|
EnhancerAtlas ID | HS091-27379 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr2:119931850-119934220 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr2:119932208-119932227 | GCATGCCCCCTGGTGGCCG | - | 6.24 | | Zfx | MA0146.2 | chr2:119934198-119934212 | GAGGCCGAGGCGGG | - | 6.01 |
|
| | 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 |
| GH02I119174 | chr2 | 119932213 | 119932271 |
|
Enhancer Sequence | GCAGGTAGGC TTTACCCTAT CAAAGCCCCC TGGGCTGGGG ACTCTGTGAA GAAGCAAGAT 60
GTGCTTGAAA CCTCCCTCTC TGCTGAAAAA TCTAGACAAG CTCCTGACCG GCTGCATTGC 120
TGCTTCAGCC CCTCCTCAGG GAAGCGGGAG GCCCTGGGTC TCTACGGGTG CTCTGTGAAA 180
GACTGCAGAG GCTGGTGGGG CTGCATTCCT GTCTGTCTGC CTAGGACAGT GCCTACTGAC 240
TTCTGACTGC TGCCCCATGG TCCAGGGCTC CAGGTACACC ACTGCAATGT CACTTTGTGC 300
TTGGGGTTCC AACTAGACAA AAGCCCCACG TTGCACAGCC CTTGAGCCGT CCCGGGTAGC 360
ATGCCCCCTG GTGGCCGTGG GCAGTTATTA CCGTTAATCC TTTCTTGCCC AGATGCCTCT 420
AGCGTAGGCC ACAGCAGCCG GCCGGGTTCG TTGTGTCTGG AAAGACCAGA GAAGGGTTCC 480
CGGAGAAAGA GGCCGTCTGA TCGGAGTTTT ATGAACCAGA GGATAAAGAA AGGAAGGGAT 540
TTCTGGGCCT CAGAAAACCA CATGCCAACG CATGGGGGTA TTAAGGATAG GGGCTCTTGA 600
ACGCCCAGGC TGGTAAAATC TAGAACGGCA GAGGGAGGAG GGGTAATTTT TCTGGTTGGT 660
AGAAATAAAG TGGGGATGAG GAAGAGCACG AAAGTCTGTC GGCAAACCTG AAAGTGGGAG 720
CGAGCTTTTG TCAAATCCAG GGTCAACCTG AGCTCTCATT AATTGGGAAA CTGGAGAGTC 780
AGATCCTCTA AAGAAAGTGG AAATATTTGT TCTAAAGAAC CCCTGCCAGG TCCCCGTTTA 840
CGTGACTCAT AAAGAGGCCT TCAGGCAGAA AGGATCCCAG TGCACCAGTA ACAGAAGGGC 900
TCCAGGACCA GAGGGAATGG ACAGGGAACC ACCACCCACA CCAAGCACAG GCCCATTGTC 960
GGCATGAGGA GCCTCGCCCC TGCAGATCAC CTCCCAGAGG GGAGCGGATC AGAGATTAAA 1020
TTCCACACCT TTCTACAAAA TCATAGCAGT TTGAAAGTGC CAAGGGGAGT AGGTGAGGAG 1080
GTTTCGAGGC ATGTATGCAG CCGTTTGGAG ACACCAGCCA TGTCGCCTGA GTTTTCTGAT 1140
GTAATCCTCA TAACAACCAT TCCAGATTTA AGTGATTAGT CCTGTTTTAC AGATGGGGAA 1200
ACTGAAGCTC AGAGAGGTTA AGCAACTTCC CCAAGGTCAT ACAGTAGCCA AGTAGCATAA 1260
GTGGTATTCG AACCCAGTTC TATTTGGAGC CTTCACAGGC TTTTTGCTGC ATTCCACAAG 1320
AGTCTGTATA TTCAGAAGCA AGTCTTCCAC AGCCATCATA AGTCATCCTC ACAGCCGGCT 1380
GGCAGGGAGG GAACATTGCC ACTGTAGCTG GGATCATAGA TATCGTGGTC TCCATTTGAC 1440
GGATAAGACT GAGGTCTGGA AGAGAGTCAG TCAGTCTGTG TGATAAGCCT GAACCACCCT 1500
CTCCTTCAGT TCCTCCCCTA ACCCAACATC CTCCGGGTCT GGAAGGACAG TGTCTTGAGC 1560
AACTTCTTGC AGCTATACTT CTCCAGCTAA TAGTCTAGAA AACCGAGCCT GGTCCCGAGT 1620
CTCCTCCTCG GGGTACGAGC CGAGGGCACT GATGGGGGTC AGGAGGTGCT GGCTAAAAGA 1680
CGGTGGTGCA GGTGCCCCTG GCTTTAAGCG CGCCCAGGTT ATAAAAAGCT TGGTTCCCAT 1740
GCTGGCCCTA ATTCTCCATG CACTGAGTAC CTTAGGTCCC TTCTCTGGGT CTGTTGCTCC 1800
CCTGTAAAAC AAGGGGGTGG GAGAAATGAC CTTCAAGCTC AAACACCATA TGTCCACCTG 1860
GGTTGGTATA GCAGATTGCA TTAGTTTGTT AGGACTGTTT TAACAAATGC CACAGACTGA 1920
GTGGCTTAAA CAACAGACAT TTATTCTCTC ACAGCTCTGG AGGCTGGAAG TCTGAGATCA 1980
AGGCAGTGGC TGGCAGGGTT GTTTCTCCTG AGGCCTCTCT CCTTGTAGCC ACCCCTCTTC 2040
TCCCTGTGTC TTCACATGGT TGTCCCTGTG TGTGTGTGTC TGTGTCCTAA TCACCTCTTC 2100
TTATAAGGAC ACCAGTCACA GAGGATTACC GGCCACCCAT AGGACTTCAT TTTACCTTAA 2160
TTATCTCTTT AAAGTCTCCA TCTCCAAATT AGTCACATTC TGAGGTACTG GGAGTGAGGA 2220
CTTAAACATA CGAATTTGGA GGATAGGACA CAATTCAGCC TATAACACAG ATAGAAGACA 2280
CTGCTCATTT TAAAAAAGAA GTAGCAGGCT GGGCGCAGTG GCCCATACCT GTAATCGCAG 2340
CACTTTGGGA GGCCGAGGCG GGAGGATCAC 2370
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