| Tag | Content |
|---|
EnhancerAtlas ID | HS073-05611 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr16:81577920-81579240 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr16:81578514-81578529 | ACAGGACAAAGTTCA | + | 6.16 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_09239 | chr16:81577187-81579212 | CD14 | | SE_23105 | chr16:81577970-81578888 | Colon_Crypt_1 | | SE_24089 | chr16:81578073-81578570 | Colon_Crypt_2 | | SE_31484 | chr16:81577978-81578973 | Gastric | | SE_42333 | chr16:81576170-81579192 | Lung | | SE_52343 | chr16:81577917-81579114 | Small_Intestine |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH16I081542 | chr16 | 81575894 | 81578858 |
|
Enhancer Sequence | CTCAATTTTT TAATTGCAAA GTCTCTTTGG TGCTATGTGT GTGGCGTGAA CACGTGAGGG 60
CATTATTTTG AAAGAATTAC TGATAGGACT CTGTCTCATC CTCAGGGGGT AAGTGTGTGT 120
GTGTGTGTGC GCGCACACAG GAAACCTCTT GTTTTTAAAT ATTTCCTTCT CCAAACAGCC 180
TGCCGCTGAC CTTCCCGGCC TCTGTGTGGC TCTCAGGCCA CCTCCTTATT GCTATATCTT 240
GGAGCCTAAG GACTTCTATT TCTGCTCTGG GTCCAGTGCA GGGTGCCAGG ACCACCACAG 300
GGGTGCATGT GTGCATGTGT GTGTGCCTGT GTGTGTGTGT GTATGTTTGA ATATGTGTGG 360
TGTATGGGTA TTTGTATGTG TGTATATGTT TGTGGAATGT TGTGTGTATA TGTGCATGTG 420
TGTGTGTGCG TGTATTTGTG TATGTGTGGA GTGTTGCGTG TGTGCACGTG TGTGTGGAGA 480
GGGTGTATGT GTGAGATGTG TGTATGCCAT GTGTGTGCGT GCATGGAGGG CTCTGCTTCC 540
GGTTTCTGGG GTTGAGTAAC TTTATGAGTG GTACTTAAAA CCCTTCTGTT GTCCACAGGA 600
CAAAGTTCAA CCCCTCATTT TTTTGGCAGA GAAGGCTGCC AAATTGGGGC CAGACTCAAT 660
CTTTTCATTT TCATCTCCTG CCAGTTCCTT ACCAGACACC CTGTGCTCCA GCCACAAACG 720
ACCTTTTGCT GTTGCCCAAA AGAGCCCATG ATCTTGTAAA CTCCTAGACT CCTAGAAGAT 780
GCCAGGCCCA CAGCCAGGGT TCCCCTTTCC GCTTTCCCTG CTCAGCTCAT ACTGGTGCGA 840
AACTCTCCCA GGCCTGCCCT CCTCCCTGCA GGGTGCCTTA GCTTCTTCCA TCCTTTGAGA 900
CAGGCTGACC ACAGGTACTG TGGTGTTTGA TTTAATGCAT TCGTTATCTC AGGATTTGCT 960
GCGCTTCTAG AGAAGTCCTG CAGACGAACC CGTCCTTGTA TCACCAGCGC CTAGCATGGT 1020
GCCTGGAAGA GGGTGGGTGC TTGATGCTTC TCGCAGTGAA GGAGCAGAAG CTTAGGTTCT 1080
GTACTAAGAT GATGCTTATA TTGTGTAGCT AAAAGGGACC GTGCACACAA CAGTGACAAC 1140
ATCAGTAATA ACGTTTACTG AGCGTCTCCT GTGTGAAGAG TCCCTGTGCT CAGTGCTCTA 1200
TGAATGGCAT TTAATCCACA CAGCTTATGT GGCGAGCTCC AGCATCCTCC TCCATCTACA 1260
GATGGAAGCA TGAGGCTGGA GAGAAGTGAC TTGGTCCAGA CCACACAGCA CGGGGCGGAC 1320
|
