Tag | Content |
---|
EnhancerAtlas ID | HS095-19840 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr22:42695830-42697400 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr22:42696059-42696077 | CGTTCCTTCGTTCCTTCG | - | 6.54 | EWSR1-FLI1 | MA0149.1 | chr22:42696055-42696073 | CTTTCGTTCCTTCGTTCC | - | 6.95 | SPI1 | MA0080.4 | chr22:42697165-42697179 | GAAATGCGGAAGTT | + | 6.68 | SPIB | MA0081.2 | chr22:42697167-42697179 | AATGCGGAAGTT | + | 6.27 | ZNF263 | MA0528.1 | chr22:42695935-42695956 | GAGGAAGAAAGGAGAGGAGGG | + | 6.03 | ZNF263 | MA0528.1 | chr22:42695830-42695851 | AGAGAAGGGGGAGAAGGAAGC | + | 6.08 | ZNF263 | MA0528.1 | chr22:42695944-42695965 | AGGAGAGGAGGGGAAGGAAGG | + | 6.1 | ZNF263 | MA0528.1 | chr22:42695953-42695974 | GGGGAAGGAAGGGCGGGGAGG | + | 6.26 | ZNF263 | MA0528.1 | chr22:42695956-42695977 | GAAGGAAGGGCGGGGAGGGGG | + | 6.33 | ZNF263 | MA0528.1 | chr22:42695938-42695959 | GAAGAAAGGAGAGGAGGGGAA | + | 6.36 | ZNF263 | MA0528.1 | chr22:42695947-42695968 | AGAGGAGGGGAAGGAAGGGCG | + | 6.4 | ZNF263 | MA0528.1 | chr22:42695839-42695860 | GGAGAAGGAAGCGGAGGGGAG | + | 6.69 | ZNF263 | MA0528.1 | chr22:42695836-42695857 | GGGGGAGAAGGAAGCGGAGGG | + | 6.79 | ZNF263 | MA0528.1 | chr22:42695853-42695874 | AGGGGAGGAGGGAGGAGGGAA | + | 6.84 | ZNF263 | MA0528.1 | chr22:42695966-42695987 | CGGGGAGGGGGAGGGGGAGGG | + | 7.01 | ZNF263 | MA0528.1 | chr22:42695914-42695935 | GGAGGAGGGGGAAAGGGAGCA | + | 7.5 | ZNF263 | MA0528.1 | chr22:42695856-42695877 | GGAGGAGGGAGGAGGGAAAAG | + | 7.69 | ZNF263 | MA0528.1 | chr22:42695908-42695929 | GGTGGAGGAGGAGGGGGAAAG | + | 8.08 | ZNF263 | MA0528.1 | chr22:42695911-42695932 | GGAGGAGGAGGGGGAAAGGGA | + | 9.32 |
|
| Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
SE_23330 | chr22:42695863-42698813 | Colon_Crypt_1 | SE_23842 | chr22:42695766-42696384 | Colon_Crypt_2 | SE_23842 | chr22:42696407-42698797 | Colon_Crypt_2 | SE_25072 | chr22:42695921-42698957 | Colon_Crypt_3 | SE_50938 | chr22:42695852-42698100 | Sigmoid_Colon | SE_56829 | chr22:42695891-42696837 | VACO_400 | SE_56829 | chr22:42697117-42697976 | VACO_400 | SE_65474 | chr22:42695910-42696986 | Pancreatic_islets |
|
| 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 |
GH22I042298 | chr22 | 42694880 | 42697851 |
|
Enhancer Sequence | AGAGAAGGGG GAGAAGGAAG CGGAGGGGAG GAGGGAGGAG GGAAAAGACA GAAAGGGGTA 60 GAAGGGAAGC TTGGAGCGGG TGGAGGAGGA GGGGGAAAGG GAGCAGAGGA AGAAAGGAGA 120 GGAGGGGAAG GAAGGGCGGG GAGGGGGAGG GGGAGGGGCG CGCTGAAATC ACCCGCAACA 180 TCAAAGCCTT CCCCAGCCGC AAAGCAGTCA CGTGCAGCCT GGTTCCTTTC GTTCCTTCGT 240 TCCTTCGCTG GTAGAAGCCG CTGGGCCTGG GGCTGCTGAA GGAATTTTAA AACGAGGCAG 300 ATTGTCTGGA ATATCAGGGG GTTAGGGGAA TGCGGTTTTA TCTCAAGGCA GGGTAAGGGG 360 AGGCAGGTTT TGAAACCTGT TCCCCCAAGG AGAGCGGCAG GGCTTTGGGG CCTCTGCTAG 420 GAGGCTGGGC AGGTGGCCAA GAGTGAAGAC CACCCAGCTA CTCCTGCCGG TGAGAGCTCG 480 TGGCTGGGCC AGCCCAGATA TCAACAGAAG CCAGAAATCT AGATTTGTAT GTGAAAACTT 540 CCCTGTTTTA ATTTTGGCTC AAACTAAAAA AAAAAAGAAA AAAAGCGCCA CATGGGCCAA 600 ATAGAGCATG TCCTGACTGG GGCCCAGAAC CTCGGTCACC TCCCACTTCT GATGGTGGGC 660 AGCAACGCTT TTGTTTCCCA GGGGGCACTG AGGCCCAGGA AGGGAAAGGC ACTTGTTCAG 720 GGACACACAC AGTGAGTGCT CAAGGGGTGC GGGCTAAGAC TTGGGGTCTC AGGACTCCCA 780 TGCCTGAAGC CTCCTGCGGT CAGCAGCCCA AGGGGCAGGG CTGTGGCTGC TGGGAAAGGG 840 AAGTATAGGG AGGTTAGTGG CAGGGGAGGG TCTCAGAAAA CCCCTCGTCC AGCCCAGGGC 900 CAACACACTC AGCCCCACTC ATCACCCTGA TGACTAACCC AGGCCTGCCT CTCTGCCTTT 960 GCCTCTGCTC AGCCCATCCT CCCTATCCAC TCCTGACATT CCCTCCTCCC CCTGCCAAGA 1020 CCTGGGCAGC TTCCCCTCCC CCGAGCCCCA CCTGCAGAAT GCACCATGCA TTCAACCATT 1080 CATTCTTCTG TTGCTCCCCA AGGCCCTGAG TCAGCCTTAA CCCCACCTTC AGAGGCCAGG 1140 ACAGGGGAGG GTGTTTAGGA TAGAGAGGTG TGGCCTCCAA GGAGGAAGCA GCTACCTCTG 1200 TAGGGTGGCG GTAGGGGAGT CTCCCCAAAG GAAGGTCCTA GGGCAGAGCA TGGCATCTGC 1260 ACTTACCAGG GTGGAGGTGT AAATGGCTGC TGGAAGCCAG AGGCAAGGCT GGGAGGAGGT 1320 GGATGTGGGG GTTCAGAAAT GCGGAAGTTT ATCTTGCGGG CACTAGGGAG CCGTTGGAGG 1380 TGTGTAAGCA GGAGAGAGGT CGGCTCAGAT CTTCACTATG GGGCTGTCAG GACAAGGCGA 1440 GGATGGAGTC ATTCATAGGT TCAACAAGTG TTTGCTGAGC ACTTACTCTG TGCCACGCCC 1500 CAGGGAGACA GAGGAGAGCC AGACAGACAA GGCGTGCACC TTGGGGAGAC AGACGTGACC 1560 ACACAACCAC 1570
|