| Tag | Content |
|---|
EnhancerAtlas ID | HS003-26158 | Organism | Homo sapiens | Tissue/cell | A549 | Coordinate | chr2:75146330-75147790 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr2:75147046-75147065 | GAGCCTCCAGGTGGCGCTC | + | 6.12 |
| | | 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 |
| GH02I074919 | chr2 | 75146728 | 75147550 |
| Enhancer Sequence | CACTAAGCCT GGCAAAATCC TGCCCATTCT TTAAGATTTA ATATATATCA CGTTTTCCTG 60
CGGTACTTCC TGGACTTCCC TTCGGACGCC TCTGGTCCCC AGTCTGGCTC CTTCTTAGGC 120
CTGTCCCGTA ATTCTAAGCT TGTCTGGCTG TCCTTCCACT ATGAGCTCTT TGGGAGCAGG 180
ATCTCTGTTT GGTTCCATTC TTTTTGGTGC CTTGAACAGT ACCTGGCACC AATAAACACC 240
TTAAGGAATG ACCACATTCC TTATTCCCTC CTTTGTATCC ACCTCTTTCC TAGCCCTTAG 300
TGTTGCACAT TGTTGATGGC CTGTCTTCCC CATCACGCTA TTAATGCCCT GGGAAACAAG 360
ACATTATCTT TATTTCTCCC CACGTCGCCA GAGCCTAACA CACAGTGGCT CCATCTCCGC 420
TCACTGCAAC TTCCGCCTCT CGGGTTCAAG CGATTCTTGT GCCTCAGCCT CATCATGAGT 480
AGCTGGGATT ACAGGTGTGC GCCACCGTGC CCGGCTAATT TTTGTATTTT TAGTAGAGAT 540
GGGGTTTCGC CATGTTGGCC AGGCTGGTCT CCAACTCCTG ACCTCAAGTG ATCCGCCCGT 600
CTCGGTCTCC CAAAGTGCTG GGATTACAGG CTTGAACCAT CGCTCCAGGC CTCGATAAAT 660
GTTTAATGAA TAAAACGATG AAAGGACCCG TCGCCTCCTA AATGCAGATC TCGAGGGAGC 720
CTCCAGGTGG CGCTCGCCGC TCGGAGAAGC AGGGAGTCGG TGCGCCGCAG CTCCGGCAGG 780
CGTCTGGGAG GTGGTCGCCT CCTCACCTGC CCAGGCGGCC GTCCCCCGGG AGCGGGTGGC 840
GGTGACCTCA GGACTGACGC ACTGCCTCCT CCGGGCGGGT GCGCAGCCTG CGTCAGGGGC 900
GCTGTTCTCC CTGTGCTCTT GGACCCCGCA GTTGTTTTAG GAACATTCAC TGGAGAGCGA 960
GAAGGGGGCC GCCTTCCGGT GCCCGGTGGG CAACACCTAA GCCGCGGTGT TTACTGGTGA 1020
GGGAGTCGGC TGTCTGCTGG CGGCTGTGAC AGCTGCAACA CGCCACACAA AGATGTTATT 1080
TACCTGTCAT ATTAATGATA GTGTTAGCAA GTGCGTGGCA CGTCCAGTAC TTTTTTTTTT 1140
TTTTGAGACG GAGTCTCGTT CTGTCGCCCA GGCTGGAGTG CAATGGCGCG ATCTGGGTTG 1200
ACAGCAACCC CCGCCTCCCG GGTTCAAGCG ATTCTCCTGC CTCAGCCTCT CGAGTAGCTG 1260
GGATTACAGG AGCCCATGAC GAAGGCCGGC TAATTTTTTG TATTTTTAGT AGAGACGGGG 1320
TTTCACCGTG TTGGCCAGGA TGGTCTGGAT CACCTGACCT AGTGATCCTC CCGCCCCCGC 1380
CTCCTAAAGT GCTGTCCAGC ACTATTCTAA CTGCTATGTA CACATTTACT CAAAGGTACA 1440
TAAGATAATA CAAAATAAAA 1460
|
| |
|
|
|
