| Tag | Content |
|---|
EnhancerAtlas ID | HS170-04042 |
Organism | Homo sapiens |
Tissue/cell | RS4-11 |
Coordinate | chr9:128207960-128210170 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| POU6F1 | MA0628.1 | chr9:128208362-128208372 | ATTAATTAAT | + | 6.02 | | POU6F1 | MA0628.1 | chr9:128208362-128208372 | ATTAATTAAT | - | 6.02 | | ZNF263 | MA0528.1 | chr9:128210140-128210161 | GGAGAAGGGTGAAAAAGAGGA | + | 6.53 | | Znf423 | MA0116.1 | chr9:128209760-128209775 | GGAACCCTGGGGGGC | + | 6.36 | | Znf423 | MA0116.1 | chr9:128209760-128209775 | GGAACCCTGGGGGGC | - | 6.66 |
|
| | 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 |
| GH09I125446 | chr9 | 128208699 | 128209695 |
|
Enhancer Sequence | ACAAGGACTG AGAATAAGAT GAGGGGCTTT GGGACTCCCA GGCTCAGGCC CATGGGGGCT 60
GCCCCGGCCT ATCGGCACTG TTATCCTTGG GTTCTAGGAG ACTCCTGTGG CCTTCCAAGA 120
AATTCTTCTT TCGCCTTAAG CTACTGAAGT TGGTTTCCAT TACTGGCAAG CAAAGGAACA 180
GTGCCCAAGA GAGACACGTA GTCAGTATTC AGTAAACCTT CCTAGACCAA GGAGCAGCAG 240
GTGACATCTC TAATATACAG GTCTCCTGCA AAACGCCCAG AAATGACCTT CCCTAGTCTT 300
TCGACAGACC TTAGTGTCTG TAAGATTAAA ATTCAGCATA TCCTTTCTAT TAGTCCTTCT 360
CATCCGTTGT CCTTTTAATT GAAGCAGCGG CTGGTCATAG TTATTAATTA ATAATATATC 420
ACCCATATTA CTGTAAGTTC ACCTCTTTCC TGGAGAAATC TTCTTGGGGA CTTTACAGTA 480
GCTAATTTTT CAGATCTCCA AAAATAAACT GATATATGTT GTACATTTGT GGCCAGAAAA 540
GTTGAGCCAC TGGTATTTTA TCCTGGAAAC ATCATTATGA TGTACTAATT GTGACTATAA 600
ATCCTAAATT GAAAAAATTA CCTAATAATT TCTGAAAAAC CTCACTTTCA GACACTTGAC 660
AAATTTAGCC TGATTCTAAA TCATGGTACT AAAATGTGAG AATTCCTGAC TGGAAGCTAG 720
TCACTCTGTT AACATATAAA TTCTGTGTTT CTAATAAGGA GGTGGACCTT ACACAGAGGC 780
ATCTGTGTGT GCGTCTGTAT CTATTCACAT TCACAGGATC TACCCCACAA CATCAGAATC 840
TTGTCGGTGA CATCCCTGTG TGGAGGAACA ATGCGGGCAC CTTTGTTGGC CATGCTGTGA 900
ACAAGCACAG CCATCTACAA AGGACACAGG GCTGTGAAGG ACAAAGAGAC ACCCCCTCCA 960
GGAGGCATTC CTGCTGACAA CTGGTCACGA CACACAAAGA CACCAGGGCC TGGGGCTAGA 1020
AAGAACCAGA AGGTCTTAGG GAGACCCACA GACCCGAAGC TTCGGGGTTC ACTGACCACT 1080
TTGATAAGAC AGCTTATGGA CTGTCCACAC CACCTGCTCC CGCTTGTCAC TGACAAAACC 1140
AAACCAAACC TCAAAGCACT AAAGCATGTT TTGCCTGAAC AATTGAGACA CTGTTAAAAA 1200
GGTTTCCTGC ACTTTAAGCA GAGCCCAATC TATACACAGC ACATGTAATA AGTAGTCTGC 1260
AAGGCCTAAG AGCCCCAGAA AGGAAGCGTT GACACTGTCC CCTTGGGACT ATGGTGCTTG 1320
TGAAGCATGT CAATTGTGGG CTGACAGAGG GGAGGCCTGT GGTTCATCTG CACAGTCACG 1380
TGAAAAAAAC AAAAAAATCA TACCAAGCCA AGTCTCCTGA AAGGCTGCAT ATTTGAACCA 1440
AGTAACCTCA AATCCCGTCC TCTGAATTTT GAATGTATTT GGTTGCATGT GGAGGCTGTG 1500
TGTGTCTCCT GCCTATCCCC AGGGCTCATT CCAGCACCCA TCTGAGGAAG AGTGAAGCAG 1560
GTGAGGAGGA GGAAGAGTCC CAACATTCCC CCACTCTCCC TCAAGCCTCC GGTCTGTTTG 1620
TCCTTTCCAG TGAAAGCACT CACGCCATAG GAGAGGGGAA CAGAGGGCAG AGAACGTTCT 1680
GTGGAGCACT TGTGTTTGGA CTTGAACAAT GACACAGCTG CAAAGTTAAT CACTGGGCCG 1740
AGGCACGGTG GACAGCCACA GCAGACAGCC CCCTCTTGCT CTCTGCAAGG AGTGATGAGC 1800
GGAACCCTGG GGGGCAAGGG CAGGTTAAGA TCAGCAGCCA TGCTGGGCCA TAGGACATGG 1860
GGCGGACTCA CTCCGCGGGC GTTTCTGCCC CGAGTTCCCC TCGCTAGCAG CCCTGTTTCG 1920
CTGGGCGGCC AGAAGGGCAG TTTTCCTCAG TCTGGGCTCT GCCAGGAGCA TGGGCTAGAG 1980
CAAAGGACAG AGAAATGAAC ACCGAGAGTC AAATATGATG AGCGTGAAGA AGGTAAACGC 2040
AGGGAGCTGC CGTGGAGACA CCAAGGCAGA AGCACCTGGC CAGAGGTGGA GAAGAGCCAC 2100
TAGGGACAGT TTCTTGGGAG GAGCTGACAC CTCCGCAGTT TTGGAGGAGG GCAGGGAGTC 2160
AGCTGGGTAA AGGTGAGGGT GGAGAAGGGT GAAAAAGAGG AAGATGCCAC 2210
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