| Tag | Content |
|---|
EnhancerAtlas ID | HS118-11254 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr20:17606610-17607990 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| E2F6 | MA0471.1 | chr20:17607810-17607821 | CTTTCCCGCCC | - | 6.32 | | ZNF263 | MA0528.1 | chr20:17607847-17607868 | GGAGGATGGGGGAGGGAAGGG | + | 7.55 | | Zfx | MA0146.2 | chr20:17607814-17607828 | CCCGCCCAGGCCTG | + | 6.74 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_23241 | chr20:17604799-17610468 | Colon_Crypt_1 | | SE_31481 | chr20:17605146-17613788 | Gastric | | SE_47483 | chr20:17606929-17608597 | Pancreas | | SE_62115 | chr20:17595320-17642758 | Toledo | | SE_65600 | chr20:17605405-17611056 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr20 | 17606951 | 17607238 | | chr20 | 17607284 | 17607662 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH20I017626 | chr20 | 17606828 | 17608589 |
|
Enhancer Sequence | CCCCAAGAGC GTCCCCAAAA GAATGAGACT CCGAGGAAGA GGTGTCAGCA GGCCAGTGGC 60
AAGGACACAC TGACAATCAC ACCCTTGGCA GCCACTGCCC GAATTCTAGA ATATCTGGGG 120
CTGAATCGCT CCTCTCTACT CCAGAGCAGG ATGGCCCAGC CTACACATAA CTTTCAGATC 180
AACTGTTTGA GAAGGAAATA AAAGCACCAA TTTCTGCCAG ACACATCTAC ATGATGCAAG 240
AAAATTCAGA TTAATCCTAA CTACAACATG AGTTCATTAT CCTAGTAATA TGCTGTGTGG 300
CCCAAGAATC TGATCTTAAA ACACAAGAGC AAAACAACAA CCTCTCTACC CCAACAAACA 360
CCACCAGGAG AAACAAAGTT TGCCCATGCT TTTTGGGAAA GGAAGGTGGA CAAGGTTTGG 420
TTGTGGGTCA TTCTGGGCCC TCAGGGCAGC TGGCTTCCTT TCCCAGTCCC CAAGCCGCAG 480
AGCCCAAATG CCAGGGAACA TGGGCTGTGG CCTGGGGAGC TGCCTCTGCT GAGAGGCACA 540
CAGGGAGGTG CTTCTTTGGT GACGAGGGTC AGGACAAGGG AACTTTGTGA ACTGATGGCC 600
TAGGACACAT CTGACCGTGT GCGAGGGAAT GCAGGACACC CTCCATGCCT CCCCCACCTA 660
CTGCTGCATG GACCCCTAGC CACGGCGGCC AGGACCTGCC TCCCCAGACT GTGGGCATGT 720
GCTACAGGAG GCGAGCCCCA GAAGTGATGG TCACAAGGAC TCCGGCCCCT GACTCGAGCC 780
ACCCCACCCA GGTGTTGGCC GGCCTTAGCA ACAGCAAATA AACACTCCCC GAACATGGCC 840
TGGCGCTGGT GCTGCTGACA CGGAGGGAAA ACAAGGTCTG GCCAGCAGTG AAGTCACCTC 900
ACAGATGGAG GAAAACAACG CTGAGACGCT GCCAGCTCTG CCCCGACGCC TCAAACCTGT 960
GCTCCAGCAG CAAGCCTGGG TTCGCCATTC TGGGTTGTGC AACCATTTTT CCTGTTAGAG 1020
TTCCTGACCT CAGCCCCTAA AATCCCTTGC TTGTACACAC AGAACCTCTG ACCAGTCAGT 1080
CCCTTCCCAC AGAGAGATGG ACAGGTGGAT GGACGGACGG CAGGTGGCAG GGGGTGCTCC 1140
CACCCTGGCT GAGGCCACTC TGGAACGATG TGATCACGAA GCTCTCTGCA AGGCCGCCTT 1200
CTTTCCCGCC CAGGCCTGTC CCGTCCTCTA AATCACCGGA GGATGGGGGA GGGAAGGGAG 1260
CCTCTGAAAG GGGCTCTTCT GCAGAGGACC TGAGCACCCT CCTGAAAACC CTGGCCCCCC 1320
AAGGGTCTTT GGTCCCCCGG GCTGAGGCTC AAGTGAGCAG GCAGGCTGCT TCCCCAGCTT 1380
|
