Tag | Content |
---|
EnhancerAtlas ID | HS091-00979 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr1:27269560-27271880 |
Target genes | Number: 15 | Name | Ensembl ID |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TBX20 | MA0689.1 | chr1:27269949-27269960 | CTTCACACCTT | - | 6.32 | TBX21 | MA0690.1 | chr1:27269950-27269960 | TTCACACCTT | - | 6.02 | TCF3 | MA0522.2 | chr1:27270127-27270137 | AACACCTGCT | + | 6.02 |
|
| 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 |
GH01I026944 | chr1 | 27270880 | 27271172 | GH01I026945 | chr1 | 27271490 | 27274089 |
|
Enhancer Sequence | GTGAGGCCCA GCCCTTCTAG CCTGGGGTGT TGATGGAAGT AGAAGGGAGG ATGTGTGCTT 60 AGTTTACTCA GGAGCCATGC TGGGGGCATT GTGGGATTAT CTTAATCCCC ATGACAACAC 120 TCTTTAAAGT AGATCTGTCT CTATTTTATT TTCTTAAAGA CAAGGTCTCA CTCTGTTGCC 180 CAGGCTGAAG TGCAGTAACA CCTTCTTAGC TCACTGCAGC CTTGAACCCT TGGGCCCAAG 240 CAATTCTCTC GCCTCGTCCT CCTGAGTAGC TAAGACTACA GGTGTACACC ACCACGCTCG 300 GCTAATTTTT GTTATTAAAT TTTTTTGTAG AGACCGGGGG GTCTCACTAT ATTTCCCAGG 360 CTGGTCTTGA ACTCCTGGCC TCAAGTGATC TTCACACCTT GGCCTCCCAA AGTGCTGAGA 420 TTACAGGCTT GAGTCAGGAA AAGAGCTCGT TGATTTACCC AAGCTCCTAC CTCTGGGAAG 480 GGGTGGAGTC AGAATTGAAA GTCTTAGTTT CTAAAGCCAC TTCTTTTTCA CTAGGTTTGT 540 ACATGCATTC AATTCATCAA ATACTTGAAC ACCTGCTCTG TGCCTGGTAC TGTTCTTGTT 600 CTAAGTGCTG GAAAGAGAAC AGTGAACAAA ACATAGGAAA ATATGTGCCC TCAGGAAGCC 660 TTCATTCTCA ACCTCACTGC CTTTACAGAG AGGTAGGACA CAGAGATCAG TAAATAAAGG 720 TGGTCTGAAA AGGGCCAAGG GTCTGAGGAG AACTTCCCAG GGCACATAAG ACCCTGTAAC 780 AGCCTGTCCG ACTGGCACTG GCTGCCTTCA CTCACTCACC CCTCCATGCC TCTGCACTTG 840 CTTTGTCGCC CAGGCTGGAG TGCAGTGGCG CGATCTCGGC TCACTGCGAG CTCCGCCTCC 900 TGGGTTCATG CCATTCTCCT GCTTCAGCCT CCAGTGTAGC TGGGACTACA GGCGCCCGCC 960 ACCATGCCTG TATTTTTTTT TTTGTCTGTT TTGTTTTCTA TTTTTTAGTA GAGACAGGGT 1020 TTCACCGTGT TAGCCAGGAT GGTCTCGATC TCCTGACCTT GTGATCCGCC CACCTCGGCC 1080 TCCCAAAGTG CTGGGATTAC AGGTGTGAGC CACCATGCCC AGCCCTTTCC CTGCCTTTTA 1140 AATTTATTTT TTATTTTTTG AGACAGGGTC TTGTTCTCAC CCAGGCTGGA ATGCAGTGGC 1200 GCAATCACGG CTTACTGCAG CCTTGACCTC CCGGGCTCAA ACGACCCTCC CACCTCAGCT 1260 TCCTGAGTAA CTGCGAGCGC CACCCTACCT GGCTAATTTT TAAATGTTTT TTGTAAAGAC 1320 AGGGTCTCAT GTTGCCCAGG CTGGTCTGAA ACTCCTGGGC TCAAGGGATC TTCCTGCCTT 1380 GGCTTCCCAA AGTGTTGGGA TTACAGGTAG GAGCCACTGC ACCTGGCACT TCCCTGCTTA 1440 AAAACTTTTT CTGGCTGGGC GTGGTAGCTC ATGCCTGTAA TCCTAGCGCT TTGGGAGGCT 1500 GAGGTGGGCA GATCACGAGG TCAGGAGTTT GAGACCAGCC TGGCCAAGAT GGCAAACCCC 1560 ATCTCTAATA AAAATACAAA AAATTAGCTG GGCATGGTGG TGGGCGCCTG TAATCCCAGC 1620 TACTTGGGAG TCTGAGGCAG GAGAATCGCT TGAACCCAGG AGGTGGAGGT TGCAGTGAGC 1680 TGACTGCACC ACTGCACATG GTGGCTCACA CCTGTAATCC CAACACTTTG GGAGACTGAG 1740 GCAGGCAGAT CATCTGAGGT CAGGAGTTTG AGACCAGCCT GGCCCAATAT GGTGAAGCCC 1800 CGTCTCTACT AAAAATACAA AAATTAGCCA GGTGTGGTGG TGCATGCCTA TAATCCCAGT 1860 TACTCGGGAG GCTGAGGCCG GAGAATTGCT TGAACCCGGG AGGCAGAGGT TGCAGTGAGC 1920 CGAGATGGTG CCACAGCACT CCAGCCTGGA CAAGAAGAAC AAGACTCCAT CTCAAAAAAT 1980 ATATATATTT ATTTTCTTCC CATTTTAAAT CTGGAATACT GCTTTGTGTC TTAAGACTCA 2040 GCCCGAGTGT CACTTTCAAA CTTTTCTCCC TCCACCCTGG ATGAATATCT CCCTTTCTGC 2100 TTTCTTCTTT CCCTTATCAC ACTGATTTGT AACTCTTTGC CTCTGTGTCT CCCCTAGCTG 2160 CAGGAAGGGC ACAGTCTTGT ACCTCTGGAT CCAGTGTAGG CCTGCAAGGG TCTCAGGTGC 2220 AGGATGTGGA TGGGAGAGAG TTTGGTTGTG AAAGGGTTAA GGGGTGATTC CTGGTGCACA 2280 GAGCAGGCCA CCTCCCACCC TCTGGTTGTT CTCTTCACAG 2320
|