| Tag | Content |
|---|
EnhancerAtlas ID | HS052-03299 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr1:204317360-204318340 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr1:204317556-204317571 | AAAGAGCAAAGTCCA | + | 6.71 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_23313 | chr1:204316827-204318459 | Colon_Crypt_1 | | SE_24138 | chr1:204317324-204318435 | Colon_Crypt_2 | | SE_28816 | chr1:204316760-204318561 | Fetal_Intestine_Large | | SE_33663 | chr1:204316787-204318512 | H2171 | | SE_50227 | chr1:204316786-204321139 | Sigmoid_Colon | | SE_52903 | chr1:204316784-204318487 | Small_Intestine | | SE_65374 | chr1:204317203-204320948 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 204317952 | 204318184 | | chr1 | 204317382 | 204317733 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I204347 | chr1 | 204316837 | 204321118 |
|
Enhancer Sequence | CATGGCTAGA GCTGAAGCTT CTTGACCCTC TGCAACCTTC TCCTCAAGCC ACGGGCCCTA 60
ATTCAGCCAT CAGCCACCCT TCAGCCCTCC CTTCAACACA GGGCAGGTTG GGCAGCTTGA 120
AGCTGAAAAG AGAATACGCC CAAACAGCAA GGAAATGTCT CCCAGCCATA AATGCCTTGC 180
CCGTTCTTCT GTTTGCAAAG AGCAAAGTCC ATTTGGGAAG GGAAGGAATG GTACCAGCTA 240
GTGAACCCCA CACAAACCAA CCCGGTCCTG AGAGATGGAC ACACAGGCTG AATTCACACA 300
GCATGGCTGA AAATGGAACC GAGCAGTGTG GATTCCTTCA TTCGCTCCTG CTTCTCATTC 360
CAGGCCTTAT CTTTATTTTA TCACAATAAA TATTTATAGG GTCAGCATTT GGCCTGGGTA 420
TTCCACAGCC ACTCGCGCCC CTCTTGCTTC AGGCACTCCC AACTCAGCCC CCAGGTGCCA 480
AACCCCCCCC CCGCCATCTC CCCCACCCTG CTGACCTTAG CCTGTGCTCA AGGCCACACT 540
TGGCAGACAT CCTGCTGACT GTCATCTCCA TTGTCAGATG GGAGATAGAC AATGAGAAAC 600
GGGCTTCTCT GGGGACTGGT TTAAGGCTTT CCTGTCAAAA AACCTCCCAG AAGCCTGAGG 660
CCTCTAGGCA TGGCCTGGGC CCCTGACACC AAGTCTGCCC TCACAGTGAG GTCCAGTTGC 720
TTGGCAACCA GAACAGCTTG TCGGGAGGGG TTAGCTTCAG CCCACGCAGC TAGCCCCACC 780
CATCCTTCCC GGCTGACTCC CCTCAGACAC GGAGGGAACA CCCAGACTGC TTCAAGCTTG 840
GCCTTCTCTT TTCACAGCTC TCCTCAGTCC CAGCCTCTGC AGTCCCTGAG ACAGCAGACA 900
AGAGGAGCCT GAGTTCCGGG CCTGGCTCCA GGCCCTCAAT TTTAAGGGGG CCAGGACAGA 960
CACCTGGGAT CTGTTTGGAT 980
|
