Tag | Content |
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EnhancerAtlas ID | HS092-13399 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr12:113763010-113765430 |
Target genes | Number: 11 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Klf1 | MA0493.1 | chr12:113764023-113764034 | AGCCACACCCA | + | 6.14 | Zfx | MA0146.2 | chr12:113763611-113763625 | CCCGCCTCGGCCTC | + | 6.01 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I113325 | chr12 | 113763225 | 113765384 |
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Enhancer Sequence | CTGCATTCAC AGCAGTTATC ACAATCTTTA TTTTGTTCAT TTCCTTGTTT ACTGAATTTT 60 ATTATTTTAG AGACCAGGTG CTTTGTCACT CAGGCTGGAG TGCAGTGGGG CAATCATGGC 120 TCACTTCAGC CTCGAACTCC TGGGCGCATG TGATCCTCCT GCCTTTGCCT CCCAAGTAGC 180 TGGGACTACA GGCATGCACC ACCACACCCA GTTAATTTTT TTAAAAATTA TTTTTTGTAG 240 AGATGGAGGT CTTGCTATGT TGCCTAGGCT GGTCTTCAAC TCCTGGCCTC AAGCCATCCT 300 CCCACCTCAG CCTCCCATTG TGCTGGGATT ATAGGCGTGA ACCACCAAAC CTGGCCTTAA 360 TTTTTTTTTT TTTTTTTGAG ACGGAGTCTC GCTCTTTCGC CCAGGCCAGA CTGCAGTGGC 420 GCTATCTCGG CTCACGGCAA GTTCCGCCTC CCAGGTTCAC ACCATTCTCC TGCCTCAGCC 480 TCCCGAGTAG CTGGGACTAC AGGCGCTCGC CACCACGCCC AGCTAATTTT TTGTATTTTT 540 AGTAGAGATG GGTTTCACCG TGTTAGCCAG GATGATCTCG ATCTCCTGAC CTTGTGATCC 600 ACCCGCCTCG GCCTCCCAAA GTGCTGGGAT TACAGGCGTG AGCCACCGCG CCCAGCCCTG 660 AATTTTTTTT GTCTGCATTC TTGTATTTGC CCTGAGCCTG GCCTGTAGTA GGGGCTTAAT 720 ACATTTGTGT TAATGGCTGC TTGAATGACT AAGTGATTTT GTGTAGCCTT TCCAACACTC 780 CTGCGAGGCA AATGGAATGA TTCCCCTTTA ACATATGGGT AAGCCAAGGG TCAGCAAACT 840 TCGGCCCCTG GACCACATCC AGCCCACCAT CTGGTTATGC ACAGCCTGCA AGCCAAGAAT 900 GATTCTTACA TTTTTAAATG GTTGGGAGAC ATAAATCAAA AGAAGAATTT TCCATGACAT 960 GTAAAATTAT ATAAAACTCA AGTTTCCATT TCCATAAATA TTTACTGGGG CACAGCCACA 1020 CCCATTCGTT GATGTACAAT CTGTGGCTAC TCAGGCACTG TGAGAGCAGT GAGTAGTTGT 1080 AGAAACCATG TAGCCCACAA AGCTGAAAAT ATTTACTGTC TAGCTCTTAT TCTATTCTTT 1140 CTTTCTTTTC TTTTTTCTTT TTTATTTACT TATTTATTTT GAGACGGAGT CTTACTCTGT 1200 TGCCCAGGCT GAAGTACAGT GGTGAGATCT CAGCTCACTG CAACCTTTGC CTCCTGGGTT 1260 CAAATTATTA TCCTGCCTCA GCCTCTGGAG GAGCTGGGAT CACAGATATG TGCCACCACG 1320 CCTGGCTGAT TTTTTTATTT TTAGTAGAGA TGGGGTTTCA CCATGTTGGC CAGGCTAGTC 1380 TCAAACTCCT GGCCTCAAGT GATCCACCAG CCTCCGCCTC CCAAAGTGCT GGGATTACAG 1440 GTGTGAGCAC TGTGACTGGC CTCTTTTCTT TCTCTCTCTT TTTTTTTTTT TGAGACAAGG 1500 TCTCACTGTT GCCCAGGCTG GAGTGCAGAA GCATGATTAT AGCTCACTGC AGCCTCAAAC 1560 TCTTAGGCTT AAGGAATTCC CCCGACTTCA ACCTCCCAAG TGGCTGGAGC TACAAATGTG 1620 AGCCCACAAC CCGGCCCTAC TATCTGGCTC TTTACAGAAA GTCTGTGCCC CAGGCTGGAG 1680 TGATGGTGTG CACATCCCAA CCCAGGCTTG GGAATCTCCA TCAACTATTC CCACCAAAAC 1740 ATGCAGATGC AAGTCTCAAG TTTCTGTCCT GAGCTTCCCT TATCCCATCC CCAGCTCCCA 1800 CCCAAAAGCA ACAGTCAGGC TGGGCTCCTT CCATACTGGG AGGGGGAGGG TTTCAGTCTT 1860 GCCCTAAGCC TGGGCCTGTG GCTTTGCTGG GGCCCAGGAA TTTCCCAGGG AGATAAAGTC 1920 ACCCAAGGGG TTTCTGACAA AGAGGGTCCC ACCCAGCACA AGGAGGAAGG ACACTAGATG 1980 GGGGCCAGGG AAGCAGGCGG GCTGCCATTT CCTCCTCTGG GAGGAACAAT AATAATCATA 2040 TTGGGAGGCA GTACAGCTCC CTCTACTGAG CCCTCCTCTC TCATGAAACT GCCTGGTTGA 2100 AATTCTAATT TGCGTCCTTC TAGGTGAGTG ATTTTGGGCA AGTAAATTAA CCTCAGTGTT 2160 CTCCTCTGAA CAATGGGGGC AATAACACCC ACAAGCCTAG ACAGGAATGG GATAAGGACA 2220 TGGAGGCCAG GCATTGTGGC TCACATCTGT AATCCCAGTG CCTGAGCCCA TGAGTTTGAG 2280 ACCAGCCTGG CCAACATGGT GAAACTCCAT CTCCACTAAA AATATAAAAA TTAGCCAGGC 2340 ACGGTGGCGT GTGCCTGTGT TCCCAGCTAC TCAGGAGGCT GAGGCAGAAT AACTTGAACC 2400 CGGGAGGCGG AGGTTGCAGT 2420
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