| Tag | Content |
|---|
EnhancerAtlas ID | HS165-03848 | Organism | Homo sapiens | Tissue/cell | Ramos | Coordinate | chr12:132254330-132256080 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2F1 | MA0017.2 | chr12:132256021-132256034 | CAGTTGACCTCTG | - | 6.15 | | ZNF263 | MA0528.1 | chr12:132255386-132255407 | CTCTCTGCCCTCCCCTCCCCC | - | 6.51 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CCGGCTAATT TTTTTGTATT TTTAGTAGAG ACGGGGTTTC ACCATGTTAG CCAAGATGGT 60
CTCAATCTGT CCTATTTATT TTTACACGTA CCCTCTCACC TCTCCTGTTT GCAGGCATTG 120
GTTTTTGAAT CTGTAGAACA TAGAAATGAG CGTTTAAATC ACTAGGATGC TCTCCCTGGA 180
TATATGTGTG TGTCTGTGTA TGCAGATTAC AGCTACCAAG CCATTTCAAC AAAAATGTAA 240
TGGTTGTAGC AGATGATGAT AAATGTCTTT AATTGCTTCT GAAACAAAAA TACTTGTAAT 300
TAAATTGGCA ATTGCCATAA AGAAAATTCA AACTCGAAAA TATTTTTAGC CTAAAACAAC 360
TTCTGGGACA GGTTACCCTT GACTTTACTA AGTATTCTAG CATCTGCTTT ACTCGCTGAT 420
GTTGAGACAT TTGACCCAGC TATGTAGTTG TGAAATTCTC GGAGTCCAGG AGGACTTGAG 480
ACAAGACCAC ATTCGGCCAC CGCACGCCCT GGGTGAGGAA GCCTGCGTGG CTGAGGGCAC 540
GTCGGCACCA GGAGGCTCAT GGCACCCCCA GGTCTGTCGG GGCCGTGGCT AGCTCGGGCT 600
GGCTCTGCAG GGTGGCATGA GGACACTCCC TTACACAAGG CCTGGCATAA CATGGCAGGA 660
ATTTTGCTGT CACCTTAAAG TTAACTGAAA ACAGCCACAG TGCAGCTTAT GTGCCTGAAG 720
GACAGTCACT TCTCTGTCTT TACTTTCTAT AAAACTGATG TATACATATG ATTTTTAAAG 780
TTCCAATGCT AGAGAAAGGT ATAAAACAAA GAGGAGAGGT CCTTTCTTTC TTGTGTATTT 840
TTTTAATTCC TGTGGAAATG GCACTTTTTA AAATTCCTCC AATTCTCTCC CTTCTGTAGA 900
GTTTGAGTTT TTAACATAAA GGTTACCATT TTACCGTTTT TAACTGTGCA GTTTATGCTG 960
GCATTAAGTA TATTCACACT GTGCAACTAT TACCACCCAA CCGTTCCCAG GATGTCCATC 1020
TTCTAAAACC AAAACTCTGT AGCCATTAAA TAGTAACTCT CTGCCCTCCC CTCCCCCAGC 1080
CCTGGCACCC ACCTGCTTGC AGCCTCTGTG AACGGGACTC CTGGGGACCG CATGTGTGTG 1140
GGATTCTGCA GTGTCTGTGC TTCTGTGCCT GGCTGACTTC ACCTAGCGTG GTATCCTCTG 1200
GGTCCAGCCA TGCAGCAGCC GCATTGGACC CCCTTCCTTT TTACAGTTGA ATGGTGCTCG 1260
GTCGTGTGCA TCTACCCCGT TTGTTTCCGA ACACTTTGGG AGGCCAAGTG AATCCTTGAG 1320
GGGAAAAACT CAATTCGATT CATGTATGTG GAGGTGTAAA ACCTCATAGG GGATCATACC 1380
CTACATATTT TTCTGACAAC TTTTTTCACT TACAGTAGAG ATCCTTCTGT TATCAATGCT 1440
TACAGTAGTG TTTGGTGTGT TACAGGCACT CGGTAGGTAT TTAGTGACCG AATGACTTTA 1500
AGTAGTTTAC CTGTAAATCA CCCCCTCTGT GTGTGCCCCT CCCCTGCTGT GGGAAATGTG 1560
AGCTGTGGGT CTGTCTTTGT GAACGATGCC GCTTTCACCC AATCTGTGTC CTGTGTCTTG 1620
TGTACTCCAG TGAGTGCACC CACGGGGGAA ATCCTCACCA TGGAATTCCT TTTTTAATTT 1680
GAGATACTGC TCAGTTGACC TCTGAAGGGA CCGTAGCAGT TTTATTTGCC CCCGTAGGGT 1740
GTGCGAACTA 1750
|
| |
|
|
|
