Tag | Content |
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EnhancerAtlas ID | HS047-01066 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr1:40282920-40284110 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXF2 | MA0030.1 | chr1:40283873-40283887 | TTTGTTTACCTTCC | - | 6.18 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_23684 | chr1:40282131-40285707 | Colon_Crypt_1 | SE_24232 | chr1:40282541-40285645 | Colon_Crypt_2 |
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| 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 |
GH01I039816 | chr1 | 40281967 | 40283916 |
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Enhancer Sequence | CTGGGGGGTG GCAGCGGCGA CGGGGGCCAT GGATTCCGGC CCCAGCCTGT GAATTCCACA 60 GACACCGCGG CTCCACACAA CCCACACCCC ACTGCACACA GAAAGGATAC GGCTGACGCT 120 TCGTGAGCGA TGCTGGTTGT CACCAAGTCA CTGGTGAAAC TGGGAGAGCG CCCCTGGTGA 180 GACGGTGTGA GGATTCATGC AAAGCACGTG ACAGAGGGAG TTTCAGGAAG TGAAGCTGTC 240 CTGTGTTGCT GCTGTTTTAT TAGTAACAGC AAGCTGCCCA GGCCCACACG AGGCAGGTGT 300 GTCTCATGAG TGTTCTACGG GAGAGGAAGT GAGGCTTAGA GGCCCAAGCC AGGAGTGGAG 360 GAGCTGCGGC TACGGGCTAC GGTGCCCATG CCCACACCTG CCTCAGGAGC GCCCTCTTCC 420 TTTGGATGAT TCTTTTTTAT AGACAGGGTC TTGCTCTGTC GCCCAAGCTG GAGTGCGGTG 480 GTGCAATCAT GGCTCCCTGC AGACTTGACC TCTTGGGCTC AGCTTCCCAA GTATCTGGAC 540 TACAAGCATG CACCACCACA CCTGGCTGAT TTTTAATTTT TTTGTAGAGA TAGGGTCTTG 600 CTATGTTGCC CAGGCTGGTC TTGAACTCCT GGACTCAAGT CCTCCTGCCT TGGCCTCCCA 660 AAGTGCTGGG ATTACAGGCG TGAGCCACCA TGCCCACCCA GCCTGGATGA TTCTTTTAGT 720 CCGTCATTCA TCCCATGAGC ATTTGTGCCA CATGTGCTCT GAGCCTGGTT CTGTGGTGGG 780 CACTGGTGCC ACCCTGGGCC CTGAGGTGCA TGAGGGGGCG GAACAAATGG AAATTGAGGC 840 AGGCTAGGCC TAGAGCCTGT GGGCTTCCTG GGACTGGGCA CTGAGCAGTG AGCTCGGGAG 900 ACAGAAGGCT GAGCCCAAGG CTGTGGGCTT GTGCCACCTC TGCCTAACCA GGGTTTGTTT 960 ACCTTCCACC CAGAATCACA TAATGGAGGT CCGTTCCTCC CCTGCACAGC ATCCTGCCCT 1020 CAGGATAGCC TCAGGGCTAC CCACACAGAT GGGAGCTGCC TCATCTGGGG CCACTCCAGG 1080 GCCGGGGGTT CTGCTGGGAA GAAGGCTCCT ACATCCTTGC CCCGCTGTCT GAAGCTGGTT 1140 TGGGCCAGTG AAGAGGAGCC TTCCCTGGCC GAACTCCTTT TGTCAGCCCA 1190
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