| Tag | Content |
|---|
EnhancerAtlas ID | HS118-17550 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr7:100994850-100996100 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr7:100996017-100996032 | GAGGTCAGAAGTTCA | + | 6.38 | | RARA | MA0729.1 | chr7:100996017-100996035 | GAGGTCAGAAGTTCAAGA | + | 6.88 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr7 | 100995496 | 100995623 | | chr7 | 100995626 | 100996011 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH07I101352 | chr7 | 100995701 | 100995970 |
|
Enhancer Sequence | GCAGAGGTTG CAGTGAGTGG AAATCGGCCA CTGCACTCCA GCCTGGGTGA CAGAGCAAGA 60
CTCCATCTTC AAAAAGACCA AAAACAAAAA CAAAATGGAC TATTGGAATA GCCATTTAAT 120
TTGCTGTCTT CCGAATATCT AGTTCACCAC TGATGTTTGA GGAAACAGGC AAGTTTATAC 180
CTGTTGGTAG GCAGAGCAAA GAAGTATTCA CTTTCATAGG GCCTGAGTGG AATTTTGGGG 240
GTGTCCAGGT AAAGAAGAAA ATTCAGGCTG GTCGAGGTGG CTCATGCCTG TAATCCCAGC 300
ACTTTGGGAG GCTGAAGTGG AGGGATTGCT TGAGTCCAGG AGCTTGAGAC CAGCCTGGGC 360
AACACAGGGA GACCCCAGTC TCTACAAAAA ATTAGCTGGG CATGGTGGTG TGTGCCTGTG 420
GTCCTAGGTA CTTGGGAGGC TGAGGTGGGA GGATCACCTG AGCCCAGGAG GTCAAGGCTG 480
CAGTGAGCCA CGATCGCTCC ACTGCCCTCC TGCCTGGGCG ACAGAGTGAG ACCATGTCTC 540
CAAAAAAAAA AAAAAAAAAA AATCAAAAGT GGAGATCTTC TATAATATCT ATATGTTCTG 600
CTTGCATCTT GCCCTGGCCA AGTAGGGAAC ACTTGCAGCA AAGCAAAGAA ATCTTTTGTT 660
TTGACTCCCC TGCTCCCTTG AGTTAACTCC AGCCCATTCC TGCGTTGTTT TGGGATCCAG 720
AACAGCTGGG AGCACAGACT GCTGGAGAAA TCAGGATGAA AACAATTCTG TTCCTACCAG 780
CACCTTCCTG AACTTCTGAG AGAATTGCAG AATCCATGTT CTATAGGGCA ATGGGTGTGG 840
TGGGGCGGAT CTCTGTTTTA GATTAACAGG AGGATTTATC ATGCCAAGAG GTCAATATTT 900
ACATTGGCTT TAGCATCATG AGTATTTACT TCTCTGTTCA GTGGCTCTCC CTGCTGACTT 960
CAGCAGAAGC AAGATCTGCT TTTTGTCTGC TGAAGAGGAT GCTGACTGAT TACGTTCTTA 1020
TCAGAAAGGT CTGGAAACAA AACTGTCACG GAGCCCACTT CCTTGGTGAA GCTTGTCTTC 1080
TTTCATCTAG AAATCTGATC TGGCCAGGCA TGGTGACTCA CGCATGTCAT CTCAGCACTG 1140
TAGAAGGCCA AGGCGGGCGG GTCACCTGAG GTCAGAAGTT CAAGACCAGC CTGACCAACA 1200
TGGTGAAACC CCGTCTCTAC TAAAAAAAAA AAAAAAAAAA AAAGAAATTA 1250
|
