| Tag | Content |
|---|
EnhancerAtlas ID | HS148-10777 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr2:233367700-233370300 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CREB1 | MA0018.3 | chr2:233367868-233367880 | CGTGACGTCACC | + | 6.32 | | CREB1 | MA0018.3 | chr2:233367868-233367880 | CGTGACGTCACC | - | 6.32 | | RFX5 | MA0510.2 | chr2:233369420-233369436 | GGTTACTATGGGAACT | + | 6.03 | | RFX5 | MA0510.2 | chr2:233369420-233369436 | GGTTACTATGGGAACT | - | 6.17 |
|
| | 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 |
| GH02I232500 | chr2 | 233365404 | 233368709 |
|
Enhancer Sequence | AGGTTTATCC GTAGGAGTCA GCCCAGTTGG GTCAAACTAA GGACCCAGTG CAGACCCCGA 60
GGCCCAGAGA CACAGGTGTG CGCACAAACA CGCACTCTGC GGAAGGCCGG GGCGGGCCTG 120
GCCGCTGCGG GACTCCTGGC CCGGCGCCCT TGACGTCAGC GGCTGGGCCG TGACGTCACC 180
TCACCGCCCC CGCCGCGCTC CCGCCCCCGC CCGCGGGCAC TCAGTCTCCG CTAATGGCAG 240
GCGACGGGGA ATGGCACATC TGTCTTGCCG GGAATTAGTT CATTGAATCA GGCGGCCCGA 300
GCTGCGGCAG CGACCTTAGC CCTGGCCCCA GGGAGGGGTC TGGGCGGGCG GCGTGGGGGA 360
GGTTCAGGCT GGAGGGCTGA GTGCGGGGAC GGGAGGAGGG GACTCACCTG GACTCGCGAG 420
GGGGACTGAG CGCTCTCCAA ATATAGGTCA ATGTCCCGCT CAGCCTCCCT CCCCCAGCAC 480
CGTGAGGACC GAGGCCTGGG GCCTGGCGCC CGCCTGGTGG ACCTCGGGGG CAGGCTGGGG 540
ACCGGGCCCC TGCGGGACGC GGCGCGGCAG GACGCTCCCC GCGCCTTTCT TTCTGCACCT 600
GCCCCTCGGG GTGGGTCCCC CTCTTTACCC TCGCTTCCCC CCGCGGGTGC CGATAAAGGC 660
GGCTAATTCC CGAGCCCGGG GAGGGAGGGG GCGACTGTTC CAGTCAACAC TTCCCCGCGC 720
TCTTCCCCGA CCCTCCCAGA GCGTTCCCGC TGCTCAGGGC GAGGAGCAGC TGCGGCCAGT 780
TTGTCCTAGC GGTTTAGGAG GCAGGGAGGT TTCCTCCAGC CTGGAGCTCT GGCTCGGGCC 840
CTCGGGCCCC AACACCTTCC CGCTGAGACC GCGGGCGTTG TCCCTGGGTC TCTCTGCCTC 900
CATTTCCCCC ACCTCCATTC TGGTTACCCC TTCCCCCCAC TCTTTCCTTC CTAACCCATG 960
AGAGCACTGG AAAGATGCTA GAAAGTCGGG CTTCTAGAGC CCCAGCCCTG CCTCTTGTTC 1020
CTGCGAGACT GTGGGCAGGT AATTTAGCCT CTCAGCCCCT TTCATCTGAC GCTGGGAAGT 1080
AATGAGGAGA CCCCACTTCT CTGGGAAGTT CAATGATATG CGTAAAGGGC TTAGAATTAG 1140
CAGATTCTGG TAGCCAGTGC GTTACGGTTT TGCACTGGGG AGGCAGAGCT GCCGCGGGAG 1200
TGTGGCTTCT CTAGAAAGAT CCCTGGGCAC TTCAGTGATG AAAGTACCAC AGTGAGGATT 1260
GTGGTGATGC AAAGGGCGGA AGAGTCTGGT GGGGCTGCCA AGTGGGCCAG GCTGGGGTCC 1320
CTCGAGATGG AGTCCCTTGA GATAGGGAGG CTCACCCACA CCAGGGATCC CACCCCAAAC 1380
TCAGGCTTCG CCTCCCTCTG CTTCTACCAG GTTGTGACAC TGACCCACTG GGCTTTTCAC 1440
ATTACTTCCA CACCTTTGCT TGGCCCTTCC CGCTTTCACC CATTGGCAAC TTAATTTTGA 1500
ATGCTTAATC CATGAACAGT ATCATCCCCA TTTCACAGAC AGGAGAAGGT TCAAAGAGGC 1560
AGAGGTTCAG AGAGGTTAAG TGACTTGCCA AAGACCTCAC AGCTATGACA TGGCATAGCT 1620
GGGATTTGAA CCCAGTGCTC TGGCCTCAAA TGTCAACTAC TCTCTAATAC TCTGCCTCAC 1680
CTCTGAGAAC CACTTAGTTG CTAGGAGACA GCAAGCTGGC GGTTACTATG GGAACTGGGC 1740
TGATGTGGAA AGTGGAGAGT TGGTGTCCAG GCAGCAATGA GAAGGCTCCA GGTAGGTTCC 1800
ACATCCCTCC CCTGTCCCTT CCATGAAGGC AGCCCTTGGC ATTCAGCTCT GGGTTCCAGA 1860
TGGCACATGT CCTGATGGGA CCTGAGGGAG GTGCAGTGAT GGTGAGTTAC GCTGGACACT 1920
GCCCTGGCAA GCCAAGAGCC CTGGTGGAGG ATGTGGTCCC AAAGATGGGT CTGAGGGGCG 1980
AGACAGGCCA GAGAACCTCA CGATCCTGCT TTCCGGACAT TTGCTGCAGT CACACCTGCC 2040
CTGCAGACAG TAGTGCAGAG CAGAGCCTTT CCTTGTGAAG TAAGGAAAAG GGAAGGCAGA 2100
ACCATGATGG GGCACAGACC CATGCCAGAG AGTTCTGGAC CCAGGAGAAC ACCTCAGTTC 2160
TCTCAACTGT AAAATGAGGA TGATACCAGC CCCTCTCTCA TAGTGTGCTG AGAAAATTGA 2220
CAAAGATACA AAGCACTATG TCTGACACAT AGACTTCACT GACTGTGTGA CCTTGGACAA 2280
GTCACTTAGC CTCTCTGAGC CTCTGTAAAA TGGGGATATT AATAGGACCT GCTTTATAGG 2340
GTTGCTGTAG GGATTCAACA TGTGCGTACA GGTAAAGGTC CTCCCAGGCT TTAAGGACTA 2400
TCTACAGTGT TTGCTGTTCT GTTTTTGTTT TGTTTTGTTT TGTTTTTTGA GACAGAGTCT 2460
TGCTCCGTCG CCCAGGCTGG AGTGCAGTGG CACAATCTCG GCTTACTGCA ACCTCCACCT 2520
TCCAGGTTCA AGTGATTCTC ATGCCTCAGC CACCTGAGTA GCTGAAATTA CAGGAGCGTG 2580
CCATCATACC CAGCTAATTT 2600
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