Tag | Content |
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EnhancerAtlas ID | HS148-04012 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr12:27747800-27749440 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RFX1 | MA0509.2 | chr12:27748386-27748402 | GGTTACCATGGCAACA | - | 7.85 | RFX1 | MA0509.2 | chr12:27748386-27748402 | GGTTACCATGGCAACA | + | 7.89 | RFX2 | MA0600.2 | chr12:27748386-27748402 | GGTTACCATGGCAACA | - | 8.01 | RFX2 | MA0600.2 | chr12:27748386-27748402 | GGTTACCATGGCAACA | + | 8.05 | RFX5 | MA0510.2 | chr12:27748386-27748402 | GGTTACCATGGCAACA | - | 8.14 | RFX5 | MA0510.2 | chr12:27748386-27748402 | GGTTACCATGGCAACA | + | 8 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_35853 | chr12:27740719-27748802 | HMEC | SE_37674 | chr12:27747408-27749920 | HSMMtube | SE_41040 | chr12:27747803-27748654 | Left_Ventricle | SE_44212 | chr12:27747510-27750092 | NHDF-Ad | SE_45579 | chr12:27743303-27750149 | Osteoblasts |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I027588 | chr12 | 27741033 | 27749438 |
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Enhancer Sequence | TGTGGCTATC ACATCAGTTG AAACAGATTA TTTTATGGCA TAGCCTACAA CAAACATATA 60 TATGGTTACT CTGCAATTGT TAATTCTTAT TAATGACCAT TAGGTGGTAG TTATTGTTTT 120 ACTAAATAAA TCTGTAGTAA ACCTGCTTTT CCATAAATCT TTGACTATGA CCCTTATTTT 180 TCTATGTGTA GGATTAATGG ACCAAACATC ACAAATATAT TACAGTCTTC TGCTGGTTGA 240 TACCAAATTA CTTTCCAGGA AGGTTTTGCT GTTTAGATGC CCATCCTCCC ATCATCTGAT 300 GACACTTTTT AGTCCAGCTT TTTCTGTGAA GCCCCGGAAA GCAAGTAGGG CTGGAAGAAT 360 GCGTGCACAC GCGCGCGCGC ACAAACACAC ACACGCGCAT ACACACATGC GTGTGCTCAC 420 ACACACACAT GCACGCAAGA CTGTCACACC CTGCTCTGGT GGCTGCCCAC ATGGAAGAAG 480 TGCTGCTAAC TCCTGAGGCA AGAAGGGGAG ACGTGAGAAA TCCTTCACAT CCCGAGTCTC 540 AGTGGCTAAA AGTCCAGCTG TCAGAAGTCT GTGTTCTGAG ACTGTTGGTT ACCATGGCAA 600 CAGAAAGACC TGAATTAGAG CCAGGAATGT GGAGAGAGAA AAGGAAAAAC GGGGATAGAA 660 AGCCACAGAA TTATCCCTTT TGCTTCCAAA ATATTCTGTG CCCTAGGCCG GGCGCAGTGG 720 CTCACGCTTA TAATCCCAGC ACTTTGGGAG GCTGAGGTGG GCGGATCACC TGAGGTCCGG 780 AGTTTGAGAC CAGCCTGACC AACATGGAGA AACCCCATCT CTACTAAAAA TACAAAATTA 840 GCCGGGTGTG GTGGCCCATG CCTGTAATCC CAGCTACTCA GGAGGCTGAG GCAGGAGAAT 900 CACTTGAACC CAGGAGGCAG AGGTTGCGGT GAGCGGAGAT AGCGCCATTG CACTCCAGCC 960 TGGGCAACAA CAGCGACACT CTGATCAACA ACAACAACAA CAACAACAAC AACAACAAAA 1020 TATATATATA TATATATATA TATATATATA TATATTTTAT GCCCATACCA TCCCGGATTG 1080 AAGAGGATTC CTCTTGAGGG TAGAAGGACG AATGCATGGA GGTTACTTCT CTCTTGTCAG 1140 GTGGCTAAGA TGGTTCCCGT CCTTAGGAGA TTTAGAGCTC TAAATAAGGG GCATGGGTAT 1200 AAATACACAC ACACACACAC ACACACACAC ACACACACAC ATATGCTTAC AAATGGCAAA 1260 AAGCCAAGAA ACACTTATCT GACCTAAAAG AACCTCAACG CATTGGAATC TATCAATTTC 1320 TAAAGATCTT TTCCAAATAT TTGTCTCCAT TTCTGCTTAA CAAGATTACA GTTAAAGTTT 1380 GCCATGACTC AGTCTCACTT TTTTCACTGT AGAACTGGCT TAAATTCGTT TGTTCTGTTA 1440 AATAAGATGT TTAAGGAATT CTGATGACAT GATAGAAGAA ATAGGCAGAG TTATAGTTAG 1500 AAAGAAGCAG ATTCTACTAC CCAATAGATG CAGCCTGGCA GGTACCCACA GACTGCCCAC 1560 AACTTCCCTG AGTGATTGTG GACCTGGATT AATCCTGGAG GCTGTTTAAG TCAGAAGTAA 1620 CATGTTCCCC AGCATTTATT 1640
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