Tag | Content |
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EnhancerAtlas ID | HS012-20331 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr5:173284880-173286080 |
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) |
Nr2f6(var.2) | MA0728.1 | chr5:173285933-173285948 | TGACCTATTGTCCTT | - | 6.51 | RARA | MA0729.1 | chr5:173285930-173285948 | ATTTGACCTATTGTCCTT | - | 6.02 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_12741 | chr5:173285333-173285506 | CD34_fetal | SE_28261 | chr5:173284904-173286711 | Fetal_Intestine | SE_28904 | chr5:173284011-173287264 | Fetal_Intestine_Large | SE_32240 | chr5:173285799-173289804 | Gastric | SE_39904 | chr5:173284824-173289875 | K562 |
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| Number: 1 | ID | Chromosome | Start | End |
GH05I173857 | chr5 | 173284313 | 173288602 |
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Enhancer Sequence | CTTTTTAAAC AAACGCAAAC TTCGCAAGCT CAGACTTGCT ACAGGATTGT AAGTCAGTAG 60 CCAAGACCTG AGAATCCATT TCTGACAGTA GAGAATTTCA GCCTTTAGAG GCATCAAGAC 120 CTGAGTTCAA GTCAGCCTGG CTGCTTTCTA GCTGTCGTCC TCTTGTGAGT AACTAAATTG 180 TGCTGAGACT CAGTTTCTCT ATCTGTAAGT TGAAGAAAAC CAGCCCTTCT CCAGATTGCC 240 ATGAGACTTA AATGCAATAA GATGTTTGGA GGTAGCTGAC AGGTGTTTAC TTTATGTGAG 300 TTCCCTCCTT CCGCTTAATC AGGAGTTTCT TATCTGGGTC AGCCTTAGGA ATGAGAGATA 360 ACTAGGTGTC ATCTGGATGG ATATAGGATG ACAGTTTAAG GGTCACCTAC ACTGGAACCG 420 AATTCACTTC ATCTGGGCTG TTAGAACACA TTCCAGACTC CTAGAATTTC TTTACTACTG 480 ACTTCATTCC AAAAAAGGAT CTGAGGCTAC AGAGTGCACG TATATATATT ACTGTTAATA 540 AAACAGGAGT AGGAATAATA GCAGCTAATG TTTATAGGGT TTGCTGTACA GCAGGTGCTG 600 TGTTAAGTGC CCTACCTCAC ATTATTTTTT CTTAAATACA GCACCCTGAC AAGCAGGCAG 660 AAGCGTATCT GCTAAGCATT GATGGCCCTT TCTGGCTCTA ATGCCAGAGC AACCCTGACT 720 TCTAGGTCAC GGTTGTAAAA TAAATTGTTG CAATGGGATC CAAAAAAGGG GGAAGTTTAT 780 ACTAGAGAGC TTTACAGTCA CAATAACAGA AATAATTTTT CCTGTAGGAG TCCCAACAGT 840 AAAGGTGTTT TTATAGCTGG GAGTTCATAA CCATAAAACC TAAAGTCACC AGCTCCTACA 900 GTGTAGAATC ACGTGGCATC TTCCTTATCA CCACCAGCTC TGACATTGGT GCAAAACATC 960 TTACGCATTT TCTAATCTTT TTTATCATCT TTTCCAGCCA ATGTTATGAT AAAGTCTTGC 1020 AATCAAAGCA AATGTTACCA CTGCAAAGCC ATTTGACCTA TTGTCCTTGT GGCTTTCTCA 1080 GCAGAGGGGC CCTGTAAGGC CAATTGTATA CCATAAATAA TCCATCAGGT TATCCAGTTG 1140 GCATAATGGG CCCTCCCACT GCAGAAGAAA AGCTTGTGGT TGAGTGTCCA AGGTCTCTCT 1200
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