Tag | Content |
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EnhancerAtlas ID | HS180-03501 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:167046380-167048020 |
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) |
Gata4 | MA0482.1 | chr1:167047481-167047492 | GGGAGATAAGA | - | 6.62 | RFX1 | MA0509.2 | chr1:167046600-167046616 | TGTAGTCATGGCAACT | + | 6.45 | RFX1 | MA0509.2 | chr1:167046600-167046616 | TGTAGTCATGGCAACT | - | 6.45 | RFX2 | MA0600.2 | chr1:167046600-167046616 | TGTAGTCATGGCAACT | - | 6.13 | RFX2 | MA0600.2 | chr1:167046600-167046616 | TGTAGTCATGGCAACT | + | 6.1 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_53129 | chr1:167047042-167047965 | Small_Intestine |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I167077 | chr1 | 167047043 | 167047965 |
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Enhancer Sequence | TGCAGTGAGC TGAGATTGCA CCACTGCACT CCAACCTGGG CAACAGAGCA AGACTCCATT 60 TCCAAAAAAA AAAAAAGAGA AGAAAACACA TTAGTCATCA TTACTAACAA GTCACCCTTC 120 ATCAGAAGGT TACTTGCTTC AATGGAGCCC TCCAGTGCCG TCTGCCCAGC TCCCAGCTAT 180 AGCAGACAGC CCATCTAGAT ATCATTTCTC ATATGCCTGG TGTAGTCATG GCAACTGCCA 240 CTGATCTTTA CTTCACCTCT TCTGTCCTTG CCTGGACCAG GGCATTTTCC CTGGAGCGCT 300 GTCCTCACGG TGACCACTCT TGGGCCTCTC CATGAACTTT ACACTGATTC TGTTCTTGTC 360 TATCACCCTG GCCACACACT ACACATTAAG GGACTTCTGC CACTGGCAGA ACCTAAATGG 420 CCCATGCACA GTTGGTCCCC AAAACTCAAG CAAATTCTAT CTGATAGTAA CAATTCTCAC 480 TCTCAAATCA AAGAGAACCA ACCCACTAAG TCATTCCTTT AGACAATGGA GTGTCTAATT 540 ACCTGCTCAC TCAAGATTAA AGGAATGTTA AGTCAACCAT CAATGGATGA AAAATGAGTC 600 ACTCTATTGA GTTAATCATT CTCAATTCCC TGTTAATCTC ATGTTATTTT AATTACATCT 660 CAATGGTACA GGCACCATAC AGGTATTTTA CAGATATTCT CTCATTTATT TTCATACTCT 720 CTTTAATGAT AGACATTTGT ATTTTCCCTA TTTTACTGGT GACATAATTG AGGTTCCAAA 780 AGGTTAAACC CTTTGCTCTA TCTAGATATG ACAGCTTGAC AGCTAACAAA TGGCAGAGCT 840 GCTGGCAAGT CCTTCAGATA GAGGCAGCCC TGGTGAGGGT ATAGGGCTGC TGCCCAACAG 900 TCAGGGAAAA GTGCTAATTT TTGCCTGCAG GGACAGGAGG ATGGTGTTTT CCTTGGCTGT 960 CAACAGAACC TATTTCCTAT TTTGTTCCTT GACCACATCA CACCCCTCAA TCTTGTCACA 1020 GAAACTCTTC TGCTTTCTTC AGTCAACCAA CAAGTATTTA ATATGTGCCT AGCATATAAA 1080 ACCAGCCCCC TGCTCTACTC AGGGAGATAA GATAGATGCC CACAAAGTCA TCTTCTTACC 1140 CTGGCAAATT AATGGACATA GACTAGCTTC ACACATACAC TTAGATCCTC TTAACCAAAT 1200 GCTAAGTACA GTATTTGCTT ATAGAAGAGA ACTCAGTGTG ACCTTTATGT AGGAAAAGAA 1260 CTAGGGCTGG CAACTGCATA GAAACAACAC CCACTATTCT CTAGCACCTC ACAGTTCTCA 1320 GGAGCCTCAC ATCCTTGTGA GAGGCGAGAC TCTGCCAAAT GGAATGGCCG AATTGGCTGT 1380 ATTCAGATTC TCTGAACATC CCCTTCCAAG GAGGGCAATA TACTCCCATC AACCACTCCT 1440 ACCACTCGTT CATTCTGTCT CCCAACTCTC CCTTTCTTCT GGTTCAGAAA CATCCCTTCG 1500 ATACTTTAAT CCCGGAGCGT GTACCGCTCT GTATCGCACA ACTTCTCCAT GGCCATTTCA 1560 GGAGGCAGCA TGGCATAGAA TTTGAATGCA CAGATTCTAG AACTAGAATG CCCCTGTTGG 1620 AACTCTGGTT CCTTTCTTTA 1640
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