Tag | Content |
---|
EnhancerAtlas ID | HS050-39872 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr2:217522760-217524740 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Hnf4a | MA0114.3 | chr2:217523728-217523744 | GCTGGACTTTAACCCG | - | 6.18 | REL | MA0101.1 | chr2:217522768-217522778 | GGAAATCCCC | - | 6.02 | 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 | TAAGACATGG AAATCCCCAG GGTTCATTGA GGGGCATTCA TTGTTTGCCA CACACAAAAT 60 GTACCCGGAG TTTGTATGTT TTGTTTTCTT AGTGTCCTCT TTCCTCTCTG CCATTTGATC 120 CTTCTTGCTA CTGTCCACAT GCATTCCTTC TTTGTCCCTT CAATTTTGTT GACTTTCTTC 180 TGCGGTGGCC TTGGAAACCA GACATCCAGA AGCCAGGCTT CCTGGAGCAG CACTGTTGTG 240 AACTGTCTCG AGGCTCCTCA CGAGATGATT CTCCCCTCAT CTTGAGTGGA AAGTGCCAAC 300 ATTTGAACAT GCTCAGCCGT GGTAACAGCT ATTAGGATGT TCAGAGCTTA TTTTCCTTGG 360 TTTCCCTGTT CTCGGTTGGG TTCCATGCTG CTGAAGTAGT AGATAACTGG GGCATTCGTC 420 ATTGTCATCA TCATCAGTGT AATAACCAGC AGCAACATGG ATATAGAATT TCTGTGCTCC 480 AGGTCGTCTT TTATTTATTT ATTTATTTAT TTATTTATTT ATTTATTTTT GAGGCAGTGT 540 CTTGCTCTGT CGCCCAGGCT GGAGTACAAT GGTGCGATCT CAGCTCACTG CAACCTCCAC 600 CTCCTGGGTT CAAGCAATTG TCCTGTGTCA CCCTTCTGAG TAGCTGGGAT TACAGGTGTG 660 TGCCACCACA CCCGGCTAAT TTTTTTGTAT TTTTAGCAGA GATGGGGTTT CACCATGTTG 720 GCCAGGCTGG TCTTGAATTC CTGACCTCAA GTGATCCACA TGCCTCAGCC TCCCAAAGTG 780 CTGGGATTAT AGGCATGAGC CACCACACCC GGCCTAAGTC ATCTTTTAAC TGCTTTTCTT 840 TCGTCATACT CTCAACAGCT CTATGAAGAA AGAACTGTTA TTATCCAGCA ACTTACAGTT 900 AAGAAAGTAG AGGCACAGAG AGGGTCTGTG TGGGGAGAAC ACGTGCAGCT GATATAGAAA 960 ATGGCAGAGC TGGACTTTAA CCCGGCTACA CCCCTTTAAC CAGAGCTGCT ACCCTGGGGA 1020 CGGCGTGCTG GCTTCTAAAG GAAGCTGCTG CATGGCAAGT GAAGAGTGAC TAGTTCTCAG 1080 GCTTGGAGGG AGGGGAAAGG ACAGGGACAG ACCCCCATCA AATGTTCCGT ATGCTGGGGC 1140 CTATGCTGGG CACGCCTTGA CAGCAGGTGC TGCTGGAGTG CCAGCACCCG GTGCTGTCCC 1200 TGGCATGGAA GAGGTGCCCC CTCCCTTAGT TGGTGAGTGA GTGAATACTC TTGTATAGAG 1260 TTACTCTAAG AATTATTCAT TTGTGTTCTA AGGGCTGTAA GTTTTTGAAG GTGCATTAAT 1320 GGGGAAGAAA AAATGTGCAA GATTGGTTGA AAAACACCCC TCTGCACCCA CCCAGATCTT 1380 GTTGGGACCT GCAGGAGAGC AGCTCTGGGT GGGAGGGTCT GGGGCTGTTT GCCGTGTCTC 1440 CAAGGGGTTG GGGCTGGGGC TCGGCGGTGT GAGGCCCTGC CCTTCTGGAG CTTGCTGGGG 1500 CTTGTCTCCT GGTTACAGCT CTGCCGTGCG ATTCAGATCC TCTCTGCCTC CTTTGGCTGG 1560 ACGTGCCTCA GCCAGAGTGA GACTGTGGCA GGCTGGAGCT GTTTTCAAGG CCTCCTTCAC 1620 CTAGGCTGTG CATACAAAAG GTTGAAGAAA GTATAAGGAG ACTTAATGGA CGCTTGTTGG 1680 ACAGACATCA CGAAGCTTCA TGCCCTGCAG TAAGCTGAAG CTATGAAGTC GAAGGAGTCA 1740 TAGTTCCTGT TCTTGGGGCT CTCAGTATAA TGGGGTTGGG GTGGGCTGCA CAGACAGACT 1800 TGGGAACGAG GGAATGTCAG TGTGGCAGAG CTGTAGCTGC CTCGGAGCAG CACTATGGGA 1860 CCTTAGGCAG GGCCAGGTGG GCAGGTACAC AGTGACAGCA GGGGGATGCT GGGACCAGGT 1920 TCTGGGTGGC GACGTGGCCT TCCACCTTCT CACTCCTTTG CCATATATGC TGCAGCCCGG 1980
|