Tag | Content |
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EnhancerAtlas ID | HS129-10372 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr13:43727260-43728870 |
Target genes | |
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) |
IRF1 | MA0050.2 | chr13:43727639-43727660 | AGAGAAAAAGAGAAAGCTAAA | - | 6.22 | IRF1 | MA0050.2 | chr13:43727712-43727733 | CAAAGGAAAGAGAAAGAGAGA | - | 6.39 |
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| Number: 1 | ID | Chromosome | Start | End |
GH13I043152 | chr13 | 43727073 | 43729513 |
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Enhancer Sequence | AATTTGAAAT CAAGGTGTCA GCAGGGCTGT GCTCCCCCTG AAGTCCCTAA AGAAGGACCC 60 TTCCTTGACT CTTCCTAGCT TCTGGTAGTT GCTGTCCATC CTTGCCATTC CTTGGCTTCC 120 ATCTGCACCA CTCCTATCGC TACCTCCATA GCCACATGGC CTTCTTCCCT CTGTGCCTTC 180 CTATCTCTGT GTGCCCTCTC CTCTTCTTAC AAGCACATTG GTCACATTAG ATCTAGGGCC 240 CACTCTAATC CCATAGGACC TCATCTTAAC TATTTATATC TGCAAGATCC TAGGTCCAAC 300 TGAGGTCACA TTCTGAGGTT CTCAGTTGGA TCTGAATTTG GGGTTGGGGA GTGCTATTTA 360 ACCCACTATA ATGGTGAAGA GAGAAAAAGA GAAAGCTAAA GGCAGAATCA TGAGACGCAC 420 GAACATTCTG GTCGTTAGTA GGGAAGTGTT AGCAAAGGAA AGAGAAAGAG AGAGAGAGAG 480 ACCACATTCC TAGCTGCTGA GAGGCCGGGT GGGGATGCAA GCAGGTAACT GTGTGTGACC 540 ATCAGAAAAC ACTGGTAACG GCAGTTGGGT GACTAACTAA TATATTTCAC CCAGGACTAG 600 AGTGGCAGTC CAGGATGCAG AACTTTCGGT GCTAAAACCC AACAGTACCA AGCACACTGG 660 AATGGTTGGA CACTCTACCT GGGAACCAGC AGTTCTATTA GAACTGAATG TGGGGAGAAC 720 GCACGGCTGA AGCTTAATGG CTTGGGGAAT GAGTAAGCCT TAAGAAATGT ACTTGCCTGG 780 GGCGTGATTC TGGTTGCGTT GTTTTTCTGA CAATTCAACC ACATTTGGAA TTTTCTTACG 840 TAGGATATGG GCTTGAGTTT TTAATTTAAA GTCTTCGGGT AAGGTCAGCT CAGTCCCTAA 900 CCACCGGACA TCGTGGAACA ACCAAGTTAT TGGAGATTAA AGTGTCCTTC AACTGTCATG 960 AATGCCACTC TGACCCTCCT TGTCTGGAGG GGACCTCCAG GGCATGCTAT TTAAATGAAC 1020 CCAATTTTGA AAGTTCACCT ATCTCTACTG AATGTGATAG CTATCTTGCT CTGCCTTCAG 1080 AGCACTTATC TTCAAAGTAT TCAGCGCCAG GCAAAAGCCT TGATTTTTCC TTGAAAAAGA 1140 AATTGTCAGG ATGTCTGAAT CCATCCAGAC CTTTGCATGT GTGATTTCAT TATTCATAGT 1200 CAGCATTCCT CTTCTGGCTT TTGATCTGTA GTTTACAGAA TGTGTGCATA AGGAGGCTCT 1260 CTTTCCCATA AACTGATCTC TTTACCCTCT CAGCCCGGAA TAACTTTCCA TTTATTCTTT 1320 TGATAAAGCG TTGATGCCGT GAGCCAGCAT ACATTAAATT TATCATGATA CAAACACAGC 1380 ACTACACTCT TATCCAGCCC AGATCAGCAA CCAGATCACT GCCAGTGCCC CTCAAGTGTC 1440 TCTGATGATG AACAGCAAAG GGGACCTGTG GAATTTCTCA CGACCATCAA ATCTGAAGAA 1500 GGAATTCTTC TGAGAGCAGT TTGCAAAGTC TATCACCAGT ATCCTGACTC TATTATTAGC 1560 TTGCAAGGTA GTTAAAGATA TCTTCTCAGC CTTGACTCAC TAATAAGCAC 1610
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