Tag | Content |
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EnhancerAtlas ID | HS050-41348 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr20:17843850-17845010 |
SNPs | Number: 3 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFAT5 | MA0606.1 | chr20:17844465-17844475 | AATGGAAAAT | - | 6.02 | NFATC1 | MA0624.1 | chr20:17844465-17844475 | AATGGAAAAT | - | 6.02 | NFATC3 | MA0625.1 | chr20:17844465-17844475 | AATGGAAAAT | - | 6.02 |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_23578 | chr20:17842906-17845060 | Colon_Crypt_1 | SE_24205 | chr20:17844073-17845043 | Colon_Crypt_2 | SE_28415 | chr20:17843159-17845332 | Fetal_Intestine | SE_29297 | chr20:17842603-17845447 | Fetal_Intestine_Large | SE_50301 | chr20:17843770-17845099 | Sigmoid_Colon | SE_52789 | chr20:17843827-17845115 | Small_Intestine |
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| Number: 1 | ID | Chromosome | Start | End |
GH20I017862 | chr20 | 17843176 | 17845306 |
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Enhancer Sequence | GGCAGATGGC ATTTTCTAAA AACAGCCACC ACAGTATCTC CCATCCCACT TGCTCTTATA 60 CAAGTGACCT TGGCACACCC CTATCGAGGG GTAAAGTCAG TGTCCCTTCA TCTTGAACCT 120 GGGCAGGCTT CTGTGACCTC CTTGGCTGGT GGAGTCCACC ATAAACCATG TCAGATAACC 180 TCATCCTCAC GGCTGGACAA GGCCACACAG CTTCTGCAGG TTTCTCTCTC TTGGCACATG 240 TGCCTTCAAA GCCGTGAGCC ATCATGTAAT AAGTTATCCC AAAGCCACCA CACACACAGG 300 CCCATGTGGA GAGAAACTGA GGCCGCCAGC CCCAGCCCCT AGCCCCACCT GAGCTCCTAG 360 AAAATCACAT CCAGGCCACA GCACTCACGA TGGCTACAAT CTGCCTTGCT CTCTAGGGTT 420 CCCCAAGGCC CAGCTCCCCG TCCCTGCTGT GTGCTCCCTG GGAAGGCTAG CTTCACCGCC 480 CCCCCATACA CCTGCCTGGG CCCAGCAGGG ATTAACAAAC AGGCCCTGGG TACAGCGCCT 540 CCTGAGCAGG ACTTAACAGT GTCTGCACAG GTCACCTGCC CAGCTCCCAG CTCCCCACCC 600 ACCCCACTCC AGAAAAATGG AAAATCCAGG GACCATCCCA GGCCCAGCTG CGCTCCAGGA 660 AGAAACCAGG CATGCTGCCA AGAATGACAC AAAATGGACT TTGGGCCGAT TGCCCAAGCT 720 GGACTACTGC CCCCACCTTC TTAGGAAGGG CACTCTTTCC GGAACCAAGG CCATAGCCTG 780 GAACAAAACC AGATGTCTGT AGAGCAGGAC ATGCCAGGTG GGAGGGGTTG CCGGGGTGTA 840 GGAGGCACAT ACTTGATGCC TCTCGCACCC TATCAGCCCA GGCAGGCAGG GTGCGGGGAG 900 GGAAGGAGAC CCCATGTGTA AGGACTATCA TCATTCTATT ACTGCAGGCA GCTGACTGCT 960 TCTGGAGGTG GACCTCTGAG GCCTCTGGCA TTCAGCCCCC TCATCCCTGC CTTCAGCAAT 1020 GGGGACAAAT CGAGGTTGGG GGGCACAACA AGCTATGCTC TCTGAAAGCA AAACAGATAA 1080 GTACAAATCA GGAAAGAATT GTTTCCTATC CTGTATTTGT GTTAGGATAC ATGTAATCTG 1140 TGGCTGGGCA CAGTGGCTCC 1160
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