Tag | Content |
---|
EnhancerAtlas ID | HS091-18712 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr17:3635760-3638110 |
Target genes | Number: 11 | Name | Ensembl ID |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr17:3636711-3636723 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr17:3636715-3636727 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr17:3636719-3636731 | GTTTGTTTGTTT | + | 6.32 | IRF1 | MA0050.2 | chr17:3636271-3636292 | TTTTGCTTTTGTTTTCATTTT | + | 6.76 | Zfx | MA0146.2 | chr17:3636958-3636972 | CCCGCCTCGGCCTC | + | 6.01 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH17I003732 | chr17 | 3635495 | 3635894 |
|
Enhancer Sequence | CTGTTAAAAG AGCAGATGAC ATTCTCTTAA AGAGCCAAAC AAAACAAAAC AAAAACGTGG 60 TTTCCTCACA GCAATTCAGC AAACATTCAC TAATTTTTCT GCCTGTCAGA CACCCTGCCA 120 GGAGCTAAAG AAATAAAGTC CACTTGGTCC CTGTCTTCCT CACAAGCCGG ACAGGCAGGG 180 TCAGCAGTAG ATCCCCGAGG AATTTAAATA CAAGGTCGAA GGGGTGCTTC TGTGAGGGAG 240 CTGCAGAGAA CAGCAGTGGA GAAATATGAA TTCCAACTCG GAGGAATTCG TAAGGTCTTC 300 CTGGGGAAGG AGGCATTTGA GCTGGGCCAT GGACTGATGC AAATATAACC CACAGCCTGG 360 CTGGAAGGCC GGCACACACC AGCACTGCCA CGTAGCCACC AGGGCTCCCC ACCTGGACCC 420 CCGAGGGGCA GGTGATGACT GCAGTGAGTT TTCTTAATTC TCCCAGGGAC GGTCCATCCC 480 TAGTTCCCCT CTAGATGCCT AGGAGATTGT TTTTTGCTTT TGTTTTCATT TTTTTGAGAT 540 GGAGTTTCAC TCTTTCGCCC AAGCTGCAGT GAAGTGGCGC GATCTCGGCT CACTGCAACC 600 TCCACCTCCC GGGTTCAAGC AATTCTCCTG CCTCAGTCTC CCAAGTAGCT GGGATTATAG 660 GTGCCCACCA CCACGCCCGG CTAATTTTTT GTATTTTTAA TAGAAACAGG GTTTCACCAT 720 GTTAGCCAGG CTGGTCTCGA ACTCCTGACC TCAAGTGATC CACCCACTTC AGCCTCCCAA 780 AGTGATGGGA TTACAGCCGT GAGCCACGGT GCCCGGCCTA GGAGATTGCT TCATTCATAT 840 AATGGATACT GTCCTAGCCC AAATAGCCTA AGATGACCGG GGACAAATCT ACAGTCCAAC 900 AAATTCAAAT TTATTGACTC ACTGCAATGA GGAAAACTAC ACTTTGGTTT TGTTTGTTTG 960 TTTGTTTGTT TTTGAGACAG AGTCCTGCTC TGTTGCCCAG GCTGGAGTGC AGTGGCGCAA 1020 TCTCAGCTCA CTCCAATCTC CACCTCCGGG TTCAAGTGAT TCTCGTGCCT CAGCCTCCCG 1080 AGTAGCTGGG ATTACAGGTG TACATCACCA CACCTGGCTA ATTTTTGTAT TTTTAGTAGA 1140 GACGGGGTTT TGCCATGTTG GCCAGGCTGG TCTCGAACTC CTGACCTCAG GTGATCCGCC 1200 CGCCTCGGCC TCCCAAAGTG CTGGGATTAC AGGCATGGGC CACTGCACCC ATCCAAAAAC 1260 TACACTATTG TGTGTATCAC TGAACAATGG AAAAGGCGGT TATTAAAGGA CTCCAGGGAA 1320 GGGTGGAGTT CAGATGAAAT GTAAATAAAG TCCTGTTTTG ATGGTAAAGC AGGGCTGAGT 1380 GTCAAGGAGT CAGTCACCAG CAGGCCAGCC TGTGAATCAG ACCCAGGGCC CGCTTCCTGG 1440 GAAACCATTA ATATGGAGTA GAAAGTTGAC AGACACTGTA TCTGAAGCTC TCTACCTCAG 1500 GTGGAAACAG ACTCTTCTCT TGGTCAAAAT GACTTACACT CTCCAGGCAA GAGGGATAGG 1560 GGTTCATAAT TACCGACGTA ACTACTTCAA ACAGCAAAGT TTTCTTTCTT GTTTTTTCTT 1620 TTGAGACAGA CTCTTGCTCT GTGGCCCAGG CTGGAGTGCA GTGGCGCAAT CTCGGCTCAC 1680 TGCAAGCTCC GCCTCCCGGG TTCACGCCAT TCTCCTGCCT CAGCCTCCCG AGTAGCTGGG 1740 ACTACAGGCA CCCGCCATCG CGCCCAGCTA ATTTTTTTTT GTATTTTTAG TAGAGACGGG 1800 GTTTCACCGT GTTAGCCAGG ATGGTCTCGA TCTCCTGACC TCGTGATCCG CCCGTCTCGG 1860 CCTCCCAAAG TGCTGGGATT ACAGGTGTGA GCCACCGTTC CCGGCCCAAA GTTTTCTGAT 1920 CTGTGATTTT AGAGAATAAA ATTTCTCAGT GCAGTGATAC TTGTCAGCCA CAGGGTGTCC 1980 TCGGGAAACA GACTGTTTCC TAGTATCTGT GTCTGTATCC AGCCTTGGGA ATGGCAGGGC 2040 AGATTTTCAC TTTCCCAGTC TAAGCTAATT TTTACTTTCT CAGTGTCTTA GGGCATTAGA 2100 CTCACTTCTC TCTCAGAACC CTGGTGAAGA AAGGGCCGCA CATAGGGAGG GTGGCACTGC 2160 AGCAGAATAT GGTGCCTCGG GAGGCATGGA GCCGGACTGG CGGGGATTTA TCTAGTTATT 2220 AACCATCTGT TGGTTGGACC AGGAGGAGGC TGGAGGCAGG GGTGCCAGTG AGGGGGCCAC 2280 CACAGAAAAG CAGGCATGCA GCGAGGGAGG GGCGTGAGGG ACCTGTTTCC ACAGCCACCG 2340 TCACAGTCAC 2350
|