| Tag | Content |
|---|
EnhancerAtlas ID | HS118-10278 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr2:111932750-111935050 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr2:111935021-111935036 | TGGCCTCTTGACCTT | - | 6.65 | | ZNF263 | MA0528.1 | chr2:111933375-111933396 | GGAGGAAGAGTGAATGGAGAG | + | 6.03 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_58584 | chr2:111874506-111933083 | Ly1 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TATGTAGATG TTAATATTGC ATCCATGTTA ATTTCCTGAT TTTGATCGCT GAACTCTGGT 60
TAGGTAAGAG GATGTCCTCA TTTTTAGGAG ATACACACTG AAGTATTTAG GGGCAAGGGG 120
CAACAGGTAA TTTACTCTCA ATGTTCAGGA GAAAAATGTG ATGTGCTTAC ATGCATGTGG 180
GGCAGGATGG AATGGTGGCA GTTGGAAGGG AGAAGGATAA AGCAAAATGT GGCAAAATGG 240
TAACATCTGG GTACTCTGGG TAAAGGCTAT AAGAAAAGTG TCTCTACTAT TTTGCAAACT 300
TTTTGTGTGT CTGAAATTAT TTCAAATAAA AAGTTAAAAA ATTAAGAGCT GTGCCTGGAT 360
TGTGGCTGTG CCTGGATTGT GGCTGTGCCT GGATTTTGGT CAGGAGTAGA AGTCAGGAGT 420
CCACCCCGGG AGACCTGGGA TGTGGACAGA GGGCAGACAG GCTTTGGAGG AAGAGGAGGG 480
AGGACTTCCT GATGTGGAAG GTGAGGGAAC AGAAGGAATC AAGGATTCTA AAGGATGATT 540
TGGGTCAGAG CAATTAGCGG GGATGGCGCT TCCTGAGAAT AGAAGCAGGA GTGGGAAGTG 600
AGATCGGTTG GGGAGGGGCT GGGGTGGAGG AAGAGTGAAT GGAGAGTTCT GTTTTGCTGG 660
ACCACGAACT CAACTCAGGG GTTATCTAGA AACAAAGGGC TGTCAATTCA TTTTAAAGGG 720
CTTTTTTTTA AGTTGAGTTT CTGGAAAGAA ACTCCAGGAA GGTGGACTGT ACCCACTGGC 780
TGCTTAGAGA AAGCCTGGAG CATGAATATT TAGACATTTG CTTTAATGAA GCACTCTCAT 840
AAGCCGGGGA AACAGGGCCT TGAGCATCTG TTCATGAGAG GTGGATGATG GCCCAGTGGC 900
GCCTATGGAG CATCTATGAA CACAGGCCAG ACAGGGCACA GGAGGGAGGT CCTCAAGCCT 960
AGAGGATGTT AGACTCCCCC AGGGGCTTTT ACAAAATACC CATACCAGAG GCCCACCTCT 1020
CTGAGTCTGT GGTGGGGGTG CAGTGTCATA TTTTTAAAGG GTCCCTAAAT GACTCCAGTG 1080
TGCAGCTGGG CTTGGGAGCT GCTGAATGAC AGCTTGCTCA AAACTGCCAG GGATGACTCC 1140
AGCAGTGGTG GGGCAGCCAC AGCAGCATCG GGTCCAGCAA TGCTCCCCAG GGACAATGCT 1200
CTGAAGGACA GCAATCAGCA AGGTGCTTTC TGTCTGTTTA AATTTCTGTT GTAGTTGCAA 1260
AATGATCAAT TCTCTTTTCT GTTTCCCTTT GCCAGTTTGC CCTGGCACAG GCATCCATGC 1320
CTCCAGCCAA ATTCAAGGTG AGTGGAGGAC AGAGTGTGCT GTAGGGCCCA AGGCCAAGGC 1380
CAAGGCCACG GCAGGGTGGA GGTGAGGTGG CCCCGGGTTG TGAGCCTGGG GAGAGCCCAG 1440
TCATCATCAG GTGAGTCAGA GCCTTCAACT GACAAACCCA AAGAACTCAG CGAGCTCAGA 1500
GACGGGAGGC GGAGCCATAG TGTGGACCCC AGAAGGGCTA GAGGTAGAAC CGAATCTGTG 1560
TGTGGCACAG GCAGTGAACG TGGGTGGATC ATGCTGTGCT TGAGCCTGGC CTTCCATAGC 1620
TCAGGAGAGT GTAGAGTGTG AGGGGAATCT CATAATCATG GGAAAAGTGT CATCATCGTC 1680
CCCTGAAAAA CAAGGACAGG AGGACACACA GGGGCAGGCT CTGAGAGAGC ACATTCAGGT 1740
GTGAGCACTT AGAAGGGAAA ATGATGATTT GTGTTGGGGA ACAGACCACA ATGCACATTG 1800
CACCCGGTTA GACACCAAGC TCTTCCAGGG GAACTTCTAC TTCTGATTGC TCAATACTAT 1860
GCAGAAATGG CCTCCGTGGG AGCCTCCACA GGCACACCCT TGCCCGCTCC AAGTCCCTCC 1920
CAGGACCAGA CTCTCTGTCC CTGCCCCAGC CAGCAAGGCT CAGAACAGTG GCTGCTCCCA 1980
GGTAACTCCC AGCCTGATTC CGGGTCCAGT CACCAAGCTC TGGGGATGGC CTTCTGATGG 2040
CTTATAGGTA AATGCTCTCA TCCCTGCTGG AAGATCCTAA TAACATTTTA AATTGTGTCT 2100
CTCTGTCTGT GGGGCTGCTA GCATTAGCCA GTGTGCCTCT GACTCAGCGG GATCTCGCCG 2160
TACCTGGCAC CTAGTAGGCA CTCAACACAC CGTTGTTGGA TGGGTGTGTG GCAACTAAAT 2220
GTCTGACGAG GACTCAGGTA AATCATCTTC TATGAAAGCC CAGTCTTTTC TTGGCCTCTT 2280
GACCTTCATC ATATGTATGT 2300
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