Tag | Content |
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EnhancerAtlas ID | HS105-21083 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr12:124499990-124501610 |
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) |
RREB1 | MA0073.1 | chr12:124500025-124500045 | TGGGTATGGGTGTGTGGTGG | - | 6.2 | Sox3 | MA0514.1 | chr12:124501546-124501556 | AAAACAAAGG | - | 6.02 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I124015 | chr12 | 124499441 | 124501917 |
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Enhancer Sequence | TAGTTGTGTG AATTCAGTGG TCGTGTGTGG GAGTATGGGT ATGGGTGTGT GGTGGAGAAT 60 TGGCTTGCAC ATTAAGCCCA GGGTGACCAT GTAATTTATT GTCCAAACTG AGCACTTGAG 120 AGTGAAGGGA GGGGGTGCTG TTGATACTCA CATCTGGACA ACAAGCCTCG AATGGGCCTT 180 TCTCGGGCAC ACTAAGGTGT GAGGACACCT TGGTCTGAGG TCACAGCCAC ACAGGTAATA 240 AATGACTCAA GTCAGGAATA ATCCATCTGG AGAGAGCACA GTCCACTGAG AGGACTGCCT 300 CAGCTCGGCT GTGGCTCTGT GTTCACGGCG AATACAGGCC CACAGCTCTT CTAAGAAAAC 360 ACCAACCTCG ATTTTCACAC ACAGTTTAAT CTTAAAATGT TGGCAGCTAA TTCCTTTTCC 420 TTGGGTGATC CATTTTGGTG CTTTCTGTGA TCTTCCTGGT GCCCCTTGGC AGTTCCTCCA 480 AGCCCTGCCC TGGCCCCTGC TGACTGCAGC CCATGCCTGG GAAGGCGTGA AGTGCTGTCA 540 GCTGAAGCAG AGGGGGCCCA CGTTCTGTGC CGCAGTCAAC AGTCTGACTG GCTGTGGCGT 600 CTACCAGCTT TGAGAGACAA GTCTGCATTG CAATTCCACC ATTGGGATGG GAGCAACCCA 660 AACTAGCCCT TCTGATGGGG GTGGGGGGTG GGGGCAAGGG TAGGTCATCT GTGATGGGAT 720 TCACTCTTGG TGAATCTGCT AGGATTTAGA GTGTGAGCCA AGATAAGTCC AGAATGACTG 780 CATGGTTTCT AACTTGGAAG CATGAATAAA CGGCAGATTG CCTCTTGCAG ATAGGAAGAA 840 CTCTTTGCAT CAGAGTCCAA CATTGAGATA GTCTACTGCG TGAGAATGTG GGCACAGCTC 900 GTCAGGCCAT CTCAGAAATT GAAGAGGGAT TACTTTGTGT TGTGTGAGCA TGGACATGAT 960 TCCTTCCAAG GGACCTTCTA GCTCTTGGCT CTGTTCTTAA AATTTTTGAA TTATTTCTCA 1020 GTCTTTGTAA TGTACTGATA TTCTCAGAAA TTTGAAAAAC TAGGTGAATG GAAAGCAAAT 1080 ATCAGAAGCA GATGGAAAAT ATACTCAGTG GTAAAATCTA GGAAAAGATG AGAAAGGTTG 1140 ATACTACTAC AGGGCAAGAG CCATATATAA ATAGCAAAGC TGAGTTAAGA TCTATGGATT 1200 AGAGAGGAAG AGAGGAAAAA TGAAGATGAT AGAGCACTTC CTCTAACCAT ATTCATTTTC 1260 TTAATTTTTC TAAACCTCAA GTTTCTCATC TTTAAAATGG TTTTGAAAAT ATCTAATTCA 1320 TGGAAATGTT GGGAGAAGTA AATAAACGTA AAGTGCCTAG CATTTAGTGC TATAACGAAT 1380 TCCTATTCCC AGTTGCCTAT TAAGGAAGAA AGGTCATGTT ATTTGGATTC CTTTTTGTTT 1440 TGCTGAGCTC TGTGGTGGGT TTGGACATCT AAAATTGGGG TAGGACCTGG AGAGGGCTGA 1500 ATTGCTCCAC ATGGTAAGAG AGAGAACTTG AATCTCCTGG GGTAGTTGGA GGTAAGAAAA 1560 CAAAGGGTAG ACTTGGAGTG GGAGAGAGGA CCAGGGAACC AGTGGAGTAG GATGGTCTGA 1620
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