| Tag | Content |
|---|
EnhancerAtlas ID | HS093-12109 |
Organism | Homo sapiens |
Tissue/cell | HL-60 |
Coordinate | chr16:81577880-81578980 |
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 | AAATGAGACC GAGGCTGGAG GGTCATGCAA GTGAAAAATA CTCAATTTTT TAATTGCAAA 60
GTCTCTTTGG TGCTATGTGT GTGGCGTGAA CACGTGAGGG CATTATTTTG AAAGAATTAC 120
TGATAGGACT CTGTCTCATC CTCAGGGGGT AAGTGTGTGT GTGTGTGTGC GCGCACACAG 180
GAAACCTCTT GTTTTTAAAT ATTTCCTTCT CCAAACAGCC TGCCGCTGAC CTTCCCGGCC 240
TCTGTGTGGC TCTCAGGCCA CCTCCTTATT GCTATATCTT GGAGCCTAAG GACTTCTATT 300
TCTGCTCTGG GTCCAGTGCA GGGTGCCAGG ACCACCACAG GGGTGCATGT GTGCATGTGT 360
GTGTGCCTGT GTGTGTGTGT GTATGTTTGA ATATGTGTGG TGTATGGGTA TTTGTATGTG 420
TGTATATGTT TGTGGAATGT TGTGTGTATA TGTGCATGTG TGTGTGTGCG TGTATTTGTG 480
TATGTGTGGA GTGTTGCGTG TGTGCACGTG TGTGTGGAGA GGGTGTATGT GTGAGATGTG 540
TGTATGCCAT GTGTGTGCGT GCATGGAGGG CTCTGCTTCC GGTTTCTGGG GTTGAGTAAC 600
TTTATGAGTG GTACTTAAAA CCCTTCTGTT GTCCACAGGA CAAAGTTCAA CCCCTCATTT 660
TTTTGGCAGA GAAGGCTGCC AAATTGGGGC CAGACTCAAT CTTTTCATTT TCATCTCCTG 720
CCAGTTCCTT ACCAGACACC CTGTGCTCCA GCCACAAACG ACCTTTTGCT GTTGCCCAAA 780
AGAGCCCATG ATCTTGTAAA CTCCTAGACT CCTAGAAGAT GCCAGGCCCA CAGCCAGGGT 840
TCCCCTTTCC GCTTTCCCTG CTCAGCTCAT ACTGGTGCGA AACTCTCCCA GGCCTGCCCT 900
CCTCCCTGCA GGGTGCCTTA GCTTCTTCCA TCCTTTGAGA CAGGCTGACC ACAGGTACTG 960
TGGTGTTTGA TTTAATGCAT TCGTTATCTC AGGATTTGCT GCGCTTCTAG AGAAGTCCTG 1020
CAGACGAACC CGTCCTTGTA TCACCAGCGC CTAGCATGGT GCCTGGAAGA GGGTGGGTGC 1080
TTGATGCTTC TCGCAGTGAA 1100
|
