| Tag | Content |
|---|
EnhancerAtlas ID | HS087-00912 |
Organism | Homo sapiens |
Tissue/cell | HEK293T |
Coordinate | chr1:47852490-47854970 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MYB | MA0100.3 | chr1:47852523-47852533 | GACAGTTGGT | - | 6.02 | | RUNX1 | MA0002.2 | chr1:47853284-47853295 | TTCTGTGGTTT | + | 6.32 | | TFAP2A | MA0003.3 | chr1:47854457-47854468 | AGCCTCAGGCA | + | 6.32 | | ZNF263 | MA0528.1 | chr1:47853835-47853856 | CCGTTTTCCTCCTCCTCCTCT | - | 6.22 | | ZNF263 | MA0528.1 | chr1:47853838-47853859 | TTTTCCTCCTCCTCCTCTTCA | - | 6.59 |
|
| | 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 |
| GH01I047388 | chr1 | 47854581 | 47854730 |
|
Enhancer Sequence | TAGCACAGAG TAGGTACTTA GTGTTGATGA ATTGACAGTT GGTGACAAAC CATAGTGAAA 60
GCTCACAAAT TAAACAGCTG CTTAGTCTGC TGCCATTCCT GAGCTCACAG AGTGAGAGGG 120
AAGTACTGCA TGCAACAGTA TCACAAATGC TCTCCCACTA AGGGAGTTGT CACATGGATG 180
GCAGCTTGGC ATAGTGGGCT TTCTATAATC TTACTTAGCA GCTGCCACTG TCTTAAAAGG 240
TGAGGAGAGG CTGGGCACGG TGGCTCATAT CTGTAATCCC AGCACTTTGG GAGGCCGAGG 300
CAGGTGGATC ACTTGAGGTC AGGTGTTCCA GACCAACCTG GCCAACATGG TGAAACCCCG 360
TCTCTACTAA AAATACAAAA CATTAACCAG GCATGGTGAC TAGTGCTTGT AGTCCCAGCT 420
ACTTAGGAGG CTGAGGCAGG AGAATTGCTT GAACCCAGGA GGTGGAAGCT GCAGTGAGCC 480
AAGATTACAC CACTGTACTC CAGCCTGGTG ACAGAGTGAG ACTCCATATC AAAACCAAAA 540
ACAAAATGGT GAGGAGAGGC CAGGGGACTA CCACCACTGT CTACAATCCT CTGAAGGGAG 600
ATGGAGTACA TGTATTCAAT GTGGGCTTGA GGGCAGAACT AGGGCAGTGG AAACAACATA 660
AGGAAGACCG TCTAAGGTCA GAGCCACCCA ACACTGAATT GGAGCGCCTG AGGACATGAT 720
CACCGTCCCT GGAAGTGTGC ACGCAGGCCC TGGATGCTTA TTTGGCAGAA TGCTTTAGTC 780
TTTCACTCTG GAGATTCTGT GGTTTGGGGA TCATCTTCTT CAAGTAGGTA TCTAAGTCTG 840
AAGTCCACCT GGAATTCCAG ACATACTCTC TGACACATAA GAGTTCCCTG TATATACAAG 900
TGGGGAGGAA AGGCTAAGGG GCATCATGAG GATCTGTGCC TTACCATAAG AACCCAAATG 960
CTGAGAAGTT TCCCTAAGCC TCTGTTTCTG CCTCCCACCC CCTCCCTGGG TGTCCTCCCC 1020
AGTGCCTGGG ATAAGTGCTT AACAAAGTTT ACTGGCATTA ATGCTGTTGG TGGGCAGGAG 1080
GTGCCCAGTT TGCATTGGAA AAGAGAGAAA CAGCAGTAGC AAAAAGATAG CAGTGAGGGA 1140
CAGGAGAGAC CCACTTAGCT GGAGGGGGTG AGGGTCCATG CACCAAATAA TGGGAGATAG 1200
GAGTATGCAA AGATAAAGCG ATAAACCTTT CATAACAGGT AAAGGAAGGT GAATTTTATC 1260
CAGTGTCTGT TTAGCTGAGT CCAGACTAGG AAGCTGGGCT GCATGAGTCA GTTTGACAAG 1320
GGCTTTTTAG ATTTAGGAGG CTGCTCCGTT TTCCTCCTCC TCCTCTTCAC TGTAAGCTGT 1380
CCCTTGAGCT GTATTCTGAA ACCCTGAATG GTTTTTCCAT CTCACTAGGG ACAGTTGGCA 1440
AACCCTCTCT GGCTTGGCCA GGGTTGGGGC TGGGCACTAG ACGAGCCGGG AGAGGAGGTG 1500
GCTCCCAGCA ATAAGCAACC CACAGAATTG TGTCTGTCAT TTAAGAAAAG TTTCTGGGTT 1560
TTCGGCTAAT TGCAAAAATA CATAATGGAT GCTTTTCGCA TCTGCTAGTT ATTCTGGAAC 1620
AGGCCTGCAT CCAAGAGCAA ACTTTAAACA AACAATAAGA TTATGGAGCT TAACTATTTC 1680
AATGTGTAAC AGAAAGCCAA GCCCCATACA CTTAAATTAC CACACATGCA CTCAGACACA 1740
AGCACACAAG AGATCACATC TGCACAAACA TACACACATA CAGATGCATG TTTTGGCATT 1800
AGTGCATGCA AATGCATACT TACATGCTAG CACCTAGTAC ATACATGCAT GCACAACTTG 1860
CACATGTGCG CAGTCACCAG CACCAATACA CATTCTCAGA CACACAAATG AACGTGCATA 1920
CACTCATACA CAAGTATACA CCAACGCATT TGGGCAACAA GACACACAGC CTCAGGCACA 1980
GATGCATTTA CACAAATCAT TCTTACTGCA ATGAGAGATA GTCCGGGGTA GGTGTGGGTG 2040
TCCTCCCAGT GCAGAGTTAA GTGAAGCAGT CCATCAGCTG GGCACTGGCT GTCCGGGTGT 2100
TACCAGGTGT AGTTATCAGT ATGGCCACCA AGAGGCGCCC AGGATCCATC CTGCATCCAC 2160
CTTTCATGGC TTCTGCCAGC TGGTCAATTG TTTCTGTACC CACAAGCCTG CATCTCCCTG 2220
TTCTGGATCC CTGCACAGAA CTAGGAGACT CCTTGATCCC AGCCCCAACC TTCCAGGATC 2280
CACTGTGCTC ATTCTCATCC TTTCCCTGTC CCACACCACC AAAACAACCA CAAGTCCCAT 2340
CCCTCCTCCC TCCTAGCAGA ACGCATGCTT CAGCACTCCC TGCTTGTCCT GTGGCTGCTC 2400
CATGGAGAAC TGGATCTGTC AGGTCTTGAT CATGATGTGA CTTCTACCTG GAACTTTTTC 2460
CACAGGAGAA GCTGTCAAAA 2480
|
