| Tag | Content |
|---|
EnhancerAtlas ID | HS091-28898 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr2:217523340-217525270 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Hnf4a | MA0114.3 | chr2:217523728-217523744 | GCTGGACTTTAACCCG | - | 6.18 | | Spz1 | MA0111.1 | chr2:217523764-217523775 | GCTGCTACCCT | - | 6.02 |
|
| | Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
| SE_01659 | chr2:217523496-217524848 | Aorta | | SE_25399 | chr2:217523543-217525271 | DND41 | | SE_26938 | chr2:217523482-217525014 | Esophagus | | SE_27936 | chr2:217522389-217524879 | Fetal_Intestine | | SE_29226 | chr2:217522134-217525039 | Fetal_Intestine_Large | | SE_31800 | chr2:217523600-217524795 | Gastric | | SE_58444 | chr2:217447610-217532079 | Ly1 | | SE_68753 | chr2:217523550-217524959 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I216657 | chr2 | 217522342 | 217524727 |
|
Enhancer Sequence | CAGCTCACTG CAACCTCCAC CTCCTGGGTT CAAGCAATTG TCCTGTGTCA CCCTTCTGAG 60
TAGCTGGGAT TACAGGTGTG TGCCACCACA CCCGGCTAAT TTTTTTGTAT TTTTAGCAGA 120
GATGGGGTTT CACCATGTTG GCCAGGCTGG TCTTGAATTC CTGACCTCAA GTGATCCACA 180
TGCCTCAGCC TCCCAAAGTG CTGGGATTAT AGGCATGAGC CACCACACCC GGCCTAAGTC 240
ATCTTTTAAC TGCTTTTCTT TCGTCATACT CTCAACAGCT CTATGAAGAA AGAACTGTTA 300
TTATCCAGCA ACTTACAGTT AAGAAAGTAG AGGCACAGAG AGGGTCTGTG TGGGGAGAAC 360
ACGTGCAGCT GATATAGAAA ATGGCAGAGC TGGACTTTAA CCCGGCTACA CCCCTTTAAC 420
CAGAGCTGCT ACCCTGGGGA CGGCGTGCTG GCTTCTAAAG GAAGCTGCTG CATGGCAAGT 480
GAAGAGTGAC TAGTTCTCAG GCTTGGAGGG AGGGGAAAGG ACAGGGACAG ACCCCCATCA 540
AATGTTCCGT ATGCTGGGGC CTATGCTGGG CACGCCTTGA CAGCAGGTGC TGCTGGAGTG 600
CCAGCACCCG GTGCTGTCCC TGGCATGGAA GAGGTGCCCC CTCCCTTAGT TGGTGAGTGA 660
GTGAATACTC TTGTATAGAG TTACTCTAAG AATTATTCAT TTGTGTTCTA AGGGCTGTAA 720
GTTTTTGAAG GTGCATTAAT GGGGAAGAAA AAATGTGCAA GATTGGTTGA AAAACACCCC 780
TCTGCACCCA CCCAGATCTT GTTGGGACCT GCAGGAGAGC AGCTCTGGGT GGGAGGGTCT 840
GGGGCTGTTT GCCGTGTCTC CAAGGGGTTG GGGCTGGGGC TCGGCGGTGT GAGGCCCTGC 900
CCTTCTGGAG CTTGCTGGGG CTTGTCTCCT GGTTACAGCT CTGCCGTGCG ATTCAGATCC 960
TCTCTGCCTC CTTTGGCTGG ACGTGCCTCA GCCAGAGTGA GACTGTGGCA GGCTGGAGCT 1020
GTTTTCAAGG CCTCCTTCAC CTAGGCTGTG CATACAAAAG GTTGAAGAAA GTATAAGGAG 1080
ACTTAATGGA CGCTTGTTGG ACAGACATCA CGAAGCTTCA TGCCCTGCAG TAAGCTGAAG 1140
CTATGAAGTC GAAGGAGTCA TAGTTCCTGT TCTTGGGGCT CTCAGTATAA TGGGGTTGGG 1200
GTGGGCTGCA CAGACAGACT TGGGAACGAG GGAATGTCAG TGTGGCAGAG CTGTAGCTGC 1260
CTCGGAGCAG CACTATGGGA CCTTAGGCAG GGCCAGGTGG GCAGGTACAC AGTGACAGCA 1320
GGGGGATGCT GGGACCAGGT TCTGGGTGGC GACGTGGCCT TCCACCTTCT CACTCCTTTG 1380
CCATATATGC TGCAGCCCGG TGATGTCTGT GGCACGAGTT TTAAAAAACT CAACTAATTG 1440
GTGCTCTTCC AGACCACAAA TGAAGAACTT TAAACTGGGG GTTATAGTGG GAGAATTTGG 1500
GGGGGTCCCA GAAAGGACTT AAACCCATTC CATGGTCAGG GCCTTTCAAA TGCATTCATC 1560
CCTCTGTGTG CCTCTGTTCT GCCCCAGCCT TGTAAGAGGG TCCCTGTCAT TCTTCTAGAG 1620
CCAGACAGCC TGATTTCAAA TCCTGAATCC ATCGCTTTTC AGATTTGTGA TCTTGGTCAA 1680
GTAACTGACC TCTGTGAGCC TCAAATTCTC CATCTCTGAA AGTTGGGGAG GGTGCTAGTA 1740
GTACCCACCT AAGAGTTAGG GTGAAGCTGA AATTGATCAT CCATATAAAT TGCTCAGCAC 1800
GGGCCCTGAC AGGCCATCAG CACTCATTAG CCGCGCGTCA TCTCCACCCT CATCATCATT 1860
ACGGTCCAGG TGGCTCCCGG AGGGCACGTC TCTCTGGGAA ACTGGACCTG GAGCTTTTCT 1920
TCCCTTCCTC 1930
|
