| Tag | Content |
|---|
EnhancerAtlas ID | HS101-37060 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr6:29780620-29782780 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr6:29781808-29781819 | GATGAGTCACC | - | 6.32 | | JUND | MA0491.1 | chr6:29781808-29781819 | GATGAGTCACC | - | 6.62 | | NEUROD2 | MA0668.1 | chr6:29782279-29782289 | GCCATATGGT | + | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr6 | 29780919 | 29780979 | | chr6 | 29781738 | 29781880 | | chr6 | 29782615 | 29782769 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH06I029813 | chr6 | 29781741 | 29781890 |
|
Enhancer Sequence | CGCACTTTTC CAGCCCCTGC CAGTCCCCTC CCGTGACTCC ATCAACATCA GCACCTGCCC 60
TGTGTCCACC ATCCATTGTG CAGTGAGTGA AAGGACCCAG GACTAAGGAA CAAGACCCAG 120
GAGGAAACTC AGTGCCCTTT CCTCCTCCTC TCAAGCCTGA CCAGCCCTGA CACAGTGAGA 180
GGCCTCCCCA AAGAGAGGCC CTGGCCCTGT CTCCATGTCC TTCCAGGTCT GGGCCAAGTC 240
ACACACAGTC CTTCTCTTCC TGAGACCCCA GGCCCTCTTC ACCTGCAGAG GCACCTGCAT 300
ACCAGGGCAG GCCCTGCACG CTGTGGGTTC TGCCCTCCAC CAGCAGCTCA CTGTTCCTCC 360
CCTCCCAGCT CTGAGCAGAC AGCTCCTAAC TAGAGATCCT ATCAGGAAGC CCTGGGGCTC 420
ACAGGCCCTG CATGGAAATA TGTGGCTGCC ATGGAGTCTG CACCTGACCT GATGCTGGGG 480
ACCCCCTTGC TCAAGGAGGC CCAGCCTGCC CTCCCCATAA CCTGCATTTG GGCTGTGCTT 540
GCTCCTGCCT GTCCACTCAA CCCTGGAAAT GCAGCTCCAC CCCAGGGCTG CTGCTTGGTG 600
AGGCTGCAAG CCCTTCCTGT CCCATTCCTA ACAGGGATTC CACCCAGGCC ACTGCCATCG 660
CAGCTCACAG GGGATCTTCT TCGCCTGTGG AGTAGGGGGT TTCTTCAGAC CCCTCATCCT 720
GAGGCTGCCT CTACGCACCC TCTGCACCTG GGGATTGCCA CTGCCACAGG CACTGTCTCC 780
CACATGGACC CTCTGAGAAA CGAAGCCCCA AATTTGACTT CCTGTTCTAT TCAACATCCT 840
TTACAACATC AGTATTGGGG GAAATCCTAT TAAGATTATC CAGCTGAAAT TATGTTGATG 900
GACACCAATA CTTAAAGCAG GAATTTTGAG AAACTAACAT GTAATTTTCA TGCCTTTTTC 960
TGGCCAATGT CCCAGTGACC TACGAGAAAA CCTTTCCTGC CTACAGGGAA CCAGAACTGA 1020
CAATCCCTCT ATAGGAGACA CCGCAGGTGA GAGCAGGAGC AACCACAGAC CTGCACTGCC 1080
CGTGCTGTGG TTGCCTCCTG GACGGGGCCC TCTTGCTGCA GGGCAGGGGA TGAACCGTCC 1140
CATCTGCCCA GGCCTGAGTG GCCAACTAAC TGTGCAATTA GGTTCAAGGA TGAGTCACCA 1200
CCACCTCACT GGCCAGACAC ACGGAAGTGG AGAAATGGCA GAAAGACTCG GGTTTCCTGG 1260
ACACCCCAGA CTCTCACTGT CCCCTGCACT GCCTCTGTCT TTGCAGAAAC TCAAAACTTT 1320
CTGCTTGCTC TTTTCCTCTC CCCTCAAACA ACCTGACTGT GGGGGAAATG ATTCTGACTG 1380
TCTCTTATTG TAAACTTACC AGGCAGCGAC TACACTAAGA ACAAAAACAT TGGCTCAGGA 1440
AAGGCAAGGT GAGGCCACAG AGCACAGAAC AAAGCCCAAA AAACAGCCCA CTGGGTACTA 1500
TGACCCTCGG GGGCTGGAAA AAGTAACACC TGGACATGGG ATGAAAACAG GGACCACAGC 1560
TGCCCTGACA GAGGGCTGGT CCCCACTCCC CAAATAGCCC AGGGACATCT GCTTATCAAC 1620
TGGTCCATAT TATCTGCAAG GAAACACAGG GAGACAGGGG CCATATGGTG GGAACCCAGA 1680
AAAAGCACGG TCTCGAGGGA CCCAGAGGAC GTGACACCCC TGAGACAGCT CCCAGATGAG 1740
GCATATGGGG AGCTGCAAAG TGGACAGAGG ATGGCCATGT GCACTCAGGA CTCTCCCTGT 1800
TACAAGGGGA CCTCAAAGGG GCTGTACACA TGGGGGCCCT CATTCTGGGC CTCGTGGGTC 1860
TTTTTCTTGA TGTCCTCCTG ATGGCTGGAG AAACAGGGGA GGGGGATGCA GAGAGGAAGG 1920
GACTAGAGGC ACCACCTCTC CTTGGATTCC TCTCCAGTTT CTAGCCCTCC CTAGATCACA 1980
TCTGCCTTTA CTATTTGCTC CCTCTGAGAT AGTGATCATC CAGGCCCTCA GCAATCAGCA 2040
CGCAATTCCC AACTCACCCA CCTGGATGCG ACCTGGTAAG CCTGAGAGAC AGAGACCGGG 2100
ATGGGGACAA AGCAGGCACC ACGGCCCTCC CTGCTGCCCA CTCCTCACCT GCAGCAGGAG 2160
|
