Tag | Content |
---|
EnhancerAtlas ID | HS002-02167 |
Organism | Homo sapiens |
Tissue/cell | A375 |
Coordinate | chr11:126470580-126473310 |
Target genes | Number: 10 | Name | Ensembl ID |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
POU2F2 | MA0507.1 | chr11:126470828-126470841 | GTTATTTGCATAT | + | 6.1 | ZNF263 | MA0528.1 | chr11:126471567-126471588 | CCCACTTGCCGCCCCTCCTCC | - | 6.27 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH11I126601 | chr11 | 126471664 | 126472530 |
|
Enhancer Sequence | AGCTCCAATG AGATGATTCC TGGTTTCTAC TAGGAATATA AGTAAAATTT GAATTTTTGC 60 CAGAATCCAA AGTATTCAAG GAAGGGCTCC TTATACACCT TTGATCATTC ACTTCCATGT 120 CTCATCTTTC AAAGCTTGGC TTAAACTTTC CTCCTCTGGG AAAAAAGACC CTGACTTCTT 180 CAGTTAGGGT TACTGTTCCC TCTCCCAGTC ACCCATCAGT TTTGTCCATA TCAGAGCATT 240 CTATTTTAGT TATTTGCATA TTCCCTTCTC TCTCTCACCC CTCCACGGAT CTCCTACCCC 300 AGGAAGGTCA GCATCCAGTG ACCTTTTCAG GAAATTACCC AGGATTTCAC AATCTTAGTC 360 AGAAGCGAAA TTTAAAACCC TTTGTCCCCC GTCCTCCCAG CCCCCCGATG TTCCAGGAAG 420 CCAAAGCACA GAGCAATCTT TCCAATCTAG GAAGCAATAA AGAAATGTAT TTATGAACCA 480 GCCTCTATCT AAGGGAGAGA ATTTATGTCT CTTCATGCTC TTGTTGACAA TAATAACTGA 540 TTGCTGCATC AATGTGATGC AATATAATTT TAAAACCCTC CAGAACAAGG ATCAGAAAAC 600 AACTGGCAGA GAGACTGAGC GGCAGCCGTG GGCATCTTGG GTTTTGCAGC TCAGCCCTGG 660 GCCTGCTAAT GCCCTGAGGC GATGGGAACA CAGCTCTGGG AGCACCTGCA ATCTCATCTT 720 GTTTCTTTCC AAGCACCAGG GAAGAAAAGC AATTTGTTTG CTCTCATACT CTAAAGATGA 780 ACTTCCCGTG CTCAATCAAA CGTTATTATC CCAATGTAAG TCAATTTACC TTTGAATTTG 840 AAGGCTATTT TCTTCCTAAA TGGCTAATTA TGGGAGATAG ATGGCTGTAA ACAGAAGTCT 900 TCTACCTCAA CACTCCGCCA GGTTTTCTCC TTATGGCACC TGAGAGAACC AGAGAAAGGA 960 GGCCTCACAG TGTCCTGGCC CCCTCTGCCC ACTTGCCGCC CCTCCTCCAT TCTTCTCATG 1020 CATCCTGCGG TGCCATTCGC CCACCCCGCC TACATTCCTG GACGCCTATT TGGAGTTTCA 1080 TCCCCCTGAA TTCCATCCCC TGCCGCGTCC ATTTCTAGGA GCTCCATTCC CTCGTGCCAT 1140 CTCCCGTTTT TAAGGACTGG ACTAAAGGTG GAGGTCTTGG CCTGAGAACC GTGCATACGG 1200 GACAGCATGA GTTTTAGGAG ACAAGGGGTC CTGTGTGTGT TTGAGATGAA ACAAGGTCAC 1260 CTGAGGCCGC CTCTTTGATT TGCCTGACAG AGTCACAGAA GCTGACCGCT GCGAGGCAGG 1320 GGCTGCGGCC TTTTCCCGTG GCATGATCAA CACCTCGCAG GAACTAATTG AATGGCCGAG 1380 TTTGTTTACT GAGAGGAGGA GTAGCCCCCT CCTTTCTCGC AAAACAAAGT CTTTCCCCAG 1440 GAGCGGTGGC AAAGAGGTCA GCCCTGGCAG CGTTTCTGTT TTGCCTTTTG ATGAAAGCCT 1500 ACTCTGGCTG CTCTGAAGAA GGGAGCTCAT TGTGTGCTCA CTGTCAGAGG TGGCTCCAGC 1560 AGGGAGGCCA CAGCCCTGGG GGCTTTTTGG GTCTTGGGGT TATGGAGCCT GTGGTGTGTG 1620 GGGTTATCTA CAGGGACTGA GCTTTCTAGC TCTTCTCCCA GAAGTCTGGC CTCTGGTCCT 1680 CTGCCCTTTC CACCTGGGCC CCAGAAGCCA TAGTAATAGC AACCTGCCTT TGTCCGGTGC 1740 CTCGTCGTCG TTTATGCAAG TCTATATACT TTATCTCACT TGATCCTCAC AACCATCCTG 1800 TGCTGTCATC CTCCCCTGAC AGATGAGGGA GAGGCCCAGA GAGGTCAAGT GCTCTGCCTG 1860 AGGTCACACA GCTAGGAAGT GACATAACTG GGACCTGCCT CCCTTTGGCT TGAACGCCTC 1920 TGATCTCTCC CGTCTGTCAC AGTCCCATCA CAGAAAGGCA GGCATGTGGC CCCGTGGTTG 1980 AAGCCCTGCC CCAGCTGTGG ATCCGCATCA CCTGGGCCAG GCTTCCAATT TATGATACTT 2040 ACTGAGACCT TGGCACCACG GCCTTGATAA ACCCCTCTGC CCTGGGCTTG AGCTTGCTGT 2100 TCTGTCGGGG GCAGTTCGCG GGGCTGGGAG GACAGGTAAG AAGGGAGGAG CTTTTCATGA 2160 GCTGCTCTGG AAAAGTTTAA GGCCATGGTA GGGTCAGCTC AGGAAAGCAC AGCAGGGCAA 2220 GGGGCAGGTA GGCCTGTCCA ACTCAGCTAA TAGCTACAGA GGTCTCAAGA AGTAATGATT 2280 GGAGGCCTGA CTGAGGCATA GAGACCAATA GGAGACGCTC TCTCTCCTAG CTCAGACCAA 2340 GGAACCCTAG AACATGCTCC TCCAAGTTCA CCCACCGTCA CCCTGCAGGG GAGGGGTCTG 2400 CCACACTCCA AAAAAGAATC AATCCACTGT GTGTTCTGTG GACTGTTATT TAGAGATGCC 2460 CCTACAGATT CCTGGAGCTG CTGGGCCCCA TGCCAGGGCA AGGATCCCAG GACTCCCTGT 2520 TTAGCATAGT ACTTTGATTA AAACAATAAA TTCCCATTGA ATACCGATGG GCAGGCAAGT 2580 GGGGGCTCAT GCCAGCCTCG GTGCCCTCCT GGCATCATCT CACAGCAACT CGTTTGGGGA 2640 GAAATACCTC CCTCCGCTGT GATGAGAACC CTCATTCCCA ATGAATGAGG GGGCAGAAGC 2700 TGCCTGGGAG CCTCAGGAAT GAGGGCATCA 2730
|