Tag | Content |
---|
EnhancerAtlas ID | HS047-10788 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr14:100873950-100875140 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr14:100874985-100874996 | GGTGACTCATC | + | 6.32 | JUND | MA0491.1 | chr14:100874985-100874996 | GGTGACTCATC | + | 6.62 | SP2 | MA0516.2 | chr14:100874356-100874373 | CTGGGGGCGGGGGTTGG | - | 6.12 | ZNF263 | MA0528.1 | chr14:100874860-100874881 | CCCCCCTCCAATCCCTGCTCC | - | 6.71 |
|
| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_23539 | chr14:100871804-100874662 | Colon_Crypt_1 | SE_24202 | chr14:100873619-100874446 | Colon_Crypt_2 | SE_25594 | chr14:100867310-100877105 | DND41 | SE_34657 | chr14:100871635-100878071 | HeLa | SE_50425 | chr14:100871853-100874504 | Sigmoid_Colon | SE_53089 | chr14:100871723-100875111 | Small_Intestine | SE_65652 | chr14:100872240-100875257 | Pancreatic_islets |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr14 | 100874667 | 100875097 | chr14 | 100873995 | 100874274 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH14I100405 | chr14 | 100871808 | 100877648 |
|
Enhancer Sequence | ACCTGTAGAC TACATGCACC CTGGCGCTCT GGGTATGTTG TTTCTGCAGG TTTGGGAGGC 60 AGCTGTCCTC CAAAGCATAC AATTACTAAG AACAGGGACC ATAGTTTCAC ACTTCAGTGC 120 CTAAACAGGC CCTGACACCC AGTTTGGCTA GGTTGAGTCT GGGTGCCAGA GATTAGAGCT 180 GGGATTGGAG ATGTAGCCCG TCCCCGTTCA GGAGCCTCTC ACGTGTATTG CCTCTCACGT 240 GTATTGTCTG TGAGTGTGCT GGGCTCCCAG ACACATATGT CACAGTGAGC TGTGGGAATG 300 ACCCTTGACT CCTATCCTGA TGGGAGTGGG AGAGGGTGCA AGAACTGGCC CTGGAGACAG 360 GGGAGGGGTT GTGAGAGCCA GAGCACAGAT GCCTGCACAC CAGGCACTGG GGGCGGGGGT 420 TGGGATGGAG AGTGTGGTGA TGGTAATGGC CTATAGTCGT GGGGGCTTGG GGACTTCTGA 480 GGGATGTGGG TAAATCTGGA GTTTTTCCTA TAGGAACGGG GAGCCATGGA ACGTGCGTGA 540 AGCGGTGTGT AAAACTGGAG AGAAAAACCC TAAGGAGACC TCATCGGACG TTCCTGTGAT 600 AATCTAGGCC TCAGGACAGG CAGACTGGGA TGCTTGTGTT ACCCCTAACT TTAGATTACT 660 CTCCCACTGC TCCCCTCCTT CACTGTAGAT TCCCACAATT TCAGTATCAA TGTAATTACA 720 ATTTAGGGGC TTAGAAACTC CTGTATTTAT TGAGAACCCA CTTAATTTAC ATATATTGAG 780 TTTCAATATT GCACAACTCT GTGTGGAGGG GTTAGGGTGG AGGAGACCTG AGATGACAGA 840 AGGCCATGTT CTCTAGGGAT GGTCTGCAGC CCTCAGTGCT GTCTCTTTTC CCTCCAGCGC 900 CCCCTCTGTG CCCCCCTCCA ATCCCTGCTC CCCCCAGTCT CTATAGCTGA AGGCTAGGAC 960 GAACTGTGGG GTTGTGAATA TTTACGCAGG CAGGCATAGG ACTCAGTGAC GCAGCTGAGA 1020 GCCACGCAAG TGTTTGGTGA CTCATCAGAC CTTCTCCAAA GACTTGTGAT ATTTTTCTCC 1080 TCTGAAGGGC CGAAAGCAAT TTGCAGTTAA TGATAGTATA TGACGCCAGA AGAGTACGCA 1140 GACCTTCCGG CTCATCTTTT CTGTGCCTTG GGTGTTTTGT TTTTGAAAAA 1190
|