Tag | Content |
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EnhancerAtlas ID | HS118-14958 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr5:55438110-55439610 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFIC | MA0161.2 | chr5:55438827-55438838 | TACTTGGCACA | + | 6.32 | TFAP2C | MA0524.2 | chr5:55438555-55438567 | AGCCCCAGGGCA | + | 6.11 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_43570 | chr5:55436888-55446191 | MM1S | SE_55628 | chr5:55438068-55439038 | Thymus | SE_55628 | chr5:55439046-55439441 | Thymus | SE_67226 | chr5:55436888-55446191 | MM1S |
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| Number: 1 | ID | Chromosome | Start | End |
GH05I056142 | chr5 | 55438281 | 55439639 |
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Enhancer Sequence | AGATCGCACC ACTGCACTCT GGCCTGGGCT ACAGAGTGAG ACTCCATTTC AGAAAACAAA 60 ACAAAACTAA ACAACAACAA CAAAAACCCA GCGATTCCAC CCTGTGAGGG CCCAGCGGGG 120 GTCTGGGAAT CTGTTGTTTT ACAAGCACTG CTGGTGATTC CATCGCAAGG CCAGGTCTAA 180 GACAGCAGCT CTACACTGGG GCTGGGATGG TGGAAGGGGG ACGCATGTCA GTCAGAATTA 240 CCTGGGGAGG TTTTTCAAAA TGCACATGCA TCCTGGATCT AGGGAATCAG AGTGCAGTGG 300 TGTTGAGGTG ACTATGTAGA AAGTGCCTGC TTCTGGTGCC ACTTTCATCT CAGCTGAGAA 360 CCAACACATG AGGAGCTTCC TGGGAGCCCA GCCAGGTTCC TCTGTGGCCA CCGCTACAGT 420 GGTGACCCCT GACCAGCCAG AGGCCAGCCC CAGGGCATGG AGTCCTGGGC AGAGACTGGC 480 AGCGATGGTG GCAGGGCAGG TGATTAGATA CTGAAAGTAT GTAGGAGGGT GCTATGGGCA 540 GGTGGAGATG ACAAAACAAG CCTTGCTCAC TGCATAGCTT TGCAGAGAAA CTGGTGCAGA 600 GAAACTGAAG CCAAGGTTAG AGGGATGAAA ACAGAGCAGT TTCCAGATCA CTTCTGTTTT 660 CCCCTTACAT CAGGCACACA TGTCAATCCT GAAAGTCCCA GGTGCCCACT TCTGCTGTAC 720 TTGGCACATG GAAATGCTGA CTGAAACCAC AGTCAGGGCA GCAGAAACTA TTCTCACAGG 780 GTCCTGGCAG TAGCTCAGAC AGGTGCCCTT TCTGGGCCAA CAGAAATCAA CTGTGGGGGT 840 GTCTGTGCTG AAGACAGAGA CGGGCTGGCA AGTTTATGCA AAGGATGCTC TCCTTGAAAA 900 AAGGAATAGA TAACTTTTAG TTAATCATTC CCCTTGAAAA TAGAAAGCAC TCGGTTACAC 960 ATTAGTGATT ATTATTCTTT CACCTTACTC TTGGTTTTGC CCTCTCTGGA CAATAGATTT 1020 CTTGAGCCTA TTCTGATTTG TTTGGTTGTG TGTATTGACG TGGACTCCCT TATGTGATAG 1080 TGATGCAGGG TCATGAGCCA CTACTTTCAC TGTCGGGTGT AGAATTCAGG ATCACCTGAA 1140 ATGACTCTGC TGGGGAGGAT TTGGAAGCAA GAAGAGAGTC AGAGAGTCAT GGTTCAAAGA 1200 CTTTGAAGGC ATTTTCCCAG CAATTCTTTG AAGGTTTACT CTGGGACACA GTAAGCCGGT 1260 AGCAAACATT GAGATGGAGA GAGAAACAGA GAGAATGAGA GGGGTATGTG TGTGTCTGTG 1320 TGTGCCACCC AAGGCAGGCT CTGCTTGATA TTTTATAACT ACTCCCCTTT GCATCTTGGC 1380 AGGGTTTCTT TTCAACAAGT GGTGGAGCTG AATCAAGAGC TGAAACCTCC ATCTTTAAAG 1440 TTTGACCTAC TCAGAAAATT GTTAACACTG CTTTCCACCA TTTAAACCTG AGACCAGTCC 1500
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